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TAGLN (transgelin)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6876
Gene nameGene Name - the full gene name approved by the HGNC.
Transgelin
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
TAGLN
SynonymsGene synonyms aliases
SM22, SM22-alpha, SMCC, TAGLN1, TGLN, WS3-10
ChromosomeChromosome number
11
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
11q23.3
SummarySummary of gene provided in NCBI Entrez Gene.
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 enc
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT021406 hsa-miR-9-5p Microarray 17612493
MIRT022018 hsa-miR-128-3p Microarray 17612493
MIRT023899 hsa-miR-1-3p Other 20458751
MIRT025891 hsa-miR-7-5p Microarray 17612493
MIRT030313 hsa-miR-26b-5p Microarray 19088304
Transcription factors
Transcription factor Regulation Reference
KLF4 Unknown 19486889
MKL1 Activation 14970199
SRF Activation 14970199
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21044950, 22245152, 32296183
GO:0005737 Component Cytoplasm IEA
GO:0007517 Process Muscle organ development TAS 9615232
GO:0030855 Process Epithelial cell differentiation IDA 21492153
GO:0051015 Function Actin filament binding IEA
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
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
Sequence
Sequence length 201
Interactions View interactions
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Breast carcinoma Breast Carcinoma rs80359671, rs11540652, rs28934575, rs28897672, rs137886232, rs193922376, rs80357783, rs80359306, rs80359405, rs80359507, rs80359598, rs80358429, rs397507683, rs397515636, rs80359451, rs397507859, rs80359709, rs80359742, rs80359205, rs80357627, rs80357004, rs80357571, rs80357767, rs80357653, rs80358086, rs80357608, rs28897696, rs41293465, rs146650273, rs63751017, rs63750617, rs63750726, rs63750199, rs63749848, rs398122618, rs398122653, rs397509211, rs80357791, rs121912666, rs587778541, rs121908698, rs536907995, rs587781302, rs140342925, rs587781506, rs587782652, rs587782849, rs587783057, rs10520699, rs11852999, rs139770721, rs374950566, rs786202800, rs863224451, rs377153250, rs747727055, rs876658804, rs780001540, rs760815829, rs878854926, rs775248597, rs886040658, rs886040192, rs786203523, rs886040319, rs397508006, rs587782011, rs1060502772, rs1555461727, rs1553333072, rs1114167702, rs1257401983, rs886040950, rs1060502759, rs774684620, rs142947311, rs1555580883, rs748513310, rs376170600, rs863224499, rs1593909229, rs748453607, rs1294578913, rs1574737047, rs1593909960, rs2081922847, rs2082559544, rs2053694038 29059430
Colonic neoplasms Malignant tumor of colon, Colonic Neoplasms rs267607789, rs774277300, rs781222233, rs1060502734, rs1060503333, rs1339238483 15059925
Esophagus neoplasm Squamous cell carcinoma of esophagus rs28934578, rs121918714, rs1567556006, rs1575166666 21517111
Unknown
Disease name Disease term dbSNP ID References
Endometrioma Endometrioma 21063030
Endometriosis Endometriosis rs1800629, rs1143634 21063030
Lipoidosis Lipoidosis 17175557, 15342952, 16919414
Malignant neoplasm Malignant Childhood Neoplasm 29059430

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