Homo sapiens (human): 7504
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
XK-related
Motif
Other DBs
NCBI-GeneID:
7504
NCBI-ProteinID:
NP_066569
OMIM:
314850
HGNC:
12811
Ensembl:
ENSG00000047597
UniProt:
P51811
LinkDB
All DBs
Position
X:37685791..37732130
Genome browser
AA seq
444 aa
AA seq
DB search
MKFPASVLASVFLFVAETTAALSLSSTYRSGGDRMWQALTLLFSLLPCALVQLTLLFVHR
DLSRDRPLVLLLHLLQLGPLFRCFEVFCIYFQSGNNEEPYVSITKKRQMPKNGLSEEIEK
EVGQAEGKLITHRSAFSRASVIQAFLGSAPQLTLQLYISVMQQDVTVGRSLLMTISLLSI
VYGALRCNILAIKIKYDEYEVKVKPLAYVCIFLWRSFEIATRVVVLVLFTSVLKTWVVVI
ILINFFSFFLYPWILFWCSGSPFPENIEKALSRVGTTIVLCFLTLLYTGINMFCWSAVQL
KIDSPDLISKSHNWYQLLVYYMIRFIENAILLLLWYLFKTDIYMYVCAPLLVLQLLIGYC
TAILFMLVFYQFFHPCKKLFSSSVSEGFQRWLRCFCWACRQQKPCEPIGKEDLQSSRDRD
ETPSSSKTSPEPGQFLNAEDLCSA
NT seq
1335 nt
NT seq
+upstream
nt +downstream
nt
atgaaattcccggcctcggtgctggcgtccgtgttcctgttcgtggccgagacaacggcg
gcgctcagcctgagcagcacctaccgctcgggcggggaccgcatgtggcaggcgctgacg
ttgcttttctcgctactgccttgcgcgctcgtgcagctcacgcttctcttcgtacaccgc
gacctcagccgcgaccgcccgctcgtactgctgctgcacctgctgcaacttgggcccctt
ttcaggtgttttgaagtcttctgcatctactttcagtcaggcaacaatgaagagccttat
gtcagtatcaccaagaagaggcaaatgccaaaaaatggcctctcagaggagattgagaag
gaggtgggccaggcagaaggcaaactaatcacccaccgatcagcgttcagccgggcgtcg
gtgatccaggctttcttgggctcagccccccagctgaccctacagctgtacataagtgtc
atgcagcaggacgtcactgttggaagaagtctcctcatgaccatatccctgttgtccatt
gtgtatggagccttgcgctgcaacatcctagccatcaaaatcaagtacgatgagtatgaa
gtcaaagtgaagcctctggcctatgtctgtatcttcctgtggaggagctttgagattgcc
actcgagttgtagtcctggtcctctttacctccgtcctgaagacctgggtggtggttata
atactcatcaacttcttcagtttcttcttgtacccctggatcctcttctggtgcagtggt
tccccattccctgagaacatagagaaggccctcagtagagtgggcaccaccattgtacta
tgctttctaactttactctatactggtatcaacatgttctgctggtctgctgtacagctg
aaaattgacagccctgacctcatcagcaagtcccataattggtaccagctactggtgtat
tacatgataagattcatcgagaatgccatcctcctcctcctgtggtatcttttcaagact
gacatctatatgtatgtgtgcgcacctctgttggtcctgcagctgctcattgggtactgc
acagccattctcttcatgcttgtattctatcagttcttccacccttgcaaaaagctcttt
tcttccagtgtttctgaaggctttcagaggtggctcaggtgtttttgctgggcctgcagg
cagcaaaaaccctgtgagccgataggaaaggaagatctacagtcatccagagatagagat
gagacaccttctagcagtaaaacaagtcctgagcctggtcagttcttgaatgctgaagat
ctctgctctgcttaa
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