Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
79012
Gene name Gene Name - the full gene name approved by the HGNC.
CaM kinase like vesicle associated
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CAMKV
Synonyms (NCBI Gene) Gene synonyms aliases
1G5, VACAMKL
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3p21.31
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT051070 hsa-miR-16-5p CLASH 23622248
MIRT050386 hsa-miR-23a-3p CLASH 23622248
MIRT050087 hsa-miR-26a-5p CLASH 23622248
MIRT049929 hsa-miR-30a-5p CLASH 23622248
MIRT048955 hsa-miR-92a-3p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004672 Function Protein kinase activity IEA
GO:0004683 Function Calcium/calmodulin-dependent protein kinase activity IBA
GO:0005516 Function Calmodulin binding IBA
GO:0005516 Function Calmodulin binding IEA
GO:0005524 Function ATP binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614993 28788 ENSG00000164076
Protein
UniProt ID Q8NCB2
Protein name CaM kinase-like vesicle-associated protein
Protein function Does not appear to have detectable kinase activity.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 24 286 Protein kinase domain Domain
Sequence
MPFGCVTLGDKKNYNQPSEVTDRYDLGQVIKTEEFCEIFRAKDKTTGKLHTCKKFQKRDG
RKVRKAAKNEIGILKMVKHPNILQLVDVFVTRKEYFIFLELATGREVFDWILDQGYYSER
DTSNVVRQVLEAVAYLHSLKIVHRNLKLENLVYYNRLKNSKIVISDFHLAKLENGLIKEP
CGTPEYLAPEVVGRQRYGRPVDCWAIGVIMYILLSGNPPFYEEVEEDDYENHDKNLFRKI
LAGDYEFDSPYWDDISQAAKDLVTRLMEVEQDQRITAEEAISHEWI
SGNAASDKNIKDGV
CAQIEKNFARAKWKKAVRVTTLMKRLRAPEQSSTAAAQSASATDTATPGAAGGATAAAAS
GATSAPEGDAARAAKSDNVAPADRSATPATDGSATPATDGSVTPATDGSITPATDGSVTP
ATDRSATPATDGRATPATEESTVPTTQSSAMLATKAAATPEPAMAQPDSTAPEGATGQAP
PSSKGEEAAGYAQESQREEAS
Sequence length 501
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Inflammatory Bowel Disease Inflammatory bowel disease (MTAG) N/A N/A GWAS