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Human (GRCh38.p14)
Description

meiosis specific nuclear structural 1 [Source:HGNC Symbol;Acc:HGNC:29636]

Gene Synonyms

FLJ11222, SPATA40

Location

Chromosome 15: 56,421,544-56,465,168 reverse strand.

GRCh38:CM000677.2

About this gene

This gene has 6 transcripts (splice variants), 206 orthologues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000260453.4MNS1-2012030495aaENSP00000260453.3
 
Protein coding
CCDS10158Q8NEH6 NM_018365.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P2TSL:1
ENST00000957022.1MNS1-2062091506aaENSP00000627081.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000876521.1MNS1-2051950494aaENSP00000546580.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT1
ENST00000876520.1MNS1-2041730495aaENSP00000546579.1
 
Protein coding
CCDS10158--GENCODE PrimaryGENCODE BasicAPPRIS P2
ENST00000566386.1MNS1-203539No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000558694.1MNS1-202584No protein-
 
Retained intron
--TSL:4