FAM3A FAM3 metabolism regulating signaling molecule A
Information
- Symbol
- FAM3A
- Type
- protein-coding
- Description
- FAM3 metabolism regulating signaling molecule A
- Entrez Gene ID
- 60343
- Genome
- hg19
- Position
- chrX:153,734,491-153,744,566
- Genome
- hg38
- Position
- chrX:154,506,160-154,516,242
- MIM
- 300492 OMIM
- HGNC
- HGNC:13749 HGNC
- Ensembl
- ENSG00000071889 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 6 |
Conflicting classifications of pathogenicity | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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16 |
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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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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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | 2.19 |
SYNONYM | DLD |
SYNONYM | DXS560S |
SYNONYM | XAP-7 |
MIM | 300492 OMIM |
HGNC | HGNC:13749 HGNC |
Ensembl | ENSG00000071889 Ensembl |
AllianceGenome | HGNC:13749 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000447601.7 | hg38 | chrX | 154,506,171 | 154,516,232 | 10,062 |
ENST00000393572.5 | hg38 | chrX | 154,506,640 | 154,516,160 | 9,521 |
ENST00000322269.10 | hg38 | chrX | 154,506,160 | 154,516,242 | 10,083 |
ENST00000359889.9 | hg38 | chrX | 154,506,159 | 154,516,236 | 10,078 |
ENST00000369643.5 | hg38 | chrX | 154,506,171 | 154,516,116 | 9,946 |
ENST00000369641.7 | hg38 | chrX | 154,506,535 | 154,516,238 | 9,704 |
ENST00000419205.5 | hg38 | chrX | 154,506,160 | 154,516,242 | 10,083 |
ENST00000322269.10 | hg19 | chrX | 153,734,491 | 153,744,566 | 10,076 |
ENST00000359889.9 | hg19 | chrX | 153,734,490 | 153,744,560 | 10,071 |
ENST00000419205.5 | hg19 | chrX | 153,734,491 | 153,744,566 | 10,076 |
ENST00000369643.5 | hg19 | chrX | 153,734,502 | 153,744,440 | 9,939 |
ENST00000369641.7 | hg19 | chrX | 153,734,866 | 153,744,562 | 9,697 |
ENST00000393572.5 | hg19 | chrX | 153,734,971 | 153,744,484 | 9,514 |
ENST00000447601.7 | hg19 | chrX | 153,734,502 | 153,744,556 | 10,055 |
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