FLACC1 flagellum associated containing coiled-coil domains 1
Information
- Symbol
- FLACC1
- Type
- protein-coding
- Description
- flagellum associated containing coiled-coil domains 1
- Entrez Gene ID
- 130540
- Genome
- hg19
- Position
- chr2:202,152,994-202,216,174
- Genome
- hg38
- Position
- chr2:201,288,271-201,351,451
- MIM
- 619796 OMIM
- HGNC
- HGNC:14439 HGNC
- Ensembl
- ENSG00000155749 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 10 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 54 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
66 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | ALS2CR12 |
| MIM | 619796 OMIM |
| HGNC | HGNC:14439 HGNC |
| Ensembl | ENSG00000155749 Ensembl |
| AllianceGenome | HGNC:14439 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000392257.8 | hg38 | chr2 | 201,288,271 | 201,357,345 | 69,075 |
| ENST00000405148.6 | hg38 | chr2 | 201,288,424 | 201,357,378 | 68,955 |
| ENST00000439709.5 | hg38 | chr2 | 201,288,430 | 201,357,398 | 68,969 |
| ENST00000286190.9 | hg38 | chr2 | 201,288,271 | 201,351,451 | 63,181 |
| ENST00000286190.9 | hg19 | chr2 | 202,152,994 | 202,216,174 | 63,181 |
| ENST00000392257.8 | hg19 | chr2 | 202,152,994 | 202,222,068 | 69,075 |
| ENST00000405148.6 | hg19 | chr2 | 202,153,147 | 202,222,101 | 68,955 |
| ENST00000439709.5 | hg19 | chr2 | 202,153,153 | 202,222,121 | 68,969 |
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