KEGG   Homo sapiens (human): 80169
Entry
80169             CDS       T01001                                 
Symbol
CTC1, AAF-132, AAF132, C17orf68, CRMCC, tmp494178
Name
(RefSeq) CST telomere replication complex component 1
  KO
K23311  CST complex subunit CTC1
Organism
hsa  Homo sapiens (human)
Network
nt06510  Telomere length regulation
  Element
N01477  Telomere elongation
Disease
H02251  Cerebroretinal microangiopathy with calcifications and cysts
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03032 DNA replication proteins [BR:hsa03032]
    80169 (CTC1)
DNA replication proteins [BR:hsa03032]
 Eukaryotic type
  DNA Replication Termination Factors
   Telomere proteins
    CST complex (animals)
     80169 (CTC1)
SSDB
Motif
Pfam: CTC1 CTC1_2 zf-4CXXC_R1
Other DBs
NCBI-GeneID: 80169
NCBI-ProteinID: NP_079375
OMIM: 613129
HGNC: 26169
Ensembl: ENSG00000178971
UniProt: Q2NKJ3
Structure
LinkDB
Position
17:complement(8224815..8248056)
AA seq 1217 aa
MAAGRAQVPSSEQAWLEDAQVFIQKTLCPAVKEPNVQLTPLVIDCVKTVWLSQGRNQGST
LPLSYSFVSVQDLKTHQRLPCCSHLSWSSSAYQAWAQEAGPNGNPLPREQLLLLGTLTDL
SADLEQECRNGSLYVRDNTGVLSCELIDLDLSWLGHLFLFPRWSYLPPARWNSSGEGHLE
LWDAPVPVFPLTISPGPVTPIPVLYPESASCLLRLRNKLRGVQRNLAGSLVRLSALVKSK
QKAYFILSLGRSHPAVTHVSIIVQVPAQLVWHRALRPGTAYVLTELRVSKIRGQRQHVWM
TSQSSRLLLLKPECVQELELELEGPLLEADPKPLPMPSNSEDKKDPESLVRYSRLLSYSG
AVTGVLNEPAGLYELDGQLGLCLAYQQFRGLRRVMRPGVCLQLQDVHLLQSVGGGTRRPV
LAPCLRGAVLLQSFSRQKPGAHSSRQAYGASLYEQLVWERQLGLPLYLWATKALEELACK
LCPHVLRHHQFLQHSSPGSPSLGLQLLAPTLDLLAPPGSPVRNAHNEILEEPHHCPLQKY
TRLQTPSSFPTLATLKEEGQRKAWASFDPKALLPLPEASYLPSCQLNRRLAWSWLCLLPS
AFCPAQVLLGVLVASSHKGCLQLRDQSGSLPCLLLAKHSQPLSDPRLIGCLVRAERFQLI
VERDVRSSFPSWKELSMPGFIQKQQARVYVQFFLADALILPVPRPCLHSATPSTPQTDPT
GPEGPHLGQSRLFLLCHKEALMKRNFCVPPGASPEVPKPALSFYVLGSWLGGTQRKEGTG
WGLPEPQGNDDNDQKVHLIFFGSSVRWFEFLHPGQVYRLIAPGPATPMLFEKDGSSCISR
RPLELAGCASCLTVQDNWTLELESSQDIQDVLDANKSLPESSLTDLLSDNFTDSLVSFSA
EILSRTLCEPLVASLWMKLGNTGAMRRCVKLTVALETAECEFPPHLDVYIEDPHLPPSLG
LLPGARVHFSQLEKRVSRSHNVYCCFRSSTYVQVLSFPPETTISIPLPHIYLAELLQGGQ
SPFQATASCHIVSVFSLQLFWVCAYCTSICRQGKCTRLGSTCPTQTAISQAIIRLLVEDG
TAEAVVTCRNHHVAAALGLCPREWASLLDFVQVPGRVVLQFAGPGAQLESSARVDEPMTM
FLWTLCTSPSVLRPIVLSFELERKPSKIVPLEPPRLQRFQCGELPFLTHVNPRLRLSCLS
IRESEYSSSLGILASSC
NT seq 3654 nt   +upstreamnt  +downstreamnt
atggcggctggccgggcccaggtcccttcctccgaacaagcctggcttgaggatgctcag
gtcttcatccaaaagaccctgtgtccagctgtcaaggagcctaatgtccagttgactcca
ttggtaattgattgtgtgaagactgtctggttgtcccagggaaggaaccaaggttctaca
ctgcccctcagctatagcttcgtctcagtacaggacctcaagactcaccagcgtctccca
tgctgcagccacctgtcgtggagcagtagtgcataccaggcctgggcccaagaggctgga
ccaaatgggaaccccctgccccgagagcagctgttacttttagggacactaacagaccta
tcggcagacttggaacaagagtgcaggaacggaagcctctatgtgagagataacactggc
gtcctgagctgtgagctcatagacctggacctttcttggttgggccatctttttctgttc
ccccgttggagttacctccctcctgccaggtggaattcctcaggggaagggcacttggag
ctgtgggatgcccctgtgccagtgtttcctttgaccatcagtcctggccccgtcacgcct
atccctgtcctctacccagagagtgcttcctgcctgctcaggctcagaaacaagctcaga
ggtgtgcagcgaaacctggctgggagtctagttcgattgagtgctctggtgaaaagtaaa
cagaaagcttacttcatcctgtctcttggtagatcacacccagctgtcacccacgtgtcc
atcatcgtgcaggtccctgcccagctggtgtggcacagagcccttcggcctggtacagcc
tatgtgctgacagaactgcgagtgtccaagatccgtggtcagcgccagcatgtttggatg
accagtcagtcctcccgtctgttgctgctgaaaccagaatgtgtgcaggagctggaactg
gagctggaaggacccctcttagaggctgaccccaagccactccccatgcccagcaactcg
gaggacaagaaggatccagaaagtcttgtccggtattctagactcctatcctattcggga
gcagtcactggcgtgttgaatgagcccgctggcctctatgagctggatgggcagctgggg
ctctgccttgcctaccagcagttccgtggccttaggcgggtgatgcgacctggagtgtgt
ctgcagctccaggatgttcacctgctccagtcagtgggaggggggacaagaaggccagtg
ctcgccccctgcctccgtggcgccgttctgcttcaaagcttctctcgtcagaagcctggg
gctcactcatcccgtcaagcctacggggcctccctgtacgagcagctggtgtgggaacgt
cagttaggacttcccctctacctgtgggctaccaaggccctggaggagctggcctgcaag
ctgtgtccccatgtgctgagacaccaccagttcctgcaacattcctctcctgggagcccc
agcctgggactgcaactcctggctcctaccctggatcttctagctccgccaggcagccct
gttcggaatgcacacaatgagatccttgaagagccacatcactgtcccctccagaaatac
actcggctgcagactccctcctccttccccactctggccaccctgaaagaagaaggacag
cgtaaggcctgggcctcctttgaccctaaggcccttctgcccctcccggaggcctcctac
ctgcccagctgccaactcaatcgccgcctggcttggtcctggctctgtctgctgccctct
gccttctgcccagcccaggttttacttggggttctggtggcttcatctcataaaggttgt
ctgcaacttcgggaccaaagtggttccctgccctgcctgctcctggccaagcactctcaa
cccctcagtgacccacggctgataggctgcctggtgcgggcagagaggtttcagttgatc
gtagagagggacgtgagaagcagcttcccttcctggaaggagctgagcatgccaggcttc
atccagaagcagcaggccagagtctatgtccagttctttctggctgatgccctgatcctg
cctgtgcccagaccctgccttcattcagcaacaccctcaacacctcagacagatcccacc
ggcccagagggaccccacctaggacagagccggctcttcttgctctgccacaaggaggcc
ctcatgaagcgtaatttttgtgtccccccaggagcaagtccagaggtgcccaagcccgcc
ctcagtttctatgtgttggggagctggcttgggggcacccagaggaaggagggtactgga
tgggggctgcccgagccccagggaaatgacgacaatgatcagaaggttcacctcattttc
tttggctcttcagtccgctggtttgagttcttgcacccgggacaggtgtaccgactcata
gctcctggccccgctacaccaatgttgtttgaaaaggatggttcatcctgcatatctcgg
cgtcctctggagttggctggctgtgcatcctgcctcactgtccaggacaactggactctg
gagcttgaaagctcccaggatatccaagatgtgctggatgcaaacaagtcattgcctgaa
tcctcactgaccgacctgctcagtgacaatttcacagattccttggtgtctttctccgct
gagattttgtcacggacactatgtgaaccccttgtggcgtctctctggatgaaactgggg
aacacgggggccatgagaaggtgtgtgaagctaacagtcgctcttgagactgctgaatgt
gaattcccccctcacctggatgtatatatagaagacccacacttgcctccctcactagga
ctacttccaggagcccgggtccacttcagccagttggagaaaagggtttccagatctcac
aatgtttattgttgtttccggtcatccacttatgtgcaggtcctgagttttccccctgag
accaccatcagcattcccctgccccacatctacctggctgaacttctgcagggtggtcag
tccccattccaggccactgcctcttgccatatcgtctctgtcttcagccttcagctcttc
tgggtgtgtgcttattgtaccagcatctgccggcagggaaagtgcactcgcctgggctcc
acttgccctacgcagacagctataagccaggccatcatcaggctcctggtggaggatggg
actgccgaagccgtggtgacctgtaggaatcaccatgtggcagcagcactagggctgtgt
cctagagagtgggcctccctcctagatttcgtccaagtgccaggcagagtggtcttgcag
tttgcagggcctggagcccaacttgagtcttcagccagggttgacgagcccatgaccatg
ttcctctggacactttgtactagcccctctgtcctccgtcctattgtgctttcttttgag
ctggaaaggaaaccgtcgaagatcgtcccattagaacctcctcggctacagcgattccag
tgtggagagctccctttcctgactcacgtgaaccccaggctccgattgtcctgcctttct
atccgagagtcagagtactccagctctctggggatccttgcttcctcctgttaa

KEGG   Homo sapiens (human): 79991
Entry
79991             CDS       T01001                                 
Symbol
STN1, AAF-44, AAF44, OBFC1, RPA-32, bA541N10.2
Name
(RefSeq) STN1 subunit of CST complex
  KO
K23312  CST complex subunit STN1
Organism
hsa  Homo sapiens (human)
Network
nt06510  Telomere length regulation
  Element
N01477  Telomere elongation
Disease
H02251  Cerebroretinal microangiopathy with calcifications and cysts
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03032 DNA replication proteins [BR:hsa03032]
    79991 (STN1)
DNA replication proteins [BR:hsa03032]
 Eukaryotic type
  DNA Replication Termination Factors
   Telomere proteins
    CST complex (animals)
     79991 (STN1)
SSDB
Motif
Pfam: STN1_2 Stn1 tRNA_anti-codon RUN
Other DBs
NCBI-GeneID: 79991
NCBI-ProteinID: NP_079204
OMIM: 613128
HGNC: 26200
Ensembl: ENSG00000107960
UniProt: Q9H668
Structure
LinkDB
Position
10:complement(103877569..103918184)
AA seq 368 aa
MQPGSSRCEEETPSLLWGLDPVFLAFAKLYIRDILDMKESRQVPGVFLYNGHPIKQVDVL
GTVIGVRERDAFYSYGVDDSTGVINCICWKKLNTESVSAAPSAARELSLTSQLKKLQETI
EQKTKIEIGDTIRVRGSIRTYREEREIHATTYYKVDDPVWNIQIARMLELPTIYRKVYDQ
PFHSSALEKEEALSNPGALDLPSLTSLLSEKAKEFLMENRVQSFYQQELEMVESLLSLAN
QPVIHSASSDQVNFKKDTTSKAIHSIFKNAIQLLQEKGLVFQKDDGFDNLYYVTREDKDL
HRKIHRIIQQDCQKPNHMEKGCHFLHILACARLSIRPGLSEAVLQQVLELLEDQSDIVST
MEHYYTAF
NT seq 1107 nt   +upstreamnt  +downstreamnt
atgcagcctggatccagccggtgtgaagaggagaccccttccctcttgtggggtttggat
cctgtgtttctagcctttgcaaaactctacatcagggatatcctggacatgaaggagtcc
cgccaggtgccaggtgtatttttgtacaatggacatccaataaaacaggtagatgtcttg
ggaactgtcattggagtgagagaaagagatgctttctacagttatggagtggatgacagc
actggagttataaactgcatctgctggaaaaagttgaatactgagtctgtatcagctgct
ccaagtgcagcaagagagctcagcttaacctcacaacttaagaagctacaagagaccatt
gagcagaaaacaaagatagagatcggggacacgatccgagtcagaggcagtatccgcaca
tacagagaagagcgagagattcatgccaccacttactataaagtggacgacccagtgtgg
aacattcaaattgcaaggatgcttgagctgcccactatctacaggaaagtttatgaccag
ccttttcacagctcagccctagagaaagaagaggcactaagcaatccaggcgccctggac
ctccccagtctcacgagtttgctgagtgaaaaagccaaagaattcctcatggagaacaga
gtgcagagcttttaccagcaggagctggaaatggtggagtctttgctgtcccttgccaat
cagcctgtgattcacagtgcctcctccgaccaagtgaattttaagaaggacaccacttcc
aaggcaattcatagtatatttaagaatgctatacaactgctgcaggaaaaaggacttgtt
ttccagaaagatgatggttttgataacctatactatgtaaccagagaagacaaagacctg
cacagaaagatccaccggatcattcagcaggactgccagaaaccaaatcacatggagaag
ggctgtcacttcctgcacatcttggcctgtgctcgcctgagcatccgcccgggcctgagc
gaggctgtgctgcagcaagttctggagctcctggaggaccagagtgacattgtcagcaca
atggagcactactacacagcgttctga

KEGG   Homo sapiens (human): 100134934
Entry
100134934         CDS       T01001                                 
Symbol
TEN1, C17orf106
Name
(RefSeq) TEN1 subunit of CST complex
  KO
K23313  CST complex subunit TEN1
Organism
hsa  Homo sapiens (human)
Network
nt06510  Telomere length regulation
  Element
N01477  Telomere elongation
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03032 DNA replication proteins [BR:hsa03032]
    100134934 (TEN1)
DNA replication proteins [BR:hsa03032]
 Eukaryotic type
  DNA Replication Termination Factors
   Telomere proteins
    CST complex (animals)
     100134934 (TEN1)
SSDB
Motif
Pfam: Ten1_2
Other DBs
NCBI-GeneID: 100134934
NCBI-ProteinID: NP_001106795
OMIM: 613130
HGNC: 37242
Ensembl: ENSG00000257949
UniProt: Q86WV5
Structure
LinkDB
Position
17:75979240..76000586
AA seq 123 aa
MMLPKPGTYYLPWEVSAGQVPDGSTLRTFGRLCLYDMIQSRVTLMAQHGSDQHQVLVCTK
LVEPFHAQVGSLYIVLGELQHQQDRGSVVKARVLTCVEGMNLPLLEQAIREQRLYKQERG
GSQ
NT seq 372 nt   +upstreamnt  +downstreamnt
atgatgctgcccaaacctgggacctattacctcccctgggaggttagtgcaggccaagtt
cctgatgggagcacgctgagaacatttggcaggttgtgcctctatgacatgattcagtcc
agagtaacactgatggctcagcacggatccgatcagcaccaggttcttgtctgtaccaag
ttggtggagcccttccacgcccaggtgggctccctgtacatcgtcctcggggagctccag
catcagcaggacagaggctccgtggtgaaggcgcgcgtgctgacctgtgtggaggggatg
aacctgcccttgttggaacaagccatccgggagcagagactgtacaagcaggagcggggc
ggcagccagtag

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