Gene
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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6876 |
Gene nameGene Name - the full gene name approved by the HGNC.
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Transgelin |
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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TAGLN |
SynonymsGene synonyms aliases
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SM22, SM22-alpha, SMCC, TAGLN1, WS3-10 |
ChromosomeChromosome number
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11 |
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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11q23.3 |
SummarySummary of gene provided in NCBI Entrez Gene.
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This gene encodes a shape change and transformation sensitive actin-binding protein which belongs to the calponin family. It is ubiquitously expressed in vascular and visceral smooth muscle, and is an early marker of smooth muscle differentiation. The encoded protein is thought to be involved in calcium-independent smooth muscle contraction. It acts as a tumor suppressor, and the loss of its expression is an early event in cell transformation and the development of some tumors, coinciding with cellular plasticity. The encoded protein has a domain architecture consisting of an N-terminal calponin homology (CH) domain and a C-terminal calponin-like (CLIK) domain. Mice with a knockout of the orthologous gene are viable and fertile but their vascular smooth muscle cells exhibit alterations in the distribution of the actin filament and changes in cytoskeletal organization. [provided by RefSeq, Aug 2017] |
miRNAmiRNA information provided by mirtarbase database.
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Transcription factors
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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
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UniProt ID |
Q01995 |
Protein name |
Transgelin (22 kDa actin-binding protein) (Protein WS3-10) (Smooth muscle protein 22-alpha) (SM22-alpha) |
Protein function |
Actin cross-linking/gelling protein (By similarity). Involved in calcium interactions and contractile properties of the cell that may contribute to replicative senescence. |
Family and domains |
Pfam
Accession |
ID |
Position in sequence |
Description |
Type |
PF00307 |
CH |
24 → 139 |
Calponin homology (CH) domain |
Domain |
PF00402 |
Calponin |
175 → 199 |
Calponin family repeat |
Repeat |
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Sequence |
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Sequence length |
201 |
Interactions |
View interactions |
Associated diseases
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Disease name |
Disease term |
References |
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Breast Carcinoma |
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Malignant tumor of colon |
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Colonic Neoplasms |
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Endometrioma |
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Endometriosis |
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Squamous cell carcinoma of esophagus |
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Lipoidosis |
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Malignant Childhood Neoplasm |
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