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Find link is a tool written by Edward Betts.Longer titles found: Solute carrier family 10 member 4 (view), Solute carrier family 16 member 12 (view), Solute carrier family 17 (vesicular glutamate transporter), member 6 (view), Solute carrier family 22 member 15 (view), Solute carrier family 30 member 10 (view), Solute carrier family 38 member 9 (view), Solute carrier family 9 member a4 (view)
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alternate case: solute carrier family
SLC38A5
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Solute carrier family 38 member 5 is a protein that in humans is encoded by the SLC38A5 gene. The protein encoded by this gene is a system N sodium-coupledSLC25A22 (727 words) [view diff] exact match in snippet view article find links to article
Solute carrier family 25 member 22 is a protein that in humans is encoded by the SLC25A22 gene. This gene encodes a mitochondrial glutamate carrier. MutationsSLC22A14 (211 words) [view diff] exact match in snippet view article find links to article
Solute carrier family 22 member 14 is a protein that in humans is encoded by the SLC22A14 gene. This gene encodes a member of the organic-cation transporterSLC17A9 (200 words) [view diff] exact match in snippet view article find links to article
Solute carrier family 17 member 9 is a protein that in humans is encoded by the SLC17A9 gene. This gene encodes a member of a family of transmembraneSLC66A3 (748 words) [view diff] exact match in snippet view article find links to article
Solute carrier family 66 member 3 is a gene in humans that encodes the protein SLC66A3. The function of the SLC66A3 protein is not yet well understoodSLC8B1 (325 words) [view diff] exact match in snippet view article find links to article
Solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 is a protein that in humans is encoded by the SLC8B1 gene. SLC24A6 belongs to aGHB receptor (1,348 words) [view diff] exact match in snippet view article find links to article
neurotransmitter and psychoactive drug γ-hydroxybutyric acid (GHB). As solute carrier family 52 member 2 (SLC52A2), it is also a transporter for riboflavin.Infantile free sialic acid storage disease (222 words) [view diff] exact match in snippet view article find links to article
sialic acid to be excreted in the urine. Mutations in the SLC17A5 (solute carrier family 17 (anion/sugar transporter), member 50) gene cause all forms ofSlc22a21 (238 words) [view diff] exact match in snippet view article find links to article
Solute carrier family 22 (organic cation transporter), member 21 is a protein that in the house mouse is encoded by the Slc22a21 gene. The gene is alsoSLC22A24 (124 words) [view diff] exact match in snippet view article find links to article
Solute carrier family 22 member 24 is a protein that in humans is encoded by the SLC22A24 gene. SLC22A24 belongs to a large family of transmembrane proteinsSLC52A3 (928 words) [view diff] exact match in snippet view article find links to article
Solute carrier family 52 (riboflavin transporter), member 3, formerly known as chromosome 20 open reading frame 54 and riboflavin transporter 2, is aDicarboxylic aminoaciduria (664 words) [view diff] exact match in snippet view article find links to article
resulting in a lack of expression of the SLC1A1 gene, a member of the solute carrier family, are found to cause development of dicarboxylic aminoaciduria inSLC9B2 (576 words) [view diff] exact match in snippet view article find links to article
Solute carrier family 9, subfamily B (NHA2, cation proton antiporter 2), member 2 is a protein that in humans is encoded by the SLC9B2 gene. Sodium–hydrogenSLC25A48 (158 words) [view diff] exact match in snippet view article find links to article
Solute carrier family 25 member 48 is a protein that in humans is encoded by the SLC25A48 gene. This gene encodes a mitochondrial choline carrier. MutationsVolixibat (244 words) [view diff] exact match in snippet view article find links to article
protein (ileal bile acid transporter), which is also called SLC10A2 (solute carrier family 10 member 2) or ASBT (apical sodium–bile acid transporter). IBATOrganic anion transporter 4 (67 words) [view diff] exact match in snippet view article find links to article
refer to either of these carrier proteins: Solute carrier family 22 member 9 (SLC22A9) Solute carrier family 22 member 11 (SLC22A11) This set index articleCream gene (4,679 words) [view diff] exact match in snippet view article find links to article
colors is the cream allele, which is at a specific locus on the solute carrier family 45 member 2 (SLC45A2) gene (previously known as MATP and OCA4, amongOSTalpha (674 words) [view diff] exact match in snippet view article find links to article
Identifiers Aliases SLC51A, OSTA, OSTalpha, solute carrier family 51 alpha subunit, solute carrier family 51 subunit alpha, PFIC6 External IDs OMIM: 612084;Augustine blood group system (446 words) [view diff] exact match in snippet view article find links to article
from the original on 2020-10-01. Retrieved 2021-01-28. "SLC29A1 solute carrier family 29 member 1 (Augustine blood group) [Homo sapiens (human)] - GeneChromosome 17 (2,248 words) [view diff] exact match in snippet view article find links to article
protein Spindle and Kinetochore Associated SLC39A11: encoding protein Solute carrier family 39 member 11 SLFN13 : encoding protein Schlafen family member 13OSTbeta (631 words) [view diff] exact match in snippet view article find links to article
Identifiers Aliases SLC51B, OSTB, OSTBETA, OSTbeta, solute carrier family 51 beta subunit, solute carrier family 51 subunit beta, PBAM2 External IDs OMIM: 612085;Cotransporter (2,288 words) [view diff] exact match in snippet view article find links to article
neurotransmitter γ-aminobutyric acid (GABA) transporters are members of the solute carrier family 6 (SLC6) of sodium- and chloride-dependent neurotransmitter receptorHP59 (912 words) [view diff] exact match in snippet view article find links to article
contains, entirely within its coding region, the Sialin Gene SLC17A5 (Solute carrier family 17 (anion/sugar transporter). Member 5, also known asSLC17A5 orSignal transducing adaptor protein (666 words) [view diff] exact match in snippet view article find links to article
– Src homology 2 domain containing adaptor protein B SLC4A1AP – solute carrier family 4 (anion exchanger), member 1, adaptor protein Wikipedia:MeSH D12C13orf16 (347 words) [view diff] case mismatch in snippet view article find links to article
step in the biosynthesis of tetrahydrobiopterin from GTP) SLC16A2 Solute Carrier Family 16 Member 2 Non-redundant, thyroid hormone transporter STEAP3 STEAPCongenital hereditary endothelial dystrophy (403 words) [view diff] exact match in snippet view article find links to article
cases linked to mutations in SLC4A11 gene. The SLC4A11 gene encodes solute carrier family 4, sodium borate transporter, member 11. Histologically, the Descemet'sFazio–Londe disease (1,035 words) [view diff] exact match in snippet view article find links to article
1016/j.braindev.2004.10.003. PMID 16122634. S2CID 32223440. "SLC52A3 solute carrier family 52 member 3 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlmSLC35F6 (558 words) [view diff] exact match in snippet view article find links to article
SLC35F6 Identifiers Aliases SLC35F6, ANT2BP, C2orf18, TANGO9, solute carrier family 35 member F6 External IDs MGI: 1922169; HomoloGene: 9896; GeneCards:Chromosome 20 (1,573 words) [view diff] exact match in snippet view article find links to article
encoding protein Shieldin complex subunit 1 SLC17A9: encoding protein Solute carrier family 17 member 9 SLC2A4RG: encoding protein SLC2A4 regulator SLX4IP:Excitatory amino acid reuptake inhibitor (479 words) [view diff] exact match in snippet view article find links to article
Science & Business Media. p. 200. ISBN 978-3-540-87912-1. "SLC1A1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, systemTMEM22 (408 words) [view diff] exact match in snippet view article find links to article
SLC35G2 Identifiers Aliases SLC35G2, TMEM22, solute carrier family 35 member G2 External IDs OMIM: 617812; MGI: 2685365; HomoloGene: 11893; GeneCards:Chromosome 13 (1,622 words) [view diff] exact match in snippet view article find links to article
cluster 1 SCEL: encoding protein Sciellin SLC46A3: encoding protein Solute carrier family 46, member 3 SLITRK1: encoding protein SLIT and NTRK-like proteinChromosome 12 (1,843 words) [view diff] exact match in snippet view article find links to article
SHMT2: encoding protein Serine hydroxymethyltransferase 2 SLC8B1: solute carrier family 8 member B1 TBC1D15: encoding protein TBC1 domain family memberDIRC2 (293 words) [view diff] exact match in snippet view article find links to article
Identifiers Aliases SLC49A4, RCC4, disrupted in renal carcinoma 2, solute carrier family 49 member 4, DIRC2 External IDs OMIM: 602773; MGI: 2387188; HomoloGene:SLC16A11 (193 words) [view diff] exact match in snippet view article find links to article
SLC16A11 Identifiers Aliases SLC16A11, MCT11, solute carrier family 16 member 11, MCT 11 External IDs OMIM: 615765; MGI: 2663709; HomoloGene: 27409; GeneCards:Chromosome 3 (1,991 words) [view diff] exact match in snippet view article find links to article
containing 5 SFMBT1: Scm-like with four mbt domains 1 SLC25A20: solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 STT3B: catalyticChromosome 19 (2,547 words) [view diff] exact match in snippet view article find links to article
encoding protein Splicing factor, arginine/serine-rich 16 SLC5A5: Solute carrier family 5 (sodium iodide symporter), member 5 STK11: Serine/threonine kinaseTetrabenazine (1,888 words) [view diff] exact match in snippet view article find links to article
inhibitor of vesicular monoamine transporter 2 (VMAT2) also known as solute carrier family 18 member 2 (SLC18A2). VMAT2 is a protein which depletes dopamineTMEM241 (855 words) [view diff] exact match in snippet view article find links to article
- NCBI]". www.ncbi.nlm.nih.gov. Retrieved 2016-02-28. "SLC35D1 solute carrier family 35 member D1 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlmSLC6A1 epileptic encephalopathy (912 words) [view diff] exact match in snippet view article find links to article
given patient. Research published in 2015 linked mutations on the solute carrier family 6 member 1 protein (SLC6A1) to developmental and epileptic encephalopathiesList of A1 genes, proteins or receptors (667 words) [view diff] exact match in snippet view article find links to article
S100 calcium binding protein A1 Sec61 alpha 1 Serum amyloid A1 Solute carrier family 35 (CMP-sialic acid transporter), member A1 Spectrin, alpha 1 SpermTafamidis (1,603 words) [view diff] exact match in snippet view article find links to article
inhibits organic anion transporter 1 and organic anion transporter 3/solute carrier family 22 member 8 so is likely to interact with non-steroidal anti-inflammatoryTMEM82 (1,200 words) [view diff] exact match in snippet view article find links to article
transmembrane protein 82 (TMEM82), mRNA". 2021-06-26. "SLC25A34 solute carrier family 25 member 34 [Homo sapiens (human)] - Gene - NCBI". www.ncbi.nlmTMEM156 (901 words) [view diff] exact match in snippet view article find links to article
outer dense fibers (specific fibers to the sperm tail) SLC17A9-solute carrier family 17, member 9 involved in vesicular storage and exocytosis of ATPEquine coat color genetics (4,824 words) [view diff] exact match in snippet view article find links to article
now identifiable by DNA test. The Cream locus is occupied by the Solute carrier family 45, member 2 (SLC45A2) gene, also called the Membrane associatedX chromosome (3,912 words) [view diff] exact match in snippet view article find links to article
Splicing factor, arginine/serine-rich 17A SLC38A5: encoding protein Solute carrier family 38 member 5 SLITRK2: encoding protein SLIT and NTRK-like proteinROS1 (3,682 words) [view diff] exact match in snippet view article find links to article
repeats and immunoglobulin-like domains 3; SDC; syndecan 4; SLC34A2; solute carrier family 34 (sodium phosphate), member 2; TPM3; tropomyosin 3 Several drugsHuman skin color (14,411 words) [view diff] exact match in snippet view article find links to article
may have carried different alleles that we cannot now detect." Solute carrier family 24 member 5 (SLC24A5) regulates calcium in melanocytes and is importantPANO1 (1,204 words) [view diff] exact match in snippet view article find links to article
nucleus, but many nuclear proteins possess their own. PANO1 overlaps solute carrier family 25 member 22 (SLC25A22). A causal link between this solute carrierKidney (7,009 words) [view diff] exact match in snippet view article find links to article
of the kidney with podocin and nephrin expressed in glomeruli, Solute carrier family protein SLC22A8 expressed in proximal tubules, calbindin expressedEvolution of the cochlea (2,455 words) [view diff] exact match in snippet view article find links to article
1038/35012009. PMID 10821263. S2CID 4409772. "Entrez Gene: SLC26A5 solute carrier family 26, member 5 (prestin)". Koeppl, C; Forge, A; Manley, GM (2004)CCDC188 (1,184 words) [view diff] case mismatch in snippet view article find links to article
ZNF519 Zinc Finger Protein 519 Transcription Factor -0.61 SLC8A1 Solute Carrier Family 8 Member A1 Calcium and sodium ion exchange mediator -0.601 SupraopticSLC35A1-CDG (1,432 words) [view diff] case mismatch in snippet view article find links to article
Antibody". www.genecards.org. Retrieved 2022-08-17. "Entry - *605634 - SOLUTE CARRIER FAMILY 35 (CMP-SIALIC ACID TRANSPORTER), MEMBER 1; SLC35A1 - OMIM". wwwCEFIP (1,678 words) [view diff] case mismatch in snippet view article find links to article
Chromosome 14 Open Reading Frame 80 Unknown Unconfirmed SLC35F4 Solute Carrier Family 35 Member F4 Solute transporter Unconfirmed LHX4 LIM Homeobox 4Glutamate receptor (6,876 words) [view diff] exact match in snippet view article find links to article
Thapar A, O'Donovan MC (June 2005). "A family based study implicates solute carrier family 1-member 3 (SLC1A3) gene in attention-deficit/hyperactivity disorder"Cause of obsessive–compulsive disorder (3,408 words) [view diff] exact match in snippet view article find links to article
except those relating to the glutamate transporter gene, SLC1A1 (solute carrier family 1, member 1), which codes for the glutamate transporter, EAAC1.FAM149B1 (1,887 words) [view diff] case mismatch in snippet view article find links to article
adds a methylphosphate cap at the 5-end of 7SK snRNA. SLC6A17 (Solute Carrier Family 6 Member 17) is a sodium-dependent vesicular transporter that isDNAJC28 (2,730 words) [view diff] exact match in snippet view article find links to article
for cellular viability Inner mitochondrial membrane 1535 SLC30A9 solute carrier family 30 member 9 Enables zinc ion transmembrane transporter activityTumor hypoxia (5,517 words) [view diff] exact match in snippet view article find links to article
include cancers of the gastric and colon. These genes include: solute carrier family 2 (GLUT1), hexokinase (HK), phosphoglucose isomerase (PGI), phosphofructokinaseAmphetamine (29,624 words) [view diff] exact match in snippet view article find links to article
and Clinical Pharmacology. Retrieved 13 November 2015. "SLC1A1 solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, systemList of human clusters of differentiation (492 words) [view diff] exact match in snippet view article find links to article
Receptor for several virus semaphorins. CD233 known as SLC4A1 (solute carrier family 4 member 1), anion exchanger 1 (AE1) or band 3 (BND3); present inBiological functions of nitric oxide (7,668 words) [view diff] exact match in snippet view article find links to article
S, Li Q, Zhong S, et al. (December 2014). "Genetic ablation of solute carrier family 7a3a leads to hepatic steatosis in zebrafish during fasting". HepatologyWDR88 (2,362 words) [view diff] exact match in snippet view article find links to article
(low density lipoprotein receptor-related protein 3), SLC7A10 (solute carrier family 7 membrane 10), and GPATCH1 (G-patch domain containing 1). The WDR88