Human (GRCh38.p14)
Description

meiosis 1 associated protein [Source:HGNC Symbol;Acc:HGNC:25183]

Gene Synonyms

C2ORF65, D6MM5E, SPATA37

Location

Chromosome 2: 74,557,883-74,648,338 reverse strand.

GRCh38:CM000664.2

About this gene

This gene has 9 transcripts (splice variants), 172 orthologues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000421985.2M1AP-2032544530aaENSP00000414882.2
 
Protein coding
CCDS33229Q8TC57-1 NM_001321739.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P4TSL:2
ENST00000290536.9M1AP-2012543530aaENSP00000290536.5
 
Protein coding
CCDS33229Q8TC57-1 -GENCODE basicAPPRIS P4TSL:1
ENST00000536235.5M1AP-2092531526aaENSP00000445662.1
 
Protein coding
CCDS62941Q8TC57-4 -GENCODE basicAPPRIS ALT2TSL:2
ENST00000409585.5M1AP-2022457526aaENSP00000386793.1
 
Protein coding
CCDS62941Q8TC57-4 -GENCODE basicAPPRIS ALT2TSL:5
ENST00000438226.5M1AP-20578993aaENSP00000408713.1
 
Nonsense mediated decay
F8WEA5 -TSL:3
ENST00000464686.5M1AP-2061691No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000478437.1M1AP-207584No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000422394.5M1AP-204576No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000485997.1M1AP-208277No protein-
 
Protein coding CDS not defined
--TSL:3