KEGG   Homo sapiens (human): 7504
Entry
7504              CDS       T01001                                 
Symbol
XK, KX, NA, NAC, X1k, XKR1
Name
(RefSeq) X-linked Kx blood group antigen, Kell and VPS13A binding protein
  KO
K19522  membrane transport protein XK
Organism
hsa  Homo sapiens (human)
Disease
H00655  McLeod syndrome
H00832  Core neuroacanthocytosis syndromes
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    7504 (XK)
Transporters [BR:hsa02000]
 Other transporters
  Electrochemical potential-driven transporters [TC:2]
   7504 (XK)
SSDB
Motif
Pfam: XK-related
Other DBs
NCBI-GeneID: 7504
NCBI-ProteinID: NP_066569
OMIM: 314850
HGNC: 12811
Ensembl: ENSG00000047597
UniProt: P51811
Position
X:37685791..37732130
AA seq 444 aa
MKFPASVLASVFLFVAETTAALSLSSTYRSGGDRMWQALTLLFSLLPCALVQLTLLFVHR
DLSRDRPLVLLLHLLQLGPLFRCFEVFCIYFQSGNNEEPYVSITKKRQMPKNGLSEEIEK
EVGQAEGKLITHRSAFSRASVIQAFLGSAPQLTLQLYISVMQQDVTVGRSLLMTISLLSI
VYGALRCNILAIKIKYDEYEVKVKPLAYVCIFLWRSFEIATRVVVLVLFTSVLKTWVVVI
ILINFFSFFLYPWILFWCSGSPFPENIEKALSRVGTTIVLCFLTLLYTGINMFCWSAVQL
KIDSPDLISKSHNWYQLLVYYMIRFIENAILLLLWYLFKTDIYMYVCAPLLVLQLLIGYC
TAILFMLVFYQFFHPCKKLFSSSVSEGFQRWLRCFCWACRQQKPCEPIGKEDLQSSRDRD
ETPSSSKTSPEPGQFLNAEDLCSA
NT seq 1335 nt   +upstreamnt  +downstreamnt
atgaaattcccggcctcggtgctggcgtccgtgttcctgttcgtggccgagacaacggcg
gcgctcagcctgagcagcacctaccgctcgggcggggaccgcatgtggcaggcgctgacg
ttgcttttctcgctactgccttgcgcgctcgtgcagctcacgcttctcttcgtacaccgc
gacctcagccgcgaccgcccgctcgtactgctgctgcacctgctgcaacttgggcccctt
ttcaggtgttttgaagtcttctgcatctactttcagtcaggcaacaatgaagagccttat
gtcagtatcaccaagaagaggcaaatgccaaaaaatggcctctcagaggagattgagaag
gaggtgggccaggcagaaggcaaactaatcacccaccgatcagcgttcagccgggcgtcg
gtgatccaggctttcttgggctcagccccccagctgaccctacagctgtacataagtgtc
atgcagcaggacgtcactgttggaagaagtctcctcatgaccatatccctgttgtccatt
gtgtatggagccttgcgctgcaacatcctagccatcaaaatcaagtacgatgagtatgaa
gtcaaagtgaagcctctggcctatgtctgtatcttcctgtggaggagctttgagattgcc
actcgagttgtagtcctggtcctctttacctccgtcctgaagacctgggtggtggttata
atactcatcaacttcttcagtttcttcttgtacccctggatcctcttctggtgcagtggt
tccccattccctgagaacatagagaaggccctcagtagagtgggcaccaccattgtacta
tgctttctaactttactctatactggtatcaacatgttctgctggtctgctgtacagctg
aaaattgacagccctgacctcatcagcaagtcccataattggtaccagctactggtgtat
tacatgataagattcatcgagaatgccatcctcctcctcctgtggtatcttttcaagact
gacatctatatgtatgtgtgcgcacctctgttggtcctgcagctgctcattgggtactgc
acagccattctcttcatgcttgtattctatcagttcttccacccttgcaaaaagctcttt
tcttccagtgtttctgaaggctttcagaggtggctcaggtgtttttgctgggcctgcagg
cagcaaaaaccctgtgagccgataggaaaggaagatctacagtcatccagagatagagat
gagacaccttctagcagtaaaacaagtcctgagcctggtcagttcttgaatgctgaagat
ctctgctctgcttaa

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (4)   
   KEGG DISEASE (2)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (21)   
   KEGG ORTHOLOGY (1)   
   RefGene (13)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
Protein sequence (5)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (3)   
DNA sequence (13)   
   RefSeq(nuc) (3)   
   GenBank (5)   
   EMBL (5)   
Protein domain (1)   
   Pfam (1)   
All databases (47)   

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