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

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Gene: SIRPA ENSBTAG00000007213

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Description

signal regulatory protein alpha [Source:NCBI gene (formerly Entrezgene);Acc:327666]

Gene Synonyms

MYD-1, PTPNS1

Location

Primary_assembly 13: 53,196,957-53,240,062 reverse strand.

ARS-UCD2.0:CM008180.2

About this gene

This gene has 5 transcripts (splice variants), 373 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000072837.2	SIRPA-205	2959	640aa	ENSBTAP00000064731.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M4J0	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000038306.4	SIRPA-201	3130	251aa	ENSBTAP00000038121.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6QPC6	-
ENSBTAT00000131575.1	SIRPA-203	2697	483aa	ENSBTAP00000079745.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SBY5	-
ENSBTAT00000009488.7	SIRPA-202	2667	510aa	ENSBTAP00000009488.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3X6M9	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSBTAT00000076193.2	SIRPA-204	2425	498aa	ENSBTAP00000057822.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LRX3	-

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Summary

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