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Protein Ontology report - solute carrier family 2, facilitated glucose transporter member 1 (human)
PR:P11166 -
http://purl.obolibrary.org/obo/PR_P11166
Protein Forms
Ontology Information
Show OBO stanza
/
GPI
PRO ID
PR:P11166
PRO name
solute carrier family 2, facilitated glucose transporter member 1 (human)
Synonyms
PRO-Short-label
:
EXACT:
hSLC2A1
Gene-based
:
RELATED:
GLUT1 | SLC2A1
Other
:
EXACT:
glucose transporter type 1, erythrocyte/brain (human) | GLUT-1 (human) | HepG2 glucose transporter (human)
Definition
"A solute carrier family 2, facilitated glucose transporter member 1 that is encoded in the genome of human." [PRO:DNx,
UniProtKB:P11166
]
PRO Category
organism-gene
Parent
PR:000015058
solute carrier family 2, facilitated glucose transporter member 1
PR:000029067
Homo sapiens protein
Gene Template
HGNC:11005
SLC2A1 (human)
Taxon
NCBITaxon:9606
Homo sapiens
Terms by PRO Category
Organism-Independent
Organism-Specific
Category
Number of Terms
Category
Number of Terms
Gene
0
Organism-Gene
1
Sequence
0
Organism-Sequence
5
Modification
0
Organism-Modification
2
Term Hierarchy
Visualization
DAG:
OLS:
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Related Cross References
Db identifiers
UniProtKB:P11166
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Protein Forms
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Compact View
Category
PRO ID
Name
Short Name
Definition
Ann.
Has Annotation?
Comp.
In Complex?
organism-gene
PR:P11166
solute carrier family 2, facilitated glucose transporter member 1 (human)
hSLC2A1
"A solute carrier family 2, facilitated glucose transporter member 1 that is encoded in the genome of human." [PRO:DNx, UniProtKB:P11166]
organism-sequence
PR:000060330
solute carrier family 2, facilitated glucose transporter member 1 sequence variant A342L (human)
hSLC2A1/var:A342L
"A solute carrier family 2, facilitated glucose transporter member 1 (human) that has a Leu residue at the position equivalent to Ala-342 of the amino acid sequence represented by UniProtKB:P11166. UniProtKB:P11166, Ala-342, CHEBI:30006." [PRO:DNx, Reactome:R-HSA-5632874]
organism-sequence
PR:000061422
solute carrier family 2, facilitated glucose transporter member 1 sequence variant K256V (human)
hSLC2A1/var:K256V
"A solute carrier family 2, facilitated glucose transporter member 1 (human) that has a Val residue at the position equivalent to Lys-256 of the amino acid sequence represented by UniProtKB:P11166. UniProtKB:P11166, Lys-256, CHEBI:30015." [PRO:DNx, Reactome:R-HSA-5632870]
organism-sequence
PR:000062458
solute carrier family 2, facilitated glucose transporter member 1 sequence variant R223P (human)
hSLC2A1/var:R223P
"A solute carrier family 2, facilitated glucose transporter member 1 (human) that has a Pro residue at the position equivalent to Arg-223 of the amino acid sequence represented by UniProtKB:P11166. UniProtKB:P11166, Arg-223, CHEBI:50342." [PRO:DNx, Reactome:R-HSA-5632825]
organism-sequence
PR:000064195
solute carrier family 2, facilitated glucose transporter member 1 sequence variant R126L (human)
hSLC2A1/var:R126L
"A solute carrier family 2, facilitated glucose transporter member 1 (human) that has a Leu residue at the position equivalent to Arg-126 of the amino acid sequence represented by UniProtKB:P11166. UniProtKB:P11166, Arg-126, CHEBI:30006." [PRO:DNx, Reactome:R-HSA-5632866]
organism-sequence
PR:P11166-1
solute carrier family 2, facilitated glucose transporter member 1 isoform 1 (human)
hSLC2A1/iso:1
"A solute carrier family 2, facilitated glucose transporter member 1 isoform 1 that is encoded in the genome of human." [PRO:DNx]
organism-modification
PR:000073324
solute carrier family 2, facilitated glucose transporter member 1 deaminated 1 (human)
hSLC2A1/Deam:1
"A solute carrier family 2, facilitated glucose transporter member 1 (human) that has been deaminated on the residue at the position equivalent to Asn-29 of the amino acid sequence represented by UniProtKB:P11166. UniProtKB:P11166, Asn-29, MOD:00684." [IEDB_epitope:1825409, PRO:DNx]
organism-modification
PR:000083602
solute carrier family 2, facilitated glucose transporter member 1 deaminated 2 (human)
hSLC2A1/Deam:2
"A solute carrier family 2, facilitated glucose transporter member 1 (human) that has been deaminated on the residue at the position equivalent to Asn-34 of the amino acid sequence represented by UniProtKB:P11166. UniProtKB:P11166, Asn-34, MOD:00684." [IEDB_epitope:1825408, PRO:DNx]
