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

Chr.1:1669154 on build GRCh38
Cytoband
1p36.33
Assay ID Hs03379294_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:

Within Intron 9
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 SLC35E2 FNDC10 NADK MMP23B SLC35E2B GNB1 MIB2 MMP23A CDK11A CDK11B
dgv8n100 Chr.1:1569349 - 1741152 on Build GRCh38 Loss SSU72 SLC35E2 FNDC10 MMP23B SLC35E2B MIB2 MMP23A CDK11A CDK11B
esv3575582 Chr.1:1624086 - 1721336 on Build GRCh38 Gain MMP23B SLC35E2B MIB2 MMP23A CDK11A CDK11B
nsv482937 Chr.1:10001 - 2368561 on Build GRCh38 Loss SAMD11 TTLL10-AS1 LOC100133331 LOC729737 MIR6859-2 LOC101928626 RNF223 ACAP3 ANKRD65 DVL1 CCNL2 TTLL10 LINC01342 TAS1R3 LOC105378592 OR4F16 SKI LOC100288069 SCNN1D UBE2J2 LOC100134822 LOC107985728 VWA1 MIR1302-2 LOC100287934 MIR6727 MMP23B ATAD3C GABRD MORN1 CALML6 MIR6726 PLEKHN1 LOC102724312 OR4F29 SLC35E2B GNB1 NOC2L LOC102725121 MIR6859-1 FAM41C FAAP20 AURKAIP1 LOC100130417 C1orf159 LOC107985729 MMP23A MIR200A FAM138A MIR6723 MTND1P23 SLC35E2 FNDC10 LOC100288175 TNFRSF4 LOC105378591 CPSF3L SDF4 AGRN LOC148413 WASH7P LOC284600 LINC01128 LOC105378949 LINC00115 LOC105378589 FAM87B MIR200B HES4 MIR429 CDK11A ISG15 MXRA8 CPTP LOC100506504 LOC100132287 MTND2P28 TMEM88B LOC100129534 MIR6808 ATAD3A TMEM52 PUSL1 LOC105378948 TMEM240 CFAP74 LOC105378947 CDK11B PRKCZ B3GALT6 TNFRSF18 MIB2 LOC107984841 OR4F5 SSU72 MRPL20 KLHL17 PERM1 DDX11L1 NADK ATAD3B FAM132A
nsv1160797 Chr.1:1566216 - 1805918 on Build GRCh38 Duplication SSU72 SLC35E2 FNDC10 NADK MMP23B SLC35E2B GNB1 MIB2 MMP23A CDK11A CDK11B
dgv2e199 Chr.1:1653096 - 1721890 on Build GRCh38 Deletion SLC35E2B MMP23A CDK11A CDK11B
esv2760410 Chr.1:1565561 - 1756248 on Build GRCh38 Gain+Loss SSU72 SLC35E2 FNDC10 NADK MMP23B SLC35E2B MIB2 MMP23A CDK11A CDK11B
esv3585008 Chr.1:1663929 - 1681002 on Build GRCh38 Loss SLC35E2B
esv3585007 Chr.1:1647187 - 1714507 on Build GRCh38 Loss SLC35E2B MMP23A CDK11A CDK11B
nsv950516 Chr.1:1663141 - 1715961 on Build GRCh38 Deletion SLC35E2B MMP23A CDK11A
esv27786 Chr.1:1632502 - 1752267 on Build GRCh38 Gain SLC35E2 NADK MMP23B SLC35E2B MMP23A CDK11A CDK11B
nsv545022 Chr.1:1665581 - 1683909 on Build GRCh38 Loss SLC35E2B
nsv10161 Chr.1:776731 - 1777210 on Build GRCh38 Gain+Loss SLC35E2 FNDC10 LOC100288175 SAMD11 TTLL10-AS1 TNFRSF4 CPSF3L RNF223 SDF4 AGRN ACAP3 ANKRD65 LOC148413 LOC284600 DVL1 LINC01128 CCNL2 TTLL10 LINC00115 FAM87B MIR200B HES4 MIR429 CDK11A ISG15 MXRA8 LINC01342 CPTP TAS1R3 LOC100288069 SCNN1D TMEM88B UBE2J2 LOC107985728 MIR6808 VWA1 ATAD3A LOC100287934 MIR6727 MMP23B ATAD3C PUSL1 LOC105378948 TMEM240 MIR6726 CDK11B PLEKHN1 B3GALT6 TNFRSF18 LOC102724312 SLC35E2B MIB2 NOC2L FAM41C AURKAIP1 SSU72 MRPL20 KLHL17 PERM1 NADK LOC100130417 C1orf159 LOC107985729 MMP23A MIR200A ATAD3B FAM132A
nsv545018 Chr.1:1638499 - 1688102 on Build GRCh38 Loss SLC35E2B CDK11B
dgv3n67 Chr.1:1653920 - 1735718 on Build GRCh38 Gain SLC35E2 SLC35E2B MMP23A CDK11A CDK11B
esv2758913 Chr.1:1389149 - 2092899 on Build GRCh38 Gain+Loss SLC35E2 FNDC10 VWA1 ATAD3A MMP23B ATAD3C GABRD TMEM52 LOC105378591 TMEM240 CFAP74 CALML6 ANKRD65 LOC148413 CDK11B PRKCZ CCNL2 LOC105378949 LOC102724312 LOC105378589 SLC35E2B GNB1 MIB2 CDK11A SSU72 MRPL20 NADK LOC107985729 MMP23A ATAD3B TMEM88B

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More Information


Set Membership:

Intragenic Intronic Non-exonic DGV Variation

Panther Classification:

Molecular Function -

secondary carrier transporter

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