Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: FAM98C ENSPTRG00000010929

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Description

family with sequence similarity 98 member C [Source:VGNC Symbol;Acc:VGNC:3632]

Location

Chromosome 19: 40,382,995-40,389,076 forward strand.

Pan_tro_3.0:CM000333.3

About this gene

This gene has 3 transcripts (splice variants), 175 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000020250.6	FAM98C-201	1408	350aa	ENSPTRP00000018730.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2WQ55 H2QG85	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,
ENSPTRT00000080365.1	FAM98C-203	807	268aa	ENSPTRP00000075481.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SEM7 A0A6D2WBX1	-
ENSPTRT00000083608.1	FAM98C-202	561	186aa	ENSPTRP00000061855.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RB55 A0A6D2WPY8	-

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Summary

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