KEGG   Homo sapiens (human): 59335
Entry
59335             CDS       T01001                                 
Symbol
PRDM12, HSAN8, PFM9
Name
(RefSeq) PR/SET domain 12
  KO
K24255  PR domain zinc finger protein 12 [EC:2.1.1.-]
Organism
hsa  Homo sapiens (human)
Disease
H00265  Hereditary sensory and autonomic neuropathy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    59335 (PRDM12)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Histone modification proteins
   HMTs (histone methyltransferases)
    HKMTs (histone lysine methyltransferases)
     59335 (PRDM12)
SSDB
Motif
Pfam: PRDM2_PR zf-H2C2_2 zf-C2H2 zf-C2H2_4 SET zf-C2H2_jaz zf-met zf-C2H2_2 zf-C2H2_6 zf-Di19 CBM_3 Elf1
Other DBs
NCBI-GeneID: 59335
NCBI-ProteinID: NP_067632
OMIM: 616458
HGNC: 13997
Ensembl: ENSG00000130711
UniProt: Q9H4Q4
Structure
Position
9:130664594..130682983
AA seq 367 aa
MMGSVLPAEALVLKTGLKAPGLALAEVITSDILHSFLYGRWRNVLGEQLFEDKSHHASPK
TAFTAEVLAQSFSGEVQKLSSLVLPAEVIIAQSSIPGEGLGIFSKTWIKAGTEMGPFTGR
VIAPEHVDICKNNNLMWEVFNEDGTVRYFIDASQEDHRSWMTYIKCARNEQEQNLEVVQI
GTSIFYKAIEMIPPDQELLVWYGNSHNTFLGIPGVPGLEEDQKKNKHEDFHPADSAAGPA
GRMRCVICHRGFNSRSNLRSHMRIHTLDKPFVCRFCNRRFSQSSTLRNHVRLHTGERPYK
CQVCQSAYSQLAGLRAHQKSARHRPPSTALQAHSPALPAPHAHAPALAAAAAAAAAAAAH
HLPAMVL
NT seq 1104 nt   +upstreamnt  +downstreamnt
atgatgggctccgtgctcccggctgaggccctggtgctcaagaccgggctgaaggcgccg
ggactggcgctggccgaggttatcacctccgacatcctgcacagcttcctgtacggccgc
tggcgcaacgtgctcggggagcagctcttcgaggacaagagccaccacgccagccccaag
acagccttcaccgccgaggtgctggcgcagtccttctccggcgaagtgcagaagctgtcc
agcctggtgctgcctgcggaggtgatcatcgctcagagctccatccctggcgagggcctc
ggcatcttctccaagacgtggatcaaggcgggaaccgagatgggccccttcaccggccgc
gtgatcgccccggagcacgtggacatctgcaagaacaacaacctcatgtgggaggtgttc
aatgaggatggcacggtgcgctacttcatcgatgccagccaggaggaccaccggagctgg
atgacctacatcaagtgtgcacgtaacgaacaggagcagaacctggaggtggtccagatc
ggcaccagcatcttctacaaggccattgagatgatcccacctgaccaggaactgctggtg
tggtacggaaactcacacaacaccttcctggggatcccaggtgtgcccgggctagaggag
gaccagaaaaagaacaagcatgaggacttccacccggcggactcggcggctggccccgcg
ggccgcatgcgatgcgtcatctgccaccgcggcttcaactcgcgcagcaacctgcgctcg
cacatgcgcatccacacgctggacaagcccttcgtgtgccgcttctgcaaccgccgcttc
agccagtcgtccacgctgcgcaaccacgtgcgcctgcacacgggcgagcgcccctacaag
tgccaggtgtgccagagcgcctactcgcagctggccggcctgcgcgcccaccagaagagc
gcgcggcaccggccgcccagcaccgcgctgcaggcacactcgcccgcgctgcccgccccg
cacgcgcacgcgcccgcgctcgccgccgccgccgccgccgccgccgccgccgccgcgcac
cacctgccggccatggtgctgtga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (9)   
   KEGG ORTHOLOGY (1)   
   RefGene (2)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
   PHAROS (1)   
Protein sequence (3)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (3)   
   RefSeq(nuc) (1)   
   GenBank (1)   
   EMBL (1)   
3D Structure (1)   
   PDB (1)   
Protein domain (12)   
   Pfam (12)   
All databases (34)   

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