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: MCF2 ENSBTAG00000004007

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Description

MCF.2 cell line derived transforming sequence [Source:VGNC Symbol;Acc:VGNC:31301]

Location

Primary_assembly X: 23,009,585-23,076,989 reverse strand.

ARS-UCD2.0:CM008197.2

About this gene

This gene has 4 transcripts (splice variants), 265 orthologues and 22 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000087494.2	MCF2-203	3091	924aa	ENSBTAP00000074455.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MJB9	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000077425.2	MCF2-204	3043	908aa	ENSBTAP00000066024.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MBI5	APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSBTAT00000005233.6	MCF2-201	2893	858aa	ENSBTAP00000005233.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MFK9	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSBTAT00000085270.2	MCF2-202	2776	819aa	ENSBTAP00000064904.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M3Z3	-

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Summary

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