abnormality of the intervertebral disk Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the intervertebral disk. (Human Phenotype Ontology, HP_0005108)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005108
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Genes

19 genes associated with the abnormality of the intervertebral disk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ANKH ANKH inorganic pyrophosphate transport regulator
ARID1A AT rich interactive domain 1A (SWI-like)
ARID1B AT rich interactive domain 1B (SWI1-like)
CHST3 carbohydrate (chondroitin 6) sulfotransferase 3
COL2A1 collagen, type II, alpha 1
DLL3 delta-like 3 (Drosophila)
HES7 hes family bHLH transcription factor 7
HGD homogentisate 1,2-dioxygenase
HOXD13 homeobox D13
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
RNU4ATAC RNA, U4atac small nuclear (U12-dependent splicing)
SHOC2 soc-2 suppressor of clear homolog (C. elegans)
SMAD3 SMAD family member 3
SMARCA4 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
SMARCB1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
SMARCE1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1
SOX11 SRY (sex determining region Y)-box 11
TRPV4 transient receptor potential cation channel, subfamily V, member 4