Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
Ontologies
- GO: Anatomical entity
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: Sntg1 ENSRNOG00000007294

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Description

syntrophin, gamma 1 [Source:RGD Symbol;Acc:1560290]

Gene Synonyms

LOC102556371, LOC500394, RGD1560290

Location

Primary_assembly 5: 15,046,102-15,583,468 forward strand.

GRCr8:CM070395.1

About this gene

This gene has 3 transcripts (splice variants), 205 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000009679.9	Sntg1-201	2327	505aa	ENSRNOP00000009679.9	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M2M1	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,
ENSRNOT00000095256.2	Sntg1-202	5396	470aa	ENSRNOP00000081625.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZSX2	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,
ENSRNOT00000153454.1	Sntg1-203	5393	473aa	ENSRNOP00000103582.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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