PRRT2 UNDEREXPRESSION Detail (hg19) (PRRT2)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr16:29,823,471-29,827,213 |
hg38 | chr16:29,812,150-29,815,892 |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
ClinVar
Clinical Significance | |
Review star | [No Data.] |
Show details |
Links
Type | Database | ID | Link |
---|---|---|---|
Gene | MIM | ||
HGNC | |||
Ensembl | |||
NCBI | |||
Gene Cards | |||
OncoKB |
Type | Database | ID | Link |
---|---|---|---|
Variant | TogoVar | ||
COSMIC | |||
MONDO |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
The exposure of human melanoma BRO cells in culture simultaneously with cisplatin (1-10 microM) and ... | MMMP | Detail |
MEK1/2 plays an important role in TNFalpha-resistance and is more important than NFkB, Akt, and p38M... | MMMP | Detail |
Overlapped Transcript Coordinates
Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
---|
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- Genome
- hg19
- Position
- chr16:29,823,471-29,827,213
- Variant Type
- cnv
Genome browser