Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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5357 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Plastin 1 |
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
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PLS1 |
SynonymsGene synonyms aliases
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DFNA76 |
ChromosomeChromosome number
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3 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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3q23 |
SummarySummary of gene provided in NCBI Entrez Gene.
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Plastins are a family of actin-binding proteins that are conserved throughout eukaryote evolution and expressed in most tissues of higher eukaryotes. In humans, two ubiquitous plastin isoforms (L and T) have been identified. The protein encoded by this ge |
SNPsSNP information provided by dbSNP.
|
SNP ID |
Visualize variation |
Clinical significance |
Consequence |
rs1560070780 |
C>T |
Pathogenic, uncertain-significance |
Missense variant, coding sequence variant |
rs1577876794 |
T>C |
Likely-pathogenic, pathogenic |
Missense variant, coding sequence variant |
rs1577888561 |
T>G |
Uncertain-significance, pathogenic |
Missense variant, coding sequence variant |
rs1577888985 |
G>A |
Uncertain-significance, pathogenic |
Missense variant, coding sequence variant |
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miRNAmiRNA 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 IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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Protein
|
UniProt ID |
Q14651 |
Protein name |
Plastin-1 (Intestine-specific plastin) (I-plastin) |
Protein function |
Actin-bundling protein. In the inner ear, it is required for stereocilia formation. Mediates liquid packing of actin filaments that is necessary for stereocilia to grow to their proper dimensions. |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF13833 |
EF-hand_8 |
3 → 43 |
EF-hand domain pair |
Domain |
PF00036 |
EF-hand_1 |
55 → 83 |
EF hand |
Domain |
PF00307 |
CH |
122 → 239 |
Calponin homology (CH) domain |
Domain |
PF00307 |
CH |
266 → 377 |
Calponin homology (CH) domain |
Domain |
PF00307 |
CH |
395 → 505 |
Calponin homology (CH) domain |
Domain |
PF00307 |
CH |
516 → 626 |
Calponin homology (CH) domain |
Domain |
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Sequence |
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Sequence length |
629 |
Interactions |
View interactions |
Associated diseases
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Unknown |
Disease name |
Disease term |
dbSNP ID |
References |
Liver neoplasms |
Liver neoplasms |
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17114358 |
Liver cancer |
Malignant neoplasm of liver |
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17114358 |
Non-syndromic sensorineural deafness |
Autosomal dominant non-syndromic sensorineural deafness type DFNA |
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