Homo sapiens (human): 63922
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Entry
63922 CDS
T01001
Symbol
CHTF18, C16orf41, C321D2.2, C321D2.3, C321D2.4, CHL12, Ctf18, RUVBL
Name
(RefSeq) chromosome transmission fidelity factor 18
KO
K11269
chromosome transmission fidelity protein 18
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
]
63922 (CHTF18)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Sister chromatid cohesion proteins
CTF18-RFC complex
63922 (CHTF18)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
AAA
AAA_5
AAA_22
RuvB_N
Rad17
AAA_16
AAA_33
nSTAND3
AAA_14
DNA_pol3_delta
AAA_28
AAA_30
AAA_18
AAA_25
AAA_17
AAA_19
IstB_IS21
AAA_7
Zeta_toxin
TniB
AAA_3
TsaE
NB-ARC
Motif
Other DBs
NCBI-GeneID:
63922
NCBI-ProteinID:
NP_071375
OMIM:
613201
HGNC:
18435
Ensembl:
ENSG00000127586
UniProt:
Q8WVB6
LinkDB
All DBs
Position
16:788620..798074
Genome browser
AA seq
975 aa
AA seq
DB search
MEDYEQELCGVEDDFHNQFAAELEVLAELEGASTPSPSGVPLFTAGRPPRTFEEALARGD
AASSPAPAASVGSSQGGARKRQVDADLQPAGSLPHAPRIKRPRLQVVKRLNFRSEEMEEP
PPPDSSPTDITPPPSPEDLAELWGHGVSEAAADVGLTRASPAARNPVLRRPPILEDYVHV
TSTEGVRAYLVLRADPMAPGVQGSLLHVPWRGGGQLDLLGVSLASLKKQVDGERRERLLQ
EAQKLSDTLHSLRSGEEEAAQPLGAPEEEPTDGQDASSHCLWVDEFAPRHYTELLSDDFT
NRCLLKWLKLWDLVVFGHERPSRKPRPSVEPARVSKEATAPGKWKSHEQVLEEMLEAGLD
PSQRPKQKVALLCGPPGLGKTTLAHVIARHAGYSVVEMNASDDRSPEVFRTRIEAATQME
SVLGAGGKPNCLVIDEIDGAPVAAINVLLSILNRKGPQEVGPQGPAVPSGGGRRRRAEGG
LLMRPIICICNDQFAPSLRQLKQQAFLLHFPPTLPSRLVQRLQEVSLRQGMRADPGVLAA
LCEKTDNDIRACINTLQFLYSRGQRELSVRDVQATRVGLKDQRRGLFSVWQEVFQLPRAQ
RRRVGQDPALPADTLLLGDGDAGSLTSASQRFYRVLHAAASAGEHEKVVQGLFDNFLRLR
LRDSSLGAVCVALDWLAFDDLLAGAAHHSQSFQLLRYPPFLPVAFHVLFASSHTPRITFP
SSQQEAQNRMSQMRNLIQTLVSGIAPATRSRATPQALLLDALCLLLDILAPKLRPVSTQL
YSTREKQQLASLVGTMLAYSLTYRQERTPDGQYIYRLEPNVEELCRFPELPARKPLTYQT
KQLIAREIEVEKMRRAEASARVENSPQVDGSPPGLEGLLGGIGEKGVHRPAPRNHEQRLE
HIMRRAAREEQPEKDFFGRVVVRSTAVPSAGDTAPEQDSVERRMGTAVGRSEVWFRFNEG
VSNAVRRSLYIRDLL
NT seq
2928 nt
NT seq
+upstream
nt +downstream
nt
atggaggactacgagcaggagctgtgcggcgtcgaggatgatttccacaaccagttcgcg
gccgagctggaggtgctggcagagctggaaggggcgtcgactccgtcgccctccggggtc
cccctgttcaccgcgggccgacccccgcggacgttcgaggaggcccttgccagaggggac
gcggcctccagtcccgccccagccgcatctgtgggcagcagccagggcggcgccaggaag
aggcaggtggacgccgacctgcagccggccgggtccctgccccacgcccccaggatcaaa
cggcctaggctgcaggtggtcaagaggctgaacttcagatcggaggagatggaggagccg
ccccctcccgactcctcgccgacggacatcaccccgccgccgagccctgaggacctcgca
gagctttggggccacggagtctcagaagctgctgccgacgtgggtctcacacgggcctca
ccagctgcccgcaatcccgtcctgaggcggccccccatcttggaggactacgtccacgtg
acatccacggagggcgtccgggcttatctggtgctgcgtgctgaccccatggccccgggg
gtgcagggctctctcctccacgtcccatggcgaggcggtggccagctggacctgctgggt
gtgtccttagcctccctgaagaagcaggtcgacggcgagcggcgggagcggctgcttcag
gaggcccagaagctttcagacaccctgcacagtctcaggtcgggggaggaggaggcagcc
cagcccttgggggcccctgaggaggagccgactgacggtcaagacgcctccagtcactgc
ctctgggtggatgagtttgcaccccgccactacacggagctgctcagtgatgacttcacc
aaccgctgcctgctcaagtggctgaagttgtgggacctggtggtgtttggccacgagagg
ccttcccggaagcccaggcccagtgttgagccggcccgggtcagcaaggaggccacagcc
ccaggcaagtggaagagccacgaacaggtgctggaggagatgctggaggctgggctggac
ccgagccagcgaccgaagcagaaggtggcactgctctgtgggcccccggggctggggaag
accaccctggcacacgtgattgcgcgtcacgcggggtactctgtggtggagatgaacgcc
agtgacgaccgtagcccggaggtcttccgcacacgcatcgaggcggccacccagatggag
tcggtgctgggtgctggcgggaagcccaactgcctggtcatcgatgagatcgacggggcc
cccgtggccgccatcaacgtcctcctgagcatcctgaaccgcaaggggccacaggaggtg
gggccacagggcccggctgtgccttcgggaggcggccgacggcgccgggcagaggggggg
ctcctcatgaggcccattatctgcatttgcaatgaccagttcgcaccgtccctgcggcag
ctgaagcagcaggccttcctgctccacttcccgccgactctgccctcgaggctggtgcag
cggctccaggaggtctccctgcggcagggcatgagggccgacccaggggtgctggccgcc
ctctgtgagaaaactgacaatgacatccgggcctgcatcaacaccctgcagttcctgtac
agccggggccagcgggagctgagcgtgcgggacgtgcaggccacacgcgtgggcctcaag
gaccagcgcagagggctcttctcggtgtggcaggaggtcttccagctgcctcgagcccag
aggcgccgtgtgggccaggaccccgccctgcctgctgacacactcctgctgggtgacggg
gacgcgggctccctcacctccgcctcacagcgattctaccgtgtcctgcatgccgctgcc
tctgcgggcgagcacgagaaggtggtccagggcttgtttgacaacttcctgcgtctgcgg
ctgcgagactccagcctgggtgctgtgtgtgtggccctcgactggctggccttcgatgac
ctgctggcgggggctgctcatcacagccagagcttccagctgctgcgctacccacccttc
ctgcccgtggccttccatgtgctgtttgcttccagccacacacccaggatcaccttcccc
agcagccagcaggaggcccagaaccggatgagccagatgaggaacctgatccagacgctg
gtgtccggcatcgcgccagccacgcgcagccgggccacgccccaggccctgctcctcgat
gccctctgcctgctcctggacattcttgcacccaagctccgccccgtgagcacacagctg
tacagcacccgtgaaaagcaacagctggccagcctggtgggcacgatgctcgcttacagc
ctgacctaccgccaggagcgcacgcccgatggccagtacatctacaggctggagccgaac
gtggaggaactctgccgcttccctgagctgcctgcccgcaagcccctcacctaccagacg
aagcagctcatcgcccgcgagatcgaggtggagaagatgcggcgggcggaggcttctgcc
cgggtagagaacagcccccaggtggatgggagccccccagggctcgagggtctgctgggg
ggcattggggagaaaggggtgcaccgacctgccccacgcaaccatgagcagcggctggag
cacatcatgaggcgagcggcccgggaggaacagcctgagaaggacttctttggacgtgtg
gtcgtcaggagcacagcagtcccgagtgcaggggacacggccccggagcaggactcagtg
gagcggcgcatgggcacagcggtgggcaggagcgaggtctggttccgcttcaacgagggt
gtctccaacgccgtgcggcgcagcctgtacatcagggacttgctctag
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