abnormal trabecular bone morphology Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal structure or form of trabecular bone. (Human Phenotype Ontology, HP_0100671)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100671
Similar Terms
Downloads & Tools

Genes

23 genes associated with the abnormal trabecular bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMER1 APC membrane recruitment protein 1
CLCN5 chloride channel, voltage-sensitive 5
CTC1 CTS telomere maintenance complex component 1
CYP27B1 cytochrome P450, family 27, subfamily B, polypeptide 1
CYP2R1 cytochrome P450, family 2, subfamily R, polypeptide 1
DKC1 dyskeratosis congenita 1, dyskerin
LMNA lamin A/C
NHP2 NHP2 ribonucleoprotein
NOP10 NOP10 ribonucleoprotein
PORCN porcupine homolog (Drosophila)
RTEL1 regulator of telomere elongation helicase 1
SLC29A3 solute carrier family 29 (equilibrative nucleoside transporter), member 3
SLC34A3 solute carrier family 34 (type II sodium/phosphate cotransporter), member 3
TERC telomerase RNA component
TERT telomerase reverse transcriptase
TINF2 TERF1 (TRF1)-interacting nuclear factor 2
TNFRSF11A tumor necrosis factor receptor superfamily, member 11a, NFKB activator
TNFRSF11B tumor necrosis factor receptor superfamily, member 11b
TRPV4 transient receptor potential cation channel, subfamily V, member 4
USB1 U6 snRNA biogenesis 1
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
WRAP53 WD repeat containing, antisense to TP53
ZMPSTE24 zinc metallopeptidase STE24