MARCKS myristoylated alanine rich protein kinase C substrate
Information
- Symbol
- MARCKS
- Type
- protein-coding
- Description
- myristoylated alanine rich protein kinase C substrate
- Entrez Gene ID
- 4082
- Genome
- hg19
- Position
- chr6:114,178,524-114,184,652
- Genome
- hg38
- Position
- chr6:113,857,345-113,863,475
- MIM
- 177061 OMIM
- HGNC
- HGNC:6759 HGNC
- Ensembl
- ENSG00000277443 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely pathogenic | 0 | 2 |
| Benign | 0 | 4 |
| Likely benign | 0 | 4 |
| not provided | 3 | 0 |
| Uncertain significance | 0 | 72 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
82 |
 |
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
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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
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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
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| Category | : |
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| 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 | 80K-L |
| SYNONYM | MACS |
| SYNONYM | PKCSL |
| SYNONYM | PRKCSL |
| MIM | 177061 OMIM |
| HGNC | HGNC:6759 HGNC |
| Ensembl | ENSG00000277443 Ensembl |
| AllianceGenome | HGNC:6759 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000612661.2 | hg38 | chr6 | 113,857,345 | 113,863,475 | 6,131 |
| ENST00000612661.2 | hg19 | chr6 | 114,178,524 | 114,184,652 | 6,129 |
| Key | Value |
|---|---|
| strand | + |
| start | 114,178,513 |
| Gene Symbol | MARCKS |
| Entrez GeneId | 4,082 |
| Chr Band | 6q22.2 |
| end | 114,184,651 |
| chr | chr6 |
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