Assay Details
Target Gene Details
Entrez Gene ID: | 91304 |
Gene Name: | transmembrane protein 259 |
Gene Aliases: |
ASBABP1, C19orf6, MBRL, MEMBRALIN, R32184_3 |
Location: |
Chr.19:1009651-1021169 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 3 - Exon 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TMEM259 | NM_001033026.1 | NP_001028198.1 | ||
NM_033420.3 | NP_219488.1 | |||
XM_005259675.2 | XP_005259732.1 | |||
XM_005259676.2 | XP_005259733.1 | |||
XM_005259677.2 | XP_005259734.1 | |||
XM_005259678.2 | XP_005259735.1 | |||
XM_017027457.1 | XP_016882946.1 | |||
AK095756.1 | ||||
BC008957.2 | AAH08957.1 | |||
BQ895919.1 | ||||
DQ005958.1 | AAY27747.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv9662 | Chr.19:893394 - 1317740 on Build GRCh38 | Gain |
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nsv1160555 | Chr.19:887275 - 1346084 on Build GRCh38 | Deletion |
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nsv578189 | Chr.19:1007994 - 1013149 on Build GRCh38 | Loss |
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esv3643383 | Chr.19:1012555 - 1069137 on Build GRCh38 | Gain |
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nsv578188 | Chr.19:923744 - 1059005 on Build GRCh38 | Loss |
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nsv469845 | Chr.19:951640 - 1144486 on Build GRCh38 | Loss |
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esv2758743 | Chr.19:951641 - 1544934 on Build GRCh38 | Gain+Loss |
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nsv953938 | Chr.19:355801 - 1104501 on Build GRCh38 | Deletion |
![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() |
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs71335287] 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)