KEGG   Homo sapiens (human): 6566
Entry
6566              CDS       T01001                                 
Symbol
SLC16A1, HHF7, MCT, MCT1, MCT1D
Name
(RefSeq) solute carrier family 16 member 1
  KO
K08179  MFS transporter, MCT family, solute carrier family 16 (monocarboxylic acid transporters), member 1
Organism
hsa  Homo sapiens (human)
Pathway
hsa04148  Efferocytosis
Network
nt06535  Efferocytosis
  Element
N01784  Glucose uptake and lactate release induced by efferocytosis
Disease
H01248  Monocarboxylate transporter 1 deficiency
H01267  Familial hyperinsulinemic hypoglycemia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09141 Transport and catabolism
   04148 Efferocytosis
    6566 (SLC16A1)
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    6566 (SLC16A1)
   04147 Exosome [BR:hsa04147]
    6566 (SLC16A1)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC16: Monocarboxylate transporter
   6566 (SLC16A1)
 Major facilitator superfamily (MFS)
  Organic acid transporters
   Monocarboxylate transporter (MCT) family [TC:2.A.1.13]
    6566 (SLC16A1)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of microglial cells
   6566 (SLC16A1)
SSDB
Motif
Pfam: MFS_1 CbtA
Other DBs
NCBI-GeneID: 6566
NCBI-ProteinID: NP_001159968
OMIM: 600682
HGNC: 10922
Ensembl: ENSG00000155380
UniProt: P53985 B4DKS0
Structure
Position
1:complement(112911847..112956196)
AA seq 500 aa
MPPAVGGPVGYTPPDGGWGWAVVIGAFISIGFSYAFPKSITVFFKEIEGIFHATTSEVSW
ISSIMLAVMYGGGPISSILVNKYGSRIVMIVGGCLSGCGLIAASFCNTVQQLYVCIGVIG
GLGLAFNLNPALTMIGKYFYKRRPLANGLAMAGSPVFLCTLAPLNQVFFGIFGWRGSFLI
LGGLLLNCCVAGALMRPIGPKPTKAGKDKSKASLEKAGKSGVKKDLHDANTDLIGRHPKQ
EKRSVFQTINQFLDLTLFTHRGFLLYLSGNVIMFFGLFAPLVFLSSYGKSQHYSSEKSAF
LLSILAFVDMVARPSMGLVANTKPIRPRIQYFFAASVVANGVCHMLAPLSTTYVGFCVYA
GFFGFAFGWLSSVLFETLMDLVGPQRFSSAVGLVTIVECCPVLLGPPLLGRLNDMYGDYK
YTYWACGVVLIISGIYLFIGMGINYRLLAKEQKANEQKKESKEEETSIDVAGKPNEVTKA
AESPDQKDTDGGPKEEESPV
NT seq 1503 nt   +upstreamnt  +downstreamnt
atgccaccagcagttggaggtccagttggatacacccccccagatggaggctggggctgg
gcagtggtaattggagctttcatttccatcggcttctcttatgcatttcccaaatcaatt
actgtcttcttcaaagagattgaaggtatattccatgccaccaccagcgaagtgtcatgg
atatcctccataatgttggctgtcatgtatggtggaggtcctatcagcagtatcctggtg
aataaatatggaagtcgtatagtcatgattgttggtggctgcttgtcaggctgtggcttg
attgcagcttctttctgtaacaccgtacagcaactatacgtctgtattggagtcattgga
ggtcttgggcttgccttcaacttgaatccagctctgaccatgattggcaagtatttctac
aagaggcgaccattggccaacggactggccatggcaggcagccctgtgttcctctgtact
ctggcccccctcaatcaggttttcttcggtatctttggatggagaggaagctttctaatt
cttgggggcttgctactaaactgctgtgttgctggagccctcatgcgaccaatcgggccc
aagccaaccaaggcagggaaagataagtctaaagcatcccttgagaaagctggaaaatct
ggtgtgaaaaaagatctgcatgatgcaaatacagatcttattggaagacaccctaaacaa
gagaaacgatcagtcttccaaacaattaatcagttcctggacttaaccctattcacccac
agaggctttttgctatacctctctggaaatgtgatcatgttttttggactctttgcacct
ttggtgtttcttagtagttatgggaagagtcagcattattctagtgagaagtctgccttc
cttctttccattctggcttttgttgacatggtagcccgaccatctatgggacttgtagcc
aacacaaagccaataagacctcgaattcagtatttctttgcggcttccgttgttgcaaat
ggagtgtgtcatatgctagcacctttatccactacctatgttggattctgtgtctatgcg
ggattctttggatttgccttcgggtggctcagctccgtattgtttgaaacattgatggac
cttgttggaccccagaggttctccagcgctgtgggattggtgaccattgtggaatgctgt
cctgtcctcctggggccaccacttttaggtcggctcaatgacatgtatggagactacaaa
tacacatactgggcatgtggcgtcgtcctaattatttcaggtatctatctcttcattggc
atgggcatcaattatcgacttttggcaaaagaacagaaagcaaacgagcagaaaaaggaa
agtaaagaggaagagaccagtatagatgttgctgggaagccaaatgaagttaccaaagca
gcagaatctccggaccagaaagacacagatggagggcccaaggaggaggaaagtccagtc
tga

  All links  
Disease (4)   
   OMIM (4)   
Gene (9)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
Protein sequence (8)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (5)   
DNA sequence (37)   
   RefSeq(nuc) (5)   
   GenBank (16)   
   EMBL (16)   
3D Structure (6)   
   PDB (6)   
Protein domain (2)   
   Pfam (2)   
All databases (66)   

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