KEGG   Homo sapiens (human): 7355
Entry
7355              CDS       T01001                                 
Symbol
SLC35A2, CDG2M, CDGX, UDP-Gal-Tr, UGALT, UGAT, UGT, UGT1, UGT2, UGTL
Name
(RefSeq) solute carrier family 35 member A2
  KO
K15272  solute carrier family 35 (UDP-sugar transporter), member A1/2/3
Organism
hsa  Homo sapiens (human)
Network
nt06015  N-Glycan biosynthesis
  Element
N00826  Transport of UDP-galactose
Disease
H00119  Congenital disorders of glycosylation type II
H00606  Early infantile epileptic encephalopathy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    7355 (SLC35A2)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC35: Nucleoside-sugar transporter
   7355 (SLC35A2)
SSDB
Motif
Pfam: Nuc_sug_transp EamA PUNUT TPT
Other DBs
NCBI-GeneID: 7355
NCBI-ProteinID: NP_005651
OMIM: 314375
HGNC: 11022
Ensembl: ENSG00000102100
UniProt: P78381
Position
X:complement(48903183..48911958)
AA seq 396 aa
MAAVGAGGSTAAPGPGAVSAGALEPGTASAAHRRLKYISLAVLVVQNASLILSIRYARTL
PGDRFFATTAVVMAEVLKGLTCLLLLFAQKRGNVKHLVLFLHEAVLVQYVDTLKLAVPSL
IYTLQNNLQYVAISNLPAATFQVTYQLKILTTALFSVLMLNRSLSRLQWASLLLLFTGVA
IVQAQQAGGGGPRPLDQNPGAGLAAVVASCLSSGFAGVYFEKILKGSSGSVWLRNLQLGL
FGTALGLVGLWWAEGTAVATRGFFFGYTPAVWGVVLNQAFGGLLVAVVVKYADNILKGFA
TSLSIVLSTVASIRLFGFHVDPLFALGAGLVIGAVYLYSLPRGAAKAIASASASASGPCV
HQQPPGQPPPPQLSSHRGDLITEPFLPKLLTKVKGS
NT seq 1191 nt   +upstreamnt  +downstreamnt
atggcagcggttggggctggtggttccaccgcggcgcccgggccaggggcggtttccgcg
ggtgcattggagccggggaccgccagtgcggctcacaggcgcctgaagtacatatcccta
gctgtgctggtggtccagaatgcctccctcatcctcagcatccgctacgcccgcacgttg
ccaggggaccgcttctttgccaccactgctgtggtcatggcggaagtgctcaaaggtctc
acctgcctgctgctgctcttcgcacagaagaggggtaacgtgaagcacctggttctcttc
ctccatgaggctgtcctggtgcagtatgtggacacgctcaagctcgcagtgccctctctc
atctacaccttgcagaataacctccagtatgttgccatctctaacctaccagctgccact
ttccaggtgacataccagctgaagatcctgaccacagcgctgttctccgtgctcatgctg
aatcgcagcctttcccggctgcagtgggcctccctgctgctcctcttcactggcgtcgcc
attgtccaggcacagcaagccggtgggggaggcccacggccactggatcagaaccctggg
gcaggcctggcagccgtcgtggcctcctgtctctcctccggcttcgcaggtgtctacttt
gagaagatcctcaaaggcagctcaggctccgtgtggctgcgcaacctgcaactgggcctc
ttcggcacagcactgggcctggtggggctctggtgggctgagggtaccgccgtggccacc
cgtggtttcttttttgggtacacacctgctgtctggggcgtggtgctcaaccaggccttc
ggcgggctactggtggctgtggttgtcaagtacgctgacaatatcctcaagggctttgcc
acctccctgtccattgtgctgtccactgttgcctccattcgcctctttggcttccacgtg
gacccattatttgcccttggcgctggactcgtcattggtgctgtctacctctacagcctt
ccccgaggtgcagccaaagccatagcctctgcctctgcctccgcctccgggccctgcgtt
caccagcagcctcccgggcagccaccaccaccgcagctgtcttcccaccgtggagacctc
atcacggagccctttctgccaaagttgctcaccaaggtgaagggttcctag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Network (2)   
   KEGG NETWORK (2)   
Disease (4)   
   KEGG DISEASE (2)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (25)   
   KEGG ORTHOLOGY (1)   
   RefGene (16)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (3)   
   OC (1)   
Protein sequence (10)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (8)   
DNA sequence (38)   
   RefSeq(nuc) (8)   
   GenBank (15)   
   EMBL (15)   
Protein domain (4)   
   Pfam (4)   
All databases (86)   

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