Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Molecular function
- GO: Cellular component
- GO: Biological process
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Bmf ENSRNOG00000007529

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Description

Bcl2 modifying factor [Source:RGD Symbol;Acc:628658]

Gene Synonyms

Bmf-pending

Location

Primary_assembly 3: 125,953,466-125,974,258 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 3 transcripts (splice variants), 174 orthologues and is associated with 2 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000150084.1	Bmf-203	2084	291aa	ENSRNOP00000111477.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000010381.6	Bmf-201	4665	271aa	ENSRNOP00000010381.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8L2Q4K3 A6HPB4	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,
ENSRNOT00000105313.2	Bmf-202	4409	190aa	ENSRNOP00000096398.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GLK7	-

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Summary

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