Genomic Map
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Target Gene Details
Entrez Gene ID: | 29071 |
Gene Name: | C1GALT1 specific chaperone 1 |
Gene Aliases: |
C1GALT2, C38H2-L1, COSMC, HSPC067, MST143, TNPS |
Location: |
Chr.X:120625674-120630150 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| C1GALT1C1 | NM_001011551.2 | 1 | 150 | NP_001011551.1 |
| NM_152692.4 | 1 | 150 | NP_689905.1 | |
| AB084170.1 | BAC41493.1 | |||
| AF161552.1 | AAF29039.1 | |||
| AF177284.1 | AAQ13670.1 | |||
| AJ238398.1 | 1 | 150 | CAC80277.1 | |
| AK290111.1 | ||||
| AY159319.1 | AAN78129.1 | |||
| AY358642.1 | AAQ89005.1 | |||
| BC011930.2 | AAH11930.1 | |||
| BC050441.1 | AAH50441.1 | |||
| BG779539.1 | 1 | 125 |
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Additional Information:
For this assay, SNP(s) [rs111295814] 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
Exonic
non-DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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