KIF13B (kinesin family member 13B)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 23303 |
| Gene name | Kinesin family member 13B |
| Gene symbol | KIF13B |
| Synonyms (NCBI Gene) |
GAKIN
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| Chromosome | 8 |
| Chromosome location | 8p12 |
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miRNA
miRNA information provided by mirtarbase database.
206
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
29
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q9NQT8 | |||||||||||||||||||||||||||||||||||
| Protein name | Kinesin-like protein KIF13B (Kinesin-like protein GAKIN) | |||||||||||||||||||||||||||||||||||
| Protein function | Involved in reorganization of the cortical cytoskeleton. Regulates axon formation by promoting the formation of extra axons. May be functionally important for the intracellular trafficking of MAGUKs and associated protein complexes. {ECO:0000269 | |||||||||||||||||||||||||||||||||||
| PDB | 2COW , 3FM8 , 3GBJ , 3MDB | |||||||||||||||||||||||||||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Ubiquitous. | |||||||||||||||||||||||||||||||||||
| Sequence |
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| Sequence length | 1826 | |||||||||||||||||||||||||||||||||||
| Interactions | View interactions | |||||||||||||||||||||||||||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
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Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
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