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See other FAM65A CNV Assays ›
Gene Symbol
FAM65A
Assay Reference Genome
Location

Chr.16:67532517 on build GRCh38
Cytoband
16q22.1
Assay ID Hs07550035_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 79567

Gene Name:

 family with sequence similarity 65 member A

Gene Aliases:

 -

Location:

 Chr.16:67528814-67546788 on Build GRCh38

Assay Gene Location:

 Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
FAM65A NM_001193522.1 NP_001180451.1
NM_001193523.1 NP_001180452.1
NM_024519.3 NP_078795.2
XM_011523321.1 XP_011521623.1
XM_011523322.1 XP_011521624.1
XM_011523325.1 XP_011521627.1
XM_011523326.1 XP_011521628.1
XM_017023663.1 XP_016879152.1
AK127792.1 BAC87139.1
AK293748.1
AK307467.1
CN401995.1
DC310605.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv833266 Chr.16:67408564 - 67571421 on Build GRCh38 Loss AGRP FAM65A ATP6V0D1 HSD11B2 CTCF LOC100505942 ZDHHC1 LOC107984813
nsv522852 Chr.16:67153308 - 68071571 on Build GRCh38 Gain RANBP10 ENKD1 LOC100505942 EXOC3L1 ELMO3 DDX28 TMEM208 CTRL PARD6A DUS2 LRRC36 TPPP3 LCAT C16orf86 MIR328 KIAA0895L E2F4 ACD FHOD1 FBXL8 CARMIL2 PLEKHG4 PSMB10 HSF4 LRRC29 ZDHHC1 KCTD19 DPEP2 ATP6V0D1 TRADD SLC9A5 AGRP FAM65A EDC4 CENPT PSKH1 NOL3 LOC105369155 CTCF SLC12A4 LOC100131303 TSNAXIP1 DPEP3 NUTF2 NRN1L THAP11 HSD11B2 GFOD2 LOC107984813
esv29734 Chr.16:67531230 - 67533773 on Build GRCh38 Loss FAM65A
esv3638889 Chr.16:67531203 - 67534341 on Build GRCh38 Loss FAM65A
nsv524363 Chr.16:67136529 - 68071571 on Build GRCh38 Loss RANBP10 ENKD1 LOC100505942 EXOC3L1 ELMO3 DDX28 TMEM208 CTRL PARD6A DUS2 LRRC36 TPPP3 LCAT C16orf86 MIR328 KIAA0895L E2F4 ACD FHOD1 C16orf70 FBXL8 CARMIL2 PLEKHG4 PSMB10 HSF4 LRRC29 ZDHHC1 KCTD19 B3GNT9 DPEP2 ATP6V0D1 TRADD SLC9A5 AGRP FAM65A EDC4 CENPT PSKH1 NOL3 LOC105369155 CTCF SLC12A4 LOC100131303 TSNAXIP1 DPEP3 NUTF2 NRN1L THAP11 HSD11B2 GFOD2 LOC107984813

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More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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