KEGG   Homo sapiens (human): 81554
Entry
81554             CDS       T01001                                 
Symbol
RCC1L, WBSCR16
Name
(RefSeq) RCC1 like
  KO
K23495  RCC1-like G exchanging factor-like protein
Organism
hsa  Homo sapiens (human)
Disease
H01439  Williams-Beuren syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    81554 (RCC1L)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    81554 (RCC1L)
SSDB
Motif
Pfam: RCC1 RCC1_2
Other DBs
NCBI-GeneID: 81554
NCBI-ProteinID: NP_110425
OMIM: 620739
HGNC: 14948
Ensembl: ENSG00000274523
UniProt: Q96I51
Structure
Position
7:complement(75027119..75073802)
AA seq 464 aa
MALVALVAGARLGRRLSGPGLGRGHWTAAGRSRSRREAAEAEAEVPVVQYVGERAARADR
VFVWGFSFSGALGVPSFVVPSSGPGPRAGARPRRRIQPVPYRLELDQKISSAACGYGFTL
LSSKTADVTKVWGMGLNKDSQLGFHRSRKDKTRGYEYVLEPSPVSLPLDRPQETRVLQVS
CGRAHSLVLTDREGVFSMGNNSYGQCGRKVVENEIYSESHRVHRMQDFDGQVVQVACGQD
HSLFLTDKGEVYSCGWGADGQTGLGHYNITSSPTKLGGDLAGVNVIQVATYGDCCLAVSA
DGGLFGWGNSEYLQLASVTDSTQVNVPRCLHFSGVGKVRQAACGGTGCAVLNGEGHVFVW
GYGILGKGPNLVESAVPEMIPPTLFGLTEFNPEIQVSRIRCGLSHFAALTNKGELFVWGK
NIRGCLGIGRLEDQYFPWRVTMPGEPVDVACGVDHMVTLAKSFI
NT seq 1395 nt   +upstreamnt  +downstreamnt
atggcgctggtggcgttggtggctggggctcggctggggcggcggctgagcgggccgggg
ctggggcgagggcactggacggcggccgggcgctcccggagccggcgcgaagcggcagaa
gccgaggcggaggtgcccgtggtccagtacgtgggcgagcgcgctgcccgcgccgatcgc
gtcttcgtgtggggcttcagcttctcgggggcgctgggcgtgccttcctttgtggtgccc
agctccgggcccgggccccgcgccggcgcccgaccgcgccgcaggatccagcccgtgccc
tatcgcctggagctggaccaaaagatttcatctgctgcttgcggctatggattcacactg
ctgtcctctaagactgcggatgttacgaaagtctgggggatgggactcaacaaagattct
cagcttggatttcacaggagccggaaagataaaacgaggggctacgagtatgtgttggag
ccctcacccgtctccctgcctctggacagacctcaggagacacgggtgctgcaggtctcc
tgcggccgagctcactctcttgtgttgactgacagggaaggagtcttcagcatgggaaac
aattcttatgggcaatgtggaagaaaggtggtcgaaaatgaaatttacagtgaaagtcac
agagtccacaggatgcaggacttcgatggccaggtggtccaggtcgcctgtggtcaggat
catagtctgttcctgacggataaaggagaagtctattcttgtggatggggtgctgatggg
caaacaggtctgggtcactacaatatcaccagctcgcccaccaagctgggtggagacctg
gcgggagtgaacgttatccaagttgccacctacggtgattgctgcctggccgtgtccgcc
gacggaggactttttggttggggaaactcggagtacctgcagctggcctctgtcactgac
tccacacaggtgaatgtgccccgctgcttacacttctcaggagtggggaaggtgcgacag
gctgcatgcggtggcacgggctgtgcagtgttaaacggagaaggacatgtttttgtctgg
ggctatggaattcttgggaaaggtccaaacctagtggaaagtgccgtccctgaaatgatt
ccacccactctctttggcttgacggagttcaacccagaaatccaggtttcccgcatccga
tgtggactcagccactttgctgcactgaccaacaaaggagagctgtttgtatggggcaag
aacatccgagggtgcctgggaatcggtcgcctggaggaccagtatttcccatggagggtg
acgatgcctggggagcctgtggacgtggcatgtggcgtggaccacatggtgaccctggcc
aagtcattcatctaa

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Ontology (2)   
   KEGG BRITE (2)   
Disease (2)   
   KEGG DISEASE (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (26)   
   KEGG ORTHOLOGY (1)   
   RefGene (7)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (13)   
   OC (1)   
Protein sequence (6)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (4)   
DNA sequence (30)   
   RefSeq(nuc) (4)   
   GenBank (13)   
   EMBL (13)   
3D Structure (1)   
   PDB (1)   
Protein domain (2)   
   Pfam (2)   
All databases (70)   

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