postnatal growth retardation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Slow or limited growth after birth. (Human Phenotype Ontology, HP_0008897)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008897
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Genes

68 genes associated with the postnatal growth retardation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTB actin, beta
ARG1 arginase 1
ATRX alpha thalassemia/mental retardation syndrome X-linked
B3GALTL beta 1,3-galactosyltransferase-like
BLM Bloom syndrome, RecQ helicase-like
BRIP1 BRCA1 interacting protein C-terminal helicase 1
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family)
CCBE1 collagen and calcium binding EGF domains 1
CDAN1 codanin 1
CDKN1C cyclin-dependent kinase inhibitor 1C (p57, Kip2)
CHD7 chromodomain helicase DNA binding protein 7
COG1 component of oligomeric golgi complex 1
COLEC11 collectin sub-family member 11
CREBBP CREB binding protein
CTC1 CTS telomere maintenance complex component 1
CUL7 cullin 7
DCX doublecortin
DHODH dihydroorotate dehydrogenase (quinone)
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19
DYM dymeclin
EBP emopamil binding protein (sterol isomerase)
ERCC6 excision repair cross-complementation group 6
ERCC8 excision repair cross-complementation group 8
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
FLNA filamin A, alpha
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GUSB glucuronidase, beta
HDAC8 histone deacetylase 8
HOXD13 homeobox D13
INSR insulin receptor
KIF7 kinesin family member 7
KMT2D lysine (K)-specific methyltransferase 2D
LHX4 LIM homeobox 4
LMNA lamin A/C
MASP1 mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor)
MBD5 methyl-CpG binding domain protein 5
MCM4 minichromosome maintenance complex component 4
MGAT2 mannosyl (alpha-1,6-)-glycoprotein beta-1,2-N-acetylglucosaminyltransferase
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
NALCN sodium leak channel, non selective
NBAS neuroblastoma amplified sequence
NSUN2 NOP2/Sun RNA methyltransferase family, member 2
PALB2 partner and localizer of BRCA2
PCNT pericentrin
PCYT1A phosphate cytidylyltransferase 1, choline, alpha
PIEZO2 piezo-type mechanosensitive ion channel component 2
PLOD3 procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3
POU1F1 POU class 1 homeobox 1
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PSPH phosphoserine phosphatase
PTEN phosphatase and tensin homolog
PTPN11 protein tyrosine phosphatase, non-receptor type 11
PYGL phosphorylase, glycogen, liver
RAB18 RAB18, member RAS oncogene family
RAB3GAP2 RAB3 GTPase activating protein subunit 2 (non-catalytic)
RTEL1 regulator of telomere elongation helicase 1
SEMA3E sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3E
SETBP1 SET binding protein 1
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SMOC1 SPARC related modular calcium binding 1
SOX2 SRY (sex determining region Y)-box 2
TBC1D20 TBC1 domain family, member 20
TBCE tubulin folding cofactor E
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TMCO1 transmembrane and coiled-coil domains 1
TSHB thyroid stimulating hormone, beta