Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: Fam118b ENSRNOG00000011543

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Description

family with sequence similarity 118, member B [Source:RGD Symbol;Acc:1307173]

Gene Synonyms

LOC315549, MGC116168, Ppp4r1l, RGD1307173

Location

Primary_assembly 8: 41,824,158-41,846,256 reverse strand.

GRCr8:CM070398.1

About this gene

This gene has 2 transcripts (splice variants), 205 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000168218.1	Fam118b-202	2104	364aa	ENSRNOP00000108617.1	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,
ENSRNOT00000015366.9	Fam118b-201	1547	350aa	ENSRNOP00000015366.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JYK2 Q4QQT2	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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