ACOT11 acyl-CoA thioesterase 11
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 24 |
Likely benign | 0 | 24 |
Uncertain significance | 0 | 166 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
214 |
![]() |
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 | BFIT |
SYNONYM | STARD14 |
SYNONYM | THEA |
SYNONYM | THEM1 |
MIM | 606803 OMIM |
HGNC | HGNC:18156 HGNC |
Ensembl | ENSG00000162390 Ensembl |
AllianceGenome | HGNC:18156 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000343744.7 | hg38 | chr1 | 54,548,228 | 54,610,329 | 62,102 |
ENST00000371316.3 | hg38 | chr1 | 54,548,228 | 54,639,192 | 90,965 |
ENST00000343744.7 | hg19 | chr1 | 55,013,901 | 55,076,002 | 62,102 |
ENST00000371316.3 | hg19 | chr1 | 55,013,901 | 55,104,865 | 90,965 |
Genome browser