Genomic Map
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Target Gene Details
Entrez Gene ID: | 4297 |
Gene Name: | lysine methyltransferase 2A |
Gene Aliases: |
ALL-1, CXXC7, HRX, HTRX1, MLL, MLL-AF9, MLL/GAS7, MLL1, MLL1A, TET1-MLL, TRX1, WDSTS |
Location: |
Chr.11:118436490-118526832 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| KMT2A | NM_001197104.1 | NP_001184033.1 | ||
| NM_005933.3 | NP_005924.2 | |||
| XM_006718839.3 | XP_006718902.2 | |||
| XM_011542829.2 | XP_011541131.1 | |||
| XM_011542830.2 | XP_011541132.1 | |||
| XM_011542831.2 | XP_011541133.1 | |||
| XM_011542833.2 | XP_011541135.1 | |||
| D14540.1 | BAA03407.1 | |||
| L04284.1 | AAA58669.1 | |||
| L04731.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv512 | Chr.11:118416012 - 118445621 on Build GRCh38 | Insertion |
 LOC100131626
KMT2A
|
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Additional Information:
For this assay, SNP(s) [rs76651078] 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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