FAM131B family with sequence similarity 131 member B
Information
- Symbol
- FAM131B
- Type
- protein-coding
- Description
- family with sequence similarity 131 member B
- Entrez Gene ID
- 9715
- Genome
- hg19
- Position
- chr7:143,050,493-143,059,806
- Genome
- hg38
- Position
- chr7:143,353,400-143,362,713
- MIM
- 619282 OMIM
- HGNC
- HGNC:22202 HGNC
- Ensembl
- ENSG00000159784 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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46 |
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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
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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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 |
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Target data | : |
MGeND data only
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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
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
MIM | 619282 OMIM |
HGNC | HGNC:22202 HGNC |
Ensembl | ENSG00000159784 Ensembl |
AllianceGenome | HGNC:22202 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409346.5 | hg38 | chr7 | 143,353,401 | 143,362,725 | 9,325 |
ENST00000443739.7 | hg38 | chr7 | 143,353,400 | 143,362,713 | 9,314 |
ENST00000409222.7 | hg38 | chr7 | 143,353,822 | 143,362,055 | 8,234 |
ENST00000409408.5 | hg38 | chr7 | 143,353,402 | 143,361,802 | 8,401 |
ENST00000409578.5 | hg38 | chr7 | 143,353,401 | 143,362,693 | 9,293 |
ENST00000443739.7 | hg19 | chr7 | 143,050,493 | 143,059,806 | 9,314 |
ENST00000409578.5 | hg19 | chr7 | 143,050,494 | 143,059,786 | 9,293 |
ENST00000409346.5 | hg19 | chr7 | 143,050,494 | 143,059,818 | 9,325 |
ENST00000409408.5 | hg19 | chr7 | 143,050,495 | 143,058,895 | 8,401 |
ENST00000409222.7 | hg19 | chr7 | 143,050,915 | 143,059,148 | 8,234 |
Key | Value |
---|---|
strand | - |
start | 143,050,492 |
Gene Symbol | FAM131B |
Entrez GeneId | 9,715 |
Chr Band | 7q34 |
end | 143,059,839 |
chr | chr7 |
Name | family with sequence similarity 131, member B |
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