From Wikipedia, the free encyclopedia
Proton myo -inositol cotransporter , also known as solute carrier family 2 member 13 is a protein that in humans is encoded by the SLC2A13 gene .[5]
References [ ]
Further reading [ ]
Uldry M, Ibberson M, Horisberger JD, Chatton JY, Riederer BM, Thorens B (August 2001). "Identification of a mammalian H(+)-myo-inositol symporter expressed predominantly in the brain" . The EMBO Journal . 20 (16): 4467–77. doi :10.1093/emboj/20.16.4467 . PMC 125574 . PMID 11500374 .
Fu GK, Wang JT, Yang J, Au-Young J, Stuve LL (July 2004). "Circular rapid amplification of cDNA ends for high-throughput extension cloning of partial genes". Genomics . 84 (1): 205–10. doi :10.1016/j.ygeno.2004.01.011 . PMID 15203218 .
Bankovic J, Stojsic J, Jovanovic D, Andjelkovic T, Milinkovic V, Ruzdijic S, Tanic N (February 2010). "Identification of genes associated with non-small-cell lung cancer promotion and progression". Lung Cancer . 67 (2): 151–9. doi :10.1016/j.lungcan.2009.04.010 . PMID 19473719 .
Di Daniel E, Mok MH, Mead E, Mutinelli C, Zambello E, Caberlotto LL, Pell TJ, Langmead CJ, Shah AJ, Duddy G, Kew JN, Maycox PR (July 2009). "Evaluation of expression and function of the H+/myo-inositol transporter HMIT" . BMC Cell Biology . 10 : 54. doi :10.1186/1471-2121-10-54 . PMC 2717050 . PMID 19607714 .
Satake W, Nakabayashi Y, Mizuta I, Hirota Y, Ito C, Kubo M, Kawaguchi T, Tsunoda T, Watanabe M, Takeda A, Tomiyama H, Nakashima K, Hasegawa K, Obata F, Yoshikawa T, Kawakami H, Sakoda S, Yamamoto M, Hattori N, Murata M, Nakamura Y, Toda T (December 2009). "Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease". Nature Genetics . 41 (12): 1303–7. doi :10.1038/ng.485 . PMID 19915576 . S2CID 205356259 .
By group
SLC1–10
(1):
high affinity glutamate and neutral amino-acid transporter
(2): (3): (4): (5): (6): (7): (8): (9): (10):
SLC10A1
SLC10A2
SLC10A3
SLC10A7
10A1
10A2
10A3
10A7
SLC11–20
(11): (12): (13): (14): (15): (16): (17): (18): (19): (20):
SLC21–30
(21):
Organic anion-transporting polypeptide
SLCO1A2
SLCO1B1
SLCO1B3
SLCO1C1
(22):
organic cation/anion/zwitterion transporter
(23): (24): (25): (26): (27): (28): (29): (30):
zinc efflux
SLC30A1
SLC30A3
SLC30A4
SLC30A7
SLC30A8
SLC31–40
(31): (32): (33): (34): (35): (36): (37): (38): (39):
metal ion transporter
SLC39A1
SLC39A2
SLC39A3
SLC39A4
SLC39A6
SLC39A7
SLC39A8
SLC39A9
SLC39A10
SLC39A12
(40):
SLC41–48
(41): (42): (43): (44): (45): (46): (47): (48):
SLCO1–4
O1A2
O1B1
O1B3
O2B1
O431
O4A1
see also solute carrier disorders
Categories :
Genes on human chromosome 12 Solute carrier family Human chromosome 12 gene stubs Membrane protein stubs