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

Configure this page

Share this page

Bookmark this page

.

Gene: Cd47 ENSRNOG00000001964

.

Description

Cd47 molecule [Source:RGD Symbol;Acc:2308]

Gene Synonyms

IAP, Itgp, MGC93490

Location

Primary_assembly 11: 64,377,926-64,438,272 reverse strand.

GRCr8:CM070401.1

About this gene

This gene has 7 transcripts (splice variants), 123 orthologues, 1 paralogue and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000078434.3	Cd47-203	1379	348aa	ENSRNOP00000071430.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2R5X3	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,
ENSRNOT00000163230.1	Cd47-206	2074	324aa	ENSRNOP00000101878.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000168684.1	Cd47-207	1927	303aa	ENSRNOP00000100420.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IQT9 P97829	-
ENSRNOT00000143411.1	Cd47-205	1819	267aa	ENSRNOP00000098805.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000078221.3	Cd47-202	1444	342aa	ENSRNOP00000068714.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2JTH4	-
ENSRNOT00000050142.7	Cd47-201	1140	307aa	ENSRNOP00000050938.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2QRJ3	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,
ENSRNOT00000098840.2	Cd47-204	1031	299aa	ENSRNOP00000082971.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6G871 A6IQU2	-

.

Summary

.

.