Description

complement receptor 2 [Source:MGI Symbol;Acc:MGI:88489]

INSDC coordinates

chromosome:GRCm38:CM000994.2:195136811:195176716:1

About this gene

This gene has 11 transcripts (splice variants), 49 orthologues, 13 paralogues and is a member of 3 Ensembl protein families.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
Cr2-202ENSMUST0000008232162071032aaENSMUSP00000080938
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS15642Q9DC83 NM_007758
NP_031784
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P2

PRINCIPAL2 - APPRIS candidate principal isoform (CCDS).

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Cr2-002ENSMUST0000019512062121026aaENSMUSP00000141538
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-A0A0A6YWG3 -GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS ALT2

ALTERNATIVE2 - APPRIS candidate principal isoform that appears to be conserved in fewer than three tested non-primate species.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Cr2-201ENSMUST000000431041044347aaENSMUSP00000044261
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-E9Q3S5 -TSL:5

Transcript Support Level 5, for transcripts that are not supported at all by either an mRNA or an EST.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
Cr2-009ENSMUST0000019343635562aaENSMUSP00000142147
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-A0A0A6YXU7 -CDS 5' incomplete5' truncation in transcript evidence prevents annotation of the start of the CDS.
Cr2-007ENSMUST0000019380120650aaENSMUSP00000141276
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-Q32M14 -GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
Cr2-006ENSMUST000001933562736735aaENSMUSP00000141706
 
Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins.
-A0A0A6YWU7 -CDS 5' incomplete5' truncation in transcript evidence prevents annotation of the start of the CDS.
Cr2-005ENSMUST00000194149751No protein-
 
Processed transcriptTranscripts that don't contain an open reading frame (ORF) and cannot be placed in one of the other categories.
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Cr2-003ENSMUST00000195722689No protein-
 
Processed transcriptTranscripts that don't contain an open reading frame (ORF) and cannot be placed in one of the other categories.
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Cr2-004ENSMUST00000195347357No protein-
 
Processed transcriptTranscripts that don't contain an open reading frame (ORF) and cannot be placed in one of the other categories.
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Cr2-001ENSMUST000001957371000No protein-
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
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Cr2-010ENSMUST00000192604974No protein-
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
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Gene-based displays