FAM171A1 (family with sequence similarity 171 member A1)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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221061 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Family with sequence similarity 171 member A1 |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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FAM171A1 |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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APCN, C10orf38 |
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Chromosome
Chromosome number
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10 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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10p13 |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene ontology information of associated ontologies with gene provided by GO database.
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Other IDs
Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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| Protein | |||||||||||
| UniProt ID | Q5VUB5 | ||||||||||
| Protein name | Protein FAM171A1 (Astroprincin) (APCN) | ||||||||||
| Protein function | Involved in the regulation of the cytoskeletal dynamics, plays a role in actin stress fiber formation. | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Expressed in heart, brain, liver, skeletal muscle, kidney and pancreas (PubMed:30312582). In brain, expressed by glia, pyramidal neurons and astrocytes (at protein level) (PubMed:30312582). Highly expressed in placental trophoblasts (P | ||||||||||
| Sequence |
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| Sequence length | 890 | ||||||||||
| 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)
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