abnormal male reproductive system physiology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal functionality of the male genital system. (Human Phenotype Ontology, HP_0012874)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012874
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Genes

59 genes associated with the abnormal male reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCD1 ATP-binding cassette, sub-family D (ALD), member 1
ANK1 ankyrin 1, erythrocytic
AR androgen receptor
ATM ATM serine/threonine kinase
AURKC aurora kinase C
BAZ1B bromodomain adjacent to zinc finger domain, 1B
BLM Bloom syndrome, RecQ helicase-like
BRCA2 breast cancer 2, early onset
BRIP1 BRCA1 interacting protein C-terminal helicase 1
C21ORF59 chromosome 21 open reading frame 59
CATSPER1 cation channel, sperm associated 1
CATSPER2 cation channel, sperm associated 2
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CLIP2 CAP-GLY domain containing linker protein 2
CNBP CCHC-type zinc finger, nucleic acid binding protein
DAZ1 deleted in azoospermia 1
DBH dopamine beta-hydroxylase (dopamine beta-monooxygenase)
DNAAF5 dynein, axonemal, assembly factor 5
ELN elastin
ERCC4 excision repair cross-complementation group 4
FANCA Fanconi anemia, complementation group A
FANCB Fanconi anemia, complementation group B
FANCC Fanconi anemia, complementation group C
FANCD2 Fanconi anemia, complementation group D2
FANCE Fanconi anemia, complementation group E
FANCF Fanconi anemia, complementation group F
FANCG Fanconi anemia, complementation group G
FANCI Fanconi anemia, complementation group I
FANCL Fanconi anemia, complementation group L
FANCM Fanconi anemia, complementation group M
FMR1 fragile X mental retardation 1
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
GUCY1A3 guanylate cyclase 1, soluble, alpha 3
HEXB hexosaminidase B (beta polypeptide)
HFE hemochromatosis
LHB luteinizing hormone beta polypeptide
LHCGR luteinizing hormone/choriogonadotropin receptor
LIMK1 LIM domain kinase 1
LMNB1 lamin B1
NANOS1 nanos homolog 1 (Drosophila)
NR5A1 nuclear receptor subfamily 5, group A, member 1
OCRL oculocerebrorenal syndrome of Lowe
PALB2 partner and localizer of BRCA2
POC1A POC1 centriolar protein A
RAD51C RAD51 paralog C
RFC2 replication factor C (activator 1) 2, 40kDa
RSPH9 radial spoke head 9 homolog (Chlamydomonas)
SCP2 sterol carrier protein 2
SLX4 SLX4 structure-specific endonuclease subunit
STEAP3 STEAP family member 3, metalloreductase
STRC stereocilin
SYCP3 synaptonemal complex protein 3
TAF4B TAF4b RNA polymerase II, TATA box binding protein (TBP)-associated factor, 105kDa
TBL2 transducin (beta)-like 2
TTR transthyretin
USP9Y ubiquitin specific peptidase 9, Y-linked
ZMYND10 zinc finger, MYND-type containing 10
ZMYND15 zinc finger, MYND-type containing 15