Short 5Th Finger Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Hypoplasia (congenital reduction in size) of the fifth finger, also known as the little finger. (Human Phenotype Ontology, HP_0009237)
External Link https://www.disgenet.org/browser/0/1/0/C1842878
Similar Terms
Downloads & Tools

Genes

18 genes associated with the disease Short 5Th Finger in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
CUL7 cullin 7
FGD1 FYVE, RhoGEF and PH domain containing 1
GJA1 gap junction protein, alpha 1, 43kDa
HDAC8 histone deacetylase 8
HOXA13 homeobox A13
KDM6A lysine (K)-specific demethylase 6A
KMT2D lysine (K)-specific methyltransferase 2D
MASP1 mannan-binding lectin serine peptidase 1 (C4/C2 activating component of Ra-reactive factor)
MEIS2 Meis homeobox 2
OBSL1 obscurin-like 1
PUF60 poly-U binding splicing factor 60KDa
RAC1 ras-related C3 botulinum toxin substrate 1 (rho family, small GTP binding protein Rac1)
RAP1A RAP1A, member of RAS oncogene family
RAP1B RAP1B, member of RAS oncogene family
SMC3 structural maintenance of chromosomes 3
TBC1D24 TBC1 domain family, member 24
TRPS1 trichorhinophalangeal syndrome I
ZMYND11 zinc finger, MYND-type containing 11