MUC15 mucin 15, cell surface associated
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 12 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 50 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
2 |
![]() |
68 |
![]() |
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 |
Type | ID |
---|---|
SYNONYM | MUC-15 |
SYNONYM | PAS3 |
SYNONYM | PASIII |
MIM | 608566 OMIM |
HGNC | HGNC:14956 HGNC |
Ensembl | ENSG00000169550 Ensembl |
AllianceGenome | HGNC:14956 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000455601.6 | hg38 | chr11 | 26,559,033 | 26,572,121 | 13,089 |
ENST00000281268.12 | hg38 | chr11 | 26,559,033 | 26,567,094 | 8,062 |
ENST00000527569.1 | hg38 | chr11 | 26,560,762 | 26,572,142 | 11,381 |
ENST00000529533.6 | hg38 | chr11 | 26,559,032 | 26,572,263 | 13,232 |
ENST00000436318.6 | hg38 | chr11 | 26,559,033 | 26,567,094 | 8,062 |
ENST00000529533.6 | hg19 | chr11 | 26,580,579 | 26,593,810 | 13,232 |
ENST00000436318.6 | hg19 | chr11 | 26,580,580 | 26,588,641 | 8,062 |
ENST00000281268.12 | hg19 | chr11 | 26,580,580 | 26,588,641 | 8,062 |
ENST00000455601.6 | hg19 | chr11 | 26,580,580 | 26,593,668 | 13,089 |
ENST00000527569.1 | hg19 | chr11 | 26,582,309 | 26,593,689 | 11,381 |
Genome browser