KEGG T01001: 63922

Homo sapiens (human): 63922

Entry

63922 CDS T01001

Gene name

CHTF18, C16orf41, C321D2.2, C321D2.3, C321D2.4, CHL12, Ctf18, RUVBL

Definition

CTF18, chromosome transmission fidelity factor 18 homolog (S. cerevisiae)

Orthology

K11269

chromosome transmission fidelity protein 18

Organism

hsa Homo sapiens (human)

Class

SSDB

Motif

Pfam:

AAA AAA_5 Rad17 AAA_22 RuvB_N AAA_17 AAA_14 AAA_19 AAA_33 AAA_16 DNA_pol3_delta IstB_IS21 Zeta_toxin AAA_18 AAA_28 AAA_25 ABC_tran DUF258 AAA_3 AAA_24 NTPase_1 TIP49 NB-ARC RNA_helicase

Other DBs

NCBI-GI:

NCBI-GeneID:

OMIM:

HGNC:

HPRD:

Ensembl:

Vega:

UniProt:

Position

16p13.3

AA seq 975 aa
MEDYEQELCGVEDDFHNQFAAELEVLAELEGASTPSPSGVPLFTAGRPPRTFEEALARGD
AASSPAPAASVGSSQGGARKRQVDADLQPAGSLPHAPRIKRPRLQVVKRLNFRSEEMEEP
PPPDSSPTDITPPPSPEDLAELWGHGVSEAAADVGLTRASPAARNPVLRRPPILEDYVHV
TSTEGVRAYLVLRADPMAPGVQGSLLHVPWRGGGQLDLLGVSLASLKKQVDGERRERLLQ
EAQKLSDTLHSLRSGEEEAAQPLGAPEEEPTDGQDASSHCLWVDEFAPRHYTELLSDDFT
NRCLLKWLKLWDLVVFGHERPSRKPRPSVEPARVSKEATAPGKWKSHEQVLEEMLEAGLD
PSQRPKQKVALLCGPPGLGKTTLAHVIARHAGYSVVEMNASDDRSPEVFRTRIEAATQME
SVLGAGGKPNCLVIDEIDGAPVAAINVLLSILNRKGPQEVGPQGPAVPSGGGRRRRAEGG
LLMRPIICICNDQFAPSLRQLKQQAFLLHFPPTLPSRLVQRLQEVSLRQGMRADPGVLAA
LCEKTDNDIRACINTLQFLYSRGQRELSVRDVQATRVGLKDQRRGLFSVWQEVFQLPRAQ
RRRVGQDPALPADTLLLGDGDAGSLTSASQRFYRVLHAAASAGEHEKVVQGLFDNFLRLR
LRDSSLGAVCVALDWLAFDDLLAGAAHHSQSFQLLRYPPFLPVAFHVLFASSHTPRITFP
SSQQEAQNRMSQMRNLIQTLVSGIAPATRSRATPQALLLDALCLLLDILAPKLRPVSTQL
YSTREKQQLASLVGTMLAYSLTYRQERTPDGQYIYRLEPNVEELCRFPELPARKPLTYQT
KQLIAREIEVEKMRRAEASARVENSPQVDGSPPGLEGLLGGIGEKGVHRPAPRNHEQRLE
HIMRRAAREEQPEKDFFGRVVVRSTAVPSAGDTAPEQDSVERRMGTAVGRSEVWFRFNEG
VSNAVRRSLYIRDLL

NT seq 2928 nt +upstreamnt +downstreamnt
atggaggactacgagcaggagctgtgcggcgtcgaggatgatttccacaaccagttcgcg
gccgagctggaggtgctggcagagctggaaggggcgtcgactccgtcgccctccggggtc
cccctgttcaccgcgggccgacccccgcggacgttcgaggaggcccttgccagaggggac
gcggcctccagtcccgccccagccgcatctgtgggcagcagccagggcggcgccaggaag
aggcaggtggacgccgacctgcagccggccgggtccctgccccacgcccccaggatcaaa
cggcctaggctgcaggtggtcaagaggctgaacttcaggtcggaggagatggaggagccg
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

All links

Disease (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (14)   
   KEGG ORTHOLOGY (1)   
   NCBI-Gene (1)   
   NCBI-GI (6)   
   UniGene (1)   
   HGNC (1)   
   HPRD (1)   
   ENSEMBL-HSA (1)   
   OC (1)   
   VEGA (1)   
Protein sequence (2)   
   UniProt (1)   
   RefSeq(pep) (1)   
DNA sequence (19)   
   RefSeq(nuc) (1)   
   GenBank (9)   
   EMBL (9)   
Protein domain (24)   
   Pfam (24)   
All databases (61)   

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