Genomic Map
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Target Gene Details
Entrez Gene ID: | 54780 |
Gene Name: | NSE4 homolog A, SMC5-SMC6 complex component |
Gene Aliases: |
C10orf86, NS4EA, NSE4A |
Location: |
Chr.10:121957088-121975228 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 6 - Exon 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NSMCE4A | NM_001167865.1 | NP_001161337.1 | ||
| NM_017615.2 | NP_060085.2 | |||
| XM_005269929.4 | XP_005269986.1 | |||
| XM_005269930.3 | XP_005269987.1 | |||
| XM_011539910.2 | XP_011538212.1 | |||
| XM_017016359.1 | XP_016871848.1 | |||
| AF258584.1 | AAG23787.1 | |||
| AK000010.1 | BAA90881.1 | |||
| AK222487.1 | BAD96207.1 | |||
| AK301658.1 | ||||
| AK308687.1 | ||||
| BC005212.1 | AAH05212.1 | |||
| BC062427.1 | AAH62427.1 |
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Additional Information:
For this assay, SNP(s) [rs149089631] 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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