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: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: C3H1orf141 ENSBTAG00000030809

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Description

chromosome 3 C1orf141 homolog [Source:NCBI gene (formerly Entrezgene);Acc:768032]

Gene Synonyms

C1orf141

Location

Primary_assembly 3: 78,193,289-78,238,376 forward strand.

ARS-UCD2.0:CM008170.2

About this gene

This gene has 1 transcript (splice variant) and 71 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000043557.3	C3H1orf141-201	1734	430aa	ENSBTAP00000041118.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q2KIL1	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,

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Summary

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