Genomic Map
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Target Gene Details
Entrez Gene ID: | 4638 |
Gene Name: | myosin light chain kinase |
Gene Aliases: |
AAT7, KRP, MLCK, MLCK1, MLCK108, MLCK210, MSTP083, MYLK1, smMLCK |
Location: |
Chr.3:123612296-123884302 on Build GRCh38 |
Assay Gene Location: | Within Exon 36 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MYLK | NM_001321309.1 | 33 | 6240 | NP_001308238.1 |
| NM_053025.3 | 34 | 6448 | NP_444253.3 | |
| NM_053026.3 | 33 | 6241 | NP_444254.3 | |
| NM_053027.3 | 33 | 6295 | NP_444255.3 | |
| NM_053028.3 | 32 | 6088 | NP_444256.3 | |
| XM_017006469.1 | 17 | 3724 | XP_016861958.1 | |
| XM_017006470.1 | 16 | 2712 | XP_016861959.1 | |
| XM_017006471.1 | 16 | 2765 | XP_016861960.1 | |
| XM_017006472.1 | 4 | 1058 | XP_016861961.1 | |
| XM_017006473.1 | 4 | 1007 | XP_016861962.1 | |
| AF172084.1 | 1 | 312 | AAQ13607.1 | |
| AK025953.1 | 1 | 219 | ||
| AK127437.1 | 1 | 1970 | ||
| BC064420.1 | 3 | 1122 | ||
| BC107783.1 | 3 | 1106 | AAI07784.1 | |
| BC113456.1 | 3 | 927 | ||
| BC113458.1 | 3 | 924 | ||
| BM723621.1 | 1 | 409 | ||
| CR749364.1 | 3 | 5908 | CAH18217.1 |
Target Gene Details
Entrez Gene ID: | 100506826 |
Gene Name: | MYLK antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.3:123585513-123630821 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MYLK-AS1 | NR_038266.2 | |||
| NR_121654.1 | ||||
| DA531919.1 | ||||
| DA714112.1 | ||||
| DB499540.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv591428 | Chr.3:123608828 - 124139902 on Build GRCh38 | Gain |
 KALRN
CCDC14
MYLK-AS1
MYLK-AS2
MYLK
MIR5002
ROPN1
|
| nsv829708 | Chr.3:123519589 - 123690957 on Build GRCh38 | Gain |
MYLK-AS1
HACD2
MYLK-AS2
MYLK
|
| nsv829709 | Chr.3:123554281 - 123748120 on Build GRCh38 | Loss |
MYLK-AS1
HACD2
MYLK-AS2
MYLK
|
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Additional Information:
For this assay, SNP(s) [rs115932105] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Exonic
Intronic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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