abnormal spermatogenesis Gene Set
Genes
17 genes associated with the abnormal spermatogenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Symbol |
Name |
AR
|
androgen receptor
|
ATM
|
ATM serine/threonine kinase
|
BLM
|
Bloom syndrome, RecQ helicase-like
|
CATSPER1
|
cation channel, sperm associated 1
|
CFTR
|
cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
|
CNBP
|
CCHC-type zinc finger, nucleic acid binding protein
|
DAZ1
|
deleted in azoospermia 1
|
HFE
|
hemochromatosis
|
NANOS1
|
nanos homolog 1 (Drosophila)
|
NR5A1
|
nuclear receptor subfamily 5, group A, member 1
|
POC1A
|
POC1 centriolar protein A
|
SCP2
|
sterol carrier protein 2
|
STEAP3
|
STEAP family member 3, metalloreductase
|
SYCP3
|
synaptonemal complex protein 3
|
TAF4B
|
TAF4b RNA polymerase II, TATA box binding protein (TBP)-associated factor, 105kDa
|
USP9Y
|
ubiquitin specific peptidase 9, Y-linked
|
ZMYND15
|
zinc finger, MYND-type containing 15
|