Human Gene SGCA (uc010wmi.2) Description and Page Index
  Description: Homo sapiens sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein) (SGCA), transcript variant 1, mRNA.
RefSeq Summary (NM_000023): This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008].
Transcript (Including UTRs)
   Position: hg19 chr17:48,243,366-48,253,293 Size: 9,928 Total Exon Count: 9 Strand: +


Page IndexSequence and LinksMalaCardsCTDRNA-Seq ExpressionMicroarray Expression
Other SpeciesmRNA DescriptionsPathwaysOther NamesModel InformationMethods
Data last updated: 2013-06-15

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr17:48,243,366-48,253,293)mRNA (may differ from genome)No protein
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
BioGPSCGAPEnsemblExonPrimerGeneNetworkH-INV
HGNCLynxPubMedStanford SOURCETreefamWikipedia

-  MalaCards Disease Associations
  MalaCards Gene Search: SGCA
Diseases sorted by gene-association score: muscular dystrophy, limb-girdle, type 2d* (1669), limb-girdle muscular dystrophy (50), autosomal recessive limb-girdle muscular dystrophy (29), muscular dystrophy (28), sarcoglycanopathies (18), autosomal recessive limb-girdle muscular dystrophy type 2f (16), muscular dystrophy, limb-girdle, type 2c (13), progressive muscular dystrophy (13), dmd-associated dilated cardiomyopathy (11), becker muscular dystrophy (10), autosomal recessive limb-girdle muscular dystrophy type 2e (10), autosomal recessive limb-girdle muscular dystrophy type 2b (10), walker-warburg syndrome (8), muscular dystrophy, limb-girdle, type 2a (8), muscular dystrophy, congenital merosin-deficient (6), subependymal glioma (5), muscle tissue disease (5), dilated cardiomyopathy (4), myopathy (4), muscle eye brain disease (4), duchenne muscular dystrophy (3), arrhythmogenic right ventricular cardiomyopathy (3), cardiomyopathy (3), muscular dystrophy, congenital (1)
* = Manually curated disease association

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 99.78 RPKM in Muscle - Skeletal
Total median expression: 574.35 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologNo orthologNo orthologNo orthologNo ortholog
      
      
      
      
      

-  Descriptions from all associated GenBank mRNAs
  AK300710 - Homo sapiens cDNA FLJ56722 complete cds, highly similar to Alpha-sarcoglycan precursor.
L46810 - Human adhalin mRNA with an R266C mutation causing a mild form of autosomal recessive limb-girdle muscular dystrophy.
L35853 - Homo sapiens adhalin-35 mRNA, complete cds.
L34355 - Homo sapiens clone p4 50 kD dystrophin-associated glycoprotein precursor mRNA, complete cds.
AK293614 - Homo sapiens cDNA FLJ50751 complete cds, highly similar to Alpha-sarcoglycan precursor.
AK290622 - Homo sapiens cDNA FLJ75653 complete cds, highly similar to Homo sapiens sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein) (SGCA), mRNA.
BC025702 - Homo sapiens sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein), mRNA (cDNA clone MGC:34551 IMAGE:5222483), complete cds.
U08895 - Human adhalin (DAG2) mRNA, complete cds.
AB464188 - Synthetic construct DNA, clone: pF1KB6524, Homo sapiens SGCA gene for sarcoglycan alpha, without stop codon, in Flexi system.
DQ893777 - Synthetic construct Homo sapiens clone IMAGE:100008237; FLH167478.01L; RZPDo839B0389D sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein) (SGCA) gene, encodes complete protein.
CU693018 - Synthetic construct Homo sapiens gateway clone IMAGE:100019192 5' read SGCA mRNA.
KJ892132 - Synthetic construct Homo sapiens clone ccsbBroadEn_01526 SGCA gene, encodes complete protein.
KR710659 - Synthetic construct Homo sapiens clone CCSBHm_00015445 SGCA (SGCA) mRNA, encodes complete protein.
KR710660 - Synthetic construct Homo sapiens clone CCSBHm_00015454 SGCA (SGCA) mRNA, encodes complete protein.
KR710661 - Synthetic construct Homo sapiens clone CCSBHm_00015475 SGCA (SGCA) mRNA, encodes complete protein.
KR710662 - Synthetic construct Homo sapiens clone CCSBHm_00015485 SGCA (SGCA) mRNA, encodes complete protein.
KU178331 - Homo sapiens sarcoglycan alpha isoform 1 (SGCA) mRNA, partial cds.
KU178332 - Homo sapiens sarcoglycan alpha isoform 2 (SGCA) mRNA, partial cds.
JD104733 - Sequence 85757 from Patent EP1572962.
JD392480 - Sequence 373504 from Patent EP1572962.
JD133975 - Sequence 114999 from Patent EP1572962.
JD174967 - Sequence 155991 from Patent EP1572962.
JD155332 - Sequence 136356 from Patent EP1572962.
JD401100 - Sequence 382124 from Patent EP1572962.
JD159310 - Sequence 140334 from Patent EP1572962.
JD108417 - Sequence 89441 from Patent EP1572962.
JD446028 - Sequence 427052 from Patent EP1572962.
JD350026 - Sequence 331050 from Patent EP1572962.

-  Biochemical and Signaling Pathways
  KEGG - Kyoto Encyclopedia of Genes and Genomes
hsa05410 - Hypertrophic cardiomyopathy (HCM)
hsa05412 - Arrhythmogenic right ventricular cardiomyopathy (ARVC)
hsa05414 - Dilated cardiomyopathy
hsa05416 - Viral myocarditis

-  Other Names for This Gene
  Alternate Gene Symbols: AK300710
UCSC ID: uc010wmi.2
RefSeq Accession: NM_000023

-  Gene Model Information
 
category: nearCoding nonsense-mediated-decay: yes RNA accession: AK300710.1
exon count: 9CDS single in 3' UTR: no RNA size: 1091
ORF size: 0CDS single in intron: no Alignment % ID: 99.82
txCdsPredict score: 1471.00frame shift in genome: no % Coverage: 99.82
has start codon: yes stop codon in genome: no # of Alignments: 1
has end codon: yes retained intron: no # AT/AC introns 0
selenocysteine: no end bleed into intron: 0# strange splices: 0
Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.