Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
282973
Gene name Gene Name - the full gene name approved by the HGNC.
Janus kinase and microtubule interacting protein 3
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
JAKMIP3
Synonyms (NCBI Gene) Gene synonyms aliases
C10orf14, C10orf39, Jamip3, NECC2, bA140A10.5
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q26.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017302 hsa-miR-335-5p Microarray 18185580
MIRT611605 hsa-miR-8485 HITS-CLIP 19536157
MIRT611604 hsa-miR-329-3p HITS-CLIP 19536157
MIRT611603 hsa-miR-362-3p HITS-CLIP 19536157
MIRT611602 hsa-miR-1228-3p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005794 Component Golgi apparatus IEA
GO:0008017 Function Microtubule binding IEA
GO:0019900 Function Kinase binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611198 23523 ENSG00000188385
Protein
UniProt ID Q5VZ66
Protein name Janus kinase and microtubule-interacting protein 3 (Neuroendocrine long coiled-coil protein 2)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF16034 JAKMIP_CC3 429 626 JAKMIP CC3 domain Coiled-coil
Tissue specificity TISSUE SPECIFICITY: Specifically expressed in the CNS and endocrine tissues. Also detected in other tissues including heart, testis and prostate. {ECO:0000269|PubMed:17572408}.
Sequence
MSKRGMSSRAKGDKAEALAALQAANEDLRAKLTDIQIELQQEKSKVSKVEREKNQELRQV
REHEQHKTAVLLTELKTKLHEEKMKELQAVRETLLRQHEAELLRVIKIKDNENQRLQALL
SALRDGGPEKVKTVLLSEAKEEAKKGFEVEKVKMQQEISELKGAKRQVEEALTLVIQADK
IKAAEIRSVYHLHQEEITRIKKECEREIRRLMEEIKFKDRAVFVLERELGVQAGHAQRLQ
LQKEALDEQLSQVREADRHPGSPRRELPHAAGAGDASDHSGSPEQQLDEKDARRFQLKIA
ELSAIIRKLEDRNALLSEERNELLKRVREAESQYKPLLDKNKRLSRKNEDLSHALRRMEN
KLKFVTQENIEMRQRAGIIRRPSSLNDLDQSQDEREVDFLKLQIVEQQNLIDELSKTLET
AGYVKSVLERDKLLRFRKQRKKMAKLPKPVVVETFFGYDEEASLESDGSSVSYQTDRTDQ
TPCTPDDDLEEGMAKEETELRFRQLTMEYQALQRAYALLQEQVGGTLDAEREVKTREQLQ
AEVQRAQARIEDLEKALAEQGQDMKWIEEKQALYRRNQELVEKIKQMETEEARLRHEVQD
ARDQNELLEFRILELEERERKSPAIS
FHHTPFVDGKSPLQVYCEAEGVTDIVVAELMKKL
DILGDNANLTNEEQVVVIQARTVLTLAEKWLQQIEETEAALQRKMVDLESEKELFSKQKG
YLDEELDYRKQALDQANKHILELEAMLYDALQQEAGAKVAELLSEEEREKLKVAVEQWKR
QVMSELRERDAQILRERMELLQLAQQRIKELEERIEAQKRQIKELEEKFLFLFLFFSLAF
ILWS
Sequence length 844
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
Glioblastoma Glioblastoma N/A N/A GWAS
Metabolic Syndrome Metabolic syndrome N/A N/A GWAS