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Protein Ontology report - solute carrier family 67 member A1 (human)
PR:Q96BI1 - http://purl.obolibrary.org/obo/PR_Q96BI1
 
  Protein Forms      
Ontology Information Show OBO stanza / GPI
  PRO ID
PR:Q96BI1   
  PRO namesolute carrier family 67 member A1 (human) 
  Synonyms
PRO-Short-label: EXACT:hSLC67A1
Gene-based: RELATED:BWR1A | BWSCR1A | HET | IMPT1 | ITM | ORCTL2 | SLC22A18 | SLC22A1L | SLC67A1 | TSSC5
Other: EXACT:Beckwith-Wiedemann syndrome chromosomal region 1 candidate gene A protein (human) | efflux transporter-like protein (human) | imprinted multi-membrane-spanning polyspecific transporter-related protein 1 (human) | ORCTL-2 (human) | organic cation transporter-like protein 2 (human) | p45-Beckwith-Wiedemann region 1 A (human) | p45-BWR1A (human) | solute carrier family 22 member 1-like (human) | solute carrier family 22 member 18 (human) | tumor-suppressing STF cDNA 5 protein (human) | tumor-suppressing subchromosomal transferable fragment candidate gene 5 protein (human)
  Definition"A solute carrier family 67 member A1 that is encoded in the genome of human." [PRO:DNx, UniProtKB:Q96BI1] 
  PRO Categoryorganism-gene 
  ParentPR:000014986 solute carrier family 67 member A1
PR:000029067 Homo sapiens protein
  Gene TemplateHGNC:10964 SLC67A1 (human)
  TaxonNCBITaxon:9606 Homo sapiens
  Terms by PRO Category
Organism-Independent Organism-Specific
         Category          Number of Terms          Category          Number of Terms
         Gene0                                                  Organism-Gene 1                                        
         Sequence0                                                  Organism-Sequence 2                                        
         Modification0                                                  Organism-Modification 1                                        
  Term Hierarchy
  Visualization
DAG: OLS:
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Related Cross References

  Db identifiers
UniProtKB:Q96BI1
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Protein Forms Switch to Compact View   

Category  
PRO ID
Name
Short Name
Definition
Ann. Has Annotation?

Comp. In Complex?
organism-gene


PR:Q96BI1
solute carrier family 67 member A1 (human)
hSLC67A1
"A solute carrier family 67 member A1 that is encoded in the genome of human." [PRO:DNx, UniProtKB:Q96BI1]

organism-sequence


PR:000060283
solute carrier family 67 member A1 sequence variant L286H (human)
hSLC67A1/var:L286H
"A solute carrier family 67 member A1 (human) that has a His residue at the position equivalent to Leu-286 of the amino acid sequence represented by UniProtKB:Q96BI1. UniProtKB:Q96BI1, Leu-286, CHEBI:29979." [PRO:DNx, Reactome:R-HSA-5625583]

organism-sequence


PR:000064270
solute carrier family 67 member A1 sequence variant S233F (human)
hSLC67A1/var:S233F
"A solute carrier family 67 member A1 (human) that has a Phe residue at the position equivalent to Ser-233 of the amino acid sequence represented by UniProtKB:Q96BI1. UniProtKB:Q96BI1, Ser-233, CHEBI:29997." [PRO:DNx, Reactome:R-HSA-5625564]

organism-modification


PR:000084353
solute carrier family 67 member A1 phosphorylated 1 (human)
hSLC67A1/Phos:1
"A solute carrier family 67 member A1 (human) that has been phosphorylated on the residue at the position equivalent to Ser-144 of the amino acid sequence represented by UniProtKB:Q96BI1. UniProtKB:Q96BI1, Ser-144, MOD:00046." [IEDB_epitope:2145847, PRO:DNx]