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90161 HS6ST2

90161

HS6ST2

heparan sulfate 6-O-sulfotransferase 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition heparan sulfate 6-O-sulfotransferase 2

研究结论

Date Results Publications
2020-08-12 11:21:00 we identified a novel c.916G>C variant in the HS6ST2 gene. The mutation caused a significantly reduction in HS6ST2 6-O-sulfotransferase activity and was associated with a previously undescribed form of syndromic XLID with severe congenital myopia 30471091
2019-11-09 12:19:00 downregulated HS6ST2 targeted by miR-23b-3p promotes matrix degradation by activating p38 MAPK in chondrocytes and OA cartilage. 29899528
2018-07-07 10:16:00 RT-PCR analysis showed that the overall transcriptional activity of the main Heparan Sulfate biosynthesis-involved genes (EXT1, EXT2, NDST1, NDST2, GLCE, HS2ST1, HS3ST1, HS3ST2, HS6ST1, HS6ST2, SULF1, SULF2, HPSE) was decreased by 1.5-2-fold in Grade II-III glioma. 29104277
2014-06-21 11:11:00 HS6ST-1 and HS6ST-2 have roles in regulating the angiogenic program in ovarian cancer cells affecting HB-EGF signaling and subsequent expression of angiogenic cytokines by cancer cells 24563483
2011-07-23 10:31:00 HS6ST2 knockdown disrupts epithelial-mesenchymal transition and suggesets that HS6ST2 potentiates Notch signaling in pancreatic cancer cells. 21443520

名称对应

Type IDs
Gene
UniProtKB-ID: H6ST2_HUMAN
UniprotKB: Q96MM7
UniParc: UPI0000046171, UPI0000049037, UPI0000E59259, UPI00005B733E
EMBL: AL022159, AL022309, BC037325, AK027720, BC110620, Z81365, AK075402, AL831923, Z86064, AK056706, AB067776, BC094718, BC110621, AB067777, Z82205
Ensembl: ENSG00000171004
KO: hsa:90161
Nucleutide sequences
EMBL-CDS: BAC11597.1, BAC07183.1, CAX30811.1, BAC07184.1, AAI10622.1, AAH37325.1, BAB55322.1, AAH94718.1, AAI10621.1, BAB71260.1, CAI42774.1, CAX30812.1, CAD38583.1, CAI42775.1
Gene_ORFName: PSEC0092
Ensembl_TRS: ENST00000370836, ENST00000370833, ENST00000406696, ENST00000521489
Protein sequencees
Ensembl_PRO: ENSP00000359873, ENSP00000429473, ENSP00000359870, ENSP00000384013
RefSeq: NP_001070656.1, XP_011529710.1, XP_011529708.1, XP_011529709.1, NP_671704.3, XP_016885434.1, XP_005262548.1, XP_016885435.1
Others
UniRef100: UniRef100_Q96MM7
UniRef90: UniRef90_Q96MM7
UniRef50: UniRef50_Q96MM7
UniGene: Hs.385956
CCDS: CCDS48169.1, CCDS48170.1

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