KEGG   Homo sapiens (human): 84879
Entry
84879             CDS       T01001                                 
Symbol
MFSD2A, HsMFSD2A, MCPH15, MFSD2, NEDMISBA, NLS1, SLC59A1
Name
(RefSeq) MFSD2 lysolipid transporter A, lysophospholipid
  KO
K23894  sodium-dependent lysophosphatidylcholine symporter 1
Organism
hsa  Homo sapiens (human)
Disease
H00269  Primary microcephaly
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    84879 (MFSD2A)
Transporters [BR:hsa02000]
 Other transporters
  Electrochemical potential-driven transporters [TC:2]
   84879 (MFSD2A)
SSDB
Motif
Pfam: MFS_2 MFS_1 MP_p6
Other DBs
NCBI-GeneID: 84879
NCBI-ProteinID: NP_001129965
OMIM: 614397
HGNC: 25897
Ensembl: ENSG00000168389
UniProt: Q8NA29 Q71RE4
Structure
Position
1:39955145..39969956
AA seq 543 aa
MAKGEGAESGSAAGLLPTSILQSTERPAQVKKEPKKKKQQLSVCNKLCYALGGAPYQVTG
CALGFFLQIYLLDVAQKDEEVVFCFSSFQVGPFSASIILFVGRAWDAITDPLVGLCISKS
PWTCLGRLMPWIIFSTPLAVIAYFLIWFVPDFPHGQTYWYLLFYCLFETMVTCFHVPYSA
LTMFISTEQTERDSATAYRMTVEVLGTVLGTAIQGQIVGQADTPCFQDLNSSTVASQSAN
HTHGTTSHRETQKAYLLAAGVIVCIYIICAVILILGVREQREPYEAQQSEPIAYFRGLRL
VMSHGPYIKLITGFLFTSLAFMLVEGNFVLFCTYTLGFRNEFQNLLLAIMLSATLTIPIW
QWFLTRFGKKTAVYVGISSAVPFLILVALMESNLIITYAVAVAAGISVAAAFLLPWSMLP
DVIDDFHLKQPHFHGTEPIFFSFYVFFTKFASGVSLGISTLSLDFAGYQTRGCSQPERVK
FTLNMLVTMAPIVLILLGLLLFKMYPIDEERRRQNKKALQALRDEASSSGCSETDSTELA
SIL
NT seq 1632 nt   +upstreamnt  +downstreamnt
atggccaaaggagaaggcgccgagagcggctccgcggcggggctgctacccaccagcatc
ctccaaagcactgaacgcccggcccaggtgaagaaagaaccgaaaaagaagaaacaacag
ttgtctgtttgcaacaagctttgctatgcacttgggggagccccctaccaggtgacgggc
tgtgccctgggtttcttccttcagatctacctattggatgtggctcagaaggatgaggaa
gttgtcttttgcttctcctcattccaggtgggccctttctctgcctccatcatcctgttt
gtgggccgagcctgggatgccatcacagaccccctggtgggcctctgcatcagcaaatcc
ccctggacctgcctgggtcgccttatgccctggatcatcttctccacgcccctggccgtc
attgcctacttcctcatctggttcgtgcccgacttcccacacggccagacctattggtac
ctgcttttctattgcctctttgaaacaatggtcacgtgtttccatgttccctactcggct
ctcaccatgttcatcagcaccgagcagactgagcgggattctgccaccgcctatcggatg
actgtggaagtgctgggcacagtgctgggcacggcgatccagggacaaatcgtgggccaa
gcagacacgccttgtttccaggacctcaatagctctacagtagcttcacaaagtgccaac
catacacatggcaccacctcacacagggaaacgcaaaaggcatacctgctggcagcgggg
gtcattgtctgtatctatataatctgtgctgtcatcctgatcctgggcgtgcgggagcag
agagaaccctatgaagcccagcagtctgagccaatcgcctacttccggggcctacggctg
gtcatgagccacggcccatacatcaaacttattactggcttcctcttcacctccttggct
ttcatgctggtggaggggaactttgtcttgttttgcacctacaccttgggcttccgcaat
gaattccagaatctactcctggccatcatgctctcggccactttaaccattcccatctgg
cagtggttcttgacccggtttggcaagaagacagctgtatatgttgggatctcatcagca
gtgccatttctcatcttggtggccctcatggagagtaacctcatcattacatatgcggta
gctgtggcagctggcatcagtgtggcagctgccttcttactaccctggtccatgctgcct
gatgtcattgacgacttccatctgaagcagccccacttccatggaaccgagcccatcttc
ttctccttctatgtcttcttcaccaagtttgcctctggagtgtcactgggcatttctacc
ctcagtctggactttgcagggtaccagacccgtggctgctcgcagccggaacgtgtcaag
tttacactgaacatgctcgtgaccatggctcccatagttctcatcctgctgggcctgctg
ctcttcaaaatgtaccccattgatgaggagaggcggcggcagaataagaaggccctgcag
gcactgagggacgaggccagcagctctggctgctcagaaacagactccacagagctggct
agcatcctctag

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Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (16)   
   KEGG ORTHOLOGY (1)   
   RefGene (7)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (12)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (9)   
DNA sequence (46)   
   RefSeq(nuc) (10)   
   GenBank (18)   
   EMBL (18)   
3D Structure (1)   
   PDB (1)   
Protein domain (3)   
   Pfam (3)   
All databases (84)   

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