CLNS1A chloride nucleotide-sensitive channel 1A
Information
- Symbol
- CLNS1A
- Type
- protein-coding
- Description
- chloride nucleotide-sensitive channel 1A
- Entrez Gene ID
- 1207
- Genome
- hg19
- Position
- chr11:77,325,575-77,348,839
- Genome
- hg38
- Position
- chr11:77,614,530-77,637,794
- MIM
- 602158 OMIM
- HGNC
- HGNC:2080 HGNC
- Ensembl
- ENSG00000074201 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 16 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
16 |
 |
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
[No Data.]
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
|
| 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 | CLCI |
| SYNONYM | CLNS1B |
| SYNONYM | ICln |
| MIM | 602158 OMIM |
| HGNC | HGNC:2080 HGNC |
| Ensembl | ENSG00000074201 Ensembl |
| AllianceGenome | HGNC:2080 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000263309.7 | hg38 | chr11 | 77,616,195 | 77,637,751 | 21,557 |
| ENST00000525428.6 | hg38 | chr11 | 77,614,530 | 77,637,794 | 23,265 |
| ENST00000525064.5 | hg38 | chr11 | 77,616,195 | 77,637,772 | 21,578 |
| ENST00000532069.5 | hg38 | chr11 | 77,616,404 | 77,637,794 | 21,391 |
| ENST00000528364.1 | hg38 | chr11 | 77,618,533 | 77,637,776 | 19,244 |
| ENST00000525428.6 | hg19 | chr11 | 77,325,575 | 77,348,839 | 23,265 |
| ENST00000263309.7 | hg19 | chr11 | 77,327,240 | 77,348,796 | 21,557 |
| ENST00000525064.5 | hg19 | chr11 | 77,327,240 | 77,348,817 | 21,578 |
| ENST00000532069.5 | hg19 | chr11 | 77,327,449 | 77,348,839 | 21,391 |
| ENST00000528364.1 | hg19 | chr11 | 77,329,578 | 77,348,821 | 19,244 |
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