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IMINOGLYCINURIA

Iminoglycinuria

Medical condition

Iminoglycinuria is an autosomal recessive disorder of renal tubular transport affecting reabsorption of the amino acid glycine, and the imino acids proline

Iminoglycinuria

Kidney stone disease

Formation of mineral deposits in the kidneys

PMID 8976113. Rosenberg LE, Durant JL, Elsas LJ (June 1968). "Familial iminoglycinuria. An inborn error of renal tubular transport". The New England Journal

Kidney stone disease

Kidney_stone_disease

List of diseases (I)

Illyngophobia Ilyina–Amoashy–Grygory syndrome Imaizumi–Kuroki syndrome Iminoglycinuria Immotile cilia syndrome, due to defective radial spokes Immotile cilia

List of diseases (I)

List_of_diseases_(I)

Inborn errors of renal tubular transport

Medical condition

reabsorption.[citation needed] Examples of these disorders include Iminoglycinuria, renal tubular acidosis and Gitelman syndrome.[citation needed] v t

Inborn errors of renal tubular transport

Inborn_errors_of_renal_tubular_transport

SLC6A20

Protein-coding amino acid transporter gene in the species Homo sapiens

plasma membrane. Mutation in the SLC6A20 gene are associated with iminoglycinuria. One of a cluster of 6 genes (SLC6A20, LZTFL1, CCR9, FYCO1, CXCR6 and

SLC6A20

Proton coupled amino acid transporter

Type of protein receptors

transporters are located throughout this tissue. In hereditary disease iminoglycinuria, there is a defect in the human proton-coupled amino acid transporter

Proton coupled amino acid transporter

Proton_coupled_amino_acid_transporter

Proton-coupled amino acid transporter 2

Protein-coding gene in the species Homo sapiens

gamma-aminobutyric acid. Mutations in the SLC36A2 gene are associated with Iminoglycinuria. Proton coupled amino acid transporter GRCh38: Ensembl release 89:

Proton-coupled amino acid transporter 2

Proton-coupled_amino_acid_transporter_2

Aminomethyltransferase

Protein-coding gene in the species Homo sapiens

Kowalczuk S, Ng C, Vanslambrouck J, Rodgers H, et al. (December 2008). "Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex

Aminomethyltransferase

List of OMIM disorder codes

Ichthyosis, X-linked; 308100; STS Iminoglycinuria, digenic; 242600; SLC36A2 Iminoglycinuria, digenic; 242600; SLC6A19 Iminoglycinuria, digenic; 242600; SLC6A20

List of OMIM disorder codes

List_of_OMIM_disorder_codes

SLC6A18

Protein-coding gene in the species Homo sapiens

for sodium ions. Mutations in the SLC6A18 gene are associated with iminoglycinuria. GRCh38: Ensembl release 89: ENSG00000164363 – Ensembl, May 2017 GRCm38:

SLC6A18