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

Chr.16:67537267 on build GRCh38
Cytoband
16q22.1
Assay ID Hs05425946_cn
Size
Availability Made To Order
Catalog # 4400291
Price 475.00
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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 LOC100505942 CTCF AGRP FAM65A HSD11B2 LOC107984813 ZDHHC1 ATP6V0D1
nsv522852 Chr.16:67153308 - 68071571 on Build GRCh38 Gain PSKH1 CENPT ENKD1 ELMO3 FHOD1 AGRP EXOC3L1 HSD11B2 HSF4 CTCF THAP11 TMEM208 NRN1L FAM65A TRADD ZDHHC1 DPEP3 SLC9A5 SLC12A4 PLEKHG4 TPPP3 FBXL8 LRRC36 ATP6V0D1 MIR328 RANBP10 DDX28 LOC107984813 ACD DPEP2 LOC100505942 DUS2 GFOD2 NOL3 LOC105369155 PSMB10 C16orf86 LCAT TSNAXIP1 NUTF2 CTRL KCTD19 CARMIL2 PARD6A LRRC29 E2F4 EDC4 LOC100131303 KIAA0895L
nsv827711 Chr.16:67536103 - 67583824 on Build GRCh38 Gain CTCF FAM65A LOC107984813
nsv524363 Chr.16:67136529 - 68071571 on Build GRCh38 Loss PSKH1 CENPT ENKD1 ELMO3 FHOD1 AGRP EXOC3L1 HSD11B2 HSF4 CTCF THAP11 TMEM208 NRN1L FAM65A TRADD ZDHHC1 DPEP3 SLC9A5 SLC12A4 PLEKHG4 TPPP3 FBXL8 LRRC36 ATP6V0D1 B3GNT9 MIR328 RANBP10 DDX28 LOC107984813 ACD DPEP2 LOC100505942 DUS2 GFOD2 NOL3 LOC105369155 PSMB10 C16orf86 LCAT TSNAXIP1 C16orf70 NUTF2 CTRL KCTD19 CARMIL2 PARD6A LRRC29 E2F4 EDC4 LOC100131303 KIAA0895L

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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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