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 |
