Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: Cd37 ENSRNOG00000020699

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Description

CD37 molecule [Source:RGD Symbol;Acc:62035]

Gene Synonyms

MRC OX-44

Location

Primary_assembly 1: 104,849,166-104,861,276 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 5 transcripts (splice variants), 130 orthologues and 31 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000136795.1	Cd37-203	2448	396aa	ENSRNOP00000101719.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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 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,
ENSRNOT00000152125.1	Cd37-204	1413	365aa	ENSRNOP00000110889.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000155312.1	Cd37-205	1323	279aa	ENSRNOP00000107676.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JB01	-
ENSRNOT00000114337.2	Cd37-202	1284	294aa	ENSRNOP00000077102.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y7F5	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,
ENSRNOT00000066834.4	Cd37-201	852	252aa	ENSRNOP00000059092.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0H2UI08	-

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Summary

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