MYCL MYCL proto-oncogene, bHLH transcription factor
Information
- Symbol
- MYCL
- Type
- protein-coding
- Description
- MYCL proto-oncogene, bHLH transcription factor
- Entrez Gene ID
- 4610
- Genome
- hg19
- Position
- chr1:40,361,100-40,367,589
- Genome
- hg38
- Position
- chr1:39,895,428-39,901,917
- MIM
- 164850 OMIM
- HGNC
- HGNC:7555 HGNC
- Ensembl
- ENSG00000116990 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 128 | 0 |
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
52 |
![]() |
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 | L-Myc |
SYNONYM | LMYC |
SYNONYM | MYCL1 |
SYNONYM | bHLHe38 |
MIM | 164850 OMIM |
HGNC | HGNC:7555 HGNC |
Ensembl | ENSG00000116990 Ensembl |
AllianceGenome | HGNC:7555 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000397332.3 | hg38 | chr1 | 39,895,428 | 39,901,917 | 6,490 |
ENST00000372815.1 | hg38 | chr1 | 39,899,612 | 39,901,919 | 2,308 |
ENST00000372816.3 | hg38 | chr1 | 39,895,428 | 39,901,917 | 6,490 |
ENST00000372816.3 | hg19 | chr1 | 40,361,100 | 40,367,589 | 6,490 |
ENST00000397332.3 | hg19 | chr1 | 40,361,100 | 40,367,589 | 6,490 |
ENST00000372815.1 | hg19 | chr1 | 40,365,284 | 40,367,591 | 2,308 |
Key | Value |
---|---|
strand | - |
start | 40,361,095 |
Gene Symbol | MYCL |
Entrez GeneId | 4,610 |
Chr Band | 1p34.2 |
end | 40,367,686 |
chr | chr1 |
Name | v-myc avian myelocytomatosis viral oncogene lung carcinoma derived homolog |
Genome browser