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See other FAM177A1 CNV Assays ›
Gene Symbol
FAM177A1
Assay Reference Genome
Location

Chr.14:35083200 on build GRCh38
Cytoband
14q13.2
Assay ID Hs02516542_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 283635

Gene Name:

 family with sequence similarity 177 member A1

Gene Aliases:

 C14orf24

Location:

 Chr.14:35044907-35083383 on Build GRCh38

Assay Gene Location:

 Within Exon 7
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
FAM177A1 NM_001079519.1 7 3073 NP_001072987.1
NM_001289022.1 6 2796 NP_001275951.1
NM_173607.3 5 2743 NP_775878.2
AK096173.1 6 2684 BAC04716.1
AL833508.1 5 2657
BX640884.1 5 2746
BX640984.1 5 2694
CR749796.1 5 2743 CAH18656.1

Target Gene Details

Entrez Gene ID:

 101927178

Gene Name:

 uncharacterized LOC101927178

Gene Aliases:

 -

Location:

 Chr.14:35081081-35113130 on Build GRCh38

Assay Gene Location:

 Within Intron 1
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LOC101927178 NR_110415.1
CK904250.1
CK904251.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv564263 Chr.14:34997378 - 35087292 on Build GRCh38 Loss LOC101927178 FAM177A1 PPP2R3C SRP54
esv3892499 Chr.14:34900273 - 35107577 on Build GRCh38 Loss LOC101927178 FAM177A1 IGBP1P1 PPP2R3C SRP54
nsv564264 Chr.14:35013591 - 35263163 on Build GRCh38 Gain KIAA0391 LOC101927178 FAM177A1 PPP2R3C SRP54
nsv564265 Chr.14:35043129 - 35155625 on Build GRCh38 Loss KIAA0391 LOC101927178 FAM177A1 PPP2R3C
dgv1868n100 Chr.14:35041579 - 35287111 on Build GRCh38 Gain KIAA0391 LOC101927178 FAM177A1 PSMA6 PPP2R3C
esv3584249 Chr.14:35060670 - 35255038 on Build GRCh38 Gain KIAA0391 LOC101927178 FAM177A1 PPP2R3C
nsv1042625 Chr.14:35076888 - 35211152 on Build GRCh38 Gain KIAA0391 LOC101927178 FAM177A1 PPP2R3C

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More Information


Additional Information:

For this assay, SNP(s) [rs76897719] 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 Exonic Intronic Non-exonic DGV Variation

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