AMN1 antagonist of mitotic exit network 1 homolog

Information
Symbol
AMN1
Type
protein-coding
Description
antagonist of mitotic exit network 1 homolog
Entrez Gene ID
196394
Genome
hg19
Position
chr12:31,824,076-31,881,955
Genome
hg38
Position
chr12:31,671,142-31,729,021
MIM
620564 OMIM
HGNC
HGNC:27281 HGNC
Ensembl
ENSG00000151743 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
24
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
MIM 620564 OMIM
HGNC HGNC:27281 HGNC
Ensembl ENSG00000151743 Ensembl
AllianceGenome HGNC:27281
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000541931.5 hg38 chr12 31,672,170 31,729,110 56,941
ENST00000281471.11 hg38 chr12 31,671,142 31,729,021 57,880
ENST00000537562.5 hg38 chr12 31,671,945 31,729,010 57,066
ENST00000542781.5 hg38 chr12 31,673,552 31,729,021 55,470
ENST00000536761.5 hg38 chr12 31,672,278 31,729,021 56,744
ENST00000281471.11 hg19 chr12 31,824,076 31,881,955 57,880
ENST00000537562.5 hg19 chr12 31,824,879 31,881,944 57,066
ENST00000541931.5 hg19 chr12 31,825,104 31,882,044 56,941
ENST00000536761.5 hg19 chr12 31,825,212 31,881,955 56,744
ENST00000542781.5 hg19 chr12 31,826,486 31,881,955 55,470
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