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See other SLC35E2B CNV Assays ›
Gene Symbol
SLC35E2B
Assay Reference Genome
Location

Chr.1:1666000 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03335835_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:

728661

Gene Name:

solute carrier family 35 member E2B

Gene Aliases:

SLC35E2

Location:

Chr.1:1661478-1692804 on Build GRCh38

Assay Gene Location:

Overlaps Intron 10 - Exon 11
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
SLC35E2B NM_001110781.2 NP_001104251.1
NM_001290264.1 NP_001277193.1
XM_011542072.1 XP_011540374.1
AB007916.3
AK092311.1
AK125619.1
BC110653.1 AAI10654.1
CR936618.1 CAI56761.1
DA794179.1

Target Copy Number Variation Details

DGV Version:

Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
dgv37n54 Chr.1:1663759 - 1696548 on Build GRCh38 Loss SLC35E2B
dgv5n111 Chr.1:1575421 - 1823403 on Build GRCh38 Deletion MMP23A MIB2 NADK SLC35E2B CDK11A MMP23B SLC35E2 FNDC10 CDK11B GNB1
dgv8n100 Chr.1:1569349 - 1741152 on Build GRCh38 Loss MMP23A MIB2 SLC35E2B SSU72 CDK11A MMP23B SLC35E2 FNDC10 CDK11B
esv3575582 Chr.1:1624086 - 1721336 on Build GRCh38 Gain MMP23A MIB2 SLC35E2B CDK11A MMP23B CDK11B
nsv482937 Chr.1:10001 - 2368561 on Build GRCh38 Loss LOC729737 MRPL20 MIR429 LOC148413 LOC105378592 LOC100134822 RNF223 SLC35E2B LOC105378589 SLC35E2 LINC01128 CDK11B LOC100288175 MMP23A MIR200B LOC100129534 MIR6726 LOC105378949 PRKCZ HES4 LINC01342 AGRN TMEM88B LOC105378947 MTND2P28 KLHL17 LOC102724312 CALML6 CDK11A FAAP20 UBE2J2 VWA1 OR4F29 LOC100132287 MTND1P23 NOC2L ATAD3B FAM138A B3GALT6 LOC100130417 PLEKHN1 LOC100133331 SSU72 OR4F5 MMP23B LOC107985729 NADK ANKRD65 DVL1 FAM41C SAMD11 PERM1 MIR6859-2 LOC101928626 MIR6727 LOC105378591 LOC284600 LOC102725121 OR4F16 LOC100288069 LOC107985728 C1orf159 ACAP3 TMEM240 LOC107984841 SCNN1D SKI WASH7P MIR6723 FAM132A MIR1302-2 LOC105378948 AURKAIP1 MIR6859-1 TTLL10 TNFRSF4 CPSF3L MIB2 LOC100287934 TNFRSF18 ATAD3A LINC00115 MXRA8 LOC100506504 TMEM52 PUSL1 MIR6808 GABRD CPTP SDF4 CFAP74 FAM87B FNDC10 MIR200A DDX11L1 MORN1 ISG15 CCNL2 TTLL10-AS1 TAS1R3 GNB1 ATAD3C
nsv1160797 Chr.1:1566216 - 1805918 on Build GRCh38 Duplication MMP23A MIB2 NADK SLC35E2B SSU72 CDK11A MMP23B SLC35E2 FNDC10 CDK11B GNB1
dgv2e199 Chr.1:1653096 - 1721890 on Build GRCh38 Deletion MMP23A SLC35E2B CDK11A CDK11B
esv2760410 Chr.1:1565561 - 1756248 on Build GRCh38 Gain+Loss MMP23A MIB2 NADK SLC35E2B SSU72 CDK11A MMP23B SLC35E2 FNDC10 CDK11B
esv3585008 Chr.1:1663929 - 1681002 on Build GRCh38 Loss SLC35E2B
esv3585007 Chr.1:1647187 - 1714507 on Build GRCh38 Loss MMP23A SLC35E2B CDK11A CDK11B
nsv950516 Chr.1:1663141 - 1715961 on Build GRCh38 Deletion MMP23A SLC35E2B CDK11A
esv27786 Chr.1:1632502 - 1752267 on Build GRCh38 Gain MMP23A NADK SLC35E2B CDK11A MMP23B SLC35E2 CDK11B
nsv545022 Chr.1:1665581 - 1683909 on Build GRCh38 Loss SLC35E2B
nsv10161 Chr.1:776731 - 1777210 on Build GRCh38 Gain+Loss SAMD11 PERM1 MRPL20 MIR429 MIR6727 LOC148413 LOC284600 RNF223 LOC100288069 LOC107985728 SLC35E2B C1orf159 SLC35E2 ACAP3 LINC01128 TMEM240 CDK11B LOC100288175 MMP23A MIR200B MIR6726 SCNN1D HES4 LINC01342 FAM132A AGRN TMEM88B LOC105378948 KLHL17 LOC102724312 AURKAIP1 CDK11A TTLL10 TNFRSF4 UBE2J2 CPSF3L VWA1 MIB2 LOC100287934 TNFRSF18 ATAD3A LINC00115 MXRA8 NOC2L ATAD3B PUSL1 MIR6808 B3GALT6 CPTP LOC100130417 SDF4 PLEKHN1 SSU72 MMP23B FAM87B LOC107985729 FNDC10 NADK MIR200A ANKRD65 ISG15 CCNL2 TTLL10-AS1 DVL1 TAS1R3 FAM41C ATAD3C
nsv545018 Chr.1:1638499 - 1688102 on Build GRCh38 Loss SLC35E2B CDK11B
dgv3n67 Chr.1:1653920 - 1735718 on Build GRCh38 Gain MMP23A SLC35E2B CDK11A SLC35E2 CDK11B
esv2758913 Chr.1:1389149 - 2092899 on Build GRCh38 Gain+Loss MIB2 MRPL20 LOC105378591 ATAD3A LOC148413 SLC35E2B TMEM52 LOC105378589 ATAD3B SLC35E2 TMEM240 CDK11B MMP23A GABRD LOC105378949 PRKCZ SSU72 CFAP74 MMP23B LOC107985729 TMEM88B FNDC10 NADK ANKRD65 CCNL2 LOC102724312 CALML6 CDK11A GNB1 VWA1 ATAD3C

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More Information


Set Membership:

Intragenic Non-exonic DGV Variation

Panther Classification:

Molecular Function -

secondary carrier transporter

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