KEGG   Homo sapiens (human): 51151
Entry
51151             CDS       T01001                                 
Symbol
SLC45A2, 1A1, AIM1, MATP, OCA4, SHEP5
Name
(RefSeq) solute carrier family 45 member 2
  KO
K15378  solute carrier family 45, member 1/2/4
Organism
hsa  Homo sapiens (human)
Disease
H00168  Oculocutaneous albinism
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    51151 (SLC45A2)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC45: H+/sugar cotransporter
   51151 (SLC45A2)
SSDB
Motif
Pfam: MFS_1 MFS_2
Other DBs
NCBI-GeneID: 51151
NCBI-ProteinID: NP_057264
OMIM: 606202
HGNC: 16472
Ensembl: ENSG00000164175
UniProt: Q9UMX9 A0A076YGN1 A0A076YIB8
Position
5:complement(33944623..33984693)
AA seq 530 aa
MGSNSGQAGRHIYKSLADDGPFDSVEPPKRPTSRLIMHSMAMFGREFCYAVEAAYVTPVL
LSVGLPSSLYSIVWFLSPILGFLLQPVVGSASDHCRSRWGRRRPYILTLGVMMLVGMALY
LNGATVVAALIANPRRKLVWAISVTMIGVVLFDFAADFIDGPIKAYLFDVCSHQDKEKGL
HYHALFTGFGGALGYLLGAIDWAHLELGRLLGTEFQVMFFFSALVLTLCFTVHLCSISEA
PLTEVAKGIPPQQTPQDPPLSSDGMYEYGSIEKVKNGYVNPELAMQGAKNKNHAEQTRRA
MTLKSLLRALVNMPPHYRYLCISHLIGWTAFLSNMLFFTDFMGQIVYRGDPYSAHNSTEF
LIYERGVEVGCWGLCINSVFSSLYSYFQKVLVSYIGLKGLYFTGYLLFGLGTGFIGLFPN
VYSTLVLCSLFGVMSSTLYTVPFNLITEYHREEEKERQQAPGGDPDNSVRGKGMDCATLT
CMVQLAQILVGGGLGFLVNTAGTVVVVVITASAVALIGCCFVALFVRYVD
NT seq 1593 nt   +upstreamnt  +downstreamnt
atgggtagcaacagtgggcaggctggccgccacatctataaatccctagctgatgatggc
ccctttgactctgtggagccgcctaaaagacccaccagcagactcatcatgcacagcatg
gccatgttcggaagagagttctgctacgcggtggaggcagcgtatgtgaccccagtcctg
ctcagcgtaggtctgcccagcagcctgtacagcattgtgtggttcctcagccccatcctg
ggattcctgctgcagcccgtggtcggatcggccagcgaccactgccggtccaggtggggc
cgccggagaccctacatcctcaccctgggagtcatgatgctcgtgggcatggctctgtac
ctcaatggggctactgttgtagcagctttgattgctaacccaaggaggaagctggtttgg
gccataagtgtcaccatgataggtgtcgttctctttgattttgctgccgacttcattgat
gggcccatcaaagcctacttatttgatgtctgctcccatcaggacaaggagaagggcctc
cactaccatgccctcttcacaggttttggaggtgccctgggttaccttttgggtgctata
gactgggcccatctggagctgggaagactgttgggtacagaattccaggtcatgttcttc
ttctctgcattggtgctcactttgtgttttactgttcatctgtgcagtatctctgaagcc
ccacttacagaggttgcaaagggcattcccccacagcaaacccctcaggaccctccattg
tcatcagatggaatgtacgagtatggttctatcgagaaagttaaaaatggttacgtaaat
ccagagctggcaatgcagggagcaaaaaacaaaaatcatgctgaacagactcgcagggca
atgacattaaagtcactgctgagagcactggtgaacatgcctcctcactaccgctacctt
tgcatcagccacctcattggatggacagccttcctgtccaacatgctgttcttcacagat
ttcatgggccagattgtgtaccgcggggatccctatagtgcacacaactccacagagttt
ctcatctacgaaagaggagtcgaggttggatgttggggcttgtgcatcaactccgtgttt
tcctcactttattcttactttcagaaagttttggtatcctacattggattaaagggtctt
tacttcacgggatatttgctgtttggcctggggacgggatttattgggctcttcccgaat
gtctactccaccctggtcctgtgcagcctgtttggtgtaatgtccagcaccctgtacact
gtgccctttaacctcattactgagtaccaccgcgaggaagaaaaggagaggcagcaggcc
ccaggaggggacccagacaacagcgtgagagggaagggcatggactgcgccaccctcaca
tgcatggtgcagctggctcagatcctggtcggaggtggcctgggctttctggtcaacaca
gccgggaccgttgtcgtcgtggtgatcacagcgtctgcggtggcactgataggctgttgc
tttgtcgctctctttgttagatatgtggattag

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Ontology (2)   
   KEGG BRITE (2)   
Disease (4)   
   KEGG DISEASE (1)   
   OMIM (3)   
Genome (1)   
   KEGG GENOME (1)   
Gene (10)   
   KEGG ORTHOLOGY (1)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (11)   
   UniProt (3)   
   SWISS-PROT (1)   
   RefSeq(pep) (7)   
DNA sequence (17)   
   RefSeq(nuc) (7)   
   GenBank (5)   
   EMBL (5)   
Protein domain (2)   
   Pfam (2)   
All databases (47)   

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