Assay Details
Target Gene Details
Entrez Gene ID: | 8996 |
Gene Name: | nucleolar protein 3 |
Gene Aliases: |
ARC, FCM, MYP, NOP, NOP30 |
Location: |
Chr.16:67170497-67175737 on Build GRCh38 |
Assay Gene Location: | Within Exon 4 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
NOL3 | NM_001185057.2 | 2 | 282 | NP_001171986.1 |
NM_001276307.1 | 4 | 306 | NP_001263236.1 | |
NM_001276309.1 | 2 | 166 | NP_001263238.1 | |
NM_001276311.1 | 2 | 282 | NP_001263240.1 | |
NM_001276312.1 | 4 | 657 | NP_001263241.1 | |
NM_001276319.1 | 4 | 657 | NP_001263248.1 | |
NM_003946.6 | 2 | 282 | NP_003937.1 | |
XM_005256217.2 | 2 | 919 | XP_005256274.1 | |
XM_005256219.3 | 2 | 919 | XP_005256276.1 | |
XM_011523424.2 | 3 | 762 | XP_011521726.1 | |
XM_017023843.1 | 2 | 919 | XP_016879332.1 | |
AF043244.1 | 2 | 199 | AAC34993.1 | |
AF064599.1 | 2 | 133 | AAC18593.1 | |
AF064600.1 | 2 | 157 | AAC18594.1 | |
AK294145.1 | 4 | 622 | ||
AK314899.1 | 2 | 187 | ||
BC012798.2 | 2 | 168 | AAH12798.1 | |
BP215200.1 | 2 | 123 | ||
BQ685512.1 | 2 | 282 | ||
BT020158.1 | 1 | 80 | AAV38960.1 | |
CB959673.1 | 4 | 333 |
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 | C16orf86 AGRP ENKD1 THAP11 DDX28 CTCF EXOC3L1 NOL3 CARMIL2 LCAT FHOD1 LOC100131303 PARD6A CTRL KIAA0895L HSF4 ATP6V0D1 LRRC36 DPEP3 E2F4 EDC4 HSD11B2 ACD SLC9A5 ELMO3 LOC107984813 NRN1L DUS2 ZDHHC1 MIR328 PSKH1 NUTF2 LOC100505942 LOC105369155 GFOD2 LRRC29 SLC12A4 RANBP10 TPPP3 TRADD DPEP2 FBXL8 FAM65A PSMB10 TMEM208 CENPT TSNAXIP1 KCTD19 PLEKHG4 |
nsv827707 | Chr.16:67148355 - 67289296 on Build GRCh38 | Loss | TRADD FBXL8 SLC9A5 ELMO3 KIAA0895L EXOC3L1 HSF4 MIR328 NOL3 TMEM208 FHOD1 E2F4 B3GNT9 LOC105369155 C16orf70 LRRC29 PLEKHG4 |
nsv952044 | Chr.16:67141198 - 67244397 on Build GRCh38 | Deletion | TRADD FBXL8 ELMO3 KIAA0895L EXOC3L1 HSF4 MIR328 NOL3 TMEM208 FHOD1 E2F4 B3GNT9 LOC105369155 C16orf70 LRRC29 |
nsv1160429 | Chr.16:67161549 - 67220197 on Build GRCh38 | Deletion | NOL3 FBXL8 E2F4 ELMO3 LOC105369155 KIAA0895L EXOC3L1 LRRC29 HSF4 MIR328 |
nsv524492 | Chr.16:67174030 - 67294550 on Build GRCh38 | Loss | SLC9A5 ELMO3 KIAA0895L EXOC3L1 MIR328 NOL3 TMEM208 FHOD1 E2F4 LOC105369155 KCTD19 LRRC29 PLEKHG4 |
nsv524363 | Chr.16:67136529 - 68071571 on Build GRCh38 | Loss | C16orf86 AGRP ENKD1 THAP11 DDX28 CTCF EXOC3L1 NOL3 CARMIL2 LCAT FHOD1 C16orf70 LOC100131303 PARD6A CTRL KIAA0895L HSF4 ATP6V0D1 LRRC36 DPEP3 E2F4 EDC4 HSD11B2 ACD SLC9A5 ELMO3 LOC107984813 NRN1L DUS2 ZDHHC1 MIR328 PSKH1 NUTF2 LOC100505942 B3GNT9 LOC105369155 GFOD2 LRRC29 SLC12A4 RANBP10 TPPP3 TRADD DPEP2 FBXL8 FAM65A PSMB10 TMEM208 CENPT TSNAXIP1 KCTD19 PLEKHG4 |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |