SLC2A1

protein-coding gene in the species Homo sapiens

Wikidata entity: Q14904883

P1057 chromosome ... Q430258 (human chromosome 1) human chromosome 1
P4196 cytogenetic location String 1p34.2 ???
P1889 different from ... Q24722601 (glucose transporter, type 1) glucose transporter, type 1
P688 encodes ... Q416268 (Solute carrier family 2 member 1) Solute carrier family 2 member 1
P688 encodes ... Q21151122 (Solute carrier family 2, facilitated glucose transporter member 1) Solute carrier family 2, facilitated glucose transporter member 1
P2888 exact match Url None ???
P5572 expressed in ... Q66592418 (ectocervix) ectocervix
P5572 expressed in ... Q1978198 (tibial nerve) tibial nerve
P5572 expressed in ... Q2346242 (retinal pigment epithelium) retinal pigment epithelium
P5572 expressed in ... Q5311600 (pancreatic ductal cell) pancreatic ductal cell
P5572 expressed in ... Q6135922 (sural nerve) sural nerve
P5572 expressed in ... Q11394395 (endothelial cell) endothelial cell
P5572 expressed in ... Q66514948 (skin of abdomen) skin of abdomen
P5572 expressed in ... Q66527089 (skin of leg) skin of leg
P5572 expressed in ... Q66569011 (C1 segment) C1 segment
P5572 expressed in ... Q66574757 (olfactory zone of nasal mucosa) olfactory zone of nasal mucosa
P703 found in taxon ... Q15978631 (Homo sapiens) Homo sapiens
P692 Gene Atlas image CommonsMedia http://commons.wikimedia.org/wiki/Special:FilePath/PBB%20GE%20SLC2A1%20201249%20at%20fs.png ???
P692 Gene Atlas image CommonsMedia http://commons.wikimedia.org/wiki/Special:FilePath/PBB%20GE%20SLC2A1%20201250%20s%20at%20fs.png ???
P2293 genetic association ... Q1485893 (encephalopathy due to GLUT1 deficiency) encephalopathy due to GLUT1 deficiency
P2293 genetic association ... Q5532415 (generalized epilepsy) generalized epilepsy
P2293 genetic association ... Q7139585 (childhood onset GLUT1 deficiency syndrome 2) childhood onset GLUT1 deficiency syndrome 2
P2293 genetic association ... Q32038804 (dystonia 9) dystonia 9
P2293 genetic association ... Q55783613 (hereditary cryohydrocytosis with reduced stomatin) hereditary cryohydrocytosis with reduced stomatin
P645 genomic end String 42958893 ???
P645 genomic end String 43424530 ???
P644 genomic start String 42925353 ???
P644 genomic start String 43391052 ???
P593 HomoloGene ID String 68520 ???
P31 instance of ... Q7187 (gene) gene
P684 ortholog ... Q14904884 (Slc2a1) Slc2a1
P684 ortholog ... Q24424876 (Slc2a1) Slc2a1
P684 ortholog ... Q29688819 (R09B5.11) R09B5.11
P684 ortholog ... Q29771610 (slc2a1a) slc2a1a
P684 ortholog ... Q29771848 (slc2a1b) slc2a1b
P2548 strand orientation ... Q22809711 (reverse strand) reverse strand
P279 subclass of ... Q20747295 (protein-coding gene) protein-coding gene
External Ids
P594Ensembl gene IDENSG00000117394
P704Ensembl transcript IDENST00000372500
P704Ensembl transcript IDENST00000415851
P704Ensembl transcript IDENST00000426263
P704Ensembl transcript IDENST00000460369
P704Ensembl transcript IDENST00000475162
P704Ensembl transcript IDENST00000625233
P704Ensembl transcript IDENST00000629908
P704Ensembl transcript IDENST00000630287
P704Ensembl transcript IDENST00000630821
P704Ensembl transcript IDENST00000669445
P704Ensembl transcript IDENST00000674545
P704Ensembl transcript IDENST00000674765
P704Ensembl transcript IDENST00000675112
P704Ensembl transcript IDENST00000676097
P704Ensembl transcript IDENST00000676254
P351Entrez Gene ID6513
P353HGNC gene symbolSLC2A1
P354HGNC ID11005
P492OMIM ID138140
P492OMIM ID138140
P639RefSeq RNA IDNM_006516
P2892UMLS CUIC1335837

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log id: 2091693