Homo sapiens (human): 390594
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Entry
390594 CDS
T01001
Symbol
KBTBD13, HCG1645727, NEM6
Name
(RefSeq) kelch repeat and BTB domain containing 13
KO
K21913
kelch repeat and BTB domain-containing protein 13
Organism
hsa
Homo sapiens (human)
Disease
H00698
Nemaline myopathy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04121 Ubiquitin system [BR:
hsa04121
]
390594 (KBTBD13)
Ubiquitin system [BR:
hsa04121
]
Ubiquitin ligases (E3)
Multi subunit type E3
Cul3 complex
Adoptor and target recognizing subunit (BTB)
390594 (KBTBD13)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Kelch_1
Kelch_2
Kelch_6
Kelch_KLHDC2_KLHL20_DRC7
Kelch_3
Beta-prop_ATRN-LZTR1
BTB
NANM
Kelch_4
Motif
Other DBs
NCBI-GeneID:
390594
NCBI-ProteinID:
NP_001094832
OMIM:
613727
HGNC:
37227
Ensembl:
ENSG00000234438
UniProt:
C9JR72
LinkDB
All DBs
Position
15:65076746..65079948
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AA seq
458 aa
AA seq
DB search
MARGPQTLVQVWVGGQLFQADRALLVEHCGFFRGLFRSGMRETRAAEVRLGVLSAGGFRA
TLQVLRGDRPALAAEDELLQAVECAAFLQAPALARFLEHNLTSDNCALLCDAAAAFGLRD
VFHSAALFICDGERELAAELALPEARAYVAALRPSSYAAVSTHTPAPGFLEDASRTLCYL
DEEEDAWRTLAALPLEASTLLAGVATLGNKLYIVGGVRGASKEVVELGFCYDPDGGTWHE
FPSPHQPRYDTALAGFDGRLYAIGGEFQRTPISSVERYDPAAGCWSFVADLPQPAAGVPC
AQACGRLFVCLWRPADTTAVVEYAVRTDAWLPVAELRRPQSYGHCMVAHRDSLYVVRNGP
SDDFLHCAIDCLNLATGQWTALPGQFVNSKGALFTAVVRGDTVYTVNRMFTLLYAIEGGT
WRLLREKAGFPRPGSLQTFLLRLPPGAPGPVTSTTAEL
NT seq
1377 nt
NT seq
+upstream
nt +downstream
nt
atggcacggggtccacagaccctggtgcaggtgtgggtgggcggccagctcttccaagcc
gaccgcgccctgctggtggagcactgtggcttcttccgaggcctcttccgctccggcatg
cgggagacccgcgcagcagaggtgcgcctgggcgttctgagcgcgggaggtttccgcgcc
acgctgcaggtgctgcgcggcgaccggccggcgctggcggcggaggacgagctgctgcag
gccgtggagtgcgccgccttcctccaggcgccggcgctggctcgctttctggagcacaac
ctcacgtcggacaactgcgcattgctgtgcgacgcggccgccgccttcggcctgcgcgac
gtgttccacagtgccgcgctcttcatctgcgacggcgagcgcgagctggcggccgaactg
gcgctgcctgaggcccgcgcctacgtggcggccctgcggcccagcagctacgcggccgtg
agcacgcacacgcccgcgcccggcttcctggaggacgcctcgcgcacgctgtgttacctg
gacgaggaagaggacgcgtggcgcacgctggctgcgctgcccctggaggccagcacgttg
ctggccggggtggccacgctgggcaacaagctttacatcgtggggggcgtgcgcggcgcc
agcaaggaggtggtagagctgggcttctgctacgaccccgacggcggcacgtggcacgag
ttccccagcccgcaccagccgcgctatgacacagcgctggccggcttcgacggccgcctc
tacgccatcggcggcgaattccagaggacgcccatcagctccgtggagcgctacgaccca
gccgcgggctgctggagtttcgtggccgacctgccgcagccggccgccggcgtgccctgc
gcccaggcttgtggccgtctcttcgtgtgcctgtggcggccggccgacaccaccgccgtg
gtggagtacgcagtgcggaccgacgcgtggctgccagtggccgagctgcggcgtccgcag
agctatggccactgcatggtggcccaccgcgacagcctctatgtggtgcgcaacggacct
tccgacgacttcctgcactgcgccatcgactgtctcaacctggccacgggccagtggacg
gcgctgcccggccagttcgtcaacagcaagggagcgctcttcacggccgtggtgcgcggt
gacaccgtctatacggtcaaccgcatgttcacgctgctctacgccatcgagggcggcacc
tggcggctgctcagggagaaagccggcttcccgcggcccggctccttgcagacctttctc
ctaaggctgcctcctggcgctcctgggcctgtgacttcgacaacggcagaactgtga
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