SULT2B1 - sulfotransferase family 2B member 1 Gene

Also Known as HSST2; ARCI14

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 6820

About SULT2B1

Cytogenetic location: 19q13.33 Genomic coordinates (GRCh38): 19:48,552,172-48,599,427 (from NCBI)

This gene has 4 transcripts (splice variants), 170 orthologues, 12 paralogues and is associated with 2 phenotypes. Biased expression in esophagus (RPKM 55.8), skin (RPKM 46.5) and 4 other tissues.

Summary

Sulfotransferase Enzymes catalyze the sulfate conjugation of many Hormones, neurotransmitters, drugs, and xenobiotic compounds. These cytosolic Enzymes are different in their tissue distributions and substrate specificities. The gene structure (number and length of exons) is similar among family members. This gene sulfates dehydroepiandrosterone but not 4-nitrophenol, a typical substrate for the phenol and estrogen sulfotransferase subfamilies. Two alternatively spliced variants that encode different isoforms have been described. [provided by RefSeq, Jul 2008]

SULT2B1 Products (2)

mRNA Protein Name
NM_004605.2 NP_004596.2 sulfotransferase 2B1 isoform a
NM_177973.2 NP_814444.1 sulfotransferase 2B1 isoform b
Molecular Function GO Annotation Evidence References Source
enables cholesterol binding IDA
IDA: Inferred from direct assay
12923182 GOA
enables nucleic acid binding IMP
IMP: Inferred from mutant phenotype
12923182 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
enables small molecule binding EXP
EXP: Inferred from Experiment
12923182 GOA
enables steroid hormone binding IMP
IMP: Inferred from mutant phenotype
12923182 GOA
enables steroid sulfotransferase activity IDA
IDA: Inferred from direct assay
9799594 GOA
Biological Process GO Annotation Evidence References Source
involved in 3'-phosphoadenosine 5'-phosphosulfate metabolic process IDA
IDA: Inferred from direct assay
12923182 GOA
involved in cholesterol metabolic process IMP
IMP: Inferred from mutant phenotype
28575648 GOA
involved in negative regulation of cell population proliferation IMP
IMP: Inferred from mutant phenotype
28575648 GOA
involved in positive regulation of epidermal cell differentiation IMP
IMP: Inferred from mutant phenotype
28575648 GOA
involved in steroid metabolic process IDA
IDA: Inferred from direct assay
9799594 GOA
Cellular Component GO Annotation Evidence References Source
located in cytosol IDA
IDA: Inferred from direct assay
28575648 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SULT2B1 Protein Structure

Sulfotransfer_1

Sulfotransfer_1: Sulfotransferase domain (60 - 304)

  • 0
  • 100
  • 200
  • 300
  • 365 a.a.
Protein Preferred Names Protein Names

sulfotransferase 2B1

  • ST2B1

SULT2B1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SULT2B1 O00204 SULT1B1 Homo sapiens O43704 25910212
Intra
SULT2B1 O00204 SULT1B1 Homo sapiens O43704 32296183
Intra
SULT2B1 O00204 SULT1B1 Homo sapiens O43704 25910212
Intra
SULT2B1 O00204 SULT1B1 Homo sapiens O43704 25416956
Intra
SULT2B1 O00204 SULT1B1 Homo sapiens O43704 25910212
Intra
SULT2B1 O00204 SULT1B1 Homo sapiens O43704 25416956
Intra
SULT2B1 O00204 SULT1B1 Homo sapiens O43704 32296183
Intra
SULT2B1 O00204 SULT1B1 Homo sapiens O43704 32296183
Intra
SULT2B1 O00204 ACYP2 Homo sapiens P14621 25416956
Intra
SULT2B1 O00204 ZNF497 Homo sapiens Q6ZNH5 32296183
Intra
SULT2B1 O00204 ZNF497 Homo sapiens Q6ZNH5 32296183
Intra
SULT2B1 O00204 ZNF497 Homo sapiens Q6ZNH5 32296183
Intra
SULT2B1 O00204 SRP72 Homo sapiens O76094 32296183
Intra
SULT2B1 O00204 SRP72 Homo sapiens O76094 32296183
Intra
SULT2B1 O00204 SRP72 Homo sapiens O76094 32296183
Intra
SULT2B1 O00204 REL Homo sapiens Q04864-2 32296183
Intra
SULT2B1 O00204 REL Homo sapiens Q04864-2 32296183
Intra
SULT2B1 O00204 REL Homo sapiens Q04864-2 32296183
Intra
SULT2B1 O00204 FLACC1 Homo sapiens Q96Q35-2 25910212
Intra
SULT2B1 O00204 FLACC1 Homo sapiens Q96Q35-2 25910212
Intra
SULT2B1 O00204 FLACC1 Homo sapiens Q96Q35-2 25910212
Intra
SULT2B1 O00204 FLACC1 Homo sapiens Q96Q35-2 32296183
Intra
SULT2B1 O00204 FLACC1 Homo sapiens Q96Q35-2 32296183
Intra
SULT2B1 O00204 FLACC1 Homo sapiens Q96Q35-2 32296183
Intra
SULT2B1 O00204 KLHL8 Homo sapiens Q9P2G9-2 32296183
Intra
SULT2B1 O00204 KLHL8 Homo sapiens Q9P2G9-2 32296183
Intra
SULT2B1 O00204 KLHL8 Homo sapiens Q9P2G9-2 32296183
Intra
SULT2B1 O00204 SULT1C3 Homo sapiens Q6IMI6 32296183
Intra
SULT2B1 O00204 SULT1C3 Homo sapiens Q6IMI6 32296183
Intra
SULT2B1 O00204 SULT1C3 Homo sapiens Q6IMI6 32296183
Intra
SULT2B1 O00204 PRICKLE3 Homo sapiens O43900 25416956
Intra
SULT2B1 O00204 PRICKLE3 Homo sapiens O43900 25416956
Intra
SULT2B1 O00204 SULT1A1 Homo sapiens P50225 25910212
Intra
SULT2B1 O00204 SULT1A1 Homo sapiens P50225 31515488
Intra
SULT2B1 O00204 SULT1A1 Homo sapiens P50225 25910212
Intra
SULT2B1 O00204 SULT1A1 Homo sapiens P50225 25910212
Intra
SULT2B1 O00204 SULT1A1 Homo sapiens P50225 25416956
Intra
SULT2B1 O00204 DDIT4L Homo sapiens Q96D03 32296183
Intra
SULT2B1 O00204 DDIT4L Homo sapiens Q96D03 32296183
Intra
SULT2B1 O00204 DDIT4L Homo sapiens Q96D03 32296183
Intra
SULT2B1 O00204 FLACC1 Homo sapiens Q96Q35 16189514
Intra
SULT2B1 O00204 FLACC1 Homo sapiens Q96Q35 25416956
Intra
SULT2B1 O00204 FLACC1 Homo sapiens Q96Q35 25416956
Intra
SULT2B1 O00204 FLACC1 Homo sapiens Q96Q35 19060904
Intra
SULT2B1 O00204 FLACC1 Homo sapiens Q96Q35 19060904
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant SULT2B1 Proteins

Cat. No. Product Name Accession Purity
HY-P76666 SULT2B1 Protein, Human (His) O00204-1 (D2-S365) ≥ 90%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Ichthyosis, Congenital, Autosomal Recessive 14
  • ARCI14

  • Autosomal Recessive Congenital Ichthyosis 14

Ichthyosis, Congenital, Autosomal Recessive 1
  • Collodion Fetus

  • Autosomal Recessive Congenital Ichthyosis 1

  • ARCI1

  • Ichthyosis Congenita

  • Lamellar Exfoliation Of Newborn

  • Desquamation Of Newborn

  • Ichthyosis Congenita Ii

  • Shcb

  • Icr2

  • Bathing Suit Ichthyosis

  • Li1

  • Self-Healing Collodion Baby

  • Ichthyosis, Congenital, Autosomal Recessive 1, With Bathing Suit Distribution

  • Collodion Baby, Self-Healing

  • Ichthyosis, Lamellar, 1, Formerly

  • Li1, Formerly

  • Ichthyosis Lamellar 1

  • Lamellar Ichthyosis, Type 1

  • Bsi

  • Autosomal Recessive Congenital Ichthyosis 1 With Bathing Suit Distribution

  • Autosomal Recessive Congenital Ichthyosis Tgm1-Related

  • Lamellar Ichthyosis 1

  • Non-Erythrodermic Ichthyosis

  • Ichthyosis, Congenital, Autosomal Recessive, Type 1

  • Congenital Ichthyosis

Ichthyosis, Congenital, Autosomal Recessive 2
  • Autosomal Recessive Congenital Ichthyosis 2

  • ARCI2

  • Ncie1

  • Ichthyosiform Erythroderma, Congenital

  • Collodion Baby, Self-Healing

  • Ichthyosiform Erythroderma, Nonbullous Congenital, 1, Formerly

  • Ncie1, Formerly

  • Ichthyosiform Erythroderma, Brocq Congenital, Nonbullous Form, Formerly

  • Brocq Congenital Ichthyosiform Erythroderma Nonbullous Form

  • Nonbullous Congenital Ichthyosiform Erythroderma 1

  • Cie

  • Ichthyosiform Erythroderma Brocq Congenital Non-Bullous Form

  • Iecn1

  • Non-Bullous Congenital Ichthyosiform Erythroderma Type 1

  • Self-Healing Collodion Baby

  • Ichthyosis, Congenital, Autosomal Recessive, Type 2

  • Ichthyosiform Erythroderma, Congenital, Nonbullous, 1

Autosomal Recessive Congenital Ichthyosis
  • Lamellar Ichthyosis

  • Congenital Ichthyosiform Erythroderma

  • Li

  • Congenital Nonbullous Ichthyosiform Erythroderma

  • Arci

  • Congenital Lamellar Ichthyosis

  • Nonbullous Congenital Ichthyosiform Erythroderma

  • Cie

  • Congenital Non-Bullous Ichthyosiform Erythroderma

  • Erythrodermic Ichthyosis

  • Nbcie

  • Ncie

  • Non-Bullous Congenital Ichthyosiform Erythroderma

  • Collodion Baby

  • Ichthyosis, Lamellar

  • Non Bullous Congenital Ichthyosiform Erythroderma

  • Ichthyosiform Erythroderma, Brocq Congenital, Nonbullous Form

  • Ichthyosiform Erythroderma, Congenital, Nonbullous, 1

  • Collodion Baby Syndrome

  • Ichthyoses, Lamellar

  • Nbie

  • Nonbullous Ichthyosiform Erythroderma

  • Classic Lamellar Ichthyosis

  • Ichthyosiform Erythroderma Nonbullous Congenital

  • Ichthyosiform Erythroderma Congenital

  • Ichthyosis, Congenital, Autosomal Recessive

  • Ichthyosiform Erythroderma, Congenital

  • Collodion Fetus

  • Non-Bullous Ichthyosiform Erythroderma

Ichthyosis
  • Ichthyoses

  • Non-Syndromic Ichthyosis

  • Congenital Ichthyosis

Ichthyosis, Congenital, Autosomal Recessive 4b
  • Harlequin Ichthyosis

  • Autosomal Recessive Congenital Ichthyosis 4b

  • Hi

  • Harlequin Fetus

  • ARCI4B

  • Ichthyosis Congenita, Harlequin Fetus Type

  • Harlequin Type Ichthyosis

  • 'Harlequin Fetus'

  • Harlequin Type Ichthyosis Congenita

  • Harlequin Type Ichthyosis Fetalis

  • Harlequin Baby Syndrome

  • Ichthyosis Congenita, Harlequin Type

  • Ichthyosis Fetalis, Harlequin Type

  • Ichthyosis Congenita Harlequin Fetus Type

  • Ichthyosis, Harlequin

  • Ichthyosis, Congenital, Autosomal Recessive, Type 4b

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus SULT2B1 VGNC VGNC:65837
Rattus norvegicus SULT2B1 RGD RGD:1308882
Mus musculus SULT2B1 MGD MGI:1926342
Canis familiaris SULT2B1 VGNC VGNC:46979
Bos taurus SULT2B1 VGNC VGNC:35468
Others SULT2B1 NCBI