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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  - Gene tree
  - Orthologues
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- GO: Anatomical entity
Phenotypes
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ID History
- Gene history

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Gene: C23H6orf136 ENSBTAG00000006958

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Description

chromosome 23 C6orf136 homolog [Source:VGNC Symbol;Acc:VGNC:53961]

Location

Primary_assembly 23: 28,349,054-28,353,973 reverse strand.

ARS-UCD2.0:CM008190.2

About this gene

This gene has 3 transcripts (splice variants) and 195 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000105714.1	C23H6orf136-202	1602	406aa	ENSBTAP00000102906.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9U016	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 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,
ENSBTAT00000035893.4	C23H6orf136-203	1292	347aa	ENSBTAP00000035760.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MVB5	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,
ENSBTAT00000119108.1	C23H6orf136-201	728	181aa	ENSBTAP00000086411.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SM96	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,

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Summary

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