• THAT   AND
  • THAT   AND


Sequence in raw or FASTA format:

Database:

Blast Method:

 
 


SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein) [Homo sapiens (human)]


Clone ID RefSeq Accession Definition Vector Stock Status *Turnaround time Price Order
OHu26253 NM_000231 Homo sapiens sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein) (SGCG), mRNA. pcDNA3.1+-DYK On-demand 7-9 $159.00
OHu47253 XM_006719861 PREDICTED: Homo sapiens sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein) (SGCG), transcript variant X2, mRNA. pcDNA3.1+-DYK On-demand 7-9 $159.00
OHu47254 XM_005266505 PREDICTED: Homo sapiens sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein) (SGCG), transcript variant X1, mRNA. pcDNA3.1+-DYK On-demand 7-9 $159.00
OHu26253C NM_000231 Homo sapiens sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein) (SGCG), mRNA. Customized vector On-demand 7-9 $209.00
OHu47253C XM_006719861 PREDICTED: Homo sapiens sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein) (SGCG), transcript variant X2, mRNA. Customized vector On-demand 7-9 $209.00
OHu47254C XM_005266505 PREDICTED: Homo sapiens sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein) (SGCG), transcript variant X1, mRNA. Customized vector On-demand 7-9 $209.00

*Business Day

Related Services

Gene Symbol SGCG
Entrez Gene ID 6445
Full Name sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
Synonyms A4, DAGA4, DMDA, DMDA1, LGMD2C, MAM, SCARMD2, SCG3, TYPE
General protein information
Preferred Names
gamma-sarcoglycan
Names
gamma-sarcoglycan
35DAG
gamma-SG
gamma sarcoglycan
35kD dystrophin-associated glycoprotein
35 kDa dystrophin-associated glycoprotein
Gene Type protein-coding
Organism Homo sapiens (human)
Genome

13

13q12

Summary This gene encodes gamma-sarcoglycan, one of several sarcolemmal transmembrane glycoproteins that interact with dystrophin. The dystrophin-glycoprotein complex (DGC) spans the sarcolemma and is comprised of dystrophin, syntrophin, alpha- and beta-dystroglycans and sarcoglycans. The DGC provides a structural link between the subsarcolemmal cytoskeleton and the extracellular matrix of muscle cells. Defects in the encoded protein can lead to early onset autosomal recessive muscular dystrophy, in particular limb-girdle muscular dystrophy, type 2C (LGMD2C). [provided by RefSeq, Oct 2008].
Disorder

MIM: 608896

Muscular dystrophy, limb-girdle, type 2C, 253700 (3)

mRNA Protein Product Sequence Price Select
NM_000231, 209529740 NP_000222, 4557847 gamma-sarcoglycan ORF Sequence $300.00
XM_005266505, 530402603 XP_005266562, 530402604 gamma-sarcoglycan isoform X1 ORF Sequence $300.00
XM_006719861, 578824991 XP_006719924, 578824992 gamma-sarcoglycan isoform X2 ORF Sequence $300.00
KEGG
hsa05416Viral myocarditis
hsa05412Arrhythmogenic right ventricular cardiomyopathy (ARVC)
hsa05414Dilated cardiomyopathy
hsa05410Hypertrophic cardiomyopathy (HCM)
WikiPathways
WP2118Arrhythmogenic right ventricular cardiomyopathy
Homo sapiens (human)SGCGNP_000222.1
Pan troglodytes (chimpanzee)SGCGXP_001151216.1
Macaca mulatta (Rhesus monkey)LOC721411XP_001117551.2
Canis lupus familiaris (dog)SGCGNP_001014298.1
Bos taurus (cattle)SGCGNP_001068712.1
Mus musculus (house mouse)SgcgNP_036022.1
Rattus norvegicus (Norway rat)SgcgNP_001006994.1
Gallus gallus (chicken)SGCGXP_417139.2
Danio rerio (zebrafish)sgcgNP_001003748.1
Danio rerio (zebrafish)LOC100538014XP_003200060.1
Xenopus (Silurana) tropicalis (western clawed frog)sgcgNP_001072908.1
Process
IDNameEvidence
GO:0007517muscle organ developmentTAS
Component
IDNameEvidence
GO:0005737cytoplasmIEA
GO:0005856cytoskeletonIEA
GO:0005886plasma membraneTAS
GO:0016012sarcoglycan complexIEA
GO:0016021integral component of membraneIEA
GO:0042383sarcolemmaIEA
Function
IDNameEvidence
GO:0005515protein bindingIPI
GeneCards SGCG
UniProt Q13326
Vega OTTHUMG00000016563
MIM 608896
Ensembl ENSG00000102683
HGNC 10809
HPRD 07039

GeneRIFs: Gene References Into Functions What's a GeneRIF?

Interactant

Our customer service representatives are available 24 hours a day, Monday through Friday; please contact us anytime for assistance.