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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SSRP1 ENSG00000149136

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Description

structure specific recognition protein 1 [Source:HGNC Symbol;Acc:11327]

Gene Synonyms

FACT, FACT80, T160

Location

Chromosome 11: 57,093,459-57,103,351 reverse strand.

GRCh37:CM000673.1

About this gene

This gene has 4 transcripts (splice variants) and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000278412.2	SSRP1-001	2819	709aa	ENSP00000278412.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS7952	E9PMD4 E9PPZ7 Q08945	NM_003146.2	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000526696.1	SSRP1-004	1007	192aa	ENSP00000431154.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E9PMD4 E9PPZ7	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000529002.1	SSRP1-003	844	154aa	ENSP00000434546.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		E9PPZ7	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,
ENST00000293880.5	SSRP1-002	6296	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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