Homo sapiens Gene: XK
Summary
InnateDB Gene IDBG-55754.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol XK
Gene Name X-linked Kx blood group (McLeod syndrome)
Synonyms KX; MCLDS; NA; NAC; X1k; XKR1
Species Homo sapiens
Ensembl Gene ENSG00000047597
Encoded Proteins
X-linked Kx blood group (McLeod syndrome)
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. [provided by RefSeq, Jul 2008]
This locus controls the synthesis of the Kell blood group \'precursor substance\' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome X:37685759-37732130
Strand Forward strand
Band p21.1
Transcripts
ENST00000378616 ENSP00000367879
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
Experimentally validated
Total 5 [view]
Protein-Protein 2 [view]
Protein-DNA 3 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005215 transporter activity
GO:0005515 protein binding
Biological Process
GO:0006810 transport
GO:0006865 amino acid transport
Cellular Component
GO:0016021 integral component of membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt P51811
TrEMBL Q2Z218
UniProt Splice Variant
Entrez Gene 7504
UniGene Hs.78919
RefSeq NM_021083
HUGO HGNC:12811
OMIM 314850
CCDS CCDS14241
HPRD
IMGT
EMBL AB214532 AY534238 BC036019 DQ062746 Z32684
GenPept AAH36019 AAT07087 AAY43132 BAE48708 CAA83632
RNA Seq Atlas 7504