KEGG   Homo sapiens (human): 10058
Entry
10058             CDS       T01001                                 
Symbol
ABCB6, ABC, LAN, MTABC3, PRP, umat
Name
(RefSeq) ATP binding cassette subfamily B member 6 (LAN blood group)
  KO
K05661  ATP-binding cassette, subfamily B (MDR/TAP), member 6
Organism
hsa  Homo sapiens (human)
Pathway
hsa02010  ABC transporters
Disease
H00232  Hereditary stomatocytosis
H01027  Microphthalmia
H02001  Familial pseudohyperkalemia
H02350  Dyschromatosis universalis hereditaria
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09131 Membrane transport
   02010 ABC transporters
    10058 (ABCB6)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    10058 (ABCB6)
Transporters [BR:hsa02000]
 ABC transporters, eukaryotic type
  ABCB (MDR/TAP) subfamily
   ABCB6, 7 subgroups
    10058 (ABCB6)
SSDB
Motif
Pfam: MTABC_N ABC_tran ABC_membrane SMC_N AAA_22 AAA_16 RsgA_GTPase AAA_21 AAA_29 AAA SbcC_Walker_B AAA_30 ATP-synt_ab Septin Zeta_toxin
Other DBs
NCBI-GeneID: 10058
NCBI-ProteinID: NP_005680
OMIM: 605452
HGNC: 47
Ensembl: ENSG00000115657
UniProt: Q9NP58
Structure
Position
2:complement(219209772..219218958)
AA seq 842 aa
MVTVGNYCEAEGPVGPAWMQDGLSPCFFFTLVPSTRMALGTLALVLALPCRRRERPAGAD
SLSWGAGPRISPYVLQLLLATLQAALPLAGLAGRVGTARGAPLPSYLLLASVLESLAGAC
GLWLLVVERSQARQRLAMGIWIKFRHSPGLLLLWTVAFAAENLALVSWNSPQWWWARADL
GQQVQFSLWVLRYVVSGGLFVLGLWAPGLRPQSYTLQVHEEDQDVERSQVRSAAQQSTWR
DFGRKLRLLSGYLWPRGSPALQLVVLICLGLMGLERALNVLVPIFYRNIVNLLTEKAPWN
SLAWTVTSYVFLKFLQGGGTGSTGFVSNLRTFLWIRVQQFTSRRVELLIFSHLHELSLRW
HLGRRTGEVLRIADRGTSSVTGLLSYLVFNVIPTLADIIIGIIYFSMFFNAWFGLIVFLC
MSLYLTLTIVVTEWRTKFRRAMNTQENATRARAVDSLLNFETVKYYNAESYEVERYREAI
IKYQGLEWKSSASLVLLNQTQNLVIGLGLLAGSLLCAYFVTEQKLQVGDYVLFGTYIIQL
YMPLNWFGTYYRMIQTNFIDMENMFDLLKEETEVKDLPGAGPLRFQKGRIEFENVHFSYA
DGRETLQDVSFTVMPGQTLALVGPSGAGKSTILRLLFRFYDISSGCIRIDGQDISQVTQA
SLRSHIGVVPQDTVLFNDTIADNIRYGRVTAGNDEVEAAAQAAGIHDAIMAFPEGYRTQV
GERGLKLSGGEKQRVAIARTILKAPGIILLDEATSALDTSNERAIQASLAKVCANRTTIV
VAHRLSTVVNADQILVIKDGCIVERGRHEALLSRGGVYADMWQLQQGQEETSEDTKPQTM
ER
NT seq 2529 nt   +upstreamnt  +downstreamnt
atggtgactgtgggcaactactgcgaggccgaagggcccgtgggtccggcctggatgcag
gatggcctgagtccctgcttcttcttcacgctcgtgccctcgacgcggatggctctgggg
actctggccttggtgctggctcttccctgcagacgccgggagcggcccgctggtgctgat
tcgctgtcttggggggccggccctcgcatctctccctacgtgctgcagctgcttctggcc
acacttcaggcggcgctgcccctggccggcctggctggccgggtgggcactgcccggggg
gccccactgccaagctatctacttctggcctccgtgctggagagtctggccggcgcctgt
ggcctgtggctgcttgtcgtggagcggagccaggcacggcagcgtctggcaatgggcatc
tggatcaagttcaggcacagccctggtctcctgctcctctggactgtggcgtttgcagct
gagaacttggccctggtgtcttggaacagcccacagtggtggtgggcaagggcagacttg
ggccagcaggttcagtttagcctgtgggtgctgcggtatgtggtctctggagggctgttt
gtcctgggtctctgggcccctggacttcgtccccagtcctatacattgcaggttcatgaa
gaggaccaagatgtggaaaggagccaggttcggtcagcagcccaacagtctacctggcga
gattttggcaggaagctccgcctcctgagtggctacctgtggcctcgagggagtccagct
ctgcagctggtggtgctcatctgcctggggctcatgggtttggaacgggcactcaatgtg
ttggtgcctatattctataggaacattgtgaacttgctgactgagaaggcaccttggaac
tctctggcctggactgttaccagttacgtcttcctcaagttcctccaggggggtggcact
ggcagtacaggcttcgtgagcaacctgcgcaccttcctgtggatccgggtgcagcagttc
acgtctcggcgggtggagctgctcatcttctcccacctgcacgagctctcactgcgctgg
cacctggggcgccgcacaggggaggtgctgcggatcgcggatcggggcacatccagtgtc
acagggctgctcagctacctggtgttcaatgtcatccccacgctggccgacatcatcatt
ggcatcatctacttcagcatgttcttcaacgcctggtttggcctcattgtgttcctgtgc
atgagtctttacctcaccctgaccattgtggtcactgagtggagaaccaagtttcgtcgt
gctatgaacacacaggagaacgctacccgggcacgagcagtggactctctgctaaacttc
gagacggtgaagtattacaacgccgagagttacgaagtggaacgctatcgagaggccatc
atcaaatatcagggtttggagtggaagtcgagcgcttcactggttttactaaatcagacc
cagaacctggtgattgggctcgggctcctcgccggctccctgctttgcgcatactttgtc
actgagcagaagctacaggttggggactatgtgctctttggcacctacattatccagctg
tacatgcccctcaattggtttggcacctactacaggatgatccagaccaacttcattgac
atggagaacatgtttgacttgctgaaagaggagacagaagtgaaggaccttcctggagca
gggccccttcgctttcagaagggccgtattgagtttgagaacgtgcacttcagctatgcc
gatgggcgggagactctgcaggacgtgtctttcactgtgatgcctggacagacacttgcc
ctggtgggcccatctggggcagggaagagcacaattttgcgcctgctgtttcgcttctac
gacatcagctctggctgcatccgaatagatgggcaggacatttcacaggtgacccaggcc
tctctccggtctcacattggagttgtgccccaagacactgtcctctttaatgacaccatc
gccgacaatatccgttacggccgtgtcacagctgggaatgatgaggtggaggctgctgct
caggctgcaggcatccatgatgccattatggctttccctgaagggtacaggacacaggtg
ggcgagcggggactgaagctgagcggcggggagaagcagcgcgtcgccattgcccgcacc
atcctcaaggctccgggcatcattctgctggatgaggcaacgtcagcgctggatacatct
aatgagagggccatccaggcttctctggccaaagtctgtgccaaccgcaccaccatcgta
gtggcacacaggctctcaactgtggtcaatgctgaccagatcctcgtcatcaaggatggc
tgcatcgtggagaggggacgacacgaggctctgttgtcccgaggtggggtgtatgctgac
atgtggcagctgcagcagggacaggaagaaacctctgaagacactaagcctcagaccatg
gaacggtga

  All links  
Disease (5)   
   OMIM (5)   
Gene (13)   
   RefGene (7)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (62)   
   RefSeq(nuc) (2)   
   GenBank (30)   
   EMBL (30)   
3D Structure (16)   
   PDB (16)   
Protein domain (15)   
   Pfam (15)   
All databases (115)   

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