Homo sapiens (human): 93166
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Entry
93166 CDS
T01001
Symbol
PRDM6, KMT8C, PDA3, PRISM
Name
(RefSeq) PR/SET domain 6
KO
K20795
[histone H4]-lysine20 N-methyltransferase PRDM6 [EC:
2.1.1.361
]
Organism
hsa
Homo sapiens (human)
Pathway
hsa00310
Lysine degradation
hsa01100
Metabolic pathways
Disease
H01630
Patent ductus arteriosus
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09100 Metabolism
09105 Amino acid metabolism
00310 Lysine degradation
93166 (PRDM6)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
93166 (PRDM6)
03036 Chromosome and associated proteins [BR:
hsa03036
]
93166 (PRDM6)
Enzymes [BR:
hsa01000
]
2. Transferases
2.1 Transferring one-carbon groups
2.1.1 Methyltransferases
2.1.1.361 [histone H4]-lysine20 N-methyltransferase
93166 (PRDM6)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Zinc finger
Cys2His2 PRDM
93166 (PRDM6)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Histone modification proteins
HMTs (histone methyltransferases)
HKMTs (histone lysine methyltransferases)
93166 (PRDM6)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PRDM2_PR
zf-C2H2
zf-H2C2_2
zf-C2H2_4
SET
zf-C2H2_jaz
Zap1_zf1
zf-C2H2_11
Motif
Other DBs
NCBI-GeneID:
93166
NCBI-ProteinID:
NP_001129711
OMIM:
616982
HGNC:
9350
Ensembl:
ENSG00000061455
UniProt:
Q9NQX0
LinkDB
All DBs
Position
5:123089241..123194266
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AA seq
595 aa
AA seq
DB search
MLKPGDPGGSAFLKVDPAYLQHWQQLFPHGGAGPLKGSGAAGLLSAPQPLQPPPPPPPPE
RAEPPPDSLRPRPASLSSASSTPASSSTSASSASSCAAAAAAAALAGLSALPVSQLPVFA
PLAAAAVAAEPLPPKELCLGATSGPGPVKCGGGGGGGGEGRGAPRFRCSAEELDYYLYGQ
QRMEIIPLNQHTSDPNNRCDMCADNRNGECPMHGPLHSLRRLVGTSSAAAAAPPPELPEW
LRDLPREVCLCTSTVPGLAYGICAAQRIQQGTWIGPFQGVLLPPEKVQAGAVRNTQHLWE
IYDQDGTLQHFIDGGEPSKSSWMRYIRCARHCGEQNLTVVQYRSNIFYRACIDIPRGTEL
LVWYNDSYTSFFGIPLQCIAQDENLNVPSTVMEAMCRQDALQPFNKSSKLAPTTQQRSVV
FPQTPCSRNFSLLDKSGPIESGFNQINVKNQRVLASPTSTSQLHSEFSDWHLWKCGQCFK
TFTQRILLQMHVCTQNPDRPYQCGHCSQSFSQPSELRNHVVTHSSDRPFKCGYCGRAFAG
ATTLNNHIRTHTGEKPFKCERCERSFTQATQLSRHQRMPNECKPITESPESIEVD
NT seq
1788 nt
NT seq
+upstream
nt +downstream
nt
atgctgaagcccggagaccccggcggttcggccttcctcaaagtggacccagcctacctg
cagcactggcagcaactcttccctcacggaggcgcaggcccgctcaagggcagcggcgcc
gcgggtctcctgagcgcgccgcagcctcttcagccgccgccgccgcccccgcccccggag
cgcgctgagcctccgccggacagcctgcgcccgcggcccgcctctctctcctccgcctcg
tccacgccggcttcctcttccacctccgcctcctccgcctcctcctgcgctgctgcggcc
gctgccgccgcgctggctggtctctcggccctgccggtgtcgcagctgccggtgttcgcg
cctctagccgccgctgccgtcgccgccgagccgctgccccccaaggaactgtgcctcggc
gccacctccggccccgggcccgtcaagtgcggtggtggtggcggcggcggcggggagggt
cgcggcgccccgcgcttccgctgcagcgcagaggagctggactattacctgtatggccag
cagcgcatggagatcatcccgctcaaccagcacaccagcgaccccaacaaccgttgcgac
atgtgcgcggacaaccgcaacggcgagtgccctatgcatgggccactgcactcgctgcgc
cggcttgtgggcaccagcagcgctgcggccgccgcgcccccgccggagctgccggagtgg
ctgcgggacctgcctcgcgaggtgtgcctctgcaccagtactgtgcccggcctggcctac
ggcatctgcgcggcgcagaggatccagcaaggcacctggattggacctttccaaggcgtg
cttctgcccccagagaaggtgcaggcaggcgccgtgaggaacacgcagcatctctgggag
atatatgaccaggatgggacactacagcactttattgatggtggggaacctagtaagtcg
agctggatgaggtatatccgatgtgcaaggcactgcggagaacagaatctaacagtagtt
cagtacaggtcgaatatattctaccgagcctgtatagatatccctaggggcaccgagctt
ctggtgtggtacaatgacagctatacgtctttctttgggatccccttacaatgcattgcc
caggatgaaaacttaaatgtcccttcaacggtaatggaagccatgtgcagacaagacgcc
ctgcagcccttcaacaaaagcagcaaactcgcccctaccacccagcagcgctccgttgtt
ttcccccagactccgtgcagcaggaacttctctcttctggataagtctgggcccattgaa
tcaggatttaatcaaatcaacgtgaaaaaccagcgagtcctggcaagcccaacttccaca
agccagctccactcggagttcagtgactggcatctttggaaatgtgggcagtgctttaag
actttcacccagcggatcctcttacagatgcacgtgtgcacgcagaaccccgacagaccc
taccaatgcggccactgctcccagtccttttcccagccttcagaactgaggaaccacgtg
gtcactcactctagtgaccggcctttcaagtgcggctactgtggtcgtgcctttgccggg
gccaccaccctcaacaaccacatccgaacccacactggagaaaagcccttcaagtgcgag
aggtgtgagaggagcttcacgcaggccacccagctgagccgacaccagcggatgcccaat
gagtgcaagccaataactgagagcccagaatcaatcgaagtggattaa
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