Human (GRCh38.p14)
Description

minichromosome maintenance 9 homologous recombination repair factor [Source:HGNC Symbol;Acc:HGNC:21484]

Gene Synonyms

C6ORF61, DJ329L24.3, FLJ20170, MCMDC1, MGC35304

Location

Chromosome 6: 118,813,442-118,935,162 reverse strand.

GRCh38:CM000668.2

About this gene

This gene has 9 transcripts (splice variants), 177 orthologues, 8 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000619706.5MCM9-20952191143aaENSP00000480469.1
 
Protein coding
CCDS56447Q9NXL9-1 NM_017696.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000316316.10MCM9-20251011143aaENSP00000314505.5
 
Protein coding
CCDS56447Q9NXL9-1 -GENCODE basicAPPRIS P1TSL:5
ENST00000316068.7MCM9-2012442391aaENSP00000312870.3
 
Protein coding
CCDS5121Q9NXL9-3 -GENCODE basicTSL:1
ENST00000425154.6MCM9-204752156aaENSP00000394776.2
 
Protein coding
D6RHY8 -TSL:3CDS 3' incomplete
ENST00000458674.2MCM9-206549183aaENSP00000406576.2
 
Protein coding
H0Y6M9 -TSL:5CDS 5' and 3' incomplete
ENST00000505446.1MCM9-20747078aaENSP00000426890.1
 
Protein coding
D6RE85 -TSL:2CDS 3' incomplete
ENST00000505485.1MCM9-208825No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000368478.2MCM9-203469No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000436788.2MCM9-2057592No protein-
 
Retained intron
--TSL:2