KEGG   Homo sapiens (human): 92002
Entry
92002             CDS       T01001                                 
Symbol
CCNQ, CycM, FAM58A
Name
(RefSeq) cyclin Q
  KO
K23964  cyclin-Q
Organism
hsa  Homo sapiens (human)
Disease
H01156  STAR syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    92002 (CCNQ)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Centrosome formation proteins
   Cyclins
    92002 (CCNQ)
SSDB
Motif
Pfam: Cyclin_N CycT2-like_C
Other DBs
NCBI-GeneID: 92002
NCBI-ProteinID: NP_689487
OMIM: 300708
HGNC: 28434
Ensembl: ENSG00000262919
UniProt: Q8N1B3
Position
X:complement(153587925..153599139)
AA seq 248 aa
MEAPEGGGGGPAARGPEGQPAPEARVHFRVARFIMEAGVKLGMRSIPIATACTIYHKFFC
ETNLDAYDPYLIAMSSIYLAGKVEEQHLRTRDIINVSNRYFNPSGEPLELDSRFWELRDS
IVQCELLMLRVLRFQVSFQHPHKYLLHYLVSLQNWLNRHSWQRTPVAVTAWALLRDSYHG
ALCLRFQAQHIAVAVLYLALQVYGVEVPAEVEAEKPWWQVFNDDLTKPIIDNIVSDLIQI
YTMDTEIP
NT seq 747 nt   +upstreamnt  +downstreamnt
atggaagccccggagggcggcggaggggggcctgcagcgcggggcccggaggggcagccg
gcgcccgaagccagggtgcacttccgagtggcgaggttcatcatggaggcaggtgtcaag
ctagggatgcggtccattcccattgccactgcttgcaccatttaccataagttcttttgc
gagaccaacctggacgcctatgacccttacctgattgccatgtcttcaatttacttggcc
ggcaaagtggaagagcagcacctgcggactcgtgacatcatcaatgtgtccaacaggtac
tttaacccaagcggtgagcccctggaattggactcccgcttctgggaactccgggacagc
atcgtgcagtgtgagcttctcatgctgagagttctgcgcttccaggtctccttccagcat
ccacacaagtacctgctccactacctggtttccctccagaactggctgaaccgccacagc
tggcagcggacccctgttgccgtcaccgcctgggccctgctgcgggacagctaccatggg
gcgctgtgcctccgcttccaggcccagcacatcgccgtggcggtgctctacctggccctg
caggtctacggagttgaggtgcccgccgaggtcgaggctgagaagccgtggtggcaggtg
tttaatgacgaccttaccaagccaatcattgataatattgtgtctgatctcattcagatt
tataccatggacacagagatcccctaa

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