TSTD2 - thiosulfate sulfurtransferase like domain containing 2 Gene

Also Known as C9orf97

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 158427

About TSTD2

This gene has 6 transcripts (splice variants) and 194 orthologues. Ubiquitous expression in heart (RPKM 18.5), adrenal (RPKM 16.8) and 25 other tissues.

TSTD2 Products (1)

mRNA Protein Name
NM_139246.5 NP_640339.4 thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 2
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
25416956 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

TSTD2 Protein Structure

Rhodanese

Rhodanese: Rhodanese-like domain (298 - 389)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 516 a.a.
Protein Preferred Names Protein Names

thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 2

  • PP4189

TSTD2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
TSTD2 Q5T7W7 ZBTB14 Homo sapiens O43829 32296183
Intra
TSTD2 Q5T7W7 ZBTB14 Homo sapiens O43829 32296183
Intra
TSTD2 Q5T7W7 ZNF774 Homo sapiens Q6NX45 32296183
Intra
TSTD2 Q5T7W7 ZNF774 Homo sapiens Q6NX45 32296183
Intra
TSTD2 Q5T7W7 ZNF774 Homo sapiens Q6NX45 32296183
Intra
TSTD2 Q5T7W7 REL Homo sapiens Q04864-2 32296183
Intra
TSTD2 Q5T7W7 REL Homo sapiens Q04864-2 32296183
Intra
TSTD2 Q5T7W7 IKZF1 Homo sapiens Q13422-7 32296183
Intra
TSTD2 Q5T7W7 IKZF1 Homo sapiens Q13422-7 32296183
Intra
TSTD2 Q5T7W7 ZNF438 Homo sapiens Q7Z4V0 32296183
Intra
TSTD2 Q5T7W7 ZNF438 Homo sapiens Q7Z4V0 32296183
Intra
TSTD2 Q5T7W7 ZNF438 Homo sapiens Q7Z4V0 32296183
Intra
TSTD2 Q5T7W7 L3MBTL3 Homo sapiens Q96JM7-2 26871637
Intra
TSTD2 Q5T7W7 L3MBTL3 Homo sapiens Q96JM7-2 26871637
Intra
TSTD2 Q5T7W7 L3MBTL3 Homo sapiens Q96JM7-2 26871637
Intra
TSTD2 Q5T7W7 TCF4 Homo sapiens P15884-3 32296183
Intra
TSTD2 Q5T7W7 TCF4 Homo sapiens P15884-3 32296183
Intra
TSTD2 Q5T7W7 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
TSTD2 Q5T7W7 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
TSTD2 Q5T7W7 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
TSTD2 Q5T7W7 ISY1 Homo sapiens Q9ULR0-1 32296183
Intra
TSTD2 Q5T7W7 ISY1 Homo sapiens Q9ULR0-1 32296183
Intra
TSTD2 Q5T7W7 ISY1 Homo sapiens Q9ULR0-1 32296183
Intra
TSTD2 Q5T7W7 SSX2IP Homo sapiens Q9Y2D8 26871637
Intra
TSTD2 Q5T7W7 SSX2IP Homo sapiens Q9Y2D8 26871637
Intra
TSTD2 Q5T7W7 SSX2IP Homo sapiens Q9Y2D8 26871637
Intra
TSTD2 Q5T7W7 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
TSTD2 Q5T7W7 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
TSTD2 Q5T7W7 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
TSTD2 Q5T7W7 VPS52 Homo sapiens Q8N1B4 32296183
Intra
TSTD2 Q5T7W7 VPS52 Homo sapiens Q8N1B4 25416956
Intra
TSTD2 Q5T7W7 VPS52 Homo sapiens Q8N1B4 32296183
Intra
TSTD2 Q5T7W7 VPS52 Homo sapiens Q8N1B4 25416956
Intra
TSTD2 Q5T7W7 VPS52 Homo sapiens Q8N1B4 25416956
Intra
TSTD2 Q5T7W7 VPS52 Homo sapiens Q8N1B4 32296183
Intra
TSTD2 Q5T7W7 LHX4 Homo sapiens Q969G2 32296183
Intra
TSTD2 Q5T7W7 LHX4 Homo sapiens Q969G2 32296183
Intra
TSTD2 Q5T7W7 LHX4 Homo sapiens Q969G2 32296183
Intra
TSTD2 Q5T7W7 REL Homo sapiens Q04864 25416956
Intra
TSTD2 Q5T7W7 KIAA1328 Homo sapiens Q86T90 32296183
Intra
TSTD2 Q5T7W7 KIAA1328 Homo sapiens Q86T90 32296183
Intra
TSTD2 Q5T7W7 KIAA1328 Homo sapiens Q86T90 32296183
Intra
TSTD2 Q5T7W7 ZRANB1 Homo sapiens Q9UGI0 32296183
Intra
TSTD2 Q5T7W7 ZRANB1 Homo sapiens Q9UGI0 32296183
Intra
TSTD2 Q5T7W7 ZRANB1 Homo sapiens Q9UGI0 32296183
Intra
TSTD2 Q5T7W7 INCA1 Homo sapiens Q0VD86 32296183
Intra
TSTD2 Q5T7W7 INCA1 Homo sapiens Q0VD86 32296183
Intra
TSTD2 Q5T7W7 AGR2 Homo sapiens O95994 32296183
Intra
TSTD2 Q5T7W7 AGR2 Homo sapiens O95994 32296183
Intra
TSTD2 Q5T7W7 ZFPL1 Homo sapiens O95159 32296183
Intra
TSTD2 Q5T7W7 ZFPL1 Homo sapiens O95159 32296183
Intra
TSTD2 Q5T7W7 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
TSTD2 Q5T7W7 IKZF3 Homo sapiens Q9UKT9 26871637
Intra
TSTD2 Q5T7W7 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
TSTD2 Q5T7W7 IKZF3 Homo sapiens Q9UKT9 25416956
Intra
TSTD2 Q5T7W7 IKZF3 Homo sapiens Q9UKT9 26871637
Intra
TSTD2 Q5T7W7 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
TSTD2 Q5T7W7 IKZF3 Homo sapiens Q9UKT9 31515488
Intra
TSTD2 Q5T7W7 IKZF3 Homo sapiens Q9UKT9 26871637
Intra
TSTD2 Q5T7W7 RNF138 Homo sapiens Q8WVD3 32296183
Intra
TSTD2 Q5T7W7 RNF138 Homo sapiens Q8WVD3 32296183
Intra
TSTD2 Q5T7W7 RNF138 Homo sapiens Q8WVD3 32296183
Intra
TSTD2 Q5T7W7 PICK1 Homo sapiens Q9NRD5 32296183
Intra
TSTD2 Q5T7W7 PICK1 Homo sapiens Q9NRD5 32296183
Intra
TSTD2 Q5T7W7 PICK1 Homo sapiens Q9NRD5 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Camptodactyly-Tall Stature-Scoliosis-Hearing Loss Syndrome
  • Catshl Syndrome

  • Camptodactyly-Tall Stature-Scoliosis-Deafness Syndrome

Peptic Ulcer Perforation
  • Perforated Peptic Ulcer

  • Acute Peptic Ulcer With Perforation

  • Peptic Ulcer With Perforation

Weaver Syndrome
  • Wss

  • Weaver-Smith Syndrome

  • WVS

  • Weaver-Like Syndrome

  • Weaver-Williams Syndrome

  • Camptodactyly-Overgrowth-Unusual Facies Syndrome

  • Camptodactyly - Overgrowth - Unusual Facies

  • Ezh2 Related Overgrowth

  • Overgrowth Syndrome With Accelerated Skeletal Maturation, Unusual Facies, And Camptodactyly

  • Weaver Smith Syndrome

  • Weaver Like Syndrome

  • Weaver Williams Syndrome

  • Camptodactyly-Overgrowth-Unusual Facies

  • Weaver Syndrome 1

  • Weaver Syndrome 2

  • Wvs1

  • Wvs2

Short-Rib Thoracic Dysplasia 6 With Or Without Polydactyly
  • Majewski Syndrome

  • SRTD6

  • Srps2a

  • Short Rib-Polydactyly Syndrome, Majewski Type

  • Polydactyly With Neonatal Chondrodystrophy, Type Ii

  • Short Rib-Polydactyly Syndrome Type Iia

  • Short Rib-Polydactyly Syndrome Type 2

  • Short Rib-Polydactyly Syndrome Type Ii

  • Short Rib-Polydactyly Syndrome, Type Ii

  • Srps, Type Ii

  • Short Rib-Polydactyly Syndrome, Type Iia

  • Polydactyly With Neonatal Chondrodystrophy Type 2

  • Srps Type 2

  • Short Rib-Polydactyly Syndrome Majewski Type

  • Polydactyly With Neonatal Chondrodystrophy Type Ii

  • Short Rib-Polydactyly Syndrome 2a

  • Srps Type Ii

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
Mus musculus TSTD2 MGD MGI:3039624
Rattus norvegicus TSTD2 RGD RGD:1310893
Macaca mulatta TSTD2 VGNC VGNC:79835
Canis familiaris TSTD2 VGNC VGNC:47934
Felis catus TSTD2 VGNC VGNC:66649
Bos taurus TSTD2 VGNC VGNC:36451
Others TSTD2 NCBI