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- Gene Symbol
- DCX
- Assay Reference Genome
Location
Chr.X:111349054 on build GRCh38- Cytoband
- Xq23
Genomic Map
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Target Gene Details
Entrez Gene ID: | 1641 |
Gene Name: | doublecortin |
Gene Aliases: |
DBCN, DC, LISX, SCLH, XLIS |
Location: |
Chr.X:111293779-111412232 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DCX | NM_000555.3 | NP_000546.2 | ||
| NM_001195553.1 | NP_001182482.1 | |||
| NM_178151.2 | NP_835364.1 | |||
| NM_178152.2 | NP_835365.1 | |||
| NM_178153.2 | NP_835366.1 | |||
| XM_011530878.2 | XP_011529180.1 | |||
| XM_011530879.2 | XP_011529181.1 | |||
| XM_011530880.2 | XP_011529182.1 | |||
| XM_017029312.1 | XP_016884801.1 | |||
| AF034634.1 | AAC52037.1 | |||
| AF040254.1 | AAC31797.1 | |||
| AF040255.1 | AAC31696.1 | |||
| AJ003112.1 | CAA05867.1 | |||
| AK290455.1 | ||||
| AK297297.1 | ||||
| AK299822.1 | ||||
| BC027925.1 | AAH27925.1 |
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Additional Information:
For this assay, SNP(s) [rs140496669] 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
non-DGV Variation
|
Gene Ontology Categories:
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