abnormality of male internal genitalia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the male internal genitalia. (Human Phenotype Ontology, HP_0000022)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000022
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Genes

24 genes associated with the abnormality of male internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMH anti-Mullerian hormone
AMHR2 anti-Mullerian hormone receptor, type II
AR androgen receptor
BRCA2 breast cancer 2, early onset
BTK Bruton agammaglobulinemia tyrosine kinase
CREBBP CREB binding protein
CTLA4 cytotoxic T-lymphocyte-associated protein 4
DHH desert hedgehog
HGD homogentisate 1,2-dioxygenase
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
HNF1B HNF1 homeobox B
IGHV4-34 immunoglobulin heavy variable 4-34
KLF6 Kruppel-like factor 6
MAD1L1 MAD1 mitotic arrest deficient-like 1 (yeast)
MSR1 macrophage scavenger receptor 1
PHF6 PHD finger protein 6
PRTN3 proteinase 3
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
RNASEL ribonuclease L (2',5'-oligoisoadenylate synthetase-dependent)
SOX9 SRY (sex determining region Y)-box 9
SRY sex determining region Y
TP53 tumor protein p53
UNG uracil-DNA glycosylase
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase