DGCR6L DiGeorge syndrome critical region gene 6 like
Information
- Symbol
- DGCR6L
- Type
- protein-coding
- Description
- DiGeorge syndrome critical region gene 6 like
- Entrez Gene ID
- 85359
- Genome
- hg19
- Position
- chr22:20,301,761-20,307,583
- Genome
- hg38
- Position
- chr22:20,314,238-20,320,060
- MIM
- 609459 OMIM
- HGNC
- HGNC:18551 HGNC
- Ensembl
- ENSG00000128185 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
not provided | 14 | 0 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
2 |
![]() |
30 |
![]() |
2 |
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 | DGCR6 |
MIM | 609459 OMIM |
HGNC | HGNC:18551 HGNC |
Ensembl | ENSG00000128185 Ensembl |
AllianceGenome | HGNC:18551 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000405465.3 | hg38 | chr22 | 20,314,283 | 20,320,009 | 5,727 |
ENST00000248879.8 | hg38 | chr22 | 20,314,238 | 20,320,060 | 5,823 |
ENST00000248879.8 | hg19 | chr22 | 20,301,761 | 20,307,583 | 5,823 |
ENST00000405465.3 | hg19 | chr22 | 20,301,806 | 20,307,532 | 5,727 |
Genome browser