NALF2 NALCN channel auxiliary factor 2
Information
- Symbol
- NALF2
- Type
- protein-coding
- Description
- NALCN channel auxiliary factor 2
- Entrez Gene ID
- 27112
- Genome
- hg19
- Position
- chrX:68,724,169-68,752,351
- Genome
- hg38
- Position
- chrX:69,504,326-69,532,508
- HGNC
- HGNC:30701 HGNC
- Ensembl
- ENSG00000130054 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| not provided | 6 | 0 |
| Uncertain significance | 0 | 54 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
60 |
 |
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 | CXorf63 |
| SYNONYM | FAM155B |
| SYNONYM | TED |
| SYNONYM | TMEM28 |
| SYNONYM | bB57D9.1 |
| HGNC | HGNC:30701 HGNC |
| Ensembl | ENSG00000130054 Ensembl |
| AllianceGenome | HGNC:30701 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000252338.5 | hg38 | chrX | 69,504,326 | 69,532,508 | 28,183 |
| ENST00000252338.5 | hg19 | chrX | 68,724,169 | 68,752,351 | 28,183 |
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