The M1AP gene homepage

General information
Gene symbol M1AP
Gene name meiosis 1 associated protein
Chromosome 2
Chromosomal band p13.1
Imprinted Unknown
Genomic reference NC_000002.11
Transcript reference NM_138804.4
Associated with diseases INFM, SPGF48
Citation reference(s) -
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 14
Unique public DNA variants reported 7
Individuals with public variants 11
Hidden variants 0
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was performed by Johan den Dunnen, supported by Global Variome.
Date created August 08, 2017
Date last updated July 28, 2020
Version M1AP:200728

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL https://www.LOVD.nl/M1AP
HGNC 25183
Entrez Gene 130951
PubMed articles M1AP
OMIM - Diseases SPGF48 (spermatogenic failure, type 48)
HGMD M1AP
GeneCards M1AP
GeneTests M1AP
Orphanet M1AP


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00024854 2 transcript variant 1 NM_138804.4 NP_620159.2 14


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