Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)_R-HSA-5619102 - Wikidata - awgldk - TriplyDB

Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)_R-HSA-5619102

Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)_R-HSA-5619102

http://www.wikidata.org/entity/Q56860922

about

SLC transporter disorders

P527

Q45314471-F2F2B731-0FEF-4DA1-8075-F8A9B22B3C68

P527

Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG)_R-HSA-5619102

http://www.wikidata.org/entity/Q56860922

description

An instance of the biological ...... _R-HSA-5619102 in Homo sapiens

@en

name

Variant SLC6A20 contributes to ...... oglycinuria (IG)_R-HSA-5619102

@en

type

label

Variant SLC6A20 contributes to ...... oglycinuria (IG)_R-HSA-5619102

@en

prefLabel

Variant SLC6A20 contributes to ...... oglycinuria (IG)_R-HSA-5619102

@en

P2860

Q56860922-08962D59-539D-4A55-AC42-82703CD083DD

Q56860922-1DB17FE8-A481-4147-B077-8109D47DF288

Q56860922-722F8353-85D5-4D98-BCD9-5903F40387F5

P2888

Q56860922-05F568E8-BB48-4A44-BEA5-CF09FBFCCFD3

P31

Q56860922-792E16CD-9530-4472-B2FE-CF9396E456A0

P361

Q56860922-9EA364EE-82E1-4E36-B982-F4380801F3C1

P3937

Q56860922-0202F236-414A-4D2C-98B2-C37BD218FB59

P527

Q56860922-4A8D7644-C9A3-4B7A-82F3-5B0C1EAECA6D

P703

Q56860922-8540DF6A-6D8A-46F5-80BB-12946F66021B

P2860

Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters

Amino acid secondary transporters: toward a common transport mechanism.

The solute carrier 6 family of transporters

P2888

reactome:R-HSA-5660686

P31

biological pathway

P361

SLC transporter disorders

P3937

R-HSA-5660686

http://www.w3.org/2001/XMLSchema#string

P527

Variant SLC6A20 does not cotransport L-Pro; Na+ from extracellulare region to cytosol

P703