GHR, Somatotropin receptor, Serum-binding protein, GH-binding protein, GHBP, Growth Hormone Receptor, Growth Hormone Binding Protein, GH Receptor, Serum Binding Protein, GHIP, Receptors, Somatotropin


GHR is a receptor for pituitary gland growth hormone involved in regulating postnatal body growth. On ligand binding, couples to the JAK2/STAT5 pathway.The soluble form (GHBP) acts as a reservoir of growth hormone in plasma and may be a modulator/inhibitor of GH signaling.

KO Status

RenMab: F0

Drug Information

Launched drugs: 28
Drugs in clinical trials: 20
Latest Research Phase: Approved

Drug Name





Clinical Trials

Somatropin (rDNA origin, Genentech)

SMP-140, rhGH (Genentech)


Genentech Inc

Cystic Fibrosis, Turner Syndrome, Growth Disorders, Dwarfism, Renal Insufficiency, Chronic, Dwarfism, Pituitary, Growth hormone deficiency

Recombinant human growth hormone (Shanghai United Cell Biotechnology)


Shanghai United Cell Biotechnology Co Ltd

Growth Disorders

Somatropin biosimilar (Amega Biotech)


Amega Biotech

Growth hormone deficiency

Somatropin biosimilar (USV)


Union Square Ventures Llc

Growth hormone deficiency

Somatropin (Lilly)



Eli Lilly And Company

Failure to Thrive, Idiopathic short stature, Turner Syndrome, Malnutrition, Growth Disorders, Dwarfism, Pituitary, Dwarfism, Growth hormone deficiency

Recombinant human growth hormone (Shenzhen Kexing Biotech)


Shenzhen Kexing Biological Engineering Co Ltd

Growth hormone deficiency

Recombinant human growth hormone (BioGeneric Pharma)



Growth hormone deficiency

Somatropin biosimilar (Sedico)



Turner Syndrome, Growth hormone deficiency

Somatropin (rDNA origin, Merck Serono)



Merck Serono

HIV Infections, Idiopathic short stature, HIV Wasting Syndrome, Growth Disorders, Short Bowel Syndrome, Fetal Growth Retardation, HIV-Associated Lipodystrophy Syndrome, Fibromyalgia, Growth hormone deficiency

Somatropin biosimilar (BioPartners GmbH)

rhGH (BioPartners GmbH), SR-rhGH (BioPartners GmbH), LB-03002


Biopartners, Lg Life Sciences Ltd

Pituitary Diseases, Turner Syndrome, Prader-Willi Syndrome, Growth Disorders, Dwarfism, Pituitary, Growth hormone deficiency





The first homozygous mutation (S226I) in the highly-conserved WSXWS-like motif of the GH receptor causing Laron syndrome: suppression of GH secretion by GnRH analogue therapy not restored by dihydrotestosterone administration

Jorge A.A.L., Souza S.C.A.L., Arnhold I.J.P., Mendonca B.B.,

Clin. Endocrinol. (Oxf.) 60:36-40(2004)

Growth hormone receptor mutations in children with idiopathic short stature

Sanchez J.E., Perera E., Baumbach L., Cleveland W.W.,

J. Clin. Endocrinol. Metab. 83:4079-4083(1998)

Four contiguous amino acid substitutions, identified in patients with Laron syndrome, differently affect the binding affinity and intracellular trafficking of the growth hormone receptor

Wojcik J., Berg M.A., Esposito N., Geffner M.E., Sakati N., Reiter E.O., Dower S., Francke U., Postel-Vinay M.-C., Finidori J.,

J. Clin. Endocrinol. Metab. 83:4481-4489(1998)

Characterization of single-nucleotide polymorphisms in coding regions of human genes

Cargill M., Altshuler D., Ireland J., Sklar P., Ardlie K., Patil N., Shaw N., Lane C.R., Lim E.P., Kalyanaraman N., Nemesh J., Ziaugra L., Friedland L., Rolfe A., Warrington J., Lipshutz R., Daley G.Q., Lander E.S.,

Nat. Genet. 22:231-238(1999)

Characterisation of novel missense mutations in the GH receptor gene causing severe growth retardation

Enberg B., Luthman H., Segnestam K., Ritzen E.M., Sundstroem M., Norstedt G.,

Eur. J. Endocrinol. 143:71-76(2000)

Growth hormone receptor variant (L526I) modifies plasma HDL cholesterol phenotype in familial hypercholesterolemia: intra-familial association study in an eight-generation hyperlipidemic kindred

Takada D., Ezura Y., Ono S., Iino Y., Katayama Y., Xin Y., Wu L.L., Larringa-Shum S., Stephenson S.H., Hunt S.C., Hopkins P.N., Emi M.,

Am. J. Med. Genet. A 121:136-140(2003)

Growth hormone receptor and serum binding protein: purification, cloning and expression

Leung D.W., Spencer S.A., Cachianes G., Hammonds R.G., Collins C., Henzel W.J., Barnard R., Waters M.J., Wood W.I.,

Nature 330:537-543(1987)

Characterization of the human growth hormone receptor gene and demonstration of a partial gene deletion in two patients with Laron-type dwarfism

Godowski P.J., Leung D.W., Meacham L.R., Galgani J.P., Hellmiss R., Keret R., Rotwein P.S., Parks J.S., Laron Z., Wood W.I.,

Proc. Natl. Acad. Sci. U.S.A. 86:8083-8087(1989)

Expression of a human growth hormone (hGH) receptor isoform is predicted by tissue-specific alternative splicing of exon 3 of the hGH receptor gene transcript

Urbanek M., MacLeod J.N., Cooke N.E., Liebhaber S.A.,

Mol. Endocrinol. 6:279-287(1992)

Alternatively spliced forms in the cytoplasmic domain of the human growth hormone (GH) receptor regulate its ability to generate a soluble GH-binding protein

Dastot F., Sobrier M.-L., Duquesnoy P., Duriez B., Goossens M., Amselem S.,

Proc. Natl. Acad. Sci. U.S.A. 93:10723-10728(1996)