Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: C6orf136 ENSSSCG00000025943

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Description

chromosome 7 C6orf136 homolog [Source:NCBI gene (formerly Entrezgene);Acc:100153952]

Location

Primary_assembly 7: 23,185,599-23,190,299 forward strand.

Sscrofa11.1:CM000818.5

About this gene

This gene has 2 transcripts (splice variants) and 194 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000030985.4	C6orf136-202	1347	315aa	ENSSSCP00000024075.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1RU84	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 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,
ENSSSCT00000074839.1	C6orf136-201	730	181aa	ENSSSCP00000059963.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1VE47 A0A5G2Q9H7	-

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Summary

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