FAM90A18 family with sequence similarity 90 member A18
Information
- Symbol
- FAM90A18
- Type
- protein-coding
- Description
- family with sequence similarity 90 member A18
- Entrez Gene ID
- 441326
- Genome
- hg19
- Position
- chr8:7,580,613-7,583,623
- Genome
- hg38
- Position
- chr8:7,723,091-7,726,101
- MIM
- 613052 OMIM
- HGNC
- HGNC:32266 HGNC
- Ensembl
- ENSG00000285913 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 0 |
Ranking
ClinVar | |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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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 |
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SYNONYM | FAM90A18P |
SYNONYM | FAM90A19P |
MIM | 613052 OMIM |
HGNC | HGNC:32266 HGNC |
Ensembl | ENSG00000285913 Ensembl |
AllianceGenome | HGNC:32266 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000647769.1 | hg38 | chr8 | 7,723,091 | 7,726,101 | 3,011 |
ENST00000647769.1 | hg19 | chr8 | 7,580,613 | 7,583,623 | 3,011 |
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