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See other LRRC36 CNV Assays ›
Gene Symbol
LRRC36
Assay Reference Genome
Location

Chr.16:67344685 on build GRCh38
Cytoband
16q22.1
Assay ID Hs05467935_cn
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Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 55282

Gene Name:

 leucine rich repeat containing 36

Gene Aliases:

 RORBP70, XLHSRF2

Location:

 Chr.16:67326844-67385206 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
LRRC36 NM_018296.5 NP_060766.5
XM_005256025.2 XP_005256082.1
XM_005256026.2 XP_005256083.1
XM_005256027.2 XP_005256084.1
XM_005256028.1 XP_005256085.1
XM_011523200.1 XP_011521502.1
XM_011523202.2 XP_011521504.1
XM_011523203.1 XP_011521505.1
XM_011523205.1 XP_011521507.1
XM_011523206.2 XP_011521508.1
XM_017023400.1 XP_016878889.1
XM_017023401.1 XP_016878890.1
XM_017023402.1 XP_016878891.1
AY963267.1
BC026156.2

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv522852 Chr.16:67153308 - 68071571 on Build GRCh38 Gain KIAA0895L CTCF TRADD DUS2 SLC9A5 AGRP GFOD2 DPEP2 NUTF2 LRRC36 ELMO3 MIR328 LOC105369155 HSF4 LOC100505942 E2F4 PSMB10 ZDHHC1 RANBP10 LRRC29 CTRL SLC12A4 ACD PSKH1 LOC107984813 FHOD1 C16orf86 NOL3 DDX28 PARD6A NRN1L LOC100131303 TSNAXIP1 TMEM208 EDC4 FAM65A FBXL8 THAP11 TPPP3 CENPT DPEP3 KCTD19 EXOC3L1 HSD11B2 LCAT PLEKHG4 ATP6V0D1 ENKD1 CARMIL2
nsv833265 Chr.16:67327714 - 67373302 on Build GRCh38 Loss LRRC36
nsv572906 Chr.16:67237955 - 67368685 on Build GRCh38 Loss PLEKHG4 LRRC36 KCTD19 SLC9A5 FHOD1
nsv471092 Chr.16:67174030 - 67518392 on Build GRCh38 Gain KIAA0895L TPPP3 LOC105369155 NOL3 LOC100505942 E2F4 KCTD19 EXOC3L1 SLC9A5 AGRP HSD11B2 ZDHHC1 LRRC29 PLEKHG4 ATP6V0D1 TMEM208 LRRC36 ELMO3 FHOD1 MIR328
nsv524363 Chr.16:67136529 - 68071571 on Build GRCh38 Loss KIAA0895L CTCF TRADD DUS2 SLC9A5 AGRP GFOD2 DPEP2 NUTF2 B3GNT9 LRRC36 ELMO3 MIR328 LOC105369155 HSF4 LOC100505942 E2F4 PSMB10 ZDHHC1 RANBP10 LRRC29 CTRL SLC12A4 ACD PSKH1 LOC107984813 FHOD1 C16orf86 NOL3 DDX28 PARD6A NRN1L LOC100131303 TSNAXIP1 TMEM208 C16orf70 EDC4 FAM65A FBXL8 THAP11 TPPP3 CENPT DPEP3 KCTD19 EXOC3L1 HSD11B2 LCAT PLEKHG4 ATP6V0D1 ENKD1 CARMIL2

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More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

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