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

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Gene: MCM2 ENSBTAG00000014380

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Description

minichromosome maintenance complex component 2 [Source:VGNC Symbol;Acc:VGNC:31308]

Location

Primary_assembly 22: 59,895,766-59,912,859 reverse strand.

ARS-UCD1.3:CM008189.2

About this gene

This gene has 5 transcripts (splice variants), 205 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000133015.1	MCM2-204	3549	937aa	ENSBTAP00000074611.1	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,
ENSBTAT00000087255.2	MCM2-203	3828	929aa	ENSBTAP00000058122.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LHC9	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,
ENSBTAT00000105722.1	MCM2-201	3771	910aa	ENSBTAP00000086019.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000071333.2	MCM2-202	3741	900aa	ENSBTAP00000060188.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LKN6	-
ENSBTAT00000019121.7	MCM2-205	3469	911aa	ENSBTAP00000019121.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1N506	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,

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Summary

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