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: Anatomical entity
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: C6h14orf28 ENSRNOG00000023230

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Description

similar to human chromosome 14 open reading frame 28 [Source:RGD Symbol;Acc:1307621]

Gene Synonyms

LOC314168, RGD1307621

Location

Primary_assembly 6: 88,701,818-88,708,820 forward strand.

GRCr8:CM070396.1

About this gene

This gene has 3 transcripts (splice variants) and 175 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000101605.2	C6h14orf28-202	1629	376aa	ENSRNOP00000096306.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AS79	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,
ENSRNOT00000034756.8	C6h14orf28-201	1267	310aa	ENSRNOP00000035231.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6HBS5 D4A3H4	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,
ENSRNOT00000107979.2	C6h14orf28-203	1093	280aa	ENSRNOP00000081303.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZS88	-

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Summary

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