Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Biological process
- GO: Molecular function
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: FAM118A ENSSSCG00000000014

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Description

family with sequence similarity 118 member A [Source:VGNC Symbol;Acc:VGNC:87893]

Location

Primary_assembly 5: 4,070,701-4,101,287 reverse strand.

Sscrofa11.1:CM000816.5

About this gene

This gene has 2 transcripts (splice variants), 119 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000000015.4	FAM118A-202	2433	357aa	ENSSSCP00000000015.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D2C8E0 F1SM57	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,
ENSSSCT00000022845.3	FAM118A-201	2378	346aa	ENSSSCP00000028100.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1S1F1 I3LVE8	-

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Summary

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