1. Gene
  2. DHRSX - dehydrogenase/reductase X-linked Gene

DHRSX - dehydrogenase/reductase X-linked Gene

Homo sapiens

Also known as DHRSY; DHRS5X; DHRS5Y; DHRSXY; SDR7C6; CXorf11; SDR46C1

Gene ID: 207063 | Gene type: protein coding

About DHRSX

Cytogenetic location: Xp22.33 Genomic coordinates (GRCh38): X:2,219,506-2,500,976 (from NCBI)

This gene has 7 transcripts (splice variants), 164 orthologues and 4 paralogues. Ubiquitous expression in kidney (RPKM 6.0), liver (RPKM 5.1) and 25 other tissues.

Summary

Predicted to enable oxidoreductase activity. Involved in positive regulation of Autophagy. Located in extracellular region. [provided by Alliance of Genome Resources, Apr 2022]

DHRSX Products(1)

mRNA Protein Name
NM_145177.3 NP_660160.2 dehydrogenase/reductase SDR family member on chromosome X
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
28514442 GOA
Biological Process GO Annotation Evidence Reference Source
involved in positive regulation of autophagy IMP
IMP: Inferred from mutant phenotype
25076851 GOA
Cellular Component GO Annotation Evidence Reference Source
located in extracellular region IDA
IDA: Inferred from direct assay
25076851 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

DHRSX Protein Structure

adh_short

adh_short: short chain dehydrogenase (45 - 190)

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

dehydrogenase/reductase SDR family member on chromosome X

dehydrogenase/reductase (SDR family) X chromosome

DHRSX Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
DHRSX Q8N5I4 RETREG3 Homo sapiens Q86VR2 32296183
Intra
DHRSX Q8N5I4 RETREG3 Homo sapiens Q86VR2 32296183
Intra
DHRSX Q8N5I4 PGRMC2 Homo sapiens O15173 32296183
Intra
DHRSX Q8N5I4 PGRMC2 Homo sapiens O15173 32296183
Intra
DHRSX Q8N5I4 HSD17B11 Homo sapiens Q8NBQ5 32296183
Intra
DHRSX Q8N5I4 HSD17B11 Homo sapiens Q8NBQ5 32296183
Intra
DHRSX Q8N5I4 HSD17B11 Homo sapiens Q8NBQ5 32296183
Intra
DHRSX Q8N5I4 CMTM5 Homo sapiens Q96DZ9-2 32296183
Intra
DHRSX Q8N5I4 APOC1 Homo sapiens P02654 32296183
Intra
DHRSX Q8N5I4 APOC1 Homo sapiens P02654 32296183
Intra
DHRSX Q8N5I4 ZDHHC15 Homo sapiens Q96MV8 32296183
Intra
DHRSX Q8N5I4 ZDHHC15 Homo sapiens Q96MV8 32296183
Intra
DHRSX Q8N5I4 ZDHHC15 Homo sapiens Q96MV8 32296183
Intra
DHRSX Q8N5I4 TLCD4 Homo sapiens Q96MV1 32296183
Intra
DHRSX Q8N5I4 TLCD4 Homo sapiens Q96MV1 32296183
Intra
DHRSX Q8N5I4 TLCD4 Homo sapiens Q96MV1 32296183
Intra
DHRSX Q8N5I4 AQP6 Homo sapiens Q13520 32296183
Intra
DHRSX Q8N5I4 TMEM143 Homo sapiens Q96AN5 32296183
Intra
DHRSX Q8N5I4 TMEM143 Homo sapiens Q96AN5 32296183
Intra
DHRSX Q8N5I4 TMEM143 Homo sapiens Q96AN5 32296183
Intra
DHRSX Q8N5I4 FADS3 Homo sapiens Q9Y5Q0 32296183
Intra
DHRSX Q8N5I4 FADS3 Homo sapiens Q9Y5Q0 32296183
Intra
DHRSX Q8N5I4 FADS3 Homo sapiens Q9Y5Q0 32296183
Intra
DHRSX Q8N5I4 PIGP Homo sapiens P57054 32296183
Intra
DHRSX Q8N5I4 PIGP Homo sapiens P57054 32296183
Intra
DHRSX Q8N5I4 TMEM86B Homo sapiens Q8N661 32296183
Intra
DHRSX Q8N5I4 TMEM86B Homo sapiens Q8N661 32296183
Intra
DHRSX Q8N5I4 TMEM86B Homo sapiens Q8N661 32296183
Intra
DHRSX Q8N5I4 CIDEB Homo sapiens Q9UHD4 32296183
Intra
DHRSX Q8N5I4 CIDEB Homo sapiens Q9UHD4 32296183
Intra
DHRSX Q8N5I4 CIDEB Homo sapiens Q9UHD4 32296183
Intra
DHRSX Q8N5I4 ZBED1 Homo sapiens O96006 33961781
Intra
DHRSX Q8N5I4 ZBED1 Homo sapiens O96006 28514442
Intra
DHRSX Q8N5I4 RUSF1 Homo sapiens Q96GQ5 32296183
Intra
DHRSX Q8N5I4 RUSF1 Homo sapiens Q96GQ5 32296183
Intra
DHRSX Q8N5I4 RUSF1 Homo sapiens Q96GQ5 32296183
Intra
DHRSX Q8N5I4 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
DHRSX Q8N5I4 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
DHRSX Q8N5I4 TMEM14B Homo sapiens Q9NUH8 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Waisman Syndrome

Early-Onset Parkinsonism-Intellectual Disability Syndrome

Bgmr

Wsn

Laxova-Opitz Syndrome

WSMN

Parkinsonism, Early-Onset, With Mental Retardation

Basal Ganglion Disorder With Mental Retardation

Basal Ganglia Disorder With Intellectual Disability

Laxova Brown Hogan Syndrome

X-Linked Recessive Basal Ganglia Disorder With Intellectual Disability

Alpha-Thalassemia Myelodysplasia Syndrome

ATMDS

Acquired Hemoglobin H Disease

Alpha-Thalassemia Myelodysplasia Syndrome, Somatic

Acquired Hbh Disease

Alpha-Thalassemia-Myelodysplastic Syndrome

Hemoglobin H Disease, Acquired

Acquired Alpha-Thalassemia With Myelodysplastic Syndrome

Hemoglobin H Disease Acquired

Thalassemia, Alpha, Myelodysplasia Syndrome, Somatic

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
Canis familiaris DHRSX VGNC VGNC:54133
Mus musculus DHRSX MGD MGI:2181510
Rattus norvegicus DHRSX RGD RGD:1305017