Human (GRCh37.p13)
Description

minichromosome maintenance complex component 2 [Source:HGNC Symbol;Acc:6944]

Gene Synonyms

BM28, CCNL1, CDCL1, D3S3194, KIAA0030, MITOTIN, cdc19

Location

Chromosome 3: 127,317,066-127,341,276 forward strand.

GRCh37:CM000665.1

About this gene

This gene has 9 transcripts (splice variants), 1 paralogue and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000265056.7MCM2-0013619904aaENSP00000265056.7
 
Protein coding
CCDS3043C9J013 C9JZ21 P49736
Q9BWF4
NM_004526.3GENCODE basic
ENST00000491422.1MCM2-0052844836aaENSP00000420528.1
 
Protein coding
Q9BWF4 -CDS 5' incomplete
ENST00000480910.1MCM2-007693128aaENSP00000419802.1
 
Protein coding
C9J013 C9JZ21 -CDS 3' incomplete
ENST00000472731.1MCM2-008547103aaENSP00000418930.1
 
Protein coding
C9J013 -CDS 3' incomplete
ENST00000474964.1MCM2-0022847146aaENSP00000420007.1
 
Nonsense mediated decay
C9J013 C9JZ21 F8WDM3
--
ENST00000477668.1MCM2-003251091aaENSP00000417800.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000468414.1MCM2-0101076No protein-
 
Processed transcript
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ENST00000468659.1MCM2-009557No protein-
 
Processed transcript
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ENST00000473785.1MCM2-011684No protein-
 
Retained intron
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