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: ENSSSCG00000040498

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Description

family with sequence similarity 241 member B [Source:VGNC Symbol;Acc:VGNC:87966]

Location

Primary_assembly 14: 72,558,856-72,639,970 forward strand.

Sscrofa11.1:CM000825.5

About this gene

This gene has 2 transcripts (splice variants), 103 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000058169.3	-	829	265aa	ENSSSCP00000034585.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A286ZSN4 A0A8D0XUK5	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,
ENSSSCT00000097810.1	-	652	120aa	ENSSSCP00000075224.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A481DFA0 A0A8D1CG12	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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