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: Foxm1 ENSRNOG00000005936

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Description

forkhead box M1 [Source:RGD Symbol;Acc:61807]

Location

Primary_assembly 4: 163,325,614-163,337,172 forward strand.

GRCr8:CM070394.1

About this gene

This gene has 3 transcripts (splice variants), 209 orthologues, 34 paralogues and is associated with 14 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000008003.7	Foxm1-201	3393	771aa	ENSRNOP00000008003.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZLE1	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,
ENSRNOT00000008012.8	Foxm1-202	3885	762aa	ENSRNOP00000008012.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LN13	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,
ENSRNOT00000110534.2	Foxm1-203	3628	746aa	ENSRNOP00000088409.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A7T5	-

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Summary

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