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

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Gene: FAM107B ENSBTAG00000010023

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Description

family with sequence similarity 107 member B [Source:VGNC Symbol;Acc:VGNC:57007]

Location

Primary_assembly 13: 29,216,135-29,433,959 reverse strand.

ARS-UCD2.0:CM008180.2

About this gene

This gene has 4 transcripts (splice variants), 207 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000134761.1	FAM107B-204	1782	307aa	ENSBTAP00000084278.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SK75	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,
ENSBTAT00000094104.1	FAM107B-201	1541	171aa	ENSBTAP00000100081.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TNH3	-
ENSBTAT00000082421.2	FAM107B-202	1513	151aa	ENSBTAP00000063591.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LT30	-
ENSBTAT00000013221.4	FAM107B-203	1456	131aa	ENSBTAP00000013221.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MTK7	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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