KCNIP1 (potassium voltage-gated channel interacting protein 1)

2014-08-01  

Identity

HGNC
LOCATION
5q35.1
LOCUSID
ALIAS
KCHIP1,VABP
FUSION GENES

Other Information

Locus ID:

NCBI: 30820
MIM: 604660
HGNC: 15521
Ensembl: ENSG00000182132

Variants:

dbSNP: 30820
ClinVar: 30820
TCGA: ENSG00000182132
COSMIC: KCNIP1

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000182132ENST00000328939Q9NZI2
ENSG00000182132ENST00000377360Q9NZI2
ENSG00000182132ENST00000390656A0A0A0MS16
ENSG00000182132ENST00000411494Q9NZI2
ENSG00000182132ENST00000434108Q9NZI2
ENSG00000182132ENST00000517344E5RJY5
ENSG00000182132ENST00000520740Q9NZI2
ENSG00000182132ENST00000616807A0A087WTU8
ENSG00000182132ENST00000636734A0A1B0GTZ7

Expression (GTEx)

0
5
10
15
20
25
30

Pathways

PathwaySourceExternal ID
Muscle contractionREACTOMER-HSA-397014
Cardiac conductionREACTOMER-HSA-5576891
Phase 1 - inactivation of fast Na+ channelsREACTOMER-HSA-5576894

Protein levels (Protein atlas)

Not detected
Low
Medium
High

PharmGKB

Entity IDNameTypeEvidenceAssociationPKPDPMIDs
PA443796Coronary Artery DiseaseDiseaseClinicalAnnotationassociatedPD17700361
PA444552HypertensionDiseaseClinicalAnnotationassociatedPD17700361, 18496125, 18854753
PA451868verapamilChemicalClinicalAnnotationassociatedPD17700361, 18496125, 18854753

References

Pubmed IDYearTitleCitations
294912242018Divergent patterns of genic copy number variation in KCNIP1 gene reveal risk locus of type 2 diabetes in Chinese population.1
294912242018Divergent patterns of genic copy number variation in KCNIP1 gene reveal risk locus of type 2 diabetes in Chinese population.1
281328112017The ER-Mitochondria Tethering Complex VAPB-PTPIP51 Regulates Autophagy.200
291767902017Attention-deficit/hyperactivity disorder associated with KChIP1 rs1541665 in Kv channels accessory proteins.3
281328112017The ER-Mitochondria Tethering Complex VAPB-PTPIP51 Regulates Autophagy.200
291767902017Attention-deficit/hyperactivity disorder associated with KChIP1 rs1541665 in Kv channels accessory proteins.3
268313682016Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation.23
268313682016Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation.23
246814032014Protein aggregation due to nsSNP resulting in P56S VABP protein is associated with amyotrophic lateral sclerosis.7
247923782014First evidence of pathogenicity of V234I mutation of hVAPB found in Amyotrophic Lateral Sclerosis.11
248869042014Genome-wide copy number variation study reveals KCNIP1 as a modulator of insulin secretion.2
246814032014Protein aggregation due to nsSNP resulting in P56S VABP protein is associated with amyotrophic lateral sclerosis.7
247923782014First evidence of pathogenicity of V234I mutation of hVAPB found in Amyotrophic Lateral Sclerosis.11
248869042014Genome-wide copy number variation study reveals KCNIP1 as a modulator of insulin secretion.2
211294482011KChIP1 modulation of Kv4.3-mediated A-type K(+) currents and repetitive firing in hippocampal interneurons.14

Citation

Dessen P

KCNIP1 (potassium voltage-gated channel interacting protein 1)

Atlas Genet Cytogenet Oncol Haematol. 2014-08-01

Online version: http://atlasgeneticsoncology.org/gene/54392/gene-fusions-explorer/meetings/teaching-explorer/