AMN amnion associated transmembrane protein

Information
Symbol
AMN
Type
protein-coding
Description
amnion associated transmembrane protein
Entrez Gene ID
81693
Genome
hg19
Position
chr14:103,389,000-103,397,179
Genome
hg38
Position
chr14:102,922,663-102,930,842
MIM
605799 OMIM
HGNC
HGNC:14604 HGNC
Ensembl
ENSG00000166126 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 64
Likely pathogenic 0 56
Benign 0 68
Likely benign 0 758
Conflicting classifications of pathogenicity 0 10
Uncertain significance 0 180
Ranking
ClinVar
0
0
118
942
34
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 IGS2
SYNONYM PRO1028
SYNONYM amnionless
MIM 605799 OMIM
HGNC HGNC:14604 HGNC
Ensembl ENSG00000166126 Ensembl
AllianceGenome HGNC:14604
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000299155.10 hg38 chr14 102,922,663 102,930,842 8,180
ENST00000299155.10 hg19 chr14 103,389,000 103,397,179 8,180
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