Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Sgcb ENSRNOG00000002135

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Description

sarcoglycan, beta [Source:RGD Symbol;Acc:1594202]

Gene Synonyms

LOC680229

Location

Primary_assembly 14: 34,912,628-34,933,666 forward strand.

GRCr8:CM070404.1

About this gene

This gene has 5 transcripts (splice variants), 199 orthologues and is associated with 9 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000153322.1	Sgcb-205	5082	381aa	ENSRNOP00000098808.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical,
ENSRNOT00000141847.1	Sgcb-204	5201	308aa	ENSRNOP00000112646.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000089094.3	Sgcb-202	5001	354aa	ENSRNOP00000072001.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K1V7	-
ENSRNOT00000002921.7	Sgcb-201	4863	308aa	ENSRNOP00000002921.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4A5E5	-
ENSRNOT00000126831.1	Sgcb-203	1371	297aa	ENSRNOP00000101889.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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