Homo sapiens (human): 284252
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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 type E3
Cul3 complex
Adoptor and target recognizing subunit (BTB)
284252 (KCTD1)
BRITE hierarchy
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Paralog
Gene cluster
GFIT
Motif
Pfam:
KCTD1-15_CTD
BTB_2
H1_KCTD8_12_16
Motif
Other DBs
NCBI-GeneID:
284252
NCBI-ProteinID:
NP_001129677
OMIM:
613420
HGNC:
18249
Ensembl:
ENSG00000134504
UniProt:
Q719H9
Structure
PDB
PDBj
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All DBs
Position
18:complement(26454910..26657473)
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AA seq
257 aa
AA seq
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MSRPLITRSPASPLNNQGIPTPAQLTKSNAPVHIDVGGHMYTSSLATLTKYPESRIGRLF
DGTEPIVLDSLKQHYFIDRDGQMFRYILNFLRTSKLLIPDDFKDYTLLYEEAKYFQLQPM
LLEMERWKQDRETGRFSRPCECLVVRVAPDLGERITLSGDKSLIEEVFPEIGDVMCNSVN
AGWNHDSTHVIRFPLNGYCHLNSVQVLERLQQRGFEIVGSCGGGVDSSQFSEYVLRRELR
RTPRVPSVIRIKQEPLD
NT seq
774 nt
NT seq
+upstream
nt +downstream
nt
atgtcaagacctctgatcactagatcccctgcatctccactgaacaaccaaggcatccct
actccagcacaactcacaaaatccaatgcgcctgtccacattgatgtgggcggccacatg
tacaccagcagcctggccaccctcaccaaataccctgaatccagaatcggaagacttttt
gatggtacagagcccattgttttggacagtctcaaacagcactatttcattgacagagat
ggacagatgttcagatatatcttgaattttctacgaacatccaaactcctcattcctgat
gatttcaaggactacactttgttatatgaagaggcaaaatattttcagcttcagcccatg
ttgttggagatggaaagatggaagcaggacagagaaactggtcgattttcaaggccctgt
gagtgcctcgtcgtgcgtgtggccccagacctcggagaaaggatcacgctaagcggtgac
aaatccttgatagaagaagtatttccagagatcggcgacgtgatgtgtaactctgtcaat
gcaggctggaatcacgactcgacgcacgtcatcaggtttccactaaatggctactgtcac
ctcaactcagtccaggtcctcgagaggttgcagcaaagaggatttgaaatcgtgggctcc
tgtgggggaggagtagactcgtcccagttcagcgaatacgtccttcggcgggaactgagg
cggacgccccgtgtaccctccgtcatccggataaagcaagagcctctggactaa
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