PLCXD1 phosphatidylinositol specific phospholipase C X domain containing 1
Information
- Symbol
- PLCXD1
- Type
- protein-coding
- Description
- phosphatidylinositol specific phospholipase C X domain containing 1
- Entrez Gene ID
- 55344
- Genome
- hg19
- Position
- chrX:198,048-220,023
- Genome
- hg19
- Position
- chrY:148,048-170,023
- Genome
- hg38
- Position
- chrY:281,381-303,356
- Genome
- hg38
- Position
- chrX:281,381-303,356
- MIM
- 300974 OMIM
- HGNC
- HGNC:23148 HGNC
- Ensembl
- ENSG00000182378 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 3 | 0 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
0 |
 |
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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
|
| Search word | : | |
| 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 | : |
|
| 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 | LL0XNC01-136G2.1 |
| MIM | 300974 OMIM |
| HGNC | HGNC:23148 HGNC |
| Ensembl | ENSG00000182378 Ensembl |
| Ensembl | ENSG00000292344 Ensembl |
| AllianceGenome | HGNC:23148 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000711179.1 | hg38 | chrY | 281,381 | 303,356 | 21,976 |
| ENST00000711184.1 | hg38 | chrY | 276,322 | 303,353 | 27,032 |
| ENST00000381657.8 | hg38 | chrX | 281,381 | 303,356 | 21,976 |
| ENST00000399012.6 | hg38 | chrX | 276,322 | 303,353 | 27,032 |
| ENST00000399012.6 | hg19 | chrX | 192,989 | 220,020 | 27,032 |
| ENST00000381657.8 | hg19 | chrX | 198,048 | 220,023 | 21,976 |
| ENST00000711184.1 | hg19 | chrY | 142,989 | 170,020 | 27,032 |
| ENST00000711179.1 | hg19 | chrY | 148,048 | 170,023 | 21,976 |
Genome browser