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Human (GRCh38.p14)
Description

minichromosome maintenance 8 homologous recombination repair factor [Source:HGNC Symbol;Acc:HGNC:16147]

Gene Synonyms

C20ORF154, DJ967N21.5, MGC119522, MGC119523, MGC12866, MGC4816, REC

Location
About this transcript

This transcript has 18 exons, is annotated with 23 domains and features, is associated with 19417 variant alleles and maps to 823 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000610722.4MCM8-2057486840aaENSP00000478141.1
 
Protein coding
CCDS13094Q9UJA3-1 NM_032485.6MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000378886.6MCM8-2033835880aaENSP00000368164.2
 
Protein coding
CCDS63227Q9UJA3-4 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000378896.7MCM8-2043769840aaENSP00000368174.3
 
Protein coding
CCDS13094Q9UJA3-1 -GENCODE BasicAPPRIS P1TSL:1
ENST00000378883.5MCM8-2023574793aaENSP00000368161.1
 
Protein coding
CCDS63226Q9UJA3-2 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000265187.4MCM8-2013442824aaENSP00000265187.4
 
Protein coding
CCDS13095Q9UJA3-3 -GENCODE PrimaryGENCODE BasicTSL:1
Statistics

Exons: 18, Coding exons: 17, Transcript length: 3,574 bps, Translation length: 793 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9UJA3

CCDS

This transcript is a member of the Human CCDS set: CCDS63226

Transcript Support Level (TSL)

TSL:1

Version

ENST00000378883.5

Type

Protein coding

Annotation Method

Annotation produced by the Ensembl genebuild.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

GENCODE primary gene

This transcript is a member of the Gencode Primary gene set.