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  • › Hs01104481_cn
See other FMNL3 CNV Assays ›
Gene Symbol
FMNL3
Assay Reference Genome
Location

Chr.12:49636766 on build GRCh38
Cytoband
12q13.12
Assay ID Hs01104481_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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  • Genomic Map
  • Assay Details
  • More Information

Genomic Map

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Assay Details

Target Gene Details

Entrez Gene ID:

91010

Gene Name:

formin like 3

Gene Aliases:

FHOD3, FRL2, WBP-3, WBP3

Location:

Chr.12:49636499-49707414 on Build GRCh38

Assay Gene Location:

Within Exon 31
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
FMNL3 XM_005269218.2 27 12461 XP_005269275.1
XM_011538968.2 27 12951 XP_011537270.1
XM_011538969.2 26 12835 XP_011537271.1
XM_011538970.2 27 12950 XP_011537272.1
XM_011538971.2 27 12526 XP_011537273.1
XM_011538972.2 26 12796 XP_011537274.1
XM_011538973.2 23 11941 XP_011537275.2
XM_011538974.2 28 12283 XP_011537276.1

Target Gene Details

Entrez Gene ID:

25766

Gene Name:

pre-mRNA processing factor 40 homolog B

Gene Aliases:

HYPC

Location:

Chr.12:49622717-49644669 on Build GRCh38

Assay Gene Location:

Within Exon 18
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
PRPF40B NM_001031698.2 16 1654 NP_001026868.2
NM_012272.2 15 1944 NP_036404.1
XM_006719324.3 15 2708 XP_006719387.1
XM_006719325.3 15 2708 XP_006719388.1
XM_011538135.2 15 2708 XP_011536437.1
XM_011538136.2 15 2708 XP_011536438.1
XM_011538137.2 14 2627 XP_011536439.1
XM_011538138.2 14 2597 XP_011536440.1
XM_011538139.2 16 1648 XP_011536441.1
XM_011538140.2 16 1648 XP_011536442.1
XM_011538141.1 15 1474 XP_011536443.1
XM_011538143.2 15 1490 XP_011536445.1
XM_011538144.2 14 1363 XP_011536446.1
XM_017019135.1 15 1411 XP_016874624.1
XM_017019136.1 14 1363 XP_016874625.1
XM_017019137.1 14 1363 XP_016874626.1
XM_017019138.1 15 2708 XP_016874627.1
XM_017019139.1 11 1374 XP_016874628.1
AK027117.1 BAB15662.1
AL137459.1 2 157 CAB70747.1
AL834216.1 15 1944 CAD38898.1
BC050398.2 16 1490 AAH50398.1
BC067364.1 15 1475 AAH67364.1

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv832406 Chr.12:49466910 - 49668353 on Build GRCh38 Loss FMNL3 KCNH3 MCRS1 LOC100422296 SPATS2 PRPF40B FAM186B

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More Information


Set Membership:

Intragenic Exonic DGV Variation

Gene Ontology Categories:

Function(s) Process(es)

angiogenesis
cytoskeleton organization
regulation of cell shape
cell migration
actin cytoskeleton organization
mRNA splicing, via spliceosome
actin binding
Rho GTPase binding
GTPase activating protein binding
RNA binding

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