Genomic Map
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Target Gene Details
Entrez Gene ID: | 3070 |
Gene Name: | helicase, lymphoid-specific |
Gene Aliases: |
ICF4, LSH, Nbla10143, PASG, SMARCA6 |
Location: |
Chr.10:94545767-94613905 on Build GRCh38 |
Assay Gene Location: | Within Intron 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| HELLS | NM_001289067.1 | NP_001275996.1 | ||
| NM_001289068.1 | NP_001275997.1 | |||
| NM_001289069.1 | NP_001275998.1 | |||
| NM_001289070.1 | NP_001275999.1 | |||
| NM_001289071.1 | NP_001276000.1 | |||
| NM_001289072.1 | NP_001276001.1 | |||
| NM_001289073.1 | NP_001276002.1 | |||
| NM_001289074.1 | NP_001276003.1 | |||
| NM_001289075.1 | NP_001276004.1 | |||
| NM_018063.4 | NP_060533.2 | |||
| AB102716.1 | BAD10844.1 | |||
| AB102717.1 | BAD10845.1 | |||
| AB102718.1 | BAD10846.1 | |||
| AB102719.1 | BAD10847.1 | |||
| AB102720.1 | BAD10848.1 | |||
| AB102721.1 | BAD10849.1 | |||
| AB102722.1 | BAD10850.1 | |||
| AB102723.1 | BAD10851.1 | |||
| AB113248.1 | BAD24804.1 | |||
| AB113249.1 | BAD24805.1 | |||
| AF155827.1 | AAF82262.1 | |||
| AK308331.1 | ||||
| AK314485.1 | ||||
| BX538033.1 | CAD97978.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3546703 | Chr.10:94561744 - 94569243 on Build GRCh38 | Deletion |
 HELLS
|
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Additional Information:
For this assay, SNP(s) [rs79704832] 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
|
Gene Ontology Categories:
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