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: FAM98C ENSSSCG00000002959

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Description

family with sequence similarity 98 member C [Source:VGNC Symbol;Acc:VGNC:87999]

Location

Primary_assembly 6: 47,315,417-47,319,485 forward strand.

Sscrofa11.1:CM000817.5

About this gene

This gene has 2 transcripts (splice variants), 175 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000003282.5	FAM98C-202	1290	357aa	ENSSSCP00000003200.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1T6N2 F1RI46	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,
ENSSSCT00000079808.1	FAM98C-201	863	275aa	ENSSSCP00000070289.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1T980 A0A5G2RGF5	-

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Summary

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