ACTG1

GENERAL INFORMATION

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Gene name

ACTG1

Gene description

Actin, gamma 1

Protein class

Cytoskeleton related proteins
Disease related genes
Plasma proteins
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

10
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Cytoplasmic expression of myoepithelial cells.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data. Caution, targets protein from more than one gene. Antibody staining in cells/structures not annotated, view images.

Data reliability

Uncertain based on 2 antibodies.
HPA041264 , HPA041271
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Pancreas

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

ACTG1 (HGNC Symbol)

Synonyms

ACTG, DFNA20, DFNA26

Description

Actin, gamma 1 (HGNC Symbol)

Entrez gene summary

Actins are highly conserved proteins that are involved in various types of cell motility, and maintenance of the cytoskeleton. In vertebrates, three main groups of actin isoforms, alpha, beta and gamma have been identified. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. The beta and gamma actins co-exist in most cell types as components of the cytoskeleton, and as mediators of internal cell motility. Actin, gamma 1, encoded by this gene, is a cytoplasmic actin found in non-muscle cells. Mutations in this gene are associated with DFNA20/26, a subtype of autosomal dominant non-syndromic sensorineural progressive hearing loss. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2011]

Chromosome

17

Cytoband

q25.3

Chromosome location (bp)

81509971 - 81523847

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000184009 (version 78.38)

Entrez gene

71

UniProt

P63261 (UniProt - Evidence at protein level)

neXtProt

NX_P63261

Antibodypedia

ACTG1 antibodies


PROTEIN BROWSER

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ENST00000331925
 
ENST00000570382
 
ENST00000571691
 
ENST00000571721
 
ENST00000573283
 
ENST00000575087
 
ENST00000575659
 
ENST00000575842
 
ENST00000575994
 
ENST00000615544
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

ACTG1-001 ENSP00000331514
ENST00000331925
P63261
Show all »
Show » Show » 375 41.8 No 0
ACTG1-002 ENSP00000459124
ENST00000575087
P63261
Show all »
Show » Show » 375 41.8 No 0
ACTG1-003 ENSP00000458435
ENST00000573283
P63261
Show all »
Show » Show » 375 41.8 No 0
ACTG1-010 ENSP00000459119
ENST00000575659
I3L1U9
Show all »
Show » 214 23.8 No 0
ACTG1-011 ENSP00000460464
ENST00000575994
I3L1U9
Show all »
Show » 214 23.8 No 0
ACTG1-012 ENSP00000458162
ENST00000575842
P63261
Show all »
Show » Show » 375 41.8 No 0
ACTG1-013 ENSP00000460660
ENST00000571721
I3L3R2
Show all »
Show » 164 18 No 0
ACTG1-014 ENSP00000466346
ENST00000570382
K7EM38
Show all »
Show » 133 14.5 No 0
ACTG1-017 ENSP00000461407
ENST00000571691
I3L4N8
Show all »
Show » 242 26.9 No 0
ACTG1-201 ENSP00000477968
ENST00000615544
P63261
Show all »
Show » Show » 375 41.8 No 0