KEGG   Homo sapiens (human): 80152
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)
Disease
H02481  Syndromic disorder with short stature
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)
SSDB
Motif
Pfam: CENP-T_N CENP-T_C CENP-S CBFD_NFYB_HMF Histone Bromo_TP TFIID-18kDa
Other DBs
NCBI-GeneID: 80152
NCBI-ProteinID: NP_079358
OMIM: 611510
HGNC: 25787
Ensembl: ENSG00000102901
Pharos: Q96BT3(Tbio)
UniProt: Q96BT3 B3KPB2
Position
16:complement(67828157..67847693)
AA seq 561 aa
MADHNPDSDSTPRTLLRRVLDTADPRTPRRPRSARAGARRALLETASPRKLSGQTRTIAR
GRSHGARSVGRSAHIQASGHLEEQTPRTLLKNILLTAPESSILMPESVVKPVPAPQAVQP
SRQESSCGSLELQLPELEPPTTLAPGLLAPGRRKQRLRLSVFQQGVDQGLSLSQEPQGNA
DASSLTRSLNLTFATPLQPQSVQRPGLARRPPARRAVDVGAFLRDLRDTSLAPPNIVLED
TQPFSQPMVGSPNVYHSLPCTPHTGAEDAEQAAGRKTQSSGPGLQKNSPGKPAQFLAGEA
EEVNAFALGFLSTSSGVSGEDEVEPLHDGVEEAEKKMEEEGVSVSEMEATGAQGPSRVEE
AEGHTEVTEAEGSQGTAEADGPGASSGDEDASGRAASPESASSTPESLQARRHHQFLEPA
PAPGAAVLSSEPAEPLLVRHPPRPRTTGPRPRQDPHKAGLSHYVKLFSFYAKMPMERKAL
EMVEKCLDKYFQHLCDDLEVFAAHAGRKTVKPEDLELLMRRQGLVTDQVSLHVLVERHLP
LEYRQLLIPCAYSGNSVFPAQ
NT seq 1686 nt   +upstreamnt  +downstreamnt
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

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Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (22)   
   KEGG ORTHOLOGY (1)   
   RefGene (11)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
   PHAROS (1)   
Protein sequence (8)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (5)   
DNA sequence (35)   
   RefSeq(nuc) (5)   
   GenBank (15)   
   EMBL (15)   
Protein domain (7)   
   Pfam (7)   
All databases (78)   

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