TRHDE - thyrotropin releasing hormone degrading enzyme Gene

Also Known as PAP-II; PGPEP2; TRH-DE

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 29953

About TRHDE

Cytogenetic location: 12q21.1 Genomic coordinates (GRCh38): 12:72,087,266-72,670,758 (from NCBI)

This gene has 7 transcripts (splice variants), 241 orthologues and 11 paralogues. Broad expression in brain (RPKM 3.0), fat (RPKM 2.9) and 17 other tissues.

Summary

This gene encodes a member of the peptidase M1 family. The encoded protein is an extracellular peptidase that specifically cleaves and inactivates the neuropeptide thyrotropin-releasing hormone.[provided by RefSeq, Dec 2008]

TRHDE Products (1)

mRNA Protein Name
NM_013381.3 NP_037513.2 thyrotropin-releasing hormone-degrading ectoenzyme

TRHDE Protein Structure

Peptidase_M1

Peptidase_M1: Peptidase family M1 domain (140 - 530)

ERAP1_C

ERAP1_C: ERAP1-like C-terminal domain (678 - 999)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1024 a.a.
Protein Preferred Names Protein Names

thyrotropin-releasing hormone-degrading ectoenzyme

  • TRH-degrading ectoenzyme

Related Diseases

Diseases Alias
Thyroid Hormone Resistance, Generalized, Autosomal Dominant
  • Thyroid Hormone Resistance Syndrome

  • Thyroid Hormone Resistance

  • GRTHD

  • Gthr

  • Thyroid Hormone Unresponsiveness

  • Generalized Thyroid Hormone Resistance

  • Hyperthyroxinemia, Familial Euthyroid, Secondary To Pituitary And Peripheral Thyroid Hormones

  • Hyperthyroxinemia, Familial Euthyroid, Secondary To Pituitary And Peripheral Resistance To Thyroid Hormones

  • Refetoff Syndrome

  • Thyroid Hormone Responsiveness Defect

  • Familial Euthyroid Hyperthyroxinemia, Secondary To Pituitary And Peripheral Resistance To Thyroid Hormones

  • Thyroid Hormone Resistance, Generalized, Autosomal Recessive

Developmental And Epileptic Encephalopathy 2
  • Epileptic Encephalopathy, Early Infantile, 2

  • DEE2

  • Eiee2

  • Issx2

  • Developmental And Epileptic Encephalopathy, 2

  • Infantile Spasm Syndrome, X-Linked 2

  • Early Infantile Epileptic Encephalopathy 2

  • X-Linked Infantile Spasm Syndrome 2

  • Atypical Rett Syndrome Cdkl5-Related

  • Atypical Rett Syndrome Hanefeld Variant

  • Infantile Spasm Syndrome X-Linked 2

  • Rett Syndrome Early-Onset Seizure Variant

  • Rett Syndrome Variant With Infantile Spasms

  • Encephalopathy, Epileptic, Early Infantile, Type 2

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 TRHDE VGNC VGNC:66525
Canis familiaris TRHDE VGNC VGNC:47798
Bos taurus TRHDE VGNC VGNC:36305
Mus musculus TRHDE MGD MGI:2384311
Rattus norvegicus TRHDE RGD RGD:728895
Macaca mulatta TRHDE VGNC VGNC:79872
Others TRHDE NCBI