KEGG   Homo sapiens (human): 84320
Entry
84320             CDS       T01001                                 
Symbol
ACBD6, NEDPM
Name
(RefSeq) acyl-CoA binding domain containing 6
  KO
K27751  acyl-CoA-binding domain-containing protein 6
Organism
hsa  Homo sapiens (human)
Disease
H02397  Neurodevelopmental disorder with movement abnormalities or hypotonia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09190 Not Included in Pathway or Brite
  09193 Unclassified: signaling and cellular processes
   99995 Signaling proteins
    84320 (ACBD6)
SSDB
Motif
Pfam: ACBP Ank_2 Ank Ank_4 Ank_5 Ank_3
Other DBs
NCBI-GeneID: 84320
NCBI-ProteinID: NP_115736
OMIM: 616352
HGNC: 23339
Ensembl: ENSG00000230124
Pharos: Q9BR61(Tbio)
UniProt: Q9BR61 B2RAA8
Structure
Position
1:complement(180269653..180502577)
AA seq 282 aa
MASSFLPAGAITGDSGGELSSGDDSGEVEFPHSPEIEETSCLAELFEKAAAHLQGLIQVA
SREQLLYLYARYKQVKVGNCNTPKPSFFDFEGKQKWEAWKALGDSSPSQAMQEYIAVVKK
LDPGWNPQIPEKKGKEANTGFGGPVISSLYHEETIREEDKNIFDYCRENNIDHITKAIKS
KNVDVNVKDEEGRALLHWACDRGHKELVTVLLQHRADINCQDNEGQTALHYASACEFLDI
VELLLQSGADPTLRDQDGCLPEEVTGCKTVSLVLQRHTTGKA
NT seq 849 nt   +upstreamnt  +downstreamnt
atggcttcatcattcctgcccgcgggggccatcaccggcgacagcggtggagagctgagc
tcaggggacgactccggggaggtggagttcccccatagccctgagatcgaggagaccagt
tgcctggccgagctgtttgagaaggctgccgcgcacctgcaaggcctgattcaggtggcc
agcagggagcagctcttgtacctgtatgccaggtacaaacaggtcaaagttggaaattgt
aatactcctaaaccaagcttctttgattttgaaggaaagcaaaaatgggaagcttggaaa
gcacttggtgattcaagccccagccaagcaatgcaggaatatatcgcagtagttaaaaaa
ctagatccaggttggaatcctcagataccagagaagaaaggaaaagaagcaaatacaggt
tttggtgggccagttattagttctctatatcatgaagaaaccatcagggaagaagacaaa
aatatatttgattactgcagggaaaacaacattgaccatataaccaaagccatcaaatcg
aaaaatgtggatgtgaatgtgaaagatgaagagggtagggctctacttcactgggcctgt
gatcgaggacataaggaactagtcacagtgttgctgcaacatagagctgacattaactgt
caggacaatgaaggccaaacagctctacattatgcctctgcctgtgagtttctggatatt
gtagagctgctgctccagtctggtgctgaccccactctccgagaccaggatggctgcctg
ccagaggaggtgacaggctgcaaaacagtttctttggtgctgcagcggcacacaactggc
aaggcttaa

  All links  
Ontology (1)   
   KEGG BRITE (1)   
Disease (2)   
   KEGG DISEASE (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (10)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (2)   
   OC (1)   
   PHAROS (1)   
Protein sequence (16)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (13)   
DNA sequence (35)   
   RefSeq(nuc) (13)   
   GenBank (11)   
   EMBL (11)   
3D Structure (1)   
   PDB (1)   
Protein domain (6)   
   Pfam (6)   
All databases (72)   

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