Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
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: Fam117b ENSRNOG00000022066

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Description

family with sequence similarity 117, member B [Source:RGD Symbol;Acc:1307676]

Gene Synonyms

Als2cr13, LOC363236

Location

Primary_assembly 9: 68,834,354-68,902,543 forward strand.

GRCr8:CM070399.1

About this gene

This gene has 2 transcripts (splice variants), 218 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000031261.7	Fam117b-201	5494	584aa	ENSRNOP00000029910.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M8D5	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,
ENSRNOT00000111864.2	Fam117b-202	5401	553aa	ENSRNOP00000083133.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZYM6	-

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Summary

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