Gene: [22q131/SLC5A1] solute carrier family 5 (sodium/glucose transporter), member 1 (intestinal); congenital glucose-galactose malabsorbtion syndrome; [SGLT1 ]

FAG

[1] A gene coding for another sodium-glucose transport protein (renal?) has been mapped to chr 16 (GEM:16p112/SLC5A2).
[2] There are several genes coding for proteins of glucose transport unrelated to Na transport; see GEM:01p3/SLC2A1."

REL

GEM:21q22/SLC5A3; GEM:00.0/SLC5A4.

REF

LOC,PRO "Hediger MA &: Genomics, 4, N3, 297-300, 1989a
PRO,SEQ,PEP,MOP,EVO "Hediger MA &: PNAS, 86, N15, 5748-5752, 1989b
MUT "Martin MG &: Nature Genet, 12, 216-220, 1996
GEN "Turk E &: JBC, 269, 15204-15209, 1994
LOC,PRO "Turk E &: Genomics, 17, 752-754, 1993

KEY

horm, trp, carb, ion, mem

CLA

coding, basic

LOC

22 q13.1

MIM

MIM: 182380

SYN

SGLT1

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