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

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Gene: FEM1B ENSSSCG00000022419

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Description

fem-1 homolog B [Source:VGNC Symbol;Acc:VGNC:88083]

Location

Primary_assembly 1: 166,162,883-166,175,937 forward strand.

Sscrofa11.1:CM000812.5

About this gene

This gene has 1 transcript (splice variant), 112 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000031923.3	FEM1B-201	4610	627aa	ENSSSCP00000019736.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1ABA3 I3L6T4	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,

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Summary

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