Genomic Map
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Target Gene Details
Entrez Gene ID: | 163175 |
Gene Name: | leucine rich repeat LGI family member 4 |
Gene Aliases: |
LGIL3 |
Location: |
Chr.19:35124513-35135274 on Build GRCh38 |
Assay Gene Location: | Within Intron 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LGI4 | NM_139284.2 | NP_644813.1 | ||
| XM_011526595.1 | XP_011524897.1 | |||
| XM_017026428.1 | XP_016881917.1 | |||
| XM_017026429.1 | XP_016881918.1 | |||
| XM_017026430.1 | XP_016881919.1 | |||
| AF467954.1 | AAM49552.1 | |||
| AJ487519.1 | CAD31787.1 | |||
| AJ487959.1 | CAD32306.1 | |||
| AL832968.1 | CAH56336.1 | |||
| AY358121.1 | AAQ88488.1 | |||
| BC087848.1 | AAH87848.1 | |||
| BC136694.1 | ||||
| BC136697.1 | ||||
| BC140008.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv993226 | Chr.19:35132335 - 35132910 on Build GRCh38 | Loss |
 LGI4
|
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Additional Information:
For this assay, SNP(s) [rs116825564] 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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