Gene Gene information from NCBI Gene database.
Entrez ID 80333
Gene name Potassium voltage-gated channel interacting protein 4
Gene symbol KCNIP4
Synonyms (NCBI Gene)
CALPKCHIP4
Chromosome 4
Chromosome location 4p15.31-p15.2
Summary This gene encodes a member of the family of voltage-gated potassium (Kv) channel-interacting proteins (KCNIPs), which belong to the recoverin branch of the EF-hand superfamily. Members of the KCNIP family are small calcium binding proteins. They all have
miRNA miRNA information provided by mirtarbase database.
16
miRTarBase ID miRNA Experiments Reference
MIRT1081167 hsa-miR-4477a CLIP-seq
MIRT1081168 hsa-miR-4503 CLIP-seq
MIRT1081169 hsa-miR-4668-3p CLIP-seq
MIRT1081170 hsa-miR-4698 CLIP-seq
MIRT1081171 hsa-miR-548aa CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
33
GO ID Ontology Definition Evidence Reference
GO:0005267 Function Potassium channel activity IEA
GO:0005509 Function Calcium ion binding IBA
GO:0005509 Function Calcium ion binding IDA 11847232
GO:0005509 Function Calcium ion binding IEA
GO:0005515 Function Protein binding IPI 26871637, 32296183
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608182 30083 ENSG00000185774
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6PIL6
Protein name Kv channel-interacting protein 4 (KChIP4) (A-type potassium channel modulatory protein 4) (Calsenilin-like protein) (Potassium channel-interacting protein 4)
Protein function Regulatory subunit of Kv4/D (Shal)-type voltage-gated rapidly inactivating A-type potassium channels. Modulates KCND2 channel density, inactivation kinetics and rate of recovery from inactivation in a calcium-dependent and isoform-specific manne
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13833 EF-hand_8 99 152 EF-hand domain pair Domain
PF13499 EF-hand_7 158 234 EF-hand domain pair Domain
PF13202 EF-hand_5 209 233 EF hand Domain
Tissue specificity TISSUE SPECIFICITY: Predominantly expressed in brain. {ECO:0000269|PubMed:11847232}.
Sequence
MNVRRVESISAQLEEASSTGGFLYAQNSTKRSIKERLMKLLPCSAAKTSSPAIQNSVEDE
LEMATVRHRPEALELLEAQSKFTKKELQILYRGFKNECPSGVVNEETFKEIYSQFFPQGD
STTYAHFLFNAFDTDHNGAVSFEDFIKGLSIL
LRGTVQEKLNWAFNLYDINKDGYITKEE
MLDIMKAIYDMMGKCTYPVLKEDAPRQH
VETFFQKMDKNKDGVVTIDEFIESCQKDENIM
RSMQLFENVI
Sequence length 250
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Phase 1 - inactivation of fast Na+ channels
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
3
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
KCNIP4-related disorder Benign rs2322688, rs3765122, rs3765121 RCV003979608
RCV003982094
RCV003982096
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Associate 21624954, 40631452
Arrhythmias Cardiac Associate 28575239
Cough Associate 26169577
Dementia Associate 36421848
Lung Neoplasms Associate 25644374
Pancreatic Neoplasms Associate 24419231
Pyruvate Carboxylase Deficiency Disease Associate 34593906
Renal Insufficiency Chronic Associate 34593906