Assay Details
Target Gene Details
Entrez Gene ID: | 4673 |
Gene Name: | nucleosome assembly protein 1 like 1 |
Gene Aliases: |
NAP1, NAP1L, NRP |
Location: |
Chr.12:76045383-76085033 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 7 - Exon 8 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NAP1L1 | NM_001307924.1 | NP_001294853.1 | ||
NM_004537.5 | NP_004528.1 | |||
NM_139207.3 | NP_631946.1 | |||
XM_006719425.3 | XP_006719488.1 | |||
XM_011538390.2 | XP_011536692.2 | |||
XM_011538393.2 | XP_011536695.1 | |||
XM_017019338.1 | XP_016874827.1 | |||
XM_017019339.1 | XP_016874828.1 | |||
XM_017019340.1 | XP_016874829.1 | |||
AK122670.1 | ||||
AK295147.1 | ||||
AK297500.1 | ||||
AK298936.1 | ||||
AK304787.1 | ||||
AL162068.1 | CAB82405.1 | |||
BC002387.2 | AAH02387.1 | |||
BT007023.1 | AAP35669.1 | |||
DA512918.1 | ||||
M86667.1 | AAC37544.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv559423 | Chr.12:76052528 - 76072853 on Build GRCh38 | Loss |
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More Information
Additional Information:
For this assay, SNP(s) [rs139945348] 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: |
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Panther Classification:
Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)