Urgency Of Micturition Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0085606
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Genes

38 genes associated with the disease Urgency Of Micturition in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCD1 ATP-binding cassette, sub-family D (ALD), member 1
ADAMTS16 ADAM metallopeptidase with thrombospondin type 1 motif, 16
ADH1C alcohol dehydrogenase 1C (class I), gamma polypeptide
ALDH18A1 aldehyde dehydrogenase 18 family, member A1
ATL1 atlastin GTPase 1
ATXN10 ataxin 10
ATXN2 ataxin 2
CACNA1G calcium channel, voltage-dependent, T type, alpha 1G subunit
CIT citron rho-interacting serine/threonine kinase
COQ2 coenzyme Q2 4-hydroxybenzoate polyprenyltransferase
CPT1C carnitine palmitoyltransferase 1C
DDX4 DEAD (Asp-Glu-Ala-Asp) box polypeptide 4
FA2H fatty acid 2-hydroxylase
GBA glucosidase, beta, acid
GLUD2 glutamate dehydrogenase 2
HSPD1 heat shock 60kDa protein 1 (chaperonin)
INHBA inhibin, beta A
KCNC3 potassium channel, voltage gated Shaw related subfamily C, member 3
KIF5A kinesin family member 5A
LMNB1 lamin B1
LRIG2 leucine-rich repeats and immunoglobulin-like domains 2
MAPT microtubule-associated protein tau
MARS2 methionyl-tRNA synthetase 2, mitochondrial
NIPA1 non imprinted in Prader-Willi/Angelman syndrome 1
NR4A2 nuclear receptor subfamily 4, group A, member 2
PINK1 PTEN induced putative kinase 1
RTN2 reticulon 2
SACS sacsin molecular chaperone
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SNCAIP synuclein, alpha interacting protein
SPAST spastin
SPG11 spastic paraplegia 11 (autosomal recessive)
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
TBP TATA box binding protein
TRPV4 transient receptor potential cation channel, subfamily V, member 4
WASHC5 WASH complex subunit 5
ZFYVE26 zinc finger, FYVE domain containing 26
ZNF521 zinc finger protein 521