short ulna Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the ulna. (Human Phenotype Ontology, HP_0003022)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004359
Similar Terms
Downloads & Tools

Genes

42 gene mutations causing the short ulna phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP5 bone morphogenetic protein 5
CHKB choline kinase beta
COL2A1 collagen, type II, alpha 1
ESR1 estrogen receptor 1
ESR2 estrogen receptor 2 (ER beta)
EVC Ellis van Creveld protein
EVX2 even-skipped homeobox 2
FBN1 fibrillin 1
FGF18 fibroblast growth factor 18
FGF9 fibroblast growth factor 9
FGFR3 fibroblast growth factor receptor 3
FOXC1 forkhead box C1
GDF5 growth differentiation factor 5
GLI2 GLI family zinc finger 2
GLI3 GLI family zinc finger 3
HOXA11 homeobox A11
HOXD13 homeobox D13
IFT172 intraflagellar transport 172
IHH indian hedgehog
IMPAD1 inositol monophosphatase domain containing 1
INPP4B inositol polyphosphate-4-phosphatase, type II, 105kDa
KIAA1715 KIAA1715
NABP2 nucleic acid binding protein 2
NPR2 natriuretic peptide receptor 2
PAPPA2 pappalysin 2
PDS5B PDS5 cohesin associated factor B
PHEX phosphate regulating endopeptidase homolog, X-linked
PKDCC protein kinase domain containing, cytoplasmic
POSTN periostin, osteoblast specific factor
PRKG2 protein kinase, cGMP-dependent, type II
PRRX1 paired related homeobox 1
PTHLH parathyroid hormone-like hormone
ROR2 receptor tyrosine kinase-like orphan receptor 2
RYK receptor-like tyrosine kinase
SFRP2 secreted frizzled-related protein 2
SMPD3 sphingomyelin phosphodiesterase 3, neutral membrane (neutral sphingomyelinase II)
SP8 Sp8 transcription factor
TBX15 T-box 15
TGFB2 transforming growth factor, beta 2
THRA thyroid hormone receptor, alpha
WNT5A wingless-type MMTV integration site family, member 5A
XYLT1 xylosyltransferase I