Abnormality Of The Intervertebral Disk Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An abnormality of the intervertebral disk. (Human Phenotype Ontology, HP_0005108)
External Link https://www.disgenet.org/browser/0/1/0/C4025249
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Genes

29 genes associated with the disease Abnormality Of The Intervertebral Disk in GWAS and other genetic association datasets from the DisGeNET 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)
ARID2 AT rich interactive domain 2 (ARID, RFX-like)
DLL3 delta-like 3 (Drosophila)
DPF2 D4, zinc and double PHD fingers family 2
HES7 hes family bHLH transcription factor 7
HOXD13 homeobox D13
LAGE3 L antigen family, member 3
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
NUP107 nucleoporin 107kDa
NUP133 nucleoporin 133kDa
OSGEP O-sialoglycoprotein endopeptidase
PPP1CB protein phosphatase 1, catalytic subunit, beta isozyme
RIPPLY2 ripply transcriptional repressor 2
SHOC2 soc-2 suppressor of clear homolog (C. elegans)
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
SMARCC2 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2
SMARCE1 SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1
SOX11 SRY (sex determining region Y)-box 11
SOX4 SRY (sex determining region Y)-box 4
TP53RK TP53 regulating kinase
TPRKB TP53RK binding protein
TRPV4 transient receptor potential cation channel, subfamily V, member 4
WDR4 WD repeat domain 4
WDR73 WD repeat domain 73
XYLT2 xylosyltransferase II