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Gene Symbol
HNRNPAB
Assay Reference Genome
Location

Chr.5:178210572 on build GRCh38
Cytoband
5q35.3
Assay ID Hs03046754_cn
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Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 3182

Gene Name:

 heterogeneous nuclear ribonucleoprotein A/B

Gene Aliases:

 ABBP1, HNRPAB

Location:

 Chr.5:178204507-178211183 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 7 - Exon 8
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
HNRNPAB NM_004499.3 NP_004490.2
NM_031266.2 NP_112556.2
AK054600.1
AK097657.1 BAC05134.1
AK223425.1 BAD97145.1
BC001616.1 AAH01616.1
BC002625.2 AAH02625.1
BC004561.2 AAH04561.1
BC009359.2 AAH09359.1
BC036708.2 AAH36708.1
M65028.1 AAA36575.1
U76713.1 AAC50956.1
Z36844.1

Target Gene Details

Entrez Gene ID:

 85007

Gene Name:

 5-phosphohydroxy-L-lysine phospho-lyase

Gene Aliases:

 AGXT2L2, PHLU

Location:

 Chr.5:178208474-178232822 on Build GRCh38

Assay Gene Location:

 Within Intron 12
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
PHYKPL NM_001278346.1 NP_001265275.1
NM_153373.3 NP_699204.1
NR_103508.1
NR_103509.1
NR_103510.1
XM_006714925.2 XP_006714988.1
XM_011534669.2 XP_011532971.1
XM_011534670.2 XP_011532972.1
XM_011534671.2 XP_011532973.1
XM_011534672.2 XP_011532974.1
XM_011534674.2 XP_011532976.1
XM_011534676.2 XP_011532978.1
XM_017009996.1 XP_016865485.1
XM_017009997.1 XP_016865486.1
XM_017009998.1 XP_016865487.1
XM_017009999.1 XP_016865488.1
AF318375.1 AAL55882.1
AK023470.1
AK292061.1
BC008009.1 AAH08009.1
BC037567.1 AAH37567.1
BC110335.1 AAI10336.1
HY267487.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv1019404 Chr.5:178080079 - 178432088 on Build GRCh38 Gain PHYKPL N4BP3 COL23A1 NHP2 RMND5B GMCL1P1 HNRNPAB

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More Information


Additional Information:

For this assay, SNP(s) [rs114079130] 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) Process(es)


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