Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
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: Tmem37 ENSRNOG00000047714

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Description

transmembrane protein 37 [Source:RGD Symbol;Acc:628689]

Gene Synonyms

Pr, Pr1

Location

Primary_assembly 13: 33,736,308-33,743,747 reverse strand.

GRCr8:CM070403.1

About this gene

This gene has 2 transcripts (splice variants), 147 orthologues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000098837.2	Tmem37-202	1443	256aa	ENSRNOP00000083531.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZWS5	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,
ENSRNOT00000074471.4	Tmem37-201	1863	220aa	ENSRNOP00000067466.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	M0RCX9	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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