KEGG   Homo sapiens (human): 284252
Entry
284252            CDS       T01001                                 
Symbol
KCTD1, C18orf5
Name
(RefSeq) potassium channel tetramerization domain containing 1
  KO
K21754  BTB/POZ domain-containing protein KCTD1/15
Organism
hsa  Homo sapiens (human)
Disease
H02691  Scalp-ear-nipple syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04121 Ubiquitin system [BR:hsa04121]
    284252 (KCTD1)
Ubiquitin system [BR:hsa04121]
 Ubiquitin ligases (E3)
  Multi subunit Ring-finger type E3
   Cul3 complex
    Adoptor and target recognizing subunit (BTB)
     284252 (KCTD1)
SSDB
Motif
Pfam: KCTD1-15_CTD BTB_2
Other DBs
NCBI-GeneID: 284252
NCBI-ProteinID: NP_001129677
OMIM: 613420
HGNC: 18249
Ensembl: ENSG00000134504
UniProt: Q719H9
Structure
Position
18:complement(26454910..26657473)
AA seq 257 aa
MSRPLITRSPASPLNNQGIPTPAQLTKSNAPVHIDVGGHMYTSSLATLTKYPESRIGRLF
DGTEPIVLDSLKQHYFIDRDGQMFRYILNFLRTSKLLIPDDFKDYTLLYEEAKYFQLQPM
LLEMERWKQDRETGRFSRPCECLVVRVAPDLGERITLSGDKSLIEEVFPEIGDVMCNSVN
AGWNHDSTHVIRFPLNGYCHLNSVQVLERLQQRGFEIVGSCGGGVDSSQFSEYVLRRELR
RTPRVPSVIRIKQEPLD
NT seq 774 nt   +upstreamnt  +downstreamnt
atgtcaagacctctgatcactagatcccctgcatctccactgaacaaccaaggcatccct
actccagcacaactcacaaaatccaatgcgcctgtccacattgatgtgggcggccacatg
tacaccagcagcctggccaccctcaccaaataccctgaatccagaatcggaagacttttt
gatggtacagagcccattgttttggacagtctcaaacagcactatttcattgacagagat
ggacagatgttcagatatatcttgaattttctacgaacatccaaactcctcattcctgat
gatttcaaggactacactttgttatatgaagaggcaaaatattttcagcttcagcccatg
ttgttggagatggaaagatggaagcaggacagagaaactggtcgattttcaaggccctgt
gagtgcctcgtcgtgcgtgtggccccagacctcggagaaaggatcacgctaagcggtgac
aaatccttgatagaagaagtatttccagagatcggcgacgtgatgtgtaactctgtcaat
gcaggctggaatcacgactcgacgcacgtcatcaggtttccactaaatggctactgtcac
ctcaactcagtccaggtcctcgagaggttgcagcaaagaggatttgaaatcgtgggctcc
tgtgggggaggagtagactcgtcccagttcagcgaatacgtccttcggcgggaactgagg
cggacgccccgtgtaccctccgtcatccggataaagcaagagcctctggactaa

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