Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: Shc1 ENSRNOG00000020657

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Description

SHC adaptor protein 1 [Source:RGD Symbol;Acc:620446]

Gene Synonyms

P66shc

Location

Primary_assembly 2: 177,135,659-177,147,914 forward strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 199 orthologues, 4 paralogues and is associated with 18 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000028038.8	Shc1-201	3543	579aa	ENSRNOP00000028038.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6J6G1 G3V8S2	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, 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,
ENSRNOT00000056652.6	Shc1-202	1584	457aa	ENSRNOP00000053490.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LN14	-

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Summary

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