KEGG   Homo sapiens (human): 23457
Entry
23457             CDS       T01001                                 
Symbol
ABCB9, EST122234, TAPL
Name
(RefSeq) ATP binding cassette subfamily B member 9
  KO
K05656  ATP-binding cassette, subfamily B (MDR/TAP), member 9
Organism
hsa  Homo sapiens (human)
Pathway
hsa02010  ABC transporters
hsa04142  Lysosome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09131 Membrane transport
   02010 ABC transporters
    23457 (ABCB9)
 09140 Cellular Processes
  09141 Transport and catabolism
   04142 Lysosome
    23457 (ABCB9)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    23457 (ABCB9)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    23457 (ABCB9)
Membrane trafficking [BR:hsa04131]
 Endosome - Lysosome transport
  Others
   Lysosomal membrane proteins
    23457 (ABCB9)
Transporters [BR:hsa02000]
 ABC transporters, eukaryotic type
  ABCB (MDR/TAP) subfamily
   ABCB2, 3, 8, 9, 10 subgroups
    23457 (ABCB9)
SSDB
Motif
Pfam: ABC_membrane ABC_tran SMC_N AAA_22 RsgA_GTPase AAA_16 nSTAND1 DUF4191 AAA_30 AAA_29 MCU AAA_21 AAA_23
Other DBs
NCBI-GeneID: 23457
NCBI-ProteinID: NP_062571
OMIM: 605453
HGNC: 50
Ensembl: ENSG00000150967
UniProt: Q9NP78
Position
12:complement(122918610..122975114)
AA seq 766 aa
MRLWKAVVVTLAFMSVDICVTTAIYVFSHLDRSLLEDIRHFNIFDSVLDLWAACLYRSCL
LLGATIGVAKNSALGPRRLRASWLVITLVCLFVGIYAMVKLLLFSEVRRPIRDPWFWALF
VWTYISLGASFLLWWLLSTVRPGTQALEPGAATEAEGFPGSGRPPPEQASGATLQKLLSY
TKPDVAFLVAASFFLIVAALGETFLPYYTGRAIDGIVIQKSMDQFSTAVVIVCLLAIGSS
FAAGIRGGIFTLIFARLNIRLRNCLFRSLVSQETSFFDENRTGDLISRLTSDTTMVSDLV
SQNINVFLRNTVKVTGVVVFMFSLSWQLSLVTFMGFPIIMMVSNIYGKYYKRLSKEVQNA
LARASNTAEETISAMKTVRSFANEEEEAEVYLRKLQQVYKLNRKEAAAYMYYVWGSGLTL
LVVQVSILYYGGHLVISGQMTSGNLIAFIIYEFVLGDCMESVGSVYSGLMQGVGAAEKVF
EFIDRQPTMVHDGSLAPDHLEGRVDFENVTFTYRTRPHTQVLQNVSFSLSPGKVTALVGP
SGSGKSSCVNILENFYPLEGGRVLLDGKPISAYDHKYLHRVISLVSQEPVLFARSITDNI
SYGLPTVPFEMVVEAAQKANAHGFIMELQDGYSTETGEKGAQLSGGQKQRVAMARALVRN
PPVLILDEATSALDAESEYLIQQAIHGNLQKHTVLIIAHRLSTVEHAHLIVVLDKGRVVQ
QGTHQQLLAQGGLYAKLVQRQMLGLQPAADFTAGHNEPVANGSHKA
NT seq 2301 nt   +upstreamnt  +downstreamnt
atgcggctgtggaaggcggtggtggtgactttggccttcatgagtgtggacatctgcgtg
accacggccatctatgtcttcagccacctggaccgcagcctcctggaggacatccgccac
ttcaacatctttgactcggtgctggatctctgggcagcctgcctgtaccgcagctgcctg
ctgctgggagccaccattggtgtggccaagaacagtgcgctggggccccggcggctgcgg
gcctcgtggctggtcatcaccctcgtgtgcctcttcgtgggcatctatgccatggtgaag
ctgctgctcttctcagaggtgcgcaggcccatccgggacccctggttttgggccctgttc
gtgtggacgtacatttcactcggcgcatccttcctgctctggtggctgctgtccaccgtg
cggccaggcacccaggccctggagccaggggcggccaccgaggctgagggcttccctggg
agcggccggccaccgcccgagcaggcgtctggggccacgctgcagaagctgctctcctac
accaagcccgacgtggccttcctcgtggccgcctccttcttcctcatcgtggcagctctg
ggagagaccttcctgccctactacacgggccgcgccattgatggcatcgtcatccagaaa
agcatggatcagttcagcacggctgtcgtcatcgtgtgcctgctggccattggcagctca
tttgccgcaggtattcggggcggcatttttaccctcatatttgccagactgaacattcgc
cttcgaaactgtctcttccgctcactggtgtcccaggagacaagcttctttgatgagaac
cgcacaggggacctcatctcccgcctgacctcggacaccaccatggtcagcgacctggtc
tcccagaacatcaatgtcttcctgcggaacacagtcaaggtcacgggcgtggtggtcttc
atgttcagcctctcatggcagctctccttggtcaccttcatgggcttccccatcatcatg
atggtgtccaacatctacggcaagtactacaagaggctctccaaagaggtccagaatgcc
ctggccagagcgagcaacacggcggaggagaccatcagtgccatgaagactgtccggagc
ttcgccaatgaggaggaggaggcagaggtgtacctgcggaagctgcagcaggtgtacaag
ctgaacaggaaggaggcagctgcctacatgtactacgtctggggcagcgggctcacactg
ctggtggtccaggtcagcatcctctactacgggggccaccttgtcatctcaggccagatg
accagcggcaacctcatcgccttcatcatctacgagtttgtcctgggagattgtatggag
tccgtgggctccgtctacagtggcctgatgcagggagtgggggctgctgagaaggtgttc
gagttcatcgaccggcagccgaccatggtgcacgatggcagcttggcccccgaccacctg
gagggccgggtggactttgagaatgtgaccttcacctaccgcactcggccccacacccag
gtcctgcagaatgtctccttcagcctgtcccccggcaaggtgacggccctggtggggccc
tcgggcagtgggaagagctcctgtgtcaacatcctggagaacttctaccccctggagggg
ggccgggtgctgctggacggcaagcccatcagcgcctacgaccacaagtacttgcaccgt
gtgatctccctggtgagccaggagcccgtgctgttcgcccgctccatcacggataacatc
tcctacggcctgcccactgtgcctttcgagatggtggtggaggccgcacagaaggccaat
gcccacggcttcatcatggaactccaggacggctacagcacagagacaggggagaagggc
gcccagctgtcaggtggccagaagcagcgggtggccatggcccgggctctggtgcggaac
cccccagtcctcatcctggatgaagccaccagcgctttggatgccgagagcgagtatctg
atccagcaggccatccatggcaacctgcagaagcacacggtactcatcatcgcgcaccgg
ctgagcaccgtggagcacgcgcacctcattgtggtgctggacaagggccgcgtagtgcag
cagggcacccaccagcagctgctggcccagggcggcctctacgccaagctggtgcagcgg
cagatgctggggcttcagcccgccgcagacttcacagctggccacaacgagcctgtagcc
aacggcagtcacaaggcctga

  All links  
Disease (1)   
   OMIM (1)   
Gene (12)   
   RefGene (4)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (23)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (21)   
DNA sequence (68)   
   RefSeq(nuc) (36)   
   GenBank (16)   
   EMBL (16)   
Protein domain (13)   
   Pfam (13)   
All databases (117)   

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