ATM UNDEREXPRESSION Detail (hg19) (ATM)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr11:108,093,531-108,239,829 |
hg38 | chr11:108,222,804-108,369,102 |
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 |
---|---|---|
Suppression of ATM-dependent and STAT3-mediated antiapoptotic pathway sensitizes human melanoma cell... | MMMP | Detail |
ATM silencing inhibits apoptosis induced by etoposide | MMMP | Detail |
Unlike other malignancies, ATM does not modultate radiosensitivity of melanoma cells | 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
- chr11:108,093,531-108,239,829
- Variant Type
- cnv
Genome browser