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: FEM1B ENSPTRG00000007214

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Description

fem-1 homolog B [Source:VGNC Symbol;Acc:VGNC:14641]

Location

Chromosome 15: 49,244,680-49,263,000 forward strand.

Pan_tro_3.0:CM000329.3

About this gene

This gene has 2 transcripts (splice variants), 112 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000106051.1	FEM1B-201	7313	627aa	ENSPTRP00000081740.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3SXM4 A0A6D2X9E9	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,
ENSPTRT00000013321.5	FEM1B-202	1686	561aa	ENSPTRP00000051407.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2R8B5	-

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Summary

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