Genomic Map
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Target Gene Details
Entrez Gene ID: | 387893 |
Gene Name: | lysine methyltransferase 5A |
Gene Aliases: |
PR-Set7, SET07, SET8, SETD8 |
Location: |
Chr.12:123383778-123409357 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| KMT5A | NM_001324504.1 | NP_001311433.1 | ||
| NM_001324505.1 | NP_001311434.1 | |||
| NM_020382.4 | NP_065115.3 | |||
| NR_136910.1 | ||||
| XM_006719394.3 | XP_006719457.1 | |||
| XM_011538333.2 | XP_011536635.1 | |||
| AK292645.1 | ||||
| AY102937.1 | AAM47033.1 | |||
| BC050346.1 | AAH50346.1 | |||
| HQ259683.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2746505 | Chr.12:123389563 - 123395053 on Build GRCh38 | Deletion |
 KMT5A
|
| dgv44e19 | Chr.12:123389476 - 123395147 on Build GRCh38 | Loss |
KMT5A
|
| nsv826534 | Chr.12:123375063 - 123391807 on Build GRCh38 | Gain |
KMT5A
|
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Additional Information:
For this assay, SNP(s) [rs76801833] 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
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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