Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23457
Gene name Gene Name - the full gene name approved by the HGNC.
ATP binding cassette subfamily B member 9
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ABCB9
Synonyms (NCBI Gene) Gene synonyms aliases
EST122234, TAPL
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q24.31
Summary Summary of gene provided in NCBI Entrez Gene.
The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT003169 hsa-miR-210-3p immunoprecipitaion, Microarray, qRT-PCR 19826008
MIRT018865 hsa-miR-335-5p Microarray 18185580
MIRT050137 hsa-miR-26a-5p CLASH 23622248
MIRT437432 hsa-miR-31-5p Luciferase reporter assay, qRT-PCR, Western blot 24099915
MIRT437432 hsa-miR-31-5p Luciferase reporter assay, qRT-PCR, Western blot 24099915
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002474 Process Antigen processing and presentation of peptide antigen via MHC class I IDA 17977821
GO:0005515 Function Protein binding IPI 22641697
GO:0005524 Function ATP binding IDA 15863492
GO:0005764 Component Lysosome IDA 22641697
GO:0005765 Component Lysosomal membrane HDA 17897319
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605453 50 ENSG00000150967
Protein
UniProt ID Q9NP78
Protein name ABC-type oligopeptide transporter ABCB9 (EC 7.4.2.6) (ATP-binding cassette sub-family B member 9) (ATP-binding cassette transporter 9) (ABC transporter 9 protein) (hABCB9) (TAP-like protein) (TAPL)
Protein function ATP-dependent low-affinity peptide transporter which translocates a broad spectrum of peptides from the cytosol to the lysosomal lumen for degradation (PubMed:15863492, PubMed:17977821, PubMed:18434309, PubMed:22641697, PubMed:25646430, PubMed:3
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00664 ABC_membrane 188 457 ABC transporter transmembrane region Family
PF00005 ABC_tran 522 671 ABC transporter Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in testis, and at moderate levels in brain, spinal cord, and thyroid. Not expressed in monocytes but strongly expressed during differentiation of monocytes to dendritic cells and macrophages. {ECO:0000269|PubMed:107480
Sequence
MRLWKAVVVTLAFMSVDICVTTAIYVFSHLDRSLLEDIRHFNIFDSVLDLWAACLYRSCL
LLGATIGVAKNSALGPRRLRASWLVITLVCLFVGIYAMVKLLLFSEVRRPIRDPWFWALF
VWTYISLGASFLLWWLLSTVRPGTQALEPGAATEAEGFPGSGRPPPEQASGATLQKLLSY
TKPDVAFLVAASFFLIVAALGETFLPYYTGRAIDGIVIQKSMDQFSTAVVIVCLLAIGSS
FAAGIRGGIFTLIFARLNIRLRNCLFRSLVSQETSFFDENRTGDLISRLTSDTTMVSDLV
SQNINVFLRNTVKVTGVVVFMFSLSWQLSLVTFMGFPIIMMVSNIYGKYYKRLSKEVQNA
LARASNTAEETISAMKTVRSFANEEEEAEVYLRKLQQVYKLNRKEAAAYMYYVWGSGLTL
LVVQVSILYYGGHLVISGQMTSGNLIAFIIYEFVLGD
CMESVGSVYSGLMQGVGAAEKVF
EFIDRQPTMVHDGSLAPDHLEGRVDFENVTFTYRTRPHTQVLQNVSFSLSPGKVTALVGP
SGSGKSSCVNILENFYPLEGGRVLLDGKPISAYDHKYLHRVISLVSQEPVLFARSITDNI
SYGLPTVPFEMVVEAAQKANAHGFIMELQDGYSTETGEKGAQLSGGQKQRVAMARALVRN
PPVLILDEATS
ALDAESEYLIQQAIHGNLQKHTVLIIAHRLSTVEHAHLIVVLDKGRVVQ
QGTHQQLLAQGGLYAKLVQRQMLGLQPAADFTAGHNEPVANGSHKA
Sequence length 766
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Diabetes Diabetes GWAS
Insomnia Insomnia GWAS
Associations from Text Mining
Disease Name Relationship Type References
Chorioamnionitis Stimulate 29402780
Diabetes Mellitus Type 2 Associate 25799151, 27115357
Neoplasms Associate 31083274
Ovarian Neoplasms Inhibit 31083274
Parkinson Disease Associate 28851441
Schizophrenia Associate 28552197