Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
- Paralogues
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  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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Molecular interactions
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ID History
- Gene history

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Gene: TMEM237 ENSBTAG00000017437

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Description

transmembrane protein 237 [Source:VGNC Symbol;Acc:VGNC:36050]

Location

Primary_assembly 2: 90,171,834-90,195,308 reverse strand.

ARS-UCD2.0:CM008169.2

About this gene

This gene has 9 transcripts (splice variants) and 253 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000074927.2	TMEM237-207	3296	488aa	ENSBTAP00000059069.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LIT2	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,
ENSBTAT00000123406.1	TMEM237-209	3236	468aa	ENSBTAP00000102284.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TZV0	-
ENSBTAT00000105835.1	TMEM237-204	3203	420aa	ENSBTAP00000092233.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T680	-
ENSBTAT00000101920.1	TMEM237-205	3051	403aa	ENSBTAP00000093418.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9T3P0	-
ENSBTAT00000104677.1	TMEM237-203	3041	403aa	ENSBTAP00000084657.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SH48	-
ENSBTAT00000023181.6	TMEM237-202	3038	402aa	ENSBTAP00000023181.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A452DJL2	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,
ENSBTAT00000083576.2	TMEM237-208	3023	403aa	ENSBTAP00000065499.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MAC9	-
ENSBTAT00000134952.1	TMEM237-206	2962	443aa	ENSBTAP00000077120.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S1D4	-
ENSBTAT00000106756.1	TMEM237-201	2800	389aa	ENSBTAP00000081950.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9S9I9	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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