Homo sapiens (human): 79598
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Entry
79598 CDS
T01001
Symbol
CEP97, 2810403B08Rik, LRRIQ2
Name
(RefSeq) centrosomal protein 97
KO
K16717
centrosomal protein CEP97
Organism
hsa
Homo sapiens (human)
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
79598 (CEP97)
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
79598 (CEP97)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centrosome formation proteins
Centrosome duplication proteins
Centriole replication proteins
79598 (CEP97)
Cilium and associated proteins [BR:
hsa03037
]
Primary cilia and associated proteins
Other primary cilia associated proteins
79598 (CEP97)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
LRR_9
LRR_4
LRR_8
LRR_LRWD1
IQ
LRR_EndoS
LRR_6
LRR_NXF1-5
Motif
Other DBs
NCBI-GeneID:
79598
NCBI-ProteinID:
NP_078824
OMIM:
615864
HGNC:
26244
Ensembl:
ENSG00000182504
UniProt:
Q8IW35
LinkDB
All DBs
Position
3:101724614..101770562
Genome browser
AA seq
865 aa
AA seq
DB search
MAVARVDAALPPGEGSVVNWSGQGLQKLGPNLPCEADIHTLILDKNQIIKLENLEKCKRL
IQLSVANNRLVRMMGVAKLTLLRVLNLPHNSIGCVEGLKELVHLEWLNLAGNNLKAMEQI
NSCTALQHLDLSDNNISQIGDLSKLVSLKTLLLHGNIITSLRMAPAYLPRSLAILSLAEN
EIRDLNEISFLASLTELEQLSIMNNPCVMATPSIPGFDYRPYIVSWCLNLRVLDGYVISQ
KESLKAEWLYSQGKGRAYRPGQHIQLVQYLATVCPLTSTLGLQTAEDAKLEKILSKQRFH
QRQLMNQSQNEELSPLVPVETRASLIPEHSSPVQDCQISQESEPVIQVNSWVGINSNDDQ
LFAVKNNFPASVHTTRYSRNDLHLEDIQTDEDKLNCSLLSSESTFMPVASGLSPLSPTVE
LRLQGINLGLEDDGVADESVKGLESQVLDKEEEQPLWAANENSVQMMRSEINTEVNEKAG
LLPCPEPTIISAILKDDNHSLTFFPESTEQKQSDIKKPENTQPENKETISQATSEKLPMI
LTQRSVALGQDKVALQKLNDAATKLQACWRGFYARNYNPQAKDVRYEIRLRRMQEHIVCL
TDEIRRLRKERDEERIKKFVQEEAFRFLWNQVRSLQVWQQTVDQRLSSWHTDVPPISSTL
VPSKHPLFTQSQESSCDQNADWFIASDVAPQEKSLPEFPDSGFHSSLTEQVHSLQHSLDF
EKSSTEGSESSIMGNSIDTVRYGKESDLGDVSEEHGEWNKESSNNEQDNSLLEQYLTSVQ
QLEDADERTNFDTETRDSKLHIACFPVQLDTLSDGASVDESHGISPPLQGEISQTQENSK
LNAEVQGQQPECDSTFQLLHVGVTV
NT seq
2598 nt
NT seq
+upstream
nt +downstream
nt
atggcggtggcgcgcgtggacgcggctttgcctcccggagaaggatcagtggtcaattgg
tcaggacagggactacagaaattaggtccaaatttaccctgtgaagctgatattcacact
ttgattctggataaaaatcagattattaaattggaaaatctggagaaatgcaaacgatta
atacagttatcagtagctaataatcggctggttcggatgatgggtgtggccaagctgacg
ttgcttcgtgtattaaatttgcctcataatagcattggctgtgtggaagggctaaaggaa
ctagtacatctggaatggctgaatttggcaggaaataatcttaaggccatggaacagatc
aatagctgcacagctctacagcatctcgatttatcagacaataatatatcccagataggt
gatctatctaaattggtatccctgaaaaccctgcttttacatggaaacatcatcacctct
cttagaatggcacctgcttacctacccagaagtcttgctatactttctttggcagaaaat
gaaatccgagacttaaatgagatctcttttttggcatccttaactgaattggaacagttg
tcgattatgaacaatccttgtgtgatggcaacaccatccatcccaggatttgactatcgg
ccgtacatcgtcagctggtgcctaaacctcagagtcctagatggatatgtgatttctcag
aaggaaagtttgaaagctgaatggctctatagtcaaggcaaggggagagcatatcggcct
ggccagcacatccagcttgtccaatatctggctacagtctgccccctcacttctacacta
ggtcttcaaactgcagaggatgccaaactagagaagattttgagcaaacagaggtttcac
cagaggcagttgatgaaccaaagccaaaatgaagagttgtctcctcttgttcctgttgaa
acaagggcatcccttattcctgagcattcaagccctgttcaagattgccagatatcccag
gaaagtgaacccgtcattcaagtgaattcttgggttgggataaacagtaatgatgatcag
ttatttgcggttaagaataattttccagcctctgtacacactacgagatattctcgaaat
gatctgcacctggaagacatacagacggatgaggacaagttaaactgtagtcttctctct
tcagagtctacttttatgccagttgcatcaggactgtctccactatcacctacagttgag
ctgaggctgcagggcattaacttgggcctagaagatgatggtgttgcagatgaatctgtg
aaagggctggaaagccaggtgttggataaggaagaggaacagcctttatgggctgcaaat
gagaattctgttcaaatgatgagaagtgaaatcaatacagaggtaaatgagaaagctgga
ctattaccttgtcctgagccaacaataatcagtgctatcttgaaggatgataaccacagt
cttacattttttcctgagtcaactgagcagaaacaatcagacataaagaaaccagaaaat
acacaaccagaaaataaagaaaccatatctcaagcaacttcagagaaacttcccatgatt
ttaacccagagatctgttgctttgggacaagacaaagttgcccttcagaaattaaatgat
gcagccaccaagcttcaggcctgttggcggggattttatgccaggaactacaaccctcaa
gccaaagatgtgcgttacgaaatccggctacgcagaatgcaagagcacattgtctgctta
actgatgaaataaggagattacgaaaagaaagagatgaagaacgtattaaaaaatttgta
caagaagaagctttcagattcctttggaaccaggtaaggtctctacaggtttggcaacag
acagtggaccagcgtctaagttcctggcatactgatgttcctcctatatcaagtactctt
gtgccatcgaaacatccattatttacccaaagccaggagtcctcttgtgatcaaaatgct
gattggtttattgcttctgatgtagctcctcaagagaaatcattaccagaatttccagac
tctggttttcattcctctctaacagaacaagttcattcattgcagcattctttggatttt
gagaaaagttccacagaaggcagtgaaagctccataatggggaattccattgacacagtc
agatatggcaaagaatcagatttaggggatgttagtgaagaacatggtgaatggaataag
gaaagctcaaataacgagcaggacaatagtctgcttgaacagtatttaacttcagttcaa
cagctggaagatgctgatgagaggaccaattttgatacagagacaagagatagcaaactt
cacattgcttgtttcccagtacagttagatacattgtctgacggtgcttctgtagatgag
agtcatggcatatctcctcctttgcaaggtgaaattagccagacacaagagaattctaaa
ttaaatgcagaagttcaggggcagcagccagaatgtgattctacatttcagctattgcat
gttggtgttactgtgtag
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