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: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: LOC691658 ENSRNOG00000063302

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Description

similar to anterior pharynx defective 1b homolog [Source:RGD Symbol;Acc:1597236]

Gene Synonyms

RGD1559979

Location

Primary_assembly 8: 67,341,834-67,363,864 reverse strand.

mRatBN7.2:CM026981.1

About this gene

This gene has 2 transcripts (splice variants), 192 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000117753.1	LOC691658-202	2787	257aa	ENSRNOP00000096772.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8J8XJD4	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,
ENSRNOT00000109916.1	LOC691658-201	4831	216aa	ENSRNOP00000085301.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A315	-

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Summary

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