Genomic Map
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Target Gene Details
Entrez Gene ID: | 51474 |
Gene Name: | LIM domain and actin binding 1 |
Gene Aliases: |
EPLIN, SREBP3 |
Location: |
Chr.12:50175780-50283570 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| LIMA1 | NM_001113546.1 | NP_001107018.1 | ||
| NM_016357.4 | NP_057441.1 | |||
| XM_011538455.2 | XP_011536757.1 | |||
| XM_017019430.1 | XP_016874919.1 | |||
| AB209512.1 | BAD92749.1 | |||
| AF198454.1 | AAF23755.1 | |||
| AK000372.1 | BAA91120.1 | |||
| AK222971.1 | BAD96691.1 | |||
| AK314447.1 | ||||
| AL136911.1 | CAB66845.1 | |||
| BC110815.1 | AAI10816.1 | |||
| BC136763.1 | ||||
| BP216703.1 | ||||
| BP281423.1 |
Target Gene Details
Entrez Gene ID: | 100302220 |
Gene Name: | microRNA 1293 |
Gene Aliases: |
MIRN1293, hsa-mir-1293, mir-1293 |
Location: |
Chr.12:50234142-50234212 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| MIR1293 | NR_031625.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2761738 | Chr.12:50233509 - 50442644 on Build GRCh38 | Gain |
 MIR1293
LARP4
LIMA1
FAM186A
|
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Additional Information:
For this assay, SNP(s) [rs113699072,rs115202050] 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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