Genomic Map
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Target Gene Details
Entrez Gene ID: | 4068 |
Gene Name: | SH2 domain containing 1A |
Gene Aliases: |
DSHP, EBVS, IMD5, LYP, MTCP1, SAP, SAP/SH2D1A, XLP, XLPD, XLPD1 |
Location: |
Chr.X:124346282-124373160 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SH2D1A | NM_001114937.2 | NP_001108409.1 | ||
| NM_002351.4 | NP_002342.1 | |||
| AB586694.1 | ||||
| AF072930.1 | AAC62630.1 | |||
| AF073019.1 | AAC62631.1 | |||
| AF100539.1 | AAC79712.1 | |||
| AF100540.1 | AAC79713.1 | |||
| AF100541.1 | AAC79714.1 | |||
| AF100542.1 | AAC79715.1 | |||
| AF100543.1 | AAC79716.1 | |||
| AK311645.1 | ||||
| AK311911.1 | ||||
| AL023657.1 | CAA19222.1 | |||
| BC020732.1 | AAH20732.1 | |||
| CR542031.1 | CAG46828.1 | |||
| CR542043.1 | CAG46840.1 | |||
| JX512648.1 |
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Additional Information:
For this assay, SNP(s) [rs73543044] 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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