TAB3 TGF-beta activated kinase 1 (MAP3K7) binding protein 3
Information
- Symbol
- TAB3
- Type
- protein-coding
- Description
- TGF-beta activated kinase 1 (MAP3K7) binding protein 3
- Entrez Gene ID
- 257397
- Genome
- hg19
- Position
- chrX:30,845,559-30,993,201
- Genome
- hg38
- Position
- chrX:30,827,442-30,975,084
- MIM
- 300480 OMIM
- HGNC
- HGNC:30681 HGNC
- Ensembl
- ENSG00000157625 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 6 |
not provided | 6 | 0 |
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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56 |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
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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 | MAP3K7IP3 |
SYNONYM | NAP1 |
MIM | 300480 OMIM |
HGNC | HGNC:30681 HGNC |
Ensembl | ENSG00000157625 Ensembl |
AllianceGenome | HGNC:30681 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000288422.4 | hg38 | chrX | 30,827,442 | 30,889,254 | 61,813 |
ENST00000378932.6 | hg38 | chrX | 30,830,331 | 30,975,084 | 144,754 |
ENST00000378930.7 | hg38 | chrX | 30,827,443 | 30,859,720 | 32,278 |
ENST00000378933.5 | hg38 | chrX | 30,827,442 | 30,975,084 | 147,643 |
ENST00000288422.4 | hg19 | chrX | 30,845,559 | 30,907,371 | 61,813 |
ENST00000378933.5 | hg19 | chrX | 30,845,559 | 30,993,201 | 147,643 |
ENST00000378930.7 | hg19 | chrX | 30,845,560 | 30,877,837 | 32,278 |
ENST00000378932.6 | hg19 | chrX | 30,848,448 | 30,993,201 | 144,754 |
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