Homo sapiens (human): 9978
Help
Entry
9978 CDS
T01001
Symbol
RBX1, BA554C12.1, RNF75, ROC1
Name
(RefSeq) ring-box 1
KO
K03868
E3 ubiquitin-protein ligase RBX1 [EC:
2.3.2.32
]
Organism
hsa
Homo sapiens (human)
Pathway
hsa03420
Nucleotide excision repair
hsa04066
HIF-1 signaling pathway
hsa04110
Cell cycle
hsa04114
Oocyte meiosis
hsa04120
Ubiquitin mediated proteolysis
hsa04141
Protein processing in endoplasmic reticulum
hsa04310
Wnt signaling pathway
hsa04350
TGF-beta signaling pathway
hsa04710
Circadian rhythm
hsa05131
Shigellosis
hsa05170
Human immunodeficiency virus 1 infection
hsa05200
Pathways in cancer
hsa05211
Renal cell carcinoma
Network
nt06165
Epstein-Barr virus (EBV)
nt06166
Human papillomavirus (HPV)
nt06182
Shigella
nt06225
HIF-1 signaling (cancer)
nt06230
Cell cycle (cancer)
nt06261
Gastric cancer
nt06264
Renal cell carcinoma
nt06267
Small cell lung cancer
nt06272
Prostate cancer
nt06502
Nucleotide excision repair
nt06509
DNA replication
nt06516
TNF signaling
nt06541
Cytoskeleton in neurons
nt06542
HIF signaling
Element
N00080
Loss of VHL to HIF-1 signaling pathway
N00081
Mutation-inactivated VHL to HIF-1 signaling pathway
N00091
p27-Cell cycle G1/S
N00092
Amplified MYC to p27-cell cycle G1/S
N00942
Shigella OspG to TNF-NFKB signaling pathway
N01425
Global genome NER
N01430
Transcription-coupled NER
N01473
DNA replication termination
N01855
Neurofilament regulation, ubiqutination by Gigaxonin
N01872
Proteasomal degradation of HIF by VHL complex
N01873
VHL mutation to HIF-2 signaling pathway
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09123 Folding, sorting and degradation
04141 Protein processing in endoplasmic reticulum
9978 (RBX1)
04120 Ubiquitin mediated proteolysis
9978 (RBX1)
09124 Replication and repair
03420 Nucleotide excision repair
9978 (RBX1)
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
9978 (RBX1)
04350 TGF-beta signaling pathway
9978 (RBX1)
04066 HIF-1 signaling pathway
9978 (RBX1)
09140 Cellular Processes
09143 Cell growth and death
04110 Cell cycle
9978 (RBX1)
04114 Oocyte meiosis
9978 (RBX1)
09150 Organismal Systems
09159 Environmental adaptation
04710 Circadian rhythm
9978 (RBX1)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
9978 (RBX1)
09162 Cancer: specific types
05211 Renal cell carcinoma
9978 (RBX1)
09172 Infectious disease: viral
05170 Human immunodeficiency virus 1 infection
9978 (RBX1)
09171 Infectious disease: bacterial
05131 Shigellosis
9978 (RBX1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04121 Ubiquitin system [BR:
hsa04121
]
9978 (RBX1)
03400 DNA repair and recombination proteins [BR:
hsa03400
]
9978 (RBX1)
Enzymes [BR:
hsa01000
]
2. Transferases
2.3 Acyltransferases
2.3.2 Aminoacyltransferases
2.3.2.32 cullin-RING-type E3 NEDD8 transferase
9978 (RBX1)
Ubiquitin system [BR:
hsa04121
]
Ubiquitin ligases (E3)
UBL E3 ligases
9978 (RBX1)
Multi subunit type E3
SCF complex
Ring finger protein
9978 (RBX1)
Cul2 complex
9978 (RBX1)
Cul3 complex
9978 (RBX1)
Cul4 complex
9978 (RBX1)
Cul7 complex
9978 (RBX1)
Cul8 complex
9978 (RBX1)
Cul9 complex
9978 (RBX1)
DNA repair and recombination proteins [BR:
hsa03400
]
Eukaryotic type
SSBR (single strand breaks repair)
NER (nucleotide excision repair)
GGR (global genome repair) factors
Cul4-DDB2 complex
9978 (RBX1)
TCR (transcription coupled repair) factors
Cul4-CSA complex
9978 (RBX1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
zf-rbx1
zf-ANAPC11
zf-RING_2
zf-C3HC4
zf-C3HC4_2
zf-RING_11
DUF8003
PHD_NSD
Motif
Other DBs
NCBI-GeneID:
9978
NCBI-ProteinID:
NP_055063
OMIM:
603814
HGNC:
9928
Ensembl:
ENSG00000100387
UniProt:
P62877
Structure
PDB
PDBj
LinkDB
All DBs
Position
22:40951378..40973309
Genome browser
AA seq
108 aa
AA seq
DB search
MAAAMDVDTPSGTNSGAGKKRFEVKKWNAVALWAWDIVVDNCAICRNHIMDLCIECQANQ
ASATSEECTVAWGVCNHAFHFHCISRWLKTRQVCPLDNREWEFQKYGH
NT seq
327 nt
NT seq
+upstream
nt +downstream
nt
atggcggcagcgatggatgtggataccccgagcggcaccaacagcggcgcgggcaagaag
cgctttgaagtgaaaaagtggaatgcagtagccctctgggcctgggatattgtggttgat
aactgtgccatctgcaggaaccacattatggatctttgcatagaatgtcaagctaaccag
gcgtccgctacttcagaagagtgtactgtcgcatggggagtctgtaaccatgcttttcac
ttccactgcatctctcgctggctcaaaacacgacaggtgtgtccattggacaacagagag
tgggaattccaaaagtatgggcactag
Homo sapiens (human): 8452
Help
Entry
8452 CDS
T01001
Symbol
CUL3, CUL-3, NEDAUS, PHA2E
Name
(RefSeq) cullin 3
KO
K03869
cullin 3
Organism
hsa
Homo sapiens (human)
Pathway
hsa04120
Ubiquitin mediated proteolysis
hsa04340
Hedgehog signaling pathway
Network
nt06526
MAPK signaling
nt06541
Cytoskeleton in neurons
Element
N01596
Regulation of GF-RTK-RAS-ERK signaling, RAS ubiquitination by CUL3 complex
N01855
Neurofilament regulation, ubiqutination by Gigaxonin
Disease
H00243
Renal tubular acidosis type 4
H02310
Renal tubular acidosis
H02715
Neurodevelopmental disorder with defects of ubiquitin-proteasome system
H02864
Neurodevelopmental disorder with or without autism or seizures
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09123 Folding, sorting and degradation
04120 Ubiquitin mediated proteolysis
8452 (CUL3)
09130 Environmental Information Processing
09132 Signal transduction
04340 Hedgehog signaling pathway
8452 (CUL3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04121 Ubiquitin system [BR:
hsa04121
]
8452 (CUL3)
03400 DNA repair and recombination proteins [BR:
hsa03400
]
8452 (CUL3)
Ubiquitin system [BR:
hsa04121
]
Ubiquitin ligases (E3)
Multi subunit type E3
Cul3 complex
Cullin
8452 (CUL3)
DNA repair and recombination proteins [BR:
hsa03400
]
Eukaryotic type
SSBR (single strand breaks repair)
NER (nucleotide excision repair)
Other NER factors
8452 (CUL3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cullin
Cullin_AB
Cullin_Nedd8
RhgB_N
Stu2_CTS
DUF6655
WAC_Acf1_DNA_bd
Motif
Other DBs
NCBI-GeneID:
8452
NCBI-ProteinID:
NP_003581
OMIM:
603136
HGNC:
2553
Ensembl:
ENSG00000036257
UniProt:
Q13618
Structure
PDB
PDBj
LinkDB
All DBs
Position
2:complement(224470150..224585363)
Genome browser
AA seq
768 aa
AA seq
DB search
MSNLSKGTGSRKDTKMRIRAFPMTMDEKYVNSIWDLLKNAIQEIQRKNNSGLSFEELYRN
AYTMVLHKHGEKLYTGLREVVTEHLINKVREDVLNSLNNNFLQTLNQAWNDHQTAMVMIR
DILMYMDRVYVQQNNVENVYNLGLIIFRDQVVRYGCIRDHLRQTLLDMIARERKGEVVDR
GAIRNACQMLMILGLEGRSVYEEDFEAPFLEMSAEFFQMESQKFLAENSASVYIKKVEAR
INEEIERVMHCLDKSTEEPIVKVVERELISKHMKTIVEMENSGLVHMLKNGKTEDLGCMY
KLFSRVPNGLKTMCECMSSYLREQGKALVSEEGEGKNPVDYIQGLLDLKSRFDRFLLESF
NNDRLFKQTIAGDFEYFLNLNSRSPEYLSLFIDDKLKKGVKGLTEQEVETILDKAMVLFR
FMQEKDVFERYYKQHLARRLLTNKSVSDDSEKNMISKLKTECGCQFTSKLEGMFRDMSIS
NTTMDEFRQHLQATGVSLGGVDLTVRVLTTGYWPTQSATPKCNIPPAPRHAFEIFRRFYL
AKHSGRQLTLQHHMGSADLNATFYGPVKKEDGSEVGVGGAQVTGSNTRKHILQVSTFQMT
ILMLFNNREKYTFEEIQQETDIPERELVRALQSLACGKPTQRVLTKEPKSKEIENGHIFT
VNDQFTSKLHRVKIQTVAAKQGESDPERKETRQKVDDDRKHEIEAAIVRIMKSRKKMQHN
VLVAEVTQQLKARFLPSPVVIKKRIEGLIEREYLARTPEDRKVYTYVA
NT seq
2307 nt
NT seq
+upstream
nt +downstream
nt
atgtcgaatctgagcaaaggcacgggcagccggaaggacaccaagatgcggatccgggcc
tttccgatgaccatggatgaaaaatatgtaaacagcatttgggaccttctgaaaaatgca
attcaagaaatccagcgtaagaataacagtggtcttagttttgaggagctctatagaaat
gcatatacaatggttttgcataaacatggagaaaagctctacactggactaagagaagtt
gttaccgaacatctcataaataaggtgcgagaagatgtactaaattcattgaataacaac
tttcttcaaacgctaaatcaagcttggaatgatcatcaaacagctatggtgatgattaga
gacatactaatgtacatggaccgtgtgtatgtacaacaaaataatgtggagaacgtctac
aatttgggattaattatttttcgagatcaagttgtacgttatgggtgtattagggatcat
ctacggcaaactctattggatatgattgcaagagagcggaaaggagaagtcgtagacaga
ggcgcaataagaaatgcttgccagatgttaatgattttaggtctcgaaggaagatcagtc
tatgaagaagattttgaggctccttttttggaaatgtctgcagaattttttcagatggaa
agccagaaatttttagcagaaaatagtgcttcagtatatataaagaaagtagaagctaga
attaatgaagaaatagaacgagtgatgcactgccttgacaaatcaacggaagaaccaatt
gtaaaggtggttgaaagggaactcatttccaagcacatgaagactatagtagaaatggag
aattctgggctagtacatatgttgaaaaatggaaagacagaagaccttggttgcatgtac
aagttatttagtcgtgtgccaaatggtttgaaaacaatgtgtgagtgtatgagttcctat
ttgagggagcaaggtaaagctcttgtttctgaagaaggagaaggaaagaatcctgttgac
tatatccagggcttattggatctgaagagtaggttcgatcgcttcctcctggaatcattc
aacaatgaccgtctctttaaacaaactattgcgggtgactttgagtattttctcaacctc
aactccaggtctcctgaatacctctcattatttattgatgataagctgaaaaagggagtc
aaagggctaacagaacaagaagtagaaacaatattggataaagcaatggtcctttttagg
tttatgcaagaaaaagatgtatttgaacgttattataaacaacacttggcaaggagactt
ctcacaaataaaagtgtttctgatgactctgaaaaaaacatgatatctaagttaaagact
gaatgtggatgtcagttcacgtcaaaactggaaggaatgtttagggatatgagcatctca
aacacaacgatggatgaattcaggcaacatctacaggcaactggtgtatctttaggtggt
gttgatcttacagtccgggtgctcacgacaggatattggcccactcagtcagccacacca
aagtgcaacatcccaccagcaccaagacatgcttttgagatattcagaaggttctactta
gccaaacacagtggtcgacagctcacactccagcatcatatgggttctgcagatctcaat
gccacattttatggaccagttaaaaaggaagatggatctgaagttggtgttggaggtgca
caagtaactggctctaatacacggaagcacatattgcaagtttccactttccagatgacc
atattaatgctctttaataatagagaaaaatacacatttgaggaaattcagcaagagaca
gatatccctgaaagagagcttgttagagccctacagtccctcgcctgtggtaaaccaaca
cagcgggttcttacaaaagaacccaaatcaaaggaaatagaaaatggtcatatatttaca
gttaatgatcaattcacatccaaactacacagagtcaagattcaaacagttgctgccaaa
caaggtgaatccgacccagagaggaaagaaacaaggcagaaagtagacgacgacagaaaa
catgagatagaagctgctatagtgcggataatgaaatctagaaagaagatgcagcacaat
gttctagtagcggaggtaactcagcagttgaaggcgcgattcttaccaagtccagttgtt
attaagaaacgtattgaaggacttattgagagagaatatttggcacgaacacctgaggat
cgcaaagtatacacatatgtagcataa
Homo sapiens (human): 8139
Help
Entry
8139 CDS
T01001
Symbol
GAN, GAN1, GIG, KLHL16
Name
(RefSeq) gigaxonin
KO
K10453
kelch-like protein 16 (gigaxonin)
Organism
hsa
Homo sapiens (human)
Network
nt06541
Cytoskeleton in neurons
Element
N01855
Neurofilament regulation, ubiqutination by Gigaxonin
Disease
H01259
Giant axonal neuropathy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04121 Ubiquitin system [BR:
hsa04121
]
8139 (GAN)
Ubiquitin system [BR:
hsa04121
]
Ubiquitin ligases (E3)
Multi subunit type E3
Cul3 complex
Adoptor and target recognizing subunit (BTB)
8139 (GAN)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Kelch_1
BACK
Kelch_KLHDC2_KLHL20_DRC7
Beta-prop_Calicin
BTB
Kelch_FKB95
Beta-prop_ATRN-LZTR1
Beta-prop_FBX42
Kelch_2
NANM
DUF6242_C
BTB_KLHL33
DUF1668
BTB_3
Motif
Other DBs
NCBI-GeneID:
8139
NCBI-ProteinID:
NP_071324
OMIM:
605379
HGNC:
4137
Ensembl:
ENSG00000261609
UniProt:
Q9H2C0
A0A0S2Z4W2
B3KTC3
Structure
PDB
PDBj
LinkDB
All DBs
Position
16:81314962..81390809
Genome browser
AA seq
597 aa
AA seq
DB search
MAEGSAVSDPQHAARLLRALSSFREESRFCDAHLVLDGEEIPVQKNILAAASPYIRTKLN
YNPPKDDGSTYKIELEGISVMVMREILDYIFSGQIRLNEDTIQDVVQAADLLLLTDLKTL
CCEFLEGCIAAENCIGIRDFALHYCLHHVHYLATEYLETHFRDVSSTEEFLELSPQKLKE
VISLEKLNVGNERYVFEAVIRWIAHDTEIRKVHMKDVMSALWVSGLDSSYLREQMLNEPL
VREIVKECSNIPLSQPQQGEAMLANFKPRGYSECIVTVGGEERVSRKPTAAMRCMCPLYD
PNRQLWIELAPLSMPRINHGVLSAEGFLFVFGGQDENKQTLSSGEKYDPDANTWTALPPM
NEARHNFGIVEIDGMLYILGGEDGEKELISMECYDIYSKTWTKQPDLTMVRKIGCYAAMK
KKIYAMGGGSYGKLFESVECYDPRTQQWTAICPLKERRFGAVACGVAMELYVFGGVRSRE
DAQGSEMVTCKSEFYHDEFKRWIYLNDQNLCIPASSSFVYGAVPIGASIYVIGDLDTGTN
YDYVREFKRSTGTWHHTKPLLPSDLRRTGCAALRIANCKLFRLQLQQGLFRIRVHSP
NT seq
1794 nt
NT seq
+upstream
nt +downstream
nt
atggctgagggcagtgccgtgtctgaccctcagcacgccgcgcgtctgctgcgagcgctc
agctctttccgcgaggagtctcgcttctgcgacgcgcacctggtcctcgacggggaggag
atcccggtgcagaagaacatcctggcggcggccagcccgtacatcaggacaaagttaaac
tataatcctccaaaagatgatggatcaacttataagattgaacttgaagggatatcggta
atggttatgagagagatcctggattacatcttcagtgggcagatcaggctaaatgaagat
acaatccaagatgttgttcaggcagctgacctgctgctactgacggaccttaaaaccctg
tgctgtgagtttttggaaggctgcattgctgctgagaactgtattggtatccgtgacttt
gcactacattactgcctccatcacgttcattaccttgccacagaatacctggagactcat
ttccgagacgtcagcagcacggaagaattcttagagctgagtcctcaaaagcttaaagaa
gtgatttctcttgagaagttaaacgttggcaatgaaagatatgtctttgaagcagtaatt
cgatggatagcacatgatacagaaataagaaaggtccacatgaaggatgttatgtcagct
ctgtgggtttcagggttggactccagttatttacgggaacagatgctgaatgaaccatta
gtacgagaaattgtcaaagagtgtagcaatataccgctcagccagccgcagcaaggggag
gcgatgctggccaacttcaaaccccggggctactctgagtgcatcgtgactgttggtgga
gaagagagagtttcacggaaacccacagcagcgatgcgatgcatgtgccctctctatgac
cctaacaggcagctttggatcgaactggcccctttaagcatgccgagaattaaccatgga
gttctctcagcagaaggatttttgtttgtattcgggggccaagatgaaaataagcagact
cttagctcaggagaaaagtatgatccagatgcaaatacatggacagcattgccacctatg
aacgaggcaagacataacttcggaattgtggagatagatgggatgctgtacattttggga
ggagaggatggtgaaaaggagctgatttccatggagtgttacgatatttattctaaaacc
tggacaaagcaacctgatttgaccatggtcagaaagatcggctgctatgcagctatgaaa
aagaaaatctacgccatgggtggaggctcctacggaaagctttttgagtctgtagagtgt
tatgatcccaggacccagcagtggactgccatatgtccactaaaagagaggaggtttgga
gcggtggcctgtggagttgctatggagctgtatgtgtttgggggagtccgaagtcgtgag
gacgcccagggtagcgagatggtaacttgcaagtccgagttctaccatgatgagtttaaa
aggtggatctatcttaacgaccagaatttatgcatccccgccagttcctcttttgtttat
ggagctgtacctataggagccagtatttatgttattggagatcttgatacaggtaccaat
tacgactacgtgcgtgagtttaaaagaagcacaggaacctggcaccacactaaaccactc
cttccatccgaccttcgccgtacaggatgtgcagccttacgcattgcgaattgcaagctt
ttccgcctgcagcttcagcaaggcttattccgtattcgtgttcattccccttga
Homo sapiens (human): 7321
Help
Entry
7321 CDS
T01001
Symbol
UBE2D1, E2(17)KB1, SFT, UBC4/5, UBCH5, UBCH5A
Name
(RefSeq) ubiquitin conjugating enzyme E2 D1
KO
K06689
ubiquitin-conjugating enzyme E2 D [EC:
2.3.2.23
]
Organism
hsa
Homo sapiens (human)
Pathway
hsa03083
Polycomb repressive complex
hsa04120
Ubiquitin mediated proteolysis
hsa04141
Protein processing in endoplasmic reticulum
hsa05131
Shigellosis
Network
nt06541
Cytoskeleton in neurons
Element
N01854
Neurofilament regulation, ubiqutination by TRIM2
N01855
Neurofilament regulation, ubiqutination by Gigaxonin
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09123 Folding, sorting and degradation
04141 Protein processing in endoplasmic reticulum
7321 (UBE2D1)
04120 Ubiquitin mediated proteolysis
7321 (UBE2D1)
09126 Chromosome
03083 Polycomb repressive complex
7321 (UBE2D1)
09160 Human Diseases
09171 Infectious disease: bacterial
05131 Shigellosis
7321 (UBE2D1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04121 Ubiquitin system [BR:
hsa04121
]
7321 (UBE2D1)
Enzymes [BR:
hsa01000
]
2. Transferases
2.3 Acyltransferases
2.3.2 Aminoacyltransferases
2.3.2.23 E2 ubiquitin-conjugating enzyme
7321 (UBE2D1)
Ubiquitin system [BR:
hsa04121
]
Ubiquitin-conjugating enzymes (E2)
Ubiquitin-conjugating enzymes
7321 (UBE2D1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
UQ_con
RWD
UEV
Motif
Other DBs
NCBI-GeneID:
7321
NCBI-ProteinID:
NP_003329
OMIM:
602961
HGNC:
12474
Ensembl:
ENSG00000072401
UniProt:
P51668
Structure
PDB
PDBj
LinkDB
All DBs
Position
10:58335006..58370748
Genome browser
AA seq
147 aa
AA seq
DB search
MALKRIQKELSDLQRDPPAHCSAGPVGDDLFHWQATIMGPPDSAYQGGVFFLTVHFPTDY
PFKPPKIAFTTKIYHPNINSNGSICLDILRSQWSPALTVSKVLLSICSLLCDPNPDDPLV
PDIAQIYKSDKEKYNRHAREWTQKYAM
NT seq
444 nt
NT seq
+upstream
nt +downstream
nt
atggcgctgaagaggattcagaaagaattgagtgatctacagcgcgatccacctgctcac
tgttcagctggacctgtgggagatgacttgttccactggcaagccactattatggggcct
cctgatagcgcatatcaaggtggagtcttctttctcactgtacattttccgacagattat
ccttttaaaccaccaaagattgctttcacaacaaaaatttaccatccaaacataaacagt
aatggaagtatttgtctcgatattctgaggtcacaatggtcaccagctctgactgtatca
aaagttttattgtccatatgttctctactttgtgatcctaatccagatgaccccttagta
ccagatattgcacaaatctataaatcagacaaagaaaaatacaacagacatgcaagagaa
tggactcagaaatatgcaatgtaa
DBGET
integrated database retrieval system