rough bone trabeculation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100670
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Genes

18 genes associated with the rough bone trabeculation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AMER1 APC membrane recruitment protein 1
CTC1 CTS telomere maintenance complex component 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
TERC telomerase RNA component
TERT telomerase reverse transcriptase
TINF2 TERF1 (TRF1)-interacting nuclear factor 2
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