Solute carrier family 41, member 3 is a protein that in humans is encoded by the SLC41A3 gene .[5]
Model organisms [ ] Model organisms have been used in the study of SLC41A3 function. A conditional knockout mouse line, called Slc41a3tm1a(KOMP)Wtsi [10] [11] International Knockout Mouse Consortium program — a high-throughput mutagenesis project to generate and distribute animal models of disease to interested scientists.[12] [13] [14]
Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion.[8] [15] mutant mice and one significant abnormality was observed: homozygous mutants displayed abnormal locomotor coordination.[8]
References [ ]
^ a b c GRCh38: Ensembl release 89: ENSG00000114544 - Ensembl , May 2017^ a b c GRCm38: Ensembl release 89: ENSMUSG00000030089 - Ensembl , May 2017^ "Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .^ "Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .^ "Entrez Gene: Solute carrier family 41, member 3" . Retrieved 2011-09-28 .^ "Salmonella infection data for Slc41a3" . Wellcome Trust Sanger Institute.^ "Citrobacter infection data for Slc41a3" . Wellcome Trust Sanger Institute.^ a b c Gerdin AK (2010). "The Sanger Mouse Genetics Programme: High throughput characterisation of knockout mice". Acta Ophthalmologica . 88 : 925–7. doi :10.1111/j.1755-3768.2010.4142.x . S2CID 85911512 . ^ Mouse Resources Portal , Wellcome Trust Sanger Institute.^ "International Knockout Mouse Consortium" .^ "Mouse Genome Informatics" .^ Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, Mujica AO, Thomas M, Harrow J, Cox T, Jackson D, Severin J, Biggs P, Fu J, Nefedov M, de Jong PJ, Stewart AF, Bradley A (June 2011). "A conditional knockout resource for the genome-wide study of mouse gene function" . Nature . 474 (7351): 337–42. doi :10.1038/nature10163 . PMC 3572410 PMID 21677750 . ^ Dolgin E (June 2011). "Mouse library set to be knockout" . Nature . 474 (7351): 262–3. doi :10.1038/474262a PMID 21677718 . ^ Collins FS, Rossant J, Wurst W (January 2007). "A mouse for all reasons" . Cell . 128 (1): 9–13. doi :10.1016/j.cell.2006.12.018 PMID 17218247 . S2CID 18872015 . ^ van der Weyden L, White JK, Adams DJ, Logan DW (June 2011). "The mouse genetics toolkit: revealing function and mechanism" . Genome Biology . 12 (6): 224. doi :10.1186/gb-2011-12-6-224 . PMC 3218837 PMID 21722353 .
Further reading [ ]
Wabakken T, Rian E, Kveine M, Aasheim HC (July 2003). "The human solute carrier SLC41A1 belongs to a novel eukaryotic subfamily with homology to prokaryotic MgtE Mg2+ transporters". Biochemical and Biophysical Research Communications . 306 (3): 718–24. doi :10.1016/S0006-291X(03)01030-1 . PMID 12810078 .
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
