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See other TEX101 CNV Assays ›
Gene Symbol
TEX101
Assay Reference Genome
Location

Chr.19:43415337 on build GRCh38
Cytoband
19q13.31
Assay ID Hs07143241_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 83639

Gene Name:

 testis expressed 101

Gene Aliases:

 CT131, GTPR867, NYD-SP8, PRO1884, SGRG, SPATA44, TES101RP

Location:

 Chr.19:43388611-43418615 on Build GRCh38

Assay Gene Location:

 Within Intron 5
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
TEX101 NM_001130011.1 NP_001123483.1
NM_031451.4 NP_113639.4
XM_005259303.3 XP_005259360.2
AF241268.1 AAK28327.1
AF353396.1 AAK38662.1
AY014285.1 AAK27310.1
AY359077.1 AAQ89436.1
BC001861.2 AAH01861.2

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv469666 Chr.19:43272995 - 43430182 on Build GRCh38 Loss CD177 PRG1 TEX101
nsv1057949 Chr.19:43380906 - 43431018 on Build GRCh38 Loss TEX101
esv3583431 Chr.19:43412826 - 43449282 on Build GRCh38 Loss TEX101
esv3644466 Chr.19:43383591 - 43418114 on Build GRCh38 Gain TEX101
dgv3603n100 Chr.19:43304322 - 43590925 on Build GRCh38 Gain CD177 IRGQ PRG1 ETHE1 PHLDB3 TEX101 ZNF575 LYPD3 XRCC1 PINLYP
nsv1060280 Chr.19:43362671 - 43455533 on Build GRCh38 Gain CD177 TEX101
nsv1057657 Chr.19:42798345 - 43572412 on Build GRCh38 Gain LOC100289650 PSG5 PRG1 PHLDB3 ZNF575 LYPD3 PSG4 CD177 LOC284344 PSG9 PSG1 PSG7 ETHE1 TEX101 PSG6 PSG2 XRCC1 PSG11 PSG10P
nsv509744 Chr.19:43400292 - 43476817 on Build GRCh38 Insertion PHLDB3 TEX101 LYPD3
dgv3604n100 Chr.19:43414688 - 43453235 on Build GRCh38 Loss TEX101
nsv520852 Chr.19:43380933 - 43455962 on Build GRCh38 Gain+Loss TEX101

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More Information


Additional Information:

For this assay, SNP(s) [rs73563824] 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 Intronic Non-exonic DGV Variation

Gene Ontology Categories:

Function(s)


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