FAM90A23 family with sequence similarity 90 member A23
Information
- Symbol
- FAM90A23
- Type
- protein-coding
- Description
- family with sequence similarity 90 member A23
- Entrez Gene ID
- 645572
- Genome
- hg19
- Position
- chr8:7,437,166-7,440,175
- Genome
- hg38
- Position
- chr8:7,579,644-7,582,653
- HGNC
- HGNC:32271 HGNC
- Ensembl
- ENSG00000285765 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 1 | 0 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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2 |
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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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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
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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 |
---|---|
SYNONYM | FAM90A23P |
HGNC | HGNC:32271 HGNC |
Ensembl | ENSG00000285765 Ensembl |
AllianceGenome | HGNC:32271 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000648435.1 | hg38 | chr8 | 7,579,644 | 7,582,653 | 3,010 |
ENST00000648435.1 | hg19 | chr8 | 7,437,166 | 7,440,175 | 3,010 |
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