Hs03376086_cn

• Gene Symbol: SLC35E2B
• Assay Reference Genome Location: Chr.1:1669834 on build GRCh38
• Cytoband: 1p36.33

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 8

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	1	306
	AK125619.1
	AK307886.1
	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	MMP23B CDK11A FNDC10 SLC35E2B MIB2 CDK11B MMP23A GNB1 SLC35E2 NADK
dgv8n100	Chr.1:1569349 - 1741152 on Build GRCh38	Loss	SSU72 MMP23B CDK11A FNDC10 SLC35E2B MIB2 CDK11B MMP23A SLC35E2
esv3575582	Chr.1:1624086 - 1721336 on Build GRCh38	Gain	MMP23B CDK11A SLC35E2B MIB2 CDK11B MMP23A
nsv482937	Chr.1:10001 - 2368561 on Build GRCh38	Loss	LOC107985729 RNF223 LOC100288069 NOC2L FAM132A KLHL17 CDK11A LOC100133331 TMEM52 TNFRSF18 LOC105378949 MMP23A MIR200B LOC284600 LOC148413 LOC100132287 B3GALT6 SCNN1D OR4F5 ATAD3A TMEM240 ACAP3 MTND2P28 TTLL10 PRKCZ PLEKHN1 MORN1 FAM138A GABRD VWA1 SKI SSU72 LOC102725121 OR4F29 LOC729737 FAM41C NADK MIR6859-2 MIR200A DDX11L1 MIR6808 SDF4 LOC105378592 GNB1 SLC35E2 LINC01342 LOC105378948 LOC107985728 LOC105378591 MIR6726 MTND1P23 CFAP74 LOC100134822 LOC100130417 MIB2 AURKAIP1 MIR429 MIR6859-1 CCNL2 LOC100506504 LOC101928626 MRPL20 TAS1R3 C1orf159 AGRN DVL1 TTLL10-AS1 ATAD3C LOC100129534 MMP23B LINC00115 TNFRSF4 HES4 PUSL1 LOC105378589 LOC105378947 UBE2J2 LOC102724312 MIR1302-2 LOC100287934 MXRA8 SAMD11 LOC107984841 FNDC10 ISG15 LOC100288175 CALML6 WASH7P CPSF3L CDK11B FAAP20 OR4F16 MIR6723 SLC35E2B TMEM88B ATAD3B MIR6727 PERM1 ANKRD65 FAM87B LINC01128 CPTP
nsv1160797	Chr.1:1566216 - 1805918 on Build GRCh38	Duplication	SSU72 MMP23B CDK11A FNDC10 SLC35E2B MIB2 CDK11B MMP23A GNB1 SLC35E2 NADK
dgv2e199	Chr.1:1653096 - 1721890 on Build GRCh38	Deletion	CDK11A SLC35E2B CDK11B MMP23A
esv2760410	Chr.1:1565561 - 1756248 on Build GRCh38	Gain+Loss	SSU72 MMP23B CDK11A FNDC10 SLC35E2B MIB2 CDK11B MMP23A SLC35E2 NADK
esv3585008	Chr.1:1663929 - 1681002 on Build GRCh38	Loss	SLC35E2B
esv3585007	Chr.1:1647187 - 1714507 on Build GRCh38	Loss	CDK11A SLC35E2B CDK11B MMP23A
nsv950516	Chr.1:1663141 - 1715961 on Build GRCh38	Deletion	CDK11A SLC35E2B MMP23A
esv27786	Chr.1:1632502 - 1752267 on Build GRCh38	Gain	MMP23B CDK11A SLC35E2B CDK11B MMP23A SLC35E2 NADK
nsv545022	Chr.1:1665581 - 1683909 on Build GRCh38	Loss	SLC35E2B
nsv10161	Chr.1:776731 - 1777210 on Build GRCh38	Gain+Loss	LOC107985729 RNF223 LOC100130417 LOC100288069 MIB2 NOC2L AURKAIP1 FAM132A MIR429 CCNL2 MRPL20 TAS1R3 KLHL17 C1orf159 CDK11A AGRN TNFRSF18 DVL1 TTLL10-AS1 MMP23A MIR200B ATAD3C LOC284600 LOC148413 MMP23B LINC00115 TNFRSF4 B3GALT6 SCNN1D HES4 ATAD3A PUSL1 TMEM240 ACAP3 UBE2J2 LOC102724312 TTLL10 LOC100287934 MXRA8 PLEKHN1 SAMD11 FNDC10 ISG15 LOC100288175 VWA1 SSU72 CPSF3L CDK11B FAM41C NADK MIR200A MIR6808 SDF4 SLC35E2B TMEM88B ATAD3B MIR6727 PERM1 ANKRD65 SLC35E2 LINC01342 FAM87B LOC105378948 LOC107985728 LINC01128 CPTP MIR6726
nsv545018	Chr.1:1638499 - 1688102 on Build GRCh38	Loss	SLC35E2B CDK11B
dgv3n67	Chr.1:1653920 - 1735718 on Build GRCh38	Gain	CDK11A SLC35E2B CDK11B MMP23A SLC35E2
esv2758913	Chr.1:1389149 - 2092899 on Build GRCh38	Gain+Loss	PRKCZ CFAP74 LOC107985729 FNDC10 MIB2 GABRD CALML6 VWA1 CCNL2 MRPL20 SSU72 CDK11A TMEM52 LOC105378949 CDK11B MMP23A ATAD3C NADK LOC148413 MMP23B SLC35E2B TMEM88B ATAD3B ATAD3A ANKRD65 LOC105378589 GNB1 SLC35E2 TMEM240 LOC102724312 LOC105378591

More Information

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation

Panther Classification:

Molecular Function -

secondary carrier transporter