KEGG   Homo sapiens (human): 84317
Entry
84317             CDS       T01001                                 
Symbol
CCDC115, CDG2O, ccp1
Name
(RefSeq) coiled-coil domain containing 115
  KO
K23543  coiled-coil domain-containing protein 115
Organism
hsa  Homo sapiens (human)
Disease
H00119  Congenital disorders of glycosylation type II
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    84317 (CCDC115)
Membrane trafficking [BR:hsa04131]
 Endosome - Golgi transport
  Others
   Others
    84317 (CCDC115)
SSDB
Motif
Pfam: Vma22_CCDC115 ATP-synt_D
Other DBs
NCBI-GeneID: 84317
NCBI-ProteinID: NP_115733
OMIM: 613734
HGNC: 28178
Ensembl: ENSG00000136710
UniProt: Q96NT0
Position
2:complement(130337933..130342681)
AA seq 180 aa
MAALDLRAELDSLVLQLLGDLEELEGKRTVLNARVEEGWLSLAKARYAMGAKSVGPLQYA
SHMEPQVCLHASEAQEGLQKFKVVRAGVHAPEEVGPREAGLRRRKGPTKTPEPESSEAPQ
DPLNWFGILVPHSLRQAQASFRDGLQLAADIASLQNRIDWGRSQLRGLQEKLKQLEPGAA
NT seq 543 nt   +upstreamnt  +downstreamnt
atggcggcgcttgacctgcgagcggagctggattcgctggtcctgcagctgcttggggac
ctggaggagctggaggggaaacgaacggtgttgaacgcccgggtggaggagggctggctc
tcgctcgccaaggctcgctacgcgatgggcgccaagtcggtagggcccctgcagtatgct
tcccacatggagccccaggtctgcctccacgccagcgaggcccaggagggactccagaag
ttcaaggtggtgagagctggtgtccacgccccagaggaggtggggcctcgcgaagcaggt
ctgcggaggcgcaagggccccactaagaccccagaaccggagtcctctgaggcccctcag
gaccccctgaactggtttggaatcctagttcctcacagtctacgtcaggctcaagcaagc
ttccgggatggcctgcagctggccgcagacatagccagcctccagaaccgcattgactgg
ggtcgaagccagctccggggactccaagagaaactcaagcagctggagcctggggctgcc
tga

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