Genomic Map
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Target Gene Details
Entrez Gene ID: | 22985 |
Gene Name: | apoptotic chromatin condensation inducer 1 |
Gene Aliases: |
ACINUS, ACN, fSAP152 |
Location: |
Chr.14:23058564-23095614 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 20 - Exon 20 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ACIN1 | NM_001164814.1 | NP_001158286.1 | ||
| NM_001164815.1 | NP_001158287.1 | |||
| NM_001164816.1 | NP_001158288.1 | |||
| NM_001164817.1 | NP_001158289.1 | |||
| NM_014977.3 | NP_055792.1 | |||
| XM_005267415.3 | XP_005267472.1 | |||
| XM_005267416.3 | XP_005267473.1 | |||
| XM_005267418.1 | XP_005267475.1 | |||
| AB014570.2 | BAA31645.2 | |||
| AF124726.1 | AAD56724.1 | |||
| AF124727.1 | AAD56725.1 | |||
| AF124728.1 | AAD56726.1 | |||
| AL050382.1 | CAB43681.2 | |||
| AL833228.1 | CAH10608.1 | |||
| BC140805.1 | ||||
| BX247975.1 | CAD62309.1 |
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Additional Information:
For this assay, SNP(s) [rs75417887] 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
Non-exonic
non-DGV Variation
|
Gene Ontology Categories:
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