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Gene Symbol
BIN1
Assay Reference Genome
Location

Chr.2:127048602 on build GRCh38
Cytoband
2q14.3
Assay ID Hs00587954_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 274

Gene Name:

 bridging integrator 1

Gene Aliases:

 AMPH2, AMPHL, SH3P9

Location:

 Chr.2:127048023-127107400 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 21 - Exon 22
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
BIN1 NM_001320632.1 NP_001307561.1
NM_001320633.1 NP_001307562.1
NM_001320634.1 NP_001307563.1
NM_001320640.1 NP_001307569.1
NM_001320641.1 NP_001307570.1
NM_001320642.1 NP_001307571.1
NM_004305.3 NP_004296.1
NM_139343.2 NP_647593.1
NM_139344.2 NP_647594.1
NM_139345.2 NP_647595.1
NM_139346.2 NP_647596.1
NM_139347.2 NP_647597.1
NM_139348.2 NP_647598.1
NM_139349.2 NP_647599.1
NM_139350.2 NP_647600.1
NM_139351.2 NP_647601.1
XM_005263642.3 XP_005263699.1
XM_005263643.3 XP_005263700.1
XM_005263645.2 XP_005263702.1
XM_006712425.3 XP_006712488.1
XM_006712426.3 XP_006712489.1
XM_006712427.2 XP_006712490.1
XM_006712428.3 XP_006712491.1
XM_006712429.3 XP_006712492.1
XM_006712431.3 XP_006712494.1
XM_006712432.3 XP_006712495.1
XM_006712433.3 XP_006712496.1
XM_006712434.3 XP_006712497.1
XM_011510975.2 XP_011509277.1
XM_017003819.1 XP_016859308.1
XM_017003820.1 XP_016859309.1
XM_017003821.1 XP_016859310.1
XM_017003822.1 XP_016859311.1
XM_017003823.1 XP_016859312.1
XM_017003824.1 XP_016859313.1
XM_017003825.1 XP_016859314.1
XM_017003826.1 XP_016859315.1
XM_017003827.1 XP_016859316.1
XM_017003828.1 XP_016859317.1
AF001383.1 AAB61363.1
AF004015.1 AAC51345.1
AF043898.1 AAC39710.1
AF043899.1 AAC39711.1
AF043900.1 AAC39712.1
AF043901.1 AAC39713.1
AF068914.1 AAC24126.1
AF068915.1 AAC24127.1
AF068916.1 AAC24128.1
AF068917.1 AAC23750.1
AF068918.1 AAC23751.1
AF070576.1 AAC28646.1
AK127325.1
AK295300.1
AK301153.1
AL713697.1 CAD28496.1
BC004101.2 AAH04101.1
BM805510.1
BT006865.1 AAP35511.1
DR761993.1
U68485.1 AAC17461.1
U87558.1 AAB63263.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv954812 Chr.2:127039525 - 127106424 on Build GRCh38 Deletion BIN1
nsv583032 Chr.2:127013430 - 127087159 on Build GRCh38 Loss BIN1
nsv516759 Chr.2:127039090 - 127101865 on Build GRCh38 Loss BIN1
dgv4064n100 Chr.2:127036712 - 127104681 on Build GRCh38 Gain BIN1
nsv583033 Chr.2:127043405 - 127110859 on Build GRCh38 Loss BIN1
nsv999422 Chr.2:126707071 - 127198967 on Build GRCh38 Gain CYP27C1 BIN1 LOC101929926

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