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: Cellular component
- GO: Biological process
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: C1h10orf143 ENSRNOG00000050554

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Description

similar to human chromosome 10 open reading frame 143 [Source:RGD Symbol;Acc:2318344]

Gene Synonyms

LOC100362342

Location

Primary_assembly 1: 201,561,396-201,652,127 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants) and 40 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000153904.1	C1h10orf143-202	517	112aa	ENSRNOP00000108158.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000073093.4	C1h10orf143-201	895	107aa	ENSRNOP00000067789.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HX83 M0RDT1	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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