Homo sapiens (human): 80152
Help
Entry
80152 CDS
T01001
Symbol
CENPT, C16orf56, CENP-T, SSMGA
Name
(RefSeq) centromere protein T
KO
K11512
centromere protein T
Organism
hsa
Homo sapiens (human)
Network
nt06515
Regulation of kinetochore-microtubule interactions
Element
N01525
Organization of the inner kinetochore
N01526
Organization of the outer kinetochore
Disease
H02607
Short stature and microcephaly with genital anomalies
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
80152 (CENPT)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centromeric chromatin formation proteins
Kinetochore proteins
Centromere proteins
80152 (CENPT)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
CENP-T_N
CENP-T_C
CENP-S
CBFD_NFYB_HMF
Bromo_TP
Histone
TFIID-18kDa
Motif
Other DBs
NCBI-GeneID:
80152
NCBI-ProteinID:
NP_079358
OMIM:
611510
HGNC:
25787
Ensembl:
ENSG00000102901
UniProt:
Q96BT3
B3KPB2
Structure
PDB
PDBj
LinkDB
All DBs
Position
16:complement(67828157..67847693)
Genome browser
AA seq
561 aa
AA seq
DB search
MADHNPDSDSTPRTLLRRVLDTADPRTPRRPRSARAGARRALLETASPRKLSGQTRTIAR
GRSHGARSVGRSAHIQASGHLEEQTPRTLLKNILLTAPESSILMPESVVKPVPAPQAVQP
SRQESSCGSLELQLPELEPPTTLAPGLLAPGRRKQRLRLSVFQQGVDQGLSLSQEPQGNA
DASSLTRSLNLTFATPLQPQSVQRPGLARRPPARRAVDVGAFLRDLRDTSLAPPNIVLED
TQPFSQPMVGSPNVYHSLPCTPHTGAEDAEQAAGRKTQSSGPGLQKNSPGKPAQFLAGEA
EEVNAFALGFLSTSSGVSGEDEVEPLHDGVEEAEKKMEEEGVSVSEMEATGAQGPSRVEE
AEGHTEVTEAEGSQGTAEADGPGASSGDEDASGRAASPESASSTPESLQARRHHQFLEPA
PAPGAAVLSSEPAEPLLVRHPPRPRTTGPRPRQDPHKAGLSHYVKLFSFYAKMPMERKAL
EMVEKCLDKYFQHLCDDLEVFAAHAGRKTVKPEDLELLMRRQGLVTDQVSLHVLVERHLP
LEYRQLLIPCAYSGNSVFPAQ
NT seq
1686 nt
NT seq
+upstream
nt +downstream
nt
atggctgaccacaaccctgacagcgactccacgccgcgcacgctgctgcgacgcgtgctg
gatacagcggacccgcgcaccccgcggcgaccccggagtgctcgggctggagcccggaga
gccctgcttgaaacggcttcccccaggaagttgagtggccaaacaaggacgatagccaga
gggcgttcccatggagccaggtctgttggcagatcggcccatattcaggccagtgggcac
ttggaggaacagacacctcggacgctgctgaagaacatcctactaactgccccagaatct
tccatcctgatgcctgagtcggtagtgaagccagtgccagcaccgcaggcggtccaaccc
tccagacaagagagcagttgcggcagcctggagctgcaacttcctgagctcgagcccccc
acaaccctggctccaggtctgctggcccctggcaggaggaaacagaggctgagactgtca
gtgtttcagcagggagtggaccaggggctgtctctctcccaagagcctcaagggaatgct
gatgcctcttccctcaccagatccctcaacctgacctttgccacacctcttcagccacag
tcagtgcagaggcctggcttggcccgcagacctccagcccgccgagctgtagacgtgggt
gcctttttgcgggatctgcgagatacttccctggctcctccaaacattgtgttggaggac
acccagccgttctctcagcccatggttggctcccccaacgtgtatcactccctgccctgc
acgcctcacactggggctgaagacgctgagcaggctgccggtcgcaagacacagagcagt
gggcctgggctgcagaagaatagccctgggaaaccagcccagtttctggcaggagaggca
gaggaggtcaatgcctttgctctgggcttcctgagcaccagcagtggtgtctctggagaa
gatgaagtagagcccttacacgatggagttgaagaggcagagaaaaagatggaagaagaa
ggtgtgagtgtgagtgaaatggaggcaacaggagcacaaggacccagcagggtagaagag
gctgagggacacacagaggtgacagaagcagagggatcccaggggactgctgaggctgac
gggccaggagcatcttcaggggatgaggatgcctctggcagggcagcaagtccagagtcg
gcctccagcacccctgagtctctccaggccaggcgacatcatcagtttcttgagccagcc
ccagcgcctggtgctgcagtcttatcttcagagcctgcagagcctctgttggtcaggcat
ccccctaggccccggaccaccggccccaggccccggcaagatccccacaaggctggactg
agccactatgtgaaactctttagcttctatgccaagatgcccatggagaggaaggctctt
gagatggtggagaagtgcctagataaatatttccagcatctttgtgatgatctggaggta
tttgctgctcatgctggccgcaagactgtgaagccagaggacctggagctgctgatgcgg
cggcagggcctggtcactgaccaagtctcactgcacgtgctagtggagcggcacctgccc
ctggagtaccggcagctgctcatcccctgtgcatacagtggcaactctgtcttccctgcc
cagtag
Homo sapiens (human): 387103
Help
Entry
387103 CDS
T01001
Symbol
CENPW, C6orf173, CENP-W, CUG2
Name
(RefSeq) centromere protein W
KO
K26091
centromere protein W
Organism
hsa
Homo sapiens (human)
Network
nt06515
Regulation of kinetochore-microtubule interactions
Element
N01525
Organization of the inner kinetochore
N01526
Organization of the outer kinetochore
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
387103 (CENPW)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centromeric chromatin formation proteins
Kinetochore proteins
Centromere proteins
387103 (CENPW)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
CENP-W
CBFD_NFYB_HMF
Motif
Other DBs
NCBI-GeneID:
387103
NCBI-ProteinID:
NP_001012525
OMIM:
611264
HGNC:
21488
Ensembl:
ENSG00000203760
UniProt:
Q5EE01
Structure
PDB
PDBj
LinkDB
All DBs
Position
6:126340115..126483320
Genome browser
AA seq
88 aa
AA seq
DB search
MALSTIVSQRKQIKRKAPRGFLKRVFKRKKPQLRLEKSGDLLVHLNCLLFVHRLAEESRT
NACASKCRVINKEHVLAAAKVILKKSRG
NT seq
267 nt
NT seq
+upstream
nt +downstream
nt
atggcgctgtcgaccatagtctcccagaggaagcagataaagcggaaggctccccgtggc
tttctaaagcgagtcttcaagcgaaagaagcctcaacttcgtctggagaaaagtggtgac
ttattggtccatctgaactgtttactgtttgttcatcgattagcagaagagtccaggaca
aacgcttgtgcgagtaaatgtagagtcattaacaaggagcatgtactggccgcagcaaag
gtaattctaaagaagagcagaggttag
Homo sapiens (human): 378708
Help
Entry
378708 CDS
T01001
Symbol
CENPS, APITD1, CENP-S, FAAP16, MHF1
Name
(RefSeq) centromere protein S
KO
K11511
centromere protein S
Organism
hsa
Homo sapiens (human)
Pathway
hsa03460
Fanconi anemia pathway
Network
nt06508
Interstrand crosslink repair
nt06515
Regulation of kinetochore-microtubule interactions
Element
N01464
Fanconi anemia pathway
N01525
Organization of the inner kinetochore
N01526
Organization of the outer kinetochore
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09124 Replication and repair
03460 Fanconi anemia pathway
378708 (CENPS)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
378708 (CENPS)
03400 DNA repair and recombination proteins [BR:
hsa03400
]
378708 (CENPS)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centromeric chromatin formation proteins
Kinetochore proteins
Centromere proteins
378708 (CENPS)
DNA repair and recombination proteins [BR:
hsa03400
]
Eukaryotic type
DSBR (double strand breaks repair)
FA (Fanconi anemia) pathway
FA core complex binding factors
378708 (CENPS)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
CENP-S
CENP-T_C
Histone
TFIID-31kDa
COMMD1_N
DASH_Dad2
Bromo_TP
DUF4087
Motif
Other DBs
NCBI-GeneID:
378708
NCBI-ProteinID:
NP_954988
OMIM:
609130
HGNC:
23163
Ensembl:
ENSG00000175279
UniProt:
Q8N2Z9
Structure
PDB
PDBj
LinkDB
All DBs
Position
1:10430433..10442808
Genome browser
AA seq
138 aa
AA seq
DB search
MEEEAETEEQQRFSYQQRLKAAVHYTVGCLCEEVALDKEMQFSKQTIAAISELTFRQCEN
FAKDLEMFARHAKRTTINTEDVKLLARRSNSLLKYITDKSEEIAQINLERKAQKKKKSED
GSKNSRQPAEAGVVESEN
NT seq
417 nt
NT seq
+upstream
nt +downstream
nt
atggaggaggaggcggagaccgaggagcagcagcgattctcttaccaacagaggctaaag
gcagcagttcactatactgtgggttgtctttgcgaggaagttgcattggacaaagagatg
cagttcagcaaacagaccattgcggccatttcggagctgactttccgacagtgtgaaaat
tttgccaaagaccttgaaatgtttgcaagacatgcgaaaagaaccacaattaacactgaa
gatgtgaagctcttagccaggaggagtaattcactgctaaaatacatcacagacaaaagt
gaagagattgctcagattaacctagaacgaaaagcacagaagaaaaagaagtcagaggat
ggaagcaaaaattcaaggcagccagcagaggctggagtggtggaaagtgagaattaa
Homo sapiens (human): 201254
Help
Entry
201254 CDS
T01001
Symbol
CENPX, CENP-X, D9, FAAP10, MHF2, STRA13
Name
(RefSeq) centromere protein X
KO
K15360
centromere protein X
Organism
hsa
Homo sapiens (human)
Pathway
hsa03460
Fanconi anemia pathway
Network
nt06508
Interstrand crosslink repair
nt06515
Regulation of kinetochore-microtubule interactions
Element
N01464
Fanconi anemia pathway
N01525
Organization of the inner kinetochore
N01526
Organization of the outer kinetochore
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09124 Replication and repair
03460 Fanconi anemia pathway
201254 (CENPX)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03400 DNA repair and recombination proteins [BR:
hsa03400
]
201254 (CENPX)
DNA repair and recombination proteins [BR:
hsa03400
]
Eukaryotic type
DSBR (double strand breaks repair)
FA (Fanconi anemia) pathway
FA core complex binding factors
201254 (CENPX)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
CENP-X
CBFD_NFYB_HMF
Motif
Other DBs
NCBI-GeneID:
201254
NCBI-ProteinID:
NP_001257935
OMIM:
615128
HGNC:
11422
Ensembl:
ENSG00000169689
UniProt:
A8MT69
Structure
PDB
PDBj
LinkDB
All DBs
Position
17:complement(82018703..82022878)
Genome browser
AA seq
81 aa
AA seq
DB search
MEGAGAGSGFRKELVSRLLHLHFKDDKTKVSGDALQLMVELLKVFVVEAAVRGVRQAQAE
DALRVDVDQLEKVLPQLLLDF
NT seq
246 nt
NT seq
+upstream
nt +downstream
nt
atggagggagcaggagctggatccggcttccggaaggagctggtgagcaggctgctgcac
ctgcacttcaaggatgacaagaccaaagtgagcggggacgcgctgcagctcatggtggag
ttgctgaaggtcttcgttgtggaagcagcagtccgcggcgtgcggcaggcccaggcagaa
gacgcgctccgtgtggacgtggaccagctggagaaggtgcttccgcagctgctcctggac
ttctag
DBGET
integrated database retrieval system