M1AP meiosis 1 associated protein

Information
Symbol
M1AP
Type
protein-coding
Description
meiosis 1 associated protein
Entrez Gene ID
130951
Genome
hg19
Position
chr2:74,785,010-74,875,457
Genome
hg38
Position
chr2:74,557,883-74,648,330
MIM
619098 OMIM
HGNC
HGNC:25183 HGNC
Ensembl
ENSG00000159374 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 2
Likely pathogenic 0 2
Likely benign 0 6
Conflicting classifications of pathogenicity 0 2
low penetrance 0 2
Uncertain significance 0 70
Ranking
ClinVar
0
0
0
80
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM C2orf65
SYNONYM D6Mm5e
SYNONYM SPATA37
SYNONYM SPGF48
MIM 619098 OMIM
HGNC HGNC:25183 HGNC
Ensembl ENSG00000159374 Ensembl
AllianceGenome HGNC:25183
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000421985.2 hg38 chr2 74,557,883 74,648,330 90,448
ENST00000290536.9 hg38 chr2 74,557,883 74,648,037 90,155
ENST00000409585.5 hg38 chr2 74,557,892 74,640,327 82,436
ENST00000536235.5 hg38 chr2 74,557,892 74,648,338 90,447
ENST00000290536.9 hg19 chr2 74,785,010 74,875,164 90,155
ENST00000421985.2 hg19 chr2 74,785,010 74,875,457 90,448
ENST00000409585.5 hg19 chr2 74,785,019 74,867,454 82,436
ENST00000536235.5 hg19 chr2 74,785,019 74,875,465 90,447
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