Name

GLC2A Gene

glaucoma 2, angle closure

GLC1P Gene

glaucoma 1, open angle, P

GLC1N Gene

glaucoma 1, open angle, N (juvenile-onset)

GLC1L Gene

glaucoma 1, open angle, L (adult-onset)

GLC1M Gene

glaucoma 1, open angle, M (juvenile-onset)

GLC1J Gene

glaucoma 1, open angle, J (juvenile-onset)

GLC1K Gene

glaucoma 1, open angle, K (juvenile-onset)

GLC1H Gene

glaucoma 1, open angle, H (adult-onset)

GLC1I Gene

glaucoma 1, open angle, I

GLC1D Gene

glaucoma 1, open angle, D (adult-onset)

GLC1B Gene

glaucoma 1, open angle, B (adult-onset)

GLC1C Gene

glaucoma 1, open angle, C

GPDS1 Gene

glaucoma-related pigment dispersion syndrome 1

GLC3B Gene

glaucoma 3, primary infantile, B

GLC3C Gene

glaucoma 3, primary congenital, C

IHG1 Gene

iris hypoplasia with glaucoma 1

C19ORF12 Gene

chromosome 19 open reading frame 12

This gene encodes a small transmembrane protein. Mutations in this gene are a cause of neurodegeneration with brain iron accumulation-4 (NBIA4), but the specific function of the encoded protein is unknown. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]

C10ORF88 Gene

chromosome 10 open reading frame 88

LOC100288542 Gene

chromosome 14 open reading frame 119 pseudogene

C22ORF39 Gene

chromosome 22 open reading frame 39

C22ORF31 Gene

chromosome 22 open reading frame 31

C22ORF34 Gene

chromosome 22 open reading frame 34

C1ORF189 Gene

chromosome 1 open reading frame 189

C1ORF185 Gene

chromosome 1 open reading frame 185

C1ORF186 Gene

chromosome 1 open reading frame 186

CXORF58 Gene

chromosome X open reading frame 58

CXORF56 Gene

chromosome X open reading frame 56

While this gene is well-supported by transcript data, no functional information on its protein products is currently available. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2009]

CXORF57 Gene

chromosome X open reading frame 57

C12ORF4 Gene

chromosome 12 open reading frame 4

C14ORF119 Gene

chromosome 14 open reading frame 119

C18ORF15 Gene

chromosome 18 open reading frame 15

C10ORF105 Gene

chromosome 10 open reading frame 105

C10ORF107 Gene

chromosome 10 open reading frame 107

C1ORF234 Gene

chromosome 1 open reading frame 234

C2ORF81 Gene

chromosome 2 open reading frame 81

LOC100420788 Gene

chromosome 2 open reading frame 27A pseudogene

C14ORF79 Gene

chromosome 14 open reading frame 79

C20ORF96 Gene

chromosome 20 open reading frame 96

C17ORF47 Gene

chromosome 17 open reading frame 47

C17ORF49 Gene

chromosome 17 open reading frame 49

C11ORF49 Gene

chromosome 11 open reading frame 49

C11ORF40 Gene

chromosome 11 open reading frame 40

C11ORF42 Gene

chromosome 11 open reading frame 42

C11ORF45 Gene

chromosome 11 open reading frame 45

C19ORF18 Gene

chromosome 19 open reading frame 18

C7ORF43 Gene

chromosome 7 open reading frame 43

LOC100420668 Gene

chromosome 2 open reading frame 16 pseudogene

C9ORF118 Gene

chromosome 9 open reading frame 118

C9ORF117 Gene

chromosome 9 open reading frame 117

C9ORF116 Gene

chromosome 9 open reading frame 116

C9ORF114 Gene

chromosome 9 open reading frame 114

LOC724065 Gene

chromosome 19 open reading frame 53 pseudogene

C20ORF197 Gene

chromosome 20 open reading frame 197

C1ORF100 Gene

chromosome 1 open reading frame 100

C1ORF101 Gene

chromosome 1 open reading frame 101

C1ORF105 Gene

chromosome 1 open reading frame 105

C1ORF106 Gene

chromosome 1 open reading frame 106

C1ORF109 Gene

chromosome 1 open reading frame 109

LOC100526839 Gene

chromosome 18 open reading frame 32 pseudogene

LOC100526838 Gene

chromosome 18 open reading frame 32 pseudogene

C4ORF36 Gene

chromosome 4 open reading frame 36

C4ORF32 Gene

chromosome 4 open reading frame 32

C8ORF33 Gene

chromosome 8 open reading frame 33

C8ORF31 Gene

chromosome 8 open reading frame 31

C8ORF37 Gene

chromosome 8 open reading frame 37

This gene encodes a ubiquitously expressed protein of unknown function. It has high levels of mRNA expression in the brain, heart, and retina and the protein co-localizes with polyglutamylated tubulin at the base of the primary cilium in human retinal pigment epithelial cells. Mutations in this gene have been associated with autosomal recessive cone-rod dystrophy (arCRD) and retinitis pigmentosa (arRP). [provided by RefSeq, Mar 2012]

C8ORF34 Gene

chromosome 8 open reading frame 34

C3ORF67 Gene

chromosome 3 open reading frame 67

C3ORF62 Gene

chromosome 3 open reading frame 62

C16ORF46 Gene

chromosome 16 open reading frame 46

LOC646058 Gene

chromosome 4 open reading frame 27 pseudogene

CXORF49B Gene

chromosome X open reading frame 49B

C10ORF82 Gene

chromosome 10 open reading frame 82

LOC100859919 Gene

chromosome 9 open reading frame 86 pseudogene 2

LOC100129478 Gene

chromosome 4 open reading frame 46 pseudogene

C1ORF27 Gene

chromosome 1 open reading frame 27

C9ORF92 Gene

chromosome 9 open reading frame 92

C18ORF32 Gene

chromosome 18 open reading frame 32

C7ORF34 Gene

chromosome 7 open reading frame 34

C7ORF33 Gene

chromosome 7 open reading frame 33

C7ORF31 Gene

chromosome 7 open reading frame 31

C6ORF99 Gene

chromosome 6 open reading frame 99

C19ORF66 Gene

chromosome 19 open reading frame 66

C19ORF60 Gene

chromosome 19 open reading frame 60

C19ORF68 Gene

chromosome 19 open reading frame 68

C6ORF132 Gene

chromosome 6 open reading frame 132

C6ORF136 Gene

chromosome 6 open reading frame 136

C12ORF56 Gene

chromosome 12 open reading frame 56

C12ORF50 Gene

chromosome 12 open reading frame 50

C21ORF33 Gene

chromosome 21 open reading frame 33

This gene encodes a potential mitochondrial protein that is a member of the DJ-1/PfpI gene family. This protein is overexpressed in fetal Down syndrome brain. Alternate splicing results in multiple transcript variants. [provided by RefSeq, May 2010]

LOC101241902 Gene

chromosome 4 open reading frame 46 pseudogene

C2ORF49 Gene

chromosome 2 open reading frame 49

C2ORF48 Gene

chromosome 2 open reading frame 48

C2ORF44 Gene

chromosome 2 open reading frame 44

C2ORF47 Gene

chromosome 2 open reading frame 47

C2ORF40 Gene

chromosome 2 open reading frame 40

C2ORF42 Gene

chromosome 2 open reading frame 42

C20ORF141 Gene

chromosome 20 open reading frame 141

C20ORF144 Gene

chromosome 20 open reading frame 144

LOC100505642 Gene

chromosome 9 open reading frame 85 pseudogene

C8ORF89 Gene

chromosome 8 open reading frame 89

C8ORF88 Gene

chromosome 8 open reading frame 88

C8ORF82 Gene

chromosome 8 open reading frame 82

C8ORF87 Gene

chromosome 8 open reading frame 87

C8ORF86 Gene

chromosome 8 open reading frame 86

C14ORF169 Gene

chromosome 14 open reading frame 169

C14ORF166 Gene

chromosome 14 open reading frame 166

C6ORF10 Gene

chromosome 6 open reading frame 10

C6ORF15 Gene

chromosome 6 open reading frame 15

C17ORF99 Gene

chromosome 17 open reading frame 99

C17ORF98 Gene

chromosome 17 open reading frame 98

C17ORF97 Gene

chromosome 17 open reading frame 97

C17ORF96 Gene

chromosome 17 open reading frame 96

C15ORF61 Gene

chromosome 15 open reading frame 61

C15ORF65 Gene

chromosome 15 open reading frame 65

C19ORF44 Gene

chromosome 19 open reading frame 44

C22ORF42 Gene

chromosome 22 open reading frame 42

C22ORF46 Gene

chromosome 22 open reading frame 46

C1ORF95 Gene

chromosome 1 open reading frame 95

C1ORF94 Gene

chromosome 1 open reading frame 94

CXORF21 Gene

chromosome X open reading frame 21

CXORF23 Gene

chromosome X open reading frame 23

LOC727964 Gene

chromosome 2 open reading frame 69 pseudogene

LOC100420864 Gene

chromosome 11 open reading frame 58 pseudogene

C16ORF74 Gene

chromosome 16 open reading frame 74

C16ORF70 Gene

chromosome 16 open reading frame 70

C16ORF71 Gene

chromosome 16 open reading frame 71

C16ORF72 Gene

chromosome 16 open reading frame 72

C16ORF78 Gene

chromosome 16 open reading frame 78

C14ORF28 Gene

chromosome 14 open reading frame 28

C20ORF62 Gene

chromosome 20 open reading frame 62

LOC389895 Gene

chromosome 16 open reading frame 72-like

C11ORF16 Gene

chromosome 11 open reading frame 16

C9ORF172 Gene

chromosome 9 open reading frame 172

C10ORF71 Gene

chromosome 10 open reading frame 71

C10ORF76 Gene

chromosome 10 open reading frame 76

C9ORF163 Gene

chromosome 9 open reading frame 163

C2ORF91 Gene

chromosome 2 open reading frame 91

C5ORF28 Gene

chromosome 5 open reading frame 28

C5ORF22 Gene

chromosome 5 open reading frame 22

C5ORF24 Gene

chromosome 5 open reading frame 24

C1ORF159 Gene

chromosome 1 open reading frame 159

C1ORF158 Gene

chromosome 1 open reading frame 158

C10ORF2 Gene

chromosome 10 open reading frame 2

This gene encodes a hexameric DNA helicase which unwinds short stretches of double-stranded DNA in the 5' to 3' direction and, along with mitochondrial single-stranded DNA binding protein and mtDNA polymerase gamma, is thought to play a key role in mtDNA replication. The protein localizes to the mitochondrial matrix and mitochondrial nucleoids. Mutations in this gene cause infantile onset spinocerebellar ataxia (IOSCA) and progressive external ophthalmoplegia (PEO) and are also associated with several mitochondrial depletion syndromes. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Aug 2009]

C2ORF66 Gene

chromosome 2 open reading frame 66

C3ORF18 Gene

chromosome 3 open reading frame 18

C3ORF14 Gene

chromosome 3 open reading frame 14

C3ORF17 Gene

chromosome 3 open reading frame 17

LOC647996 Gene

chromosome 9 open reading frame 172 pseudogene

C1ORF233 Gene

chromosome 1 open reading frame 233

C9ORF62 Gene

chromosome 9 open reading frame 62

C9ORF66 Gene

chromosome 9 open reading frame 66

C9ORF64 Gene

chromosome 9 open reading frame 64

C9ORF69 Gene

chromosome 9 open reading frame 69

C12ORF60 Gene

chromosome 12 open reading frame 60

C12ORF66 Gene

chromosome 12 open reading frame 66

LOC100130170 Gene

chromosome 12 open reading frame 49 pseudogene

C11ORF98 Gene

chromosome 11 open reading frame 98

C11ORF97 Gene

chromosome 11 open reading frame 97

C11ORF96 Gene

chromosome 11 open reading frame 96

C11ORF95 Gene

chromosome 11 open reading frame 95

C11ORF94 Gene

chromosome 11 open reading frame 94

C11ORF91 Gene

chromosome 11 open reading frame 91

LOC100420831 Gene

chromosome 1 open reading frame 106 pseudogene

C6ORF163 Gene

chromosome 6 open reading frame 163

C6ORF165 Gene

chromosome 6 open reading frame 165

C2ORF16 Gene

chromosome 2 open reading frame 16

C2ORF15 Gene

chromosome 2 open reading frame 15

C18ORF65 Gene

chromosome 18 open reading frame 65

C18ORF63 Gene

chromosome 18 open reading frame 63

C20ORF173 Gene

chromosome 20 open reading frame 173

LOC100420911 Gene

chromosome 14 open reading frame 166 pseudogene

C7ORF69 Gene

chromosome 7 open reading frame 69

C7ORF60 Gene

chromosome 7 open reading frame 60

C7ORF61 Gene

chromosome 7 open reading frame 61

C7ORF62 Gene

chromosome 7 open reading frame 62

C7ORF65 Gene

chromosome 7 open reading frame 65

C7ORF66 Gene

chromosome 7 open reading frame 66

LOC100287427 Gene

chromosome 18 open reading frame 21 pseudogene

LOC100287425 Gene

chromosome 7 open reading frame 73 pseudogene

C6ORF25 Gene

chromosome 6 open reading frame 25

This gene is a member of the immunoglobulin (Ig) superfamily and is located in the major histocompatibility complex (MHC) class III region. The protein encoded by this gene is a glycosylated, plasma membrane-bound cell surface receptor, but soluble isoforms encoded by some transcript variants have been found in the endoplasmic reticulum and Golgi before being secreted. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

LOC100420892 Gene

chromosome 14 open reading frame 166 pseudogene

C14ORF93 Gene

chromosome 14 open reading frame 93

C15ORF32 Gene

chromosome 15 open reading frame 32

C19ORF35 Gene

chromosome 19 open reading frame 35

C11ORF44 Gene

chromosome 11 open reading frame 44

C21ORF62 Gene

chromosome 21 open reading frame 62

C21ORF2 Gene

chromosome 21 open reading frame 2

Four alternatively spliced transcript variants encoding four different isoforms have been found for this nuclear gene. All isoforms contain leucine-rich repeats. Three of these isoforms are mitochondrial proteins and one of them lacks the target peptide, so is not located in mitochondrion. This gene is down-regulated in Down syndrome (DS) brain, which may represent mitochondrial dysfunction in DS patients. [provided by RefSeq, Sep 2012]

LOC100129667 Gene

chromosome 5 open reading frame 13 pseudogene

C22ORF15 Gene

chromosome 22 open reading frame 15

C8ORF58 Gene

chromosome 8 open reading frame 58

C8ORF59 Gene

chromosome 8 open reading frame 59

C17ORF107 Gene

chromosome 17 open reading frame 107

C10ORF126 Gene

chromosome 10 open reading frame 126

C10ORF120 Gene

chromosome 10 open reading frame 120

C10ORF128 Gene

chromosome 10 open reading frame 128

C2ORF27A Gene

chromosome 2 open reading frame 27A

C2ORF27B Gene

chromosome 2 open reading frame 27B

C21ORF58 Gene

chromosome 21 open reading frame 58

LOC100132977 Gene

chromosome 2 open reading frame 27B pseudogene

C16ORF47 Gene

chromosome 16 open reading frame 47

C3ORF70 Gene

chromosome 3 open reading frame 70

C11ORF68 Gene

chromosome 11 open reading frame 68

C11ORF65 Gene

chromosome 11 open reading frame 65

C11ORF63 Gene

chromosome 11 open reading frame 63

C10ORF25 Gene

chromosome 10 open reading frame 25

C10ORF99 Gene

chromosome 10 open reading frame 99

LOC100127912 Gene

chromosome 2 open reading frame 27B pseudogene

C9ORF131 Gene

chromosome 9 open reading frame 131

C9ORF135 Gene

chromosome 9 open reading frame 135

C9ORF139 Gene

chromosome 9 open reading frame 139

C5ORF17 Gene

chromosome 5 open reading frame 17

C5ORF15 Gene

chromosome 5 open reading frame 15

C1ORF127 Gene

chromosome 1 open reading frame 127

C1ORF122 Gene

chromosome 1 open reading frame 122

C1ORF123 Gene

chromosome 1 open reading frame 123

C4ORF51 Gene

chromosome 4 open reading frame 51

C3ORF49 Gene

chromosome 3 open reading frame 49

C17ORF112 Gene

chromosome 17 open reading frame 112

C12ORF65 Gene

chromosome 12 open reading frame 65

This nuclear gene encodes a mitochondrial matrix protein that appears to contribute to peptide chain termination in the mitochondrial translation machinery. Two different 1 bp deletions (resulting in the same premature stop codon)result in decreased mitochondrial translation, decreased levels of oxidative phosphorylation complexes and encepthalomyopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]

C9ORF50 Gene

chromosome 9 open reading frame 50

C9ORF57 Gene

chromosome 9 open reading frame 57

LOC100420839 Gene

chromosome 18 open reading frame 21 pseudogene

C20ORF196 Gene

chromosome 20 open reading frame 196

C20ORF195 Gene

chromosome 20 open reading frame 195

C19ORF84 Gene

chromosome 19 open reading frame 84

C19ORF80 Gene

chromosome 19 open reading frame 80

C19ORF81 Gene

chromosome 19 open reading frame 81

C14ORF37 Gene

chromosome 14 open reading frame 37

LOC100420683 Gene

chromosome X open reading frame 67 pseudogene

LOC100217367 Gene

chromosome 11 open reading frame 73 pseudogene

C1ORF43 Gene

chromosome 1 open reading frame 43

C20ORF57 Gene

chromosome 20 open reading frame 57

C18ORF54 Gene

chromosome 18 open reading frame 54

LOC100132570 Gene

chromosome 17 open reading frame 58 pseudogene

C7ORF13 Gene

chromosome 7 open reading frame 13

C4ORF33 Gene

chromosome 4 open reading frame 33

C12ORF10 Gene

chromosome 12 open reading frame 10

C15ORF41 Gene

chromosome 15 open reading frame 41

This gene encodes a protein with two predicted helix-turn-helix domains. Mutations in this gene were found in families with congenital dyserythropoietic anemia type Ib. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]

LOC100420738 Gene

chromosome 9 open reading frame 78 pseudogene

LOC100131279 Gene

chromosome 2 open reading frame 69 pseudogene

C17ORF104 Gene

chromosome 17 open reading frame 104

C17ORF105 Gene

chromosome 17 open reading frame 105

C17ORF102 Gene

chromosome 17 open reading frame 102

C17ORF100 Gene

chromosome 17 open reading frame 100

C21ORF59 Gene

chromosome 21 open reading frame 59

This gene a protein plays a critical role in dynein arm assembly and motile cilia function. Mutations in this gene result in primary ciliary dyskinesia. [provided by RefSeq, Nov 2013]

C10ORF90 Gene

chromosome 10 open reading frame 90

C10ORF91 Gene

chromosome 10 open reading frame 91

C10ORF95 Gene

chromosome 10 open reading frame 95

LOC284269 Gene

chromosome 9 open reading frame 86 pseudogene 1

C22ORF29 Gene

chromosome 22 open reading frame 29

C22ORF23 Gene

chromosome 22 open reading frame 23

C22ORF24 Gene

chromosome 22 open reading frame 24

CXORF49 Gene

chromosome X open reading frame 49

LOC100420966 Gene

chromosome 17 open reading frame 98 pseudogene

LOC100420967 Gene

chromosome 2 open reading frame 27B pseudogene

C6ORF1 Gene

chromosome 6 open reading frame 1

C6ORF7 Gene

chromosome 6 open reading frame 7

C14ORF105 Gene

chromosome 14 open reading frame 105

LOC100502572 Gene

chromosome 5 open reading frame 60 pseudogene

C1ORF204 Gene

chromosome 1 open reading frame 204

C20ORF85 Gene

chromosome 20 open reading frame 85

C6ORF201 Gene

chromosome 6 open reading frame 201

C17ORF70 Gene

chromosome 17 open reading frame 70

FAAP100 is a component of the Fanconi anemia (FA; MIM 277650) core complex and is required for core complex stability and FANCD2 (see MIM 227646) monoubiquitination (Ling et al., 2007 [PubMed 17396147]).[supplied by OMIM, Mar 2008]

C17ORF77 Gene

chromosome 17 open reading frame 77

C17ORF75 Gene

chromosome 17 open reading frame 75

C17ORF74 Gene

chromosome 17 open reading frame 74

C17ORF78 Gene

chromosome 17 open reading frame 78

C10ORF10 Gene

chromosome 10 open reading frame 10

The expression of this gene is induced by fasting as well as by progesterone. The protein encoded by this gene contains a t-synaptosome-associated protein receptor (SNARE) coiled-coil homology domain and a peroxisomal targeting signal. Production of the encoded protein leads to phosphorylation and activation of the transcription factor ELK1. [provided by RefSeq, Jul 2008]

C10ORF11 Gene

chromosome 10 open reading frame 11

This gene encodes a leucine-rich repeat protein. The encoded protein is thought to play a role in melanocyte differentiation. Mutations in this gene have been associated with autosomal recessive oculocutaneous albinism 7 (OCA7). Alternatively spliced transcript variants have been identified. [provided by RefSeq, Mar 2015]

C10ORF12 Gene

chromosome 10 open reading frame 12

C8ORF49 Gene

chromosome 8 open reading frame 49

C9ORF106 Gene

chromosome 9 open reading frame 106

C5ORF49 Gene

chromosome 5 open reading frame 49

C5ORF45 Gene

chromosome 5 open reading frame 45

C5ORF46 Gene

chromosome 5 open reading frame 46

C5ORF47 Gene

chromosome 5 open reading frame 47

C5ORF42 Gene

chromosome 5 open reading frame 42

The protein encoded by this gene has putative coiled-coil domains and may be a transmembrane protein. Defects in this gene are a cause of Joubert syndrome (JBTS). [provided by RefSeq, May 2012]

C8ORF22 Gene

chromosome 8 open reading frame 22

C4ORF29 Gene

chromosome 4 open reading frame 29

C4ORF22 Gene

chromosome 4 open reading frame 22

C4ORF27 Gene

chromosome 4 open reading frame 27

C4ORF26 Gene

chromosome 4 open reading frame 26

Dental enamel forms the outer cap of teeth and is the hardest substance found in vertebrates. This gene is thought to encode an extracellular matrix acidic phosphoprotein that has a function in enamel mineralization during amelogenesis. Mutations in this gene are associated with recessive hypomineralized amelogenesis imperfecta. [provided by RefSeq, Oct 2012]

C14ORF180 Gene

chromosome 14 open reading frame 180

LOC100887076 Gene

chromosome 9 open reading frame 172 pseudogene

C16ORF45 Gene

chromosome 16 open reading frame 45

LOC646408 Gene

chromosome 9 open reading frame 16 pseudogene

C16ORF58 Gene

chromosome 16 open reading frame 58

This gene encodes a putative transmembrane protein containing a conserved DUF647 domain that may be involved in protein-protein interaction. The encoded protein is related to a plant protein that participates in ultraviolet B light-sensing during root morphogenesis. [provided by RefSeq, Feb 2013]

C16ORF59 Gene

chromosome 16 open reading frame 59

C16ORF52 Gene

chromosome 16 open reading frame 52

C16ORF54 Gene

chromosome 16 open reading frame 54

C2ORF82 Gene

chromosome 2 open reading frame 82

C11ORF31 Gene

chromosome 11 open reading frame 31

This gene encodes a selenoprotein, which contains a selenocysteine (Sec) residue at its active site. The selenocysteine is encoded by the UGA codon that normally signals translation termination. The 3' UTR of selenoprotein genes have a common stem-loop structure, the sec insertion sequence (SECIS), that is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. The exact function of this gene is not known, however, selenoproteins are thought to be responsible for most biomedical effects of dietary selenium. [provided by RefSeq, Jul 2008]

C5ORF34 Gene

chromosome 5 open reading frame 34

C1ORF147 Gene

chromosome 1 open reading frame 147

LOC100506911 Gene

chromosome 6 open reading frame 35 pseudogene

LOC642614 Gene

chromosome 2 open reading frame 69 pseudogene

C6ORF183 Gene

chromosome 6 open reading frame 183

C11ORF1 Gene

chromosome 11 open reading frame 1

C1ORF174 Gene

chromosome 1 open reading frame 174

C1ORF177 Gene

chromosome 1 open reading frame 177

C1ORF35 Gene

chromosome 1 open reading frame 35

LOC100289470 Gene

chromosome 5 open reading frame 60 pseudogene

LOC101241901 Gene

chromosome 4 open reading frame 46 pseudogene

C9ORF89 Gene

chromosome 9 open reading frame 89

C9ORF84 Gene

chromosome 9 open reading frame 84

C9ORF85 Gene

chromosome 9 open reading frame 85

C1ORF68 Gene

chromosome 1 open reading frame 68

C6ORF89 Gene

chromosome 6 open reading frame 89

C12ORF49 Gene

chromosome 12 open reading frame 49

C12ORF40 Gene

chromosome 12 open reading frame 40

C12ORF43 Gene

chromosome 12 open reading frame 43

C12ORF42 Gene

chromosome 12 open reading frame 42

C12ORF45 Gene

chromosome 12 open reading frame 45

LOC100132615 Gene

chromosome 12 open reading frame 49 pseudogene

C19ORF53 Gene

chromosome 19 open reading frame 53

C19ORF52 Gene

chromosome 19 open reading frame 52

C19ORF57 Gene

chromosome 19 open reading frame 57

C19ORF54 Gene

chromosome 19 open reading frame 54

C6ORF106 Gene

chromosome 6 open reading frame 106

C20ORF194 Gene

chromosome 20 open reading frame 194

This gene encodes an uncharacterized protein with a C-terminal coiled-coil region. The gene is located on chromosome 20p13 in a 1.8 Mb region linked to a spinocerebellar ataxia phenotype, but this gene does not appear to be a disease candidate. [provided by RefSeq, Dec 2011]

C19ORF71 Gene

chromosome 19 open reading frame 71

C2ORF70 Gene

chromosome 2 open reading frame 70

C2ORF71 Gene

chromosome 2 open reading frame 71

The protein encoded by this gene is highly expressed in photoreceptors and may associate with the primary cilium of the outer segment. The encoded protein appears to undergo post-translational lipid modification. Nonsense and missense variants of this gene appear to cause a recessive form of retinitis pigmentosa. [provided by RefSeq, Jun 2010]

C2ORF73 Gene

chromosome 2 open reading frame 73

C2ORF74 Gene

chromosome 2 open reading frame 74

C2ORF76 Gene

chromosome 2 open reading frame 76

C2ORF78 Gene

chromosome 2 open reading frame 78

C6ORF120 Gene

chromosome 6 open reading frame 120

C21ORF140 Gene

chromosome 21 open reading frame 140

C7ORF49 Gene

chromosome 7 open reading frame 49

C14ORF159 Gene

chromosome 14 open reading frame 159

LOC100420743 Gene

chromosome 6 open reading frame 58 pseudogene

C17ORF89 Gene

chromosome 17 open reading frame 89

C17ORF82 Gene

chromosome 17 open reading frame 82

C17ORF80 Gene

chromosome 17 open reading frame 80

C17ORF85 Gene

chromosome 17 open reading frame 85

C15ORF59 Gene

chromosome 15 open reading frame 59

C15ORF57 Gene

chromosome 15 open reading frame 57

C15ORF56 Gene

chromosome 15 open reading frame 56

C15ORF54 Gene

chromosome 15 open reading frame 54

C15ORF53 Gene

chromosome 15 open reading frame 53

C15ORF52 Gene

chromosome 15 open reading frame 52

C8ORF76 Gene

chromosome 8 open reading frame 76

C8ORF74 Gene

chromosome 8 open reading frame 74

C16ORF86 Gene

chromosome 16 open reading frame 86

C10ORF142 Gene

chromosome 10 open reading frame 142

C8ORF4 Gene

chromosome 8 open reading frame 4

This gene encodes a small, monomeric, predominantly unstructured protein that functions as a positive regulator of the Wnt/beta-catenin signaling pathway. This protein interacts with a repressor of beta-catenin mediated transcription at nuclear speckles. It is thought to competitively block interactions of the repressor with beta-catenin, resulting in up-regulation of beta-catenin target genes. The encoded protein may also play a role in the NF-kappaB and ERK1/2 signaling pathways. Expression of this gene may play a role in the proliferation of several types of cancer including thyroid cancer, breast cancer and hematological malignancies. [provided by RefSeq, Nov 2011]

LOC100420879 Gene

chromosome 2 open reading frame 27B pseudogene

C14ORF39 Gene

chromosome 14 open reading frame 39

LOC100129574 Gene

chromosome 12 open reading frame 29 pseudogene

LOC642669 Gene

chromosome 2 open reading frame 27A pseudogene

C1ORF21 Gene

chromosome 1 open reading frame 21

C12ORF73 Gene

chromosome 12 open reading frame 73

C12ORF76 Gene

chromosome 12 open reading frame 76

C6ORF203 Gene

chromosome 6 open reading frame 203

LOC644525 Gene

chromosome 2 open reading frame 27A pseudogene

C9ORF156 Gene

chromosome 9 open reading frame 156

LOC100301521 Gene

chromosome 15 open reading frame 40 pseudogene

C9ORF153 Gene

chromosome 9 open reading frame 153

C9ORF152 Gene

chromosome 9 open reading frame 152

LOC100652967 Gene

chromosome 14 open reading frame 2 pseudogene

C2ORF80 Gene

chromosome 2 open reading frame 80

C2ORF88 Gene

chromosome 2 open reading frame 88

C5ORF38 Gene

chromosome 5 open reading frame 38

C5ORF30 Gene

chromosome 5 open reading frame 30

C1ORF145 Gene

chromosome 1 open reading frame 145

C1ORF146 Gene

chromosome 1 open reading frame 146

C1ORF141 Gene

chromosome 1 open reading frame 141

C1ORF143 Gene

chromosome 1 open reading frame 143

C3ORF20 Gene

chromosome 3 open reading frame 20

C3ORF22 Gene

chromosome 3 open reading frame 22

CXORF51B Gene

chromosome X open reading frame 51B

CXORF51A Gene

chromosome X open reading frame 51A

C9ORF72 Gene

chromosome 9 open reading frame 72

The protein encoded by this gene plays an important role in the regulation of endosomal trafficking, and has been shown to interact with Rab proteins that are involved in autophagy and endocytic transport. Expansion of a hexanucleotide repeat in non-coding sequence between alternate 5' exons in transcripts from this gene is associated with 9p-linked ALS (amyotrophic lateral sclerosis) and FTD (frontotemporal dementia) (PMID: 21944778, 21944779). Studies suggest that hexanucleotide expansions could result in the selective stabilization of repeat-containing pre-mRNA, and the accumulation of insoluble dipeptide repeat protein aggregates that could be pathogenic in FTD-ALS patients (PMID: 23393093). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Feb 2015]

C16ORF89 Gene

chromosome 16 open reading frame 89

This gene is expressed predominantly in the thyroid. Based on expression patterns similar to thyroid transcription factors and proteins, this gene may function in the development and function of the thyroid. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011]

C16ORF82 Gene

chromosome 16 open reading frame 82

C16ORF87 Gene

chromosome 16 open reading frame 87

C11ORF88 Gene

chromosome 11 open reading frame 88

C11ORF87 Gene

chromosome 11 open reading frame 87

C3ORF79 Gene

chromosome 3 open reading frame 79

C12ORF71 Gene

chromosome 12 open reading frame 71

C12ORF74 Gene

chromosome 12 open reading frame 74

C12ORF75 Gene

chromosome 12 open reading frame 75

C12ORF77 Gene

chromosome 12 open reading frame 77

C12ORF79 Gene

chromosome 12 open reading frame 79

C15ORF39 Gene

chromosome 15 open reading frame 39

C11ORF84 Gene

chromosome 11 open reading frame 84

C11ORF85 Gene

chromosome 11 open reading frame 85

C11ORF86 Gene

chromosome 11 open reading frame 86

C11ORF80 Gene

chromosome 11 open reading frame 80

C11ORF72 Gene

chromosome 11 open reading frame 72

C19ORF33 Gene

chromosome 19 open reading frame 33

C19ORF38 Gene

chromosome 19 open reading frame 38

C19ORF67 Gene

chromosome 19 open reading frame 67

C1ORF61 Gene

chromosome 1 open reading frame 61

C1ORF64 Gene

chromosome 1 open reading frame 64

C7ORF73 Gene

chromosome 7 open reading frame 73

C7ORF72 Gene

chromosome 7 open reading frame 72

C7ORF71 Gene

chromosome 7 open reading frame 71

C10ORF55 Gene

chromosome 10 open reading frame 55

C6ORF52 Gene

chromosome 6 open reading frame 52

C6ORF58 Gene

chromosome 6 open reading frame 58

LOC391636 Gene

chromosome 9 open reading frame 78 pseudogene

C15ORF26 Gene

chromosome 15 open reading frame 26

C15ORF27 Gene

chromosome 15 open reading frame 27

C19ORF26 Gene

chromosome 19 open reading frame 26

C19ORF24 Gene

chromosome 19 open reading frame 24

C19ORF25 Gene

chromosome 19 open reading frame 25

LOC647086 Gene

chromosome 20 open reading frame 27 pseudogene

LOC100129996 Gene

chromosome 6 open reading frame 203 pseudogene

C1ORF198 Gene

chromosome 1 open reading frame 198

C1ORF196 Gene

chromosome 1 open reading frame 196

C1ORF195 Gene

chromosome 1 open reading frame 195

C1ORF194 Gene

chromosome 1 open reading frame 194

CXORF65 Gene

chromosome X open reading frame 65

CXORF67 Gene

chromosome X open reading frame 67

CXORF66 Gene

chromosome X open reading frame 66

The protein encoded by this gene is predicted to be a type I membrane protein, however, its exact function is not known. [provided by RefSeq, Sep 2009]

C8ORF48 Gene

chromosome 8 open reading frame 48

C8ORF46 Gene

chromosome 8 open reading frame 46

C8ORF44 Gene

chromosome 8 open reading frame 44

C10ORF113 Gene

chromosome 10 open reading frame 113

C10ORF111 Gene

chromosome 10 open reading frame 111

C1ORF226 Gene

chromosome 1 open reading frame 226

C1ORF228 Gene

chromosome 1 open reading frame 228

LOC100505524 Gene

chromosome 5 open reading frame 63 pseudogene

LOC729141 Gene

chromosome 18 open reading frame 25 pseudogene

C9ORF3 Gene

chromosome 9 open reading frame 3

This gene encodes a member of the M1 zinc aminopeptidase family. The encoded protein is a zinc-dependent metallopeptidase that catalyzes the removal of an amino acid from the amino terminus of a protein or peptide. This protein may play a role in the generation of angiotensin IV. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2010]

C9ORF9 Gene

chromosome 9 open reading frame 9

C17ORF59 Gene

chromosome 17 open reading frame 59

C17ORF58 Gene

chromosome 17 open reading frame 58

C17ORF51 Gene

chromosome 17 open reading frame 51

C17ORF50 Gene

chromosome 17 open reading frame 50

C17ORF53 Gene

chromosome 17 open reading frame 53

C11ORF58 Gene

chromosome 11 open reading frame 58

C11ORF53 Gene

chromosome 11 open reading frame 53

C11ORF52 Gene

chromosome 11 open reading frame 52

C11ORF57 Gene

chromosome 11 open reading frame 57

C11ORF54 Gene

chromosome 11 open reading frame 54

C10ORF35 Gene

chromosome 10 open reading frame 35

C10ORF32 Gene

chromosome 10 open reading frame 32

C1ORF132 Gene

chromosome 1 open reading frame 132

C9ORF129 Gene

chromosome 9 open reading frame 129

C20ORF187 Gene

chromosome 20 open reading frame 187

C20ORF181 Gene

chromosome 20 open reading frame 181

C5ORF66 Gene

chromosome 5 open reading frame 66

C5ORF67 Gene

chromosome 5 open reading frame 67

C5ORF64 Gene

chromosome 5 open reading frame 64

C5ORF63 Gene

chromosome 5 open reading frame 63

C5ORF60 Gene

chromosome 5 open reading frame 60

LOC728024 Gene

chromosome X open reading frame 56 pseudogene

C1ORF112 Gene

chromosome 1 open reading frame 112

C1ORF111 Gene

chromosome 1 open reading frame 111

C1ORF110 Gene

chromosome 1 open reading frame 110

C1ORF116 Gene

chromosome 1 open reading frame 116

C1ORF115 Gene

chromosome 1 open reading frame 115

C4ORF47 Gene

chromosome 4 open reading frame 47

C4ORF46 Gene

chromosome 4 open reading frame 46

This gene encodes a small, conserved protein of unknown function that is expressed in a variety of tissues. There are pseudogenes for this gene on chromosomes 6, 8, 16, and X. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2013]

C4ORF45 Gene

chromosome 4 open reading frame 45

C4ORF48 Gene

chromosome 4 open reading frame 48

C3ORF58 Gene

chromosome 3 open reading frame 58

C3ORF52 Gene

chromosome 3 open reading frame 52

C3ORF56 Gene

chromosome 3 open reading frame 56

LOC441320 Gene

chromosome 11 open reading frame2 pseudogene

C9ORF24 Gene

chromosome 9 open reading frame 24

This gene encodes a nuclear- or perinuclear-localized protein with no predicted domains or similarity to other known proteins. Expression of this gene is induced during the differentiation of bronchial epithelial cells, and the encoded protein may play a role in ciliogenesis. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Nov 2011]

LOC100420928 Gene

chromosome 15 open reading frame 43 pseudogene

C14ORF2 Gene

chromosome 14 open reading frame 2

C11ORF39 Gene

chromosome 11 open reading frame 39

C14ORF1 Gene

chromosome 14 open reading frame 1

C11ORF30 Gene

chromosome 11 open reading frame 30

C20ORF27 Gene

chromosome 20 open reading frame 27

C20ORF24 Gene

chromosome 20 open reading frame 24

C14ORF132 Gene

chromosome 14 open reading frame 132

LOC100526841 Gene

chromosome 18 open reading frame 32 pseudogene

LOC441750 Gene

chromosome 12 open reading frame 49 pseudogene

C7ORF77 Gene

chromosome 7 open reading frame 77

C7ORF76 Gene

chromosome 7 open reading frame 76

C1ORF53 Gene

chromosome 1 open reading frame 53

C1ORF52 Gene

chromosome 1 open reading frame 52

C1ORF50 Gene

chromosome 1 open reading frame 50

C1ORF56 Gene

chromosome 1 open reading frame 56

C1ORF54 Gene

chromosome 1 open reading frame 54

C18ORF21 Gene

chromosome 18 open reading frame 21

C18ORF25 Gene

chromosome 18 open reading frame 25

LOC390314 Gene

chromosome 20 open reading frame 27 pseudogene

C7ORF25 Gene

chromosome 7 open reading frame 25

C7ORF26 Gene

chromosome 7 open reading frame 26

LOC100129168 Gene

chromosome 6 open reading frame 203 pseudogene

C6ORF62 Gene

chromosome 6 open reading frame 62

C12ORF29 Gene

chromosome 12 open reading frame 29

C19ORF70 Gene

chromosome 19 open reading frame 70

C19ORF73 Gene

chromosome 19 open reading frame 73

CXORF40A Gene

chromosome X open reading frame 40A

CXORF40B Gene

chromosome X open reading frame 40B

C2ORF50 Gene

chromosome 2 open reading frame 50

C2ORF57 Gene

chromosome 2 open reading frame 57

C2ORF54 Gene

chromosome 2 open reading frame 54

LOC645086 Gene

chromosome 11 open reading frame 58 pseudogene

C14ORF177 Gene

chromosome 14 open reading frame 177

C14ORF178 Gene

chromosome 14 open reading frame 178

C16ORF95 Gene

chromosome 16 open reading frame 95

LOC100129254 Gene

chromosome 3 open reading frame 38 pseudogene

C2ORF27AP2 Gene

chromosome 2 open reading frame 27A pseudogene 2

C2ORF27AP3 Gene

chromosome 2 open reading frame 27A pseudogene 3

C2ORF27AP1 Gene

chromosome 2 open reading frame 27A pseudogene 1

C1ORF210 Gene

chromosome 1 open reading frame 210

C1ORF216 Gene

chromosome 1 open reading frame 216

C17ORF62 Gene

chromosome 17 open reading frame 62

C17ORF64 Gene

chromosome 17 open reading frame 64

C17ORF67 Gene

chromosome 17 open reading frame 67

C18ORF8 Gene

chromosome 18 open reading frame 8

This gene encodes a colon cancer associated protein. [provided by RefSeq, Jan 2013]

LOC646970 Gene

chromosome 5 open reading frame 15 pseudogene

LOC100132762 Gene

chromosome 17 open reading frame 80 pseudogene

C5ORF58 Gene

chromosome 5 open reading frame 58

C5ORF56 Gene

chromosome 5 open reading frame 56

C5ORF52 Gene

chromosome 5 open reading frame 52

C5ORF51 Gene

chromosome 5 open reading frame 51

C1ORF86 Gene

chromosome 1 open reading frame 86

C1ORF87 Gene

chromosome 1 open reading frame 87

CXORF36 Gene

chromosome X open reading frame 36

C8ORF17 Gene

chromosome 8 open reading frame 17

C4ORF19 Gene

chromosome 4 open reading frame 19

C4ORF17 Gene

chromosome 4 open reading frame 17

C3ORF84 Gene

chromosome 3 open reading frame 84

CXORF38 Gene

chromosome X open reading frame 38

LOC100129989 Gene

chromosome 12 open reading frame 29 pseudogene

C9ORF16 Gene

chromosome 9 open reading frame 16

LOC100420859 Gene

chromosome 2 open reading frame 69 pseudogene

C16ORF62 Gene

chromosome 16 open reading frame 62

C20ORF78 Gene

chromosome 20 open reading frame 78

C3ORF80 Gene

chromosome 3 open reading frame 80

C11ORF24 Gene

chromosome 11 open reading frame 24

LOC100130455 Gene

chromosome 20 open reading frame 196 pseudogene

C10ORF67 Gene

chromosome 10 open reading frame 67

C10ORF62 Gene

chromosome 10 open reading frame 62

C6ORF229 Gene

chromosome 6 open reading frame 229

C6ORF222 Gene

chromosome 6 open reading frame 222

C6ORF223 Gene

chromosome 6 open reading frame 223

C6ORF226 Gene

chromosome 6 open reading frame 226

C9ORF171 Gene

chromosome 9 open reading frame 171

C9ORF170 Gene

chromosome 9 open reading frame 170

C1ORF162 Gene

chromosome 1 open reading frame 162

C1ORF167 Gene

chromosome 1 open reading frame 167

C1ORF168 Gene

chromosome 1 open reading frame 168

LOC100526840 Gene

chromosome 18 open reading frame 32 pseudogene

C2ORF83 Gene

chromosome 2 open reading frame 83

C18ORF12 Gene

chromosome 18 open reading frame 12

LOC389705 Gene

chromosome 4 open reading frame 27 pseudogene

C9ORF91 Gene

chromosome 9 open reading frame 91

LOC100289196 Gene

chromosome 7 open reading frame 73 pseudogene

C12ORF57 Gene

chromosome 12 open reading frame 57

This gene is ubiquitously expressed in human tissues. It is required for development of the human corpus callosum. Mutations in this gene are associated with Temtamy syndrome (TEMTYS). Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014]

C12ORF54 Gene

chromosome 12 open reading frame 54

C19ORF40 Gene

chromosome 19 open reading frame 40

FAAP24 is a component of the Fanconi anemia (FA) core complex (see MIM 227650), which plays a crucial role in DNA damage response (Ciccia et al., 2007 [PubMed 17289582]).[supplied by OMIM, Mar 2008]

C19ORF43 Gene

chromosome 19 open reading frame 43

C19ORF45 Gene

chromosome 19 open reading frame 45

C19ORF47 Gene

chromosome 19 open reading frame 47

C19ORF48 Gene

chromosome 19 open reading frame 48

C6ORF118 Gene

chromosome 6 open reading frame 118

C2ORF61 Gene

chromosome 2 open reading frame 61

C2ORF69 Gene

chromosome 2 open reading frame 69

C2ORF68 Gene

chromosome 2 open reading frame 68

LOC100128808 Gene

chromosome 11 open reading frame 51 pseudogene

LOC100420925 Gene

chromosome 2 open reading frame 27A pseudogene

C7ORF55 Gene

chromosome 7 open reading frame 55

C7ORF57 Gene

chromosome 7 open reading frame 57

C7ORF50 Gene

chromosome 7 open reading frame 50

C14ORF142 Gene

chromosome 14 open reading frame 142

C14ORF144 Gene

chromosome 14 open reading frame 144

LOC100288558 Gene

chromosome 4 open reading frame 46 pseudogene

LOC100420770 Gene

chromosome 12 open reading frame 10 pseudogene

LOC100420779 Gene

chromosome 16 open reading frame 70 pseudogene

LOC100420778 Gene

chromosome 2 open reading frame 27A pseudogene

C14ORF80 Gene

chromosome 14 open reading frame 80

C15ORF48 Gene

chromosome 15 open reading frame 48

This gene was first identified in a study of human esophageal squamous cell carcinoma tissues. Levels of both the message and protein are reduced in carcinoma samples. In adult human tissues, this gene is expressed in the the esophagus, stomach, small intestine, colon and placenta. Alternatively spliced transcript variants that encode the same protein have been identified. [provided by RefSeq, Jun 2012]

C15ORF40 Gene

chromosome 15 open reading frame 40

C15ORF43 Gene

chromosome 15 open reading frame 43

C21ORF91 Gene

chromosome 21 open reading frame 91

C8ORF60 Gene

chromosome 8 open reading frame 60

LOC100287212 Gene

chromosome 4 open reading frame 3 pseudogene

C4ORF50 Gene

chromosome 4 open reading frame 50

C10ORF131 Gene

chromosome 10 open reading frame 131

LOC100125409 Gene

chromosome 4 open reading frame 27 pseudogene

LOC399815 Gene

chromosome 10 open reading frame 88 pseudogene

C15ORF62 Gene

chromosome 15 open reading frame 62

C16ORF13 Gene

chromosome 16 open reading frame 13

C11ORF21 Gene

chromosome 11 open reading frame 21

C4ORF3 Gene

chromosome 4 open reading frame 3

C11ORF71 Gene

chromosome 11 open reading frame 71

C11ORF70 Gene

chromosome 11 open reading frame 70

C11ORF73 Gene

chromosome 11 open reading frame 73

C11ORF74 Gene

chromosome 11 open reading frame 74

This gene encodes a protein that was identified as a cellular interacting partner of non-structural protein 10 of the severe acute respiratory syndrome coronavirus (SARS-CoV). The encoded protein may function as a negative regulator of transcription. There is a pseudogene for this gene on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2013]

C10ORF54 Gene

chromosome 10 open reading frame 54

C10ORF53 Gene

chromosome 10 open reading frame 53

C9ORF147 Gene

chromosome 9 open reading frame 147

C9ORF142 Gene

chromosome 9 open reading frame 142

C1ORF131 Gene

chromosome 1 open reading frame 131

C1ORF134 Gene

chromosome 1 open reading frame 134

C1ORF137 Gene

chromosome 1 open reading frame 137

LOC100420789 Gene

chromosome 2 open reading frame 27A pseudogene

C3ORF33 Gene

chromosome 3 open reading frame 33

C3ORF30 Gene

chromosome 3 open reading frame 30

C3ORF36 Gene

chromosome 3 open reading frame 36

C3ORF35 Gene

chromosome 3 open reading frame 35

C3ORF38 Gene

chromosome 3 open reading frame 38

LOC389473 Gene

chromosome 5 open reading frame 13 pseudogene

C20ORF203 Gene

chromosome 20 open reading frame 203

C20ORF202 Gene

chromosome 20 open reading frame 202

C9ORF40 Gene

chromosome 9 open reading frame 40

C9ORF41 Gene

chromosome 9 open reading frame 41

C9ORF43 Gene

chromosome 9 open reading frame 43

C9ORF47 Gene

chromosome 9 open reading frame 47

C16ORF96 Gene

chromosome 16 open reading frame 96

C16ORF97 Gene

chromosome 16 open reading frame 97

C16ORF92 Gene

chromosome 16 open reading frame 92

C16ORF93 Gene

chromosome 16 open reading frame 93

C16ORF90 Gene

chromosome 16 open reading frame 90

C16ORF91 Gene

chromosome 16 open reading frame 91

LOC729930 Gene

chromosome 11 open reading frame 74 pseudogene

C12ORF80 Gene

chromosome 12 open reading frame 80

C6ORF141 Gene

chromosome 6 open reading frame 141

C1ORF74 Gene

chromosome 1 open reading frame 74

C2ORF72 Gene

chromosome 2 open reading frame 72

C18ORF42 Gene

chromosome 18 open reading frame 42

C9ORF78 Gene

chromosome 9 open reading frame 78

C1ORF220 Gene

chromosome 1 open reading frame 220

C1ORF229 Gene

chromosome 1 open reading frame 229

C9ORF173 Gene

chromosome 9 open reading frame 173

C6ORF48 Gene

chromosome 6 open reading frame 48

C6ORF47 Gene

chromosome 6 open reading frame 47

glaucoma, angle-closure; glaucoma, open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, angle-closure; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, primary open-angle; glaucoma, primary congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, primary open-angle; glaucoma, primary congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, open-angle; low tension glaucoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, open-angle; low tension glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, primary open-angle; glaucoma, normal tension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, primary open-angle; glaucoma, normal tension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma; glaucoma, open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; exfoliation syndrome; glaucoma; glaucoma, open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract; exfoliation syndrome; glaucoma; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, open-angle; low tension glaucoma; ocular hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, open-angle; low tension glaucoma; ocular hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma; glaucoma, primary open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma; glaucoma, primary open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Glaucoma, Angle-Closure Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma, Angle-Closure from the curated CTD Gene-Disease Associations dataset.

primary angle-closure glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease primary angle-closure glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

interval angle-closure glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease interval angle-closure glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

angle-closure glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease angle-closure glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

glaucoma, angle-closure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, angle-closure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

eye abnormalities; glaucoma, angle-closure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eye abnormalities; glaucoma, angle-closure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Glaucoma, Angle-Closure Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Glaucoma, Angle-Closure phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Glaucoma 1, open angle, e Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glaucoma 1, open angle, e phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glaucoma 1, open angle, O Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glaucoma 1, open angle, O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glaucoma 1, open angle, F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glaucoma 1, open angle, F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glaucoma 1, open angle, G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glaucoma 1, open angle, G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glaucoma, primary open angle, juvenile-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glaucoma, primary open angle, juvenile-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary open angle glaucoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary open angle glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary open angle glaucoma juvenile onset 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary open angle glaucoma juvenile onset 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glaucoma 1, Open Angle, J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 1, Open Angle, J from the curated CTD Gene-Disease Associations dataset.

Glaucoma 1, Open Angle, N Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 1, Open Angle, N from the curated CTD Gene-Disease Associations dataset.

GLAUCOMA 1, OPEN ANGLE, B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GLAUCOMA 1, OPEN ANGLE, B from the curated CTD Gene-Disease Associations dataset.

Glaucoma, Primary Open Angle Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma, Primary Open Angle from the curated CTD Gene-Disease Associations dataset.

Glaucoma 1, Open Angle, I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 1, Open Angle, I from the curated CTD Gene-Disease Associations dataset.

Glaucoma 1, Open Angle, K Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 1, Open Angle, K from the curated CTD Gene-Disease Associations dataset.

GLAUCOMA 1, PRIMARY OPEN ANGLE, C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GLAUCOMA 1, PRIMARY OPEN ANGLE, C from the curated CTD Gene-Disease Associations dataset.

Glaucoma, Open-Angle Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma, Open-Angle from the curated CTD Gene-Disease Associations dataset.

Glaucoma 1, Open Angle, H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 1, Open Angle, H from the curated CTD Gene-Disease Associations dataset.

Glaucoma 1, Open Angle, M Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 1, Open Angle, M from the curated CTD Gene-Disease Associations dataset.

Glaucoma 1, Open Angle, O Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 1, Open Angle, O from the curated CTD Gene-Disease Associations dataset.

Glaucoma 1, Open Angle, A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 1, Open Angle, A from the curated CTD Gene-Disease Associations dataset.

Glaucoma 1, Open Angle, D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 1, Open Angle, D from the curated CTD Gene-Disease Associations dataset.

Glaucoma 1, Open Angle, G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 1, Open Angle, G from the curated CTD Gene-Disease Associations dataset.

Glaucoma, Open-Angle Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Glaucoma, Open-Angle in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

open-angle glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease open-angle glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

primary open angle glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease primary open angle glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

glaucoma, primary open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, primary open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, open-angle; hydrophthalmos Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, open-angle; hydrophthalmos in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; glaucoma, open-angle; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; glaucoma, open-angle; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

exfoliation syndrome; glaucoma, open-angle; pigmentation disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease exfoliation syndrome; glaucoma, open-angle; pigmentation disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cataract; exfoliation syndrome; glaucoma, open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cataract; exfoliation syndrome; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, open-angle; vision disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, open-angle; vision disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, open-angle; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, open-angle; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

exfoliation syndrome; glaucoma, open-angle; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease exfoliation syndrome; glaucoma, open-angle; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of the optic nerve; glaucoma, open-angle; optic nerve diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of the optic nerve; glaucoma, open-angle; optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

primary open angle glaucoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease primary open angle glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

open-angle glaucoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease open-angle glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; glaucoma, open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bradycardia; glaucoma, open-angle; ocular hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bradycardia; glaucoma, open-angle; ocular hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

exfoliation syndrome; glaucoma, open-angle Gene Set

From GAD Gene-Disease Associations

genes associated with the disease exfoliation syndrome; glaucoma, open-angle in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease disorder of the optic nerve; glaucoma, open-angle; ocular hypertension; optic nerve diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, open-angle; ocular hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, open-angle; ocular hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

primary open-angle glaucoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease primary open-angle glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Glaucoma (primary open-angle) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Glaucoma (primary open-angle) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

open-angle glaucoma Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease open-angle glaucoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

primary open angle glaucoma Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the primary open angle glaucoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

primary open angle glaucoma Gene Set

From HPO Gene-Disease Associations

genes associated with the primary open angle glaucoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Glaucoma, Open-Angle Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Glaucoma, Open-Angle phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

glaucoma 1, open angle, 1o Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1, open angle, 1o phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1b, primary open angle, adult onset, Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1b, primary open angle, adult onset, phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1a, primary open angle Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1a, primary open angle phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1, open angle, i Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1, open angle, i phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1, open angle, p Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1, open angle, p phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1, open angle, h Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1, open angle, h phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1, open angle, m Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1, open angle, m phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1, open angle, n Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1, open angle, n phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1, open angle, e Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1, open angle, e phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1, open angle, f Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1, open angle, f phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1, open angle, g Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1, open angle, g phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1c, primary open angle Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1c, primary open angle phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1k, primary open angle, juvenile-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1k, primary open angle, juvenile-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 3a, primary open angle, congenital, juvenile, or adult onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 3a, primary open angle, congenital, juvenile, or adult onset phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 1d, primary open angle Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 1d, primary open angle phenotype from the curated OMIM Gene-Disease Associations dataset.

normal tension glaucoma, pigmentary glaucoma and exfoliation glaucoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease normal tension glaucoma, pigmentary glaucoma and exfoliation glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic closed-angle glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease chronic closed-angle glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

acute closed-angle glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease acute closed-angle glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

wide-angle glaucoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease wide-angle glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

closure Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term closure in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

planar cell polarity pathway involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the planar cell polarity pathway involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

anterior neuropore closure Gene Set

From GO Biological Process Annotations

genes participating in the anterior neuropore closure biological process from the curated GO Biological Process Annotations dataset.

tube closure Gene Set

From GO Biological Process Annotations

genes participating in the tube closure biological process from the curated GO Biological Process Annotations dataset.

regulation of establishment of planar polarity involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the regulation of establishment of planar polarity involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

regulation of planar cell polarity pathway involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the regulation of planar cell polarity pathway involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

establishment of planar polarity involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the establishment of planar polarity involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

negative regulation of planar cell polarity pathway involved in neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of planar cell polarity pathway involved in neural tube closure biological process from the curated GO Biological Process Annotations dataset.

ductus arteriosus closure Gene Set

From GO Biological Process Annotations

genes participating in the ductus arteriosus closure biological process from the curated GO Biological Process Annotations dataset.

initiation of neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the initiation of neural tube closure biological process from the curated GO Biological Process Annotations dataset.

foramen ovale closure Gene Set

From GO Biological Process Annotations

genes participating in the foramen ovale closure biological process from the curated GO Biological Process Annotations dataset.

closure of optic fissure Gene Set

From GO Biological Process Annotations

genes participating in the closure of optic fissure biological process from the curated GO Biological Process Annotations dataset.

neural tube closure Gene Set

From GO Biological Process Annotations

genes participating in the neural tube closure biological process from the curated GO Biological Process Annotations dataset.

delayed cranial suture closure Gene Set

From HPO Gene-Disease Associations

genes associated with the delayed cranial suture closure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature closure of fontanelles Gene Set

From HPO Gene-Disease Associations

genes associated with the premature closure of fontanelles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

delayed closure of the anterior fontanelle Gene Set

From HPO Gene-Disease Associations

genes associated with the delayed closure of the anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of neural tube closure Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of neural tube closure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

incomplete caudal neuropore closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the incomplete caudal neuropore closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature suture closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature suture closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural tube closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural tube closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed caudal neuropore closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed caudal neuropore closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic fissure closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal optic fissure closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed optic fissure closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed optic fissure closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed rostral neuropore closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed rostral neuropore closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

failure of conotruncal ridge closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the failure of conotruncal ridge closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature closure of the ductus arteriosus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature closure of the ductus arteriosus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed suture closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed suture closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

failure of ventral body wall closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the failure of ventral body wall closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delayed neural tube closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed neural tube closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

failure of atrioventricular cushion closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the failure of atrioventricular cushion closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

incomplete rostral neuropore closure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the incomplete rostral neuropore closure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

c-src mediated regulation of Cx43 function and closure of gap junctions Gene Set

From Reactome Pathways

proteins participating in the c-src mediated regulation of Cx43 function and closure of gap junctions pathway from the Reactome Pathways dataset.

open Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term open in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

branching involved in open tracheal system development Gene Set

From GO Biological Process Annotations

genes participating in the branching involved in open tracheal system development biological process from the curated GO Biological Process Annotations dataset.

open rectifier potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the open rectifier potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

open bite Gene Set

From HPO Gene-Disease Associations

genes associated with the open bite phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

triangular-shaped open mouth Gene Set

From HPO Gene-Disease Associations

genes associated with the triangular-shaped open mouth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior open-bite malocclusion Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior open-bite malocclusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior open bite Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior open bite phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

frontal open bite Gene Set

From HPO Gene-Disease Associations

genes associated with the frontal open bite phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

persistent open anterior fontanelle Gene Set

From HPO Gene-Disease Associations

genes associated with the persistent open anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

open mouth Gene Set

From HPO Gene-Disease Associations

genes associated with the open mouth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

open operculum Gene Set

From HPO Gene-Disease Associations

genes associated with the open operculum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Lipid transport, open beta-sheet Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lipid transport, open beta-sheet protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Vitellinogen, open beta-sheet Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Vitellinogen, open beta-sheet protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Vitellinogen, open beta-sheet, subdomain 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Vitellinogen, open beta-sheet, subdomain 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Vitellinogen, open beta-sheet, subdomain 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Vitellinogen, open beta-sheet, subdomain 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

eyelids open at birth Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the eyelids open at birth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

open neural tube Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the open neural tube phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

eyelids fail to open Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the eyelids fail to open phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

c-p angle neurinoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease c-p angle neurinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cerebellopontine angle tumor Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease cerebellopontine angle tumor in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cerebellopontine angle meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease cerebellopontine angle meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

angle Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term angle in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

angles Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term angles in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

angleclosure Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term angleclosure in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

increased carrying angle Gene Set

From HPO Gene-Disease Associations

genes associated with the increased carrying angle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

obtuse angle of mandible Gene Set

From HPO Gene-Disease Associations

genes associated with the obtuse angle of mandible phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Malocclusion, Angle Class II Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Malocclusion, Angle Class II phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Malocclusion, Angle Class I Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Malocclusion, Angle Class I phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

absent mandibular angle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent mandibular angle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal basicranium angle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal basicranium angle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mandibular angle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mandibular angle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal iridocorneal angle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal iridocorneal angle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Pseudoexfoliation glaucoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudoexfoliation glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Charcot-Marie-Tooth disease type 4B2 with early-onset glaucoma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glaucoma, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glaucoma, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glaucoma-Related Pigment Dispersion Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma-Related Pigment Dispersion Syndrome from the curated CTD Gene-Disease Associations dataset.

Glaucoma 3, primary infantile, B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 3, primary infantile, B from the curated CTD Gene-Disease Associations dataset.

GLAUCOMA 3, PRIMARY CONGENITAL, C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GLAUCOMA 3, PRIMARY CONGENITAL, C from the curated CTD Gene-Disease Associations dataset.

Glaucoma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma from the curated CTD Gene-Disease Associations dataset.

Iris hypoplasia and glaucoma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Iris hypoplasia and glaucoma from the curated CTD Gene-Disease Associations dataset.

Glaucoma 3, Primary Congenital, D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 3, Primary Congenital, D from the curated CTD Gene-Disease Associations dataset.

Glaucoma 3, Primary Congenital, A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glaucoma 3, Primary Congenital, A from the curated CTD Gene-Disease Associations dataset.

GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GLAUCOMA, NORMAL TENSION, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

Glaucoma Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Glaucoma in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

glaucoma Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease glaucoma from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

glaucoma Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease glaucoma in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

phacolytic glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease phacolytic glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

borderline glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease borderline glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

low tension glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease low tension glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

phacogenic glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease phacogenic glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

juvenile glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease juvenile glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

neovascular glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease neovascular glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

steroid-induced glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease steroid-induced glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

primary congenital glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease primary congenital glaucoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

primary congenital glaucoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease primary congenital glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

normal tension glaucoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease normal tension glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, normal tension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, normal tension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low tension glaucoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low tension glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

exfoliation syndrome; glaucoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease exfoliation syndrome; glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, primary congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, primary congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma, early-onset Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma, early-onset in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

exfoliation syndrome; glaucoma; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease exfoliation syndrome; glaucoma; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma (exfoliation) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma (exfoliation) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pseudoexfoliative glaucoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pseudoexfoliative glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glaucoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glaucoma Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term glaucoma in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Glaucoma Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Glaucoma phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Exfoliation glaucoma or exfoliation syndrome Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Exfoliation glaucoma or exfoliation syndrome phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

phacogenic glaucoma Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease phacogenic glaucoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

glaucoma Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease glaucoma in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

congenital glaucoma Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the congenital glaucoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

primary congenital glaucoma Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the primary congenital glaucoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

glaucoma Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the glaucoma phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

primary congenital glaucoma Gene Set

From HPO Gene-Disease Associations

genes associated with the primary congenital glaucoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

late onset congenital glaucoma Gene Set

From HPO Gene-Disease Associations

genes associated with the late onset congenital glaucoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

congenital glaucoma Gene Set

From HPO Gene-Disease Associations

genes associated with the congenital glaucoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

glaucoma Gene Set

From HPO Gene-Disease Associations

genes associated with the glaucoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Low Tension Glaucoma Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Low Tension Glaucoma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Glaucoma Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Glaucoma phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

{glaucoma, normal tension, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {glaucoma, normal tension, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

iris hypoplasia and glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the iris hypoplasia and glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 3, primary congenital, d Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 3, primary congenital, d phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 3, primary congenital, c Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 3, primary congenital, c phenotype from the curated OMIM Gene-Disease Associations dataset.

glaucoma 3, primary infantile, b Gene Set

From OMIM Gene-Disease Associations

genes associated with the glaucoma 3, primary infantile, b phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective CYP1B1 causes Glaucoma Gene Set

From Reactome Pathways

proteins participating in the Defective CYP1B1 causes Glaucoma pathway from the Reactome Pathways dataset.