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Reactome (instancebrowser)
Reactome: A Curated Pathway Database
Details
IdentifierUniProt:P50443
DatabaseUniProt
SpeciesHomo sapiens
DescriptionrecommendedName: Sulfate transporter alternativeName: Diastrophic dysplasia protein alternativeName: Solute carrier family 26 member 2
Links to corresponding entries in other databasesBioGPS Gene:1836
CTD Gene:1836
ENSEMBL:ENSG00000155850
GeneCards:P50443
HapMap:NM_000112
KEGG Gene:1836
NCBI Gene:1836
OMIM:222600
OMIM:226900
OMIM:256050
OMIM:600972
OMIM:606718
Orphanet:15315
PRO:P50443
RefSeq:NM_000112
RefSeq:NP_000103
UCSC human:P50443
UniProt:P50443
dbSNP Gene:1836
Other identifiers related to this sequenceS26A2_HUMAN, A8K2U3, B2R6J1, Q6N051, HGNC:10994, A_23_P250951, NM_000112, 7923357, C9JAN6, OTTHUMP00000160529, ENST00000286298, 11720105_a_at, HPA041957, 2835315, A_33_P3277447, ILMN_1801491, 2835310, AC011406, 2835313, Hs.711782, ENSP00000286298, 0001170541, 2835312, Hs.302738.0.S2_3p_at, EntrezGene:1836, PH_hs_0002583, 53999_at, 1836, AC008427, 2835314, 11754595_s_at, 39637_at, MIM:222600, MIM:606718, PF01740, CAE45819, GE661107, MIM:600972, 2835307, UPI000013DE3D, 2835317, AAA70081, SLC26A2, MIM:256050, 2835311, BAF83047, SLC26A2-001, Hs.618625, IPR002645, 205097_at, 8109194, LRG_684t1, 224959_at, 53061_at, AK312596, uc003lrh.3, BC059390, PF00916, 11720106_a_at, BX640696, CH471062, 2835301, GE87043, 2835316, MIM:226900, Hs.302738, 11754594_a_at, IPR001902, 16991010, GE58951, Hs.29981.0.S2_3p_at, AK290358, Hs.302738.0.S1_3p_at, CCDS4300, LRG_684, 224963_at, 2835308, ENSG00000155850, BAG35488, H0YA38, U14528, 2835309, EAW61755, AAH59390, NP_000103, PH_hs_0015635, U14528_at, IPR011547, A_14_P121945
Molecules with this sequenceSLC26A2 [plasma membrane] UKENBCdOOOOOORHPGUR
SLC26A2 G255E [plasma membrane] UKENBCdOOOOOORHPGUR
SLC26A2 L483P [plasma membrane] UKENBCdOOOOOORHPGUR
SLC26A2 N425D [plasma membrane] UKENBCdOOOOOORHPGUR
SLC26A2 R178* [plasma membrane] UKENBCdOOOOOORHPGUR
Represented by generalisation(s)SLC26A1,2 [plasma membrane]
SLC26A2 mutants [plasma membrane]
Processes where molecules and complexes with this sequence are involved

Transmembrane transport of small molecules

Metabolism

Disease

Modifications in molecules with this sequenceL-arginine 178 replaced with unknown
L-leucine 483 replaced with L-proline
glycine 255 replaced with L-glutamic acid
L-arginine 425 replaced with L-aspartic acid
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