Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
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: Cd302 ENSRNOG00000006623

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Description

CD302 molecule [Source:RGD Symbol;Acc:1307606]

Gene Synonyms

LOC295629, MGC108799, RGD1307606

Location

Primary_assembly 3: 65,113,102-65,164,737 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 4 transcripts (splice variants), 191 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000112941.2	Cd302-203	1907	243aa	ENSRNOP00000082148.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZVX3	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,
ENSRNOT00000008987.7	Cd302-201	1210	228aa	ENSRNOP00000008987.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LQ10 Q5FVR3	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,
ENSRNOT00000106977.2	Cd302-202	1053	219aa	ENSRNOP00000077037.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y5U8	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,
ENSRNOT00000115034.2	Cd302-204	995	235aa	ENSRNOP00000097098.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ARA5	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,

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Summary

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