Homo sapiens (human): 92002
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cyclin_N
CycT2-like_C
Motif
Other DBs
NCBI-GeneID:
92002
NCBI-ProteinID:
NP_689487
OMIM:
300708
HGNC:
28434
Ensembl:
ENSG00000262919
UniProt:
Q8N1B3
LinkDB
All DBs
Position
X:complement(153587925..153599139)
Genome browser
AA seq
248 aa
AA seq
DB search
MEAPEGGGGGPAARGPEGQPAPEARVHFRVARFIMEAGVKLGMRSIPIATACTIYHKFFC
ETNLDAYDPYLIAMSSIYLAGKVEEQHLRTRDIINVSNRYFNPSGEPLELDSRFWELRDS
IVQCELLMLRVLRFQVSFQHPHKYLLHYLVSLQNWLNRHSWQRTPVAVTAWALLRDSYHG
ALCLRFQAQHIAVAVLYLALQVYGVEVPAEVEAEKPWWQVFNDDLTKPIIDNIVSDLIQI
YTMDTEIP
NT seq
747 nt
NT seq
+upstream
nt +downstream
nt
atggaagccccggagggcggcggaggggggcctgcagcgcggggcccggaggggcagccg
gcgcccgaagccagggtgcacttccgagtggcgaggttcatcatggaggcaggtgtcaag
ctagggatgcggtccattcccattgccactgcttgcaccatttaccataagttcttttgc
gagaccaacctggacgcctatgacccttacctgattgccatgtcttcaatttacttggcc
ggcaaagtggaagagcagcacctgcggactcgtgacatcatcaatgtgtccaacaggtac
tttaacccaagcggtgagcccctggaattggactcccgcttctgggaactccgggacagc
atcgtgcagtgtgagcttctcatgctgagagttctgcgcttccaggtctccttccagcat
ccacacaagtacctgctccactacctggtttccctccagaactggctgaaccgccacagc
tggcagcggacccctgttgccgtcaccgcctgggccctgctgcgggacagctaccatggg
gcgctgtgcctccgcttccaggcccagcacatcgccgtggcggtgctctacctggccctg
caggtctacggagttgaggtgcccgccgaggtcgaggctgagaagccgtggtggcaggtg
tttaatgacgaccttaccaagccaatcattgataatattgtgtctgatctcattcagatt
tataccatggacacagagatcccctaa
DBGET
integrated database retrieval system