FASTK Fas activated serine/threonine kinase
Information
- Symbol
- FASTK
- Type
- protein-coding
- Description
- Fas activated serine/threonine kinase
- Entrez Gene ID
- 10922
- Genome
- hg19
- Position
- chr7:150,773,711-150,777,896
- Genome
- hg38
- Position
- chr7:151,076,624-151,080,809
- MIM
- 606965 OMIM
- HGNC
- HGNC:24676 HGNC
- Ensembl
- ENSG00000164896 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
48 |
![]() |
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 | FAST |
MIM | 606965 OMIM |
HGNC | HGNC:24676 HGNC |
Ensembl | ENSG00000164896 Ensembl |
AllianceGenome | HGNC:24676 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000353841.6 | hg38 | chr7 | 151,076,626 | 151,080,842 | 4,217 |
ENST00000297532.11 | hg38 | chr7 | 151,076,624 | 151,080,809 | 4,186 |
ENST00000482571.2 | hg38 | chr7 | 151,076,626 | 151,080,862 | 4,237 |
ENST00000297532.11 | hg19 | chr7 | 150,773,711 | 150,777,896 | 4,186 |
ENST00000353841.6 | hg19 | chr7 | 150,773,713 | 150,777,929 | 4,217 |
ENST00000482571.2 | hg19 | chr7 | 150,773,713 | 150,777,949 | 4,237 |
Genome browser