KEGG T01001: 2177

Homo sapiens (human): 2177

Entry

2177              CDS       T01001

Symbol

FANCD2, FA-D2, FA4, FACD, FAD, FAD2, FANCD

Name

(RefSeq) FA complementation group D2

K10891

fanconi anemia group D2 protein

Organism

hsa Homo sapiens (human)

Pathway

hsa03460

Fanconi anemia pathway

Network

nt06508 Interstrand crosslink repair

Element

N01464

Fanconi anemia pathway

N01465

Lesion bypass by TLS and DSB formation

N01466

Homologous recombination in ICLR

Disease

H00238

Fanconi anemia

Brite

KEGG Orthology (KO) [BR:hsa00001]
09120 Genetic Information Processing
  09124 Replication and repair
   03460 Fanconi anemia pathway
    2177 (FANCD2)
09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03400 DNA repair and recombination proteins [BR:hsa03400]
    2177 (FANCD2)
DNA repair and recombination proteins [BR:hsa03400]
Eukaryotic type
  DSBR (double strand breaks repair)
   FA (Fanconi anemia) pathway
    FANCD2-I complex
     2177 (FANCD2)

SSDB

Motif

Pfam:

FancD2 FANCI_S2 Trans_coact

Other DBs

NCBI-GeneID:

NCBI-ProteinID:

OMIM:

HGNC:

Ensembl:

UniProt:

Structure

LinkDB

Position

3:10026437..10101932

AA seq 1451 aa
MVSKRRLSKSEDKESLTEDASKTRKQPLSKKTKKSHIANEVEENDSIFVKLLKISGIILK
TGESQNQLAVDQIAFQKKLFQTLRRHPSYPKIIEEFVSGLESYIEDEDSFRNCLLSCERL
QDEEASMGASYSKSLIKLLLGIDILQPAIIKTLFEKLPEYFFENKNSDEINIPRLIVSQL
KWLDRVVDGKDLTTKIMQLISIAPENLQHDIITSLPEILGDSQHADVGKELSDLLIENTS
LTVPILDVLSSLRLDPNFLLKVRQLVMDKLSSIRLEDLPVIIKFILHSVTAMDTLEVISE
LREKLDLQHCVLPSRLQASQVKLKSKGRASSSGNQESSGQSCIILLFDVIKSAIRYEKTI
SEAWIKAIENTASVSEHKVFDLVMLFIIYSTNTQTKKYIDRVLRNKIRSGCIQEQLLQST
FSVHYLVLKDMCSSILSLAQSLLHSLDQSIISFGSLLYKYAFKFFDTYCQQEVVGALVTH
ICSGNEAEVDTALDVLLELVVLNPSAMMMNAVFVKGILDYLDNISPQQIRKLFYVLSTLA
FSKQNEASSHIQDDMHLVIRKQLSSTVFKYKLIGIIGAVTMAGIMAADRSESPSLTQERA
NLSDEQCTQVTSLLQLVHSCSEQSPQASALYYDEFANLIQHEKLDPKALEWVGHTICNDF
QDAFVVDSCVVPEGDFPFPVKALYGLEEYDTQDGIAINLLPLLFSQDFAKDGGPVTSQES
GQKLVSPLCLAPYFRLLRLCVERQHNGNLEEIDGLLDCPIFLTDLEPGEKLESMSAKERS
FMCSLIFLTLNWFREIVNAFCQETSPEMKGKVLTRLKHIVELQIILEKYLAVTPDYVPPL
GNFDVETLDITPHTVTAISAKIRKKGKIERKQKTDGSKTSSSDTLSEEKNSECDPTPSHR
GQLNKEFTGKEEKTSLLLHNSHAFFRELDIEVFSILHCGLVTKFILDTEMHTEATEVVQL
GPPELLFLLEDLSQKLESMLTPPIARRVPFLKNKGSRNIGFSHLQQRSAQEIVHCVFQLL
TPMCNHLENIHNYFQCLAAENHGVVDGPGVKVQEYHIMSSCYQRLLQIFHGLFAWSGFSQ
PENQNLLYSALHVLSSRLKQGEHSQPLEELLSQSVHYLQNFHQSIPSFQCALYLIRLLMV
ILEKSTASAQNKEKIASLARQFLCRVWPSGDKEKSNISNDQLHALLCIYLEHTESILKAI
EEIAGVGVPELINSPKDASSSTFPTLTRHTFVVFFRVMMAELEKTVKKIEPGTAADSQQI
HEEKLLYWNMAVRDFSILINLIKVFDSHPVLHVCLKYGRLFVEAFLKQCMPLLDFSFRKH
REDVLSLLETFQLDTRLLHHLCGHSKIHQDTRLTQHVPLLKKTLELLVCRVKAMLTLNNC
REAFWLGNLKNRDLQGEEIKSQNSQESTADESEDDMSSQASKSKATEDGEEDEVSAGEKE
QDSDESYDDSD

NT seq 4356 nt +upstreamnt +downstreamnt
atggtttccaaaagaagactgtcaaaatctgaggataaagagagcctgacagaagatgcc
tccaaaaccaggaagcaaccactttccaaaaagacaaagaaatctcatattgctaatgaa
gttgaagaaaatgacagcatctttgtaaagcttcttaagatatcaggaattattcttaaa
acgggagagagtcagaatcaactagctgtggatcaaatagctttccaaaagaagctcttt
cagaccctgaggagacacccttcctatcccaaaataatagaagaatttgttagtggcctg
gagtcttacattgaggatgaagacagtttcaggaactgccttttgtcttgtgagcgtctg
caggatgaggaagccagtatgggtgcatcttattctaagagtctcatcaaactgcttctg
gggattgacatactgcagcctgccattatcaaaaccttatttgagaagttgccagaatat
ttttttgaaaacaagaacagtgatgaaatcaacatacctcgactcattgtcagtcaacta
aaatggcttgacagagttgtggatggcaaggacctcaccaccaagatcatgcagctgatc
agtattgctccagagaacctgcagcatgacatcatcaccagcctacctgagatcctaggg
gattcccagcacgctgatgtggggaaagaactcagtgacctactgatagagaatacttca
ctcactgtcccaatcctggatgtcctttcaagcctccgacttgacccaaacttcctattg
aaggttcgccagttggtgatggataagttgtcgtctattagattggaggatttacctgtg
ataataaagttcattcttcattccgtaacagccatggatacacttgaggtaatttctgag
cttcgggagaagttggatctgcagcattgtgttttgccatcacggttacaggcttcccaa
gtaaagttgaaaagtaaaggacgagcaagttcctcaggaaatcaagaaagcagcggtcag
agctgtattattctcctctttgatgtaataaagtcagctattagatatgagaaaaccatt
tcagaagcctggattaaggcaattgaaaacactgcctcagtatctgaacacaaggtgttt
gacctggtgatgcttttcatcatctatagcaccaatactcagacaaagaagtacattgac
agggtgctaagaaataagattcgatcaggctgcattcaagaacagctgctccagagtaca
ttctctgttcattacttagttcttaaggatatgtgttcatccattctgtcgctggctcag
agtttgcttcactctctagaccagagtataatttcatttggcagtctcctatacaaatat
gcatttaagttttttgacacgtactgccagcaggaagtggttggtgccttagtgacccat
atctgcagtgggaatgaagctgaagttgatactgccttagatgtccttctagagttggta
gtgttaaacccatctgctatgatgatgaatgctgtctttgtaaagggcattttagattat
ctggataacatatcccctcagcaaatacgaaaactcttctatgttctcagcacactggca
tttagcaaacagaatgaagccagcagccacatccaggatgacatgcacttggtgataaga
aagcagctctctagcaccgtattcaagtacaagctcattgggattattggtgctgtgacc
atggctggcatcatggcggcagacagaagtgaatcacctagtttgacccaagagagagcc
aacctgagcgatgagcagtgcacacaggtgacctccttgttgcagttggttcattcctgc
agtgagcagtctcctcaggcctctgcactttactatgatgaatttgccaacctgatccaa
catgaaaagctggatccaaaagccctggaatgggttgggcataccatctgtaatgatttc
caggatgccttcgtagtggactcctgtgttgttccggaaggtgactttccatttcctgtg
aaagcactgtacggactggaagaatacgacactcaggatgggattgccataaacctcctg
ccgctgctgttttctcaggactttgcaaaagatgggggtccggtgacctcacaggaatca
ggccaaaaattggtgtctccgctgtgcctggctccgtatttccggttactgagactttgt
gtggagagacagcataacggaaacttggaggagattgatggtctactagattgtcctata
ttcctaactgacctggagcctggagagaagttggagtccatgtctgctaaagagcgttca
ttcatgtgttctctcatatttcttactctcaactggttccgagagattgtaaatgccttc
tgccaggaaacatcacctgagatgaaggggaaggtgctcactcggttaaagcacattgta
gaattgcaaataatcctggaaaagtacttggcagtcaccccagactatgtccctcctctt
ggaaactttgatgtggaaactttagatataacacctcatactgttactgctatttcagca
aaaatcagaaagaaaggaaaaatagaaaggaaacaaaaaacagatggcagcaagacatcc
tcctctgacacactttcagaagagaaaaattcagaatgtgaccctacgccatctcataga
ggccagctaaacaaggagttcacagggaaggaagaaaagacatcattgttactacataat
tcccatgcttttttccgagagctggacattgaggtcttctctattctacattgtggactt
gtgacgaagttcatcttagatactgaaatgcacactgaagctacagaagttgtgcaactt
gggccccctgagctgcttttcttgctggaagatctctcccagaagctggagagtatgctg
acacctcctattgccaggagagtcccctttctcaagaacaaaggaagccggaatattgga
ttctcacatctccaacagagatctgcccaagaaattgttcattgtgtttttcaactgctg
accccaatgtgtaaccacctggagaacattcacaactattttcagtgtttagctgctgag
aatcacggtgtagttgatggaccaggagtgaaagttcaggagtaccacataatgtcttcc
tgctatcagaggctgctgcagatttttcatgggctttttgcttggagtggattttctcaa
cctgaaaatcagaatttactgtattcagccctccatgtccttagtagccgactgaaacag
ggagaacacagccagcctttggaggaactactcagccagagcgtccattacttgcagaat
ttccatcaaagcattcccagtttccagtgtgctctttatctcatcagacttttgatggtt
attttggagaaatcaacagcttctgctcagaacaaagaaaaaattgcttcccttgccaga
caattcctctgtcgggtgtggccaagtggggataaagagaagagcaacatctctaatgac
cagctccatgctctgctctgtatctacctggagcacacagagagcattctgaaggccata
gaggagattgctggtgttggtgtcccagaactgatcaactctcctaaagatgcatcttcc
tccacattccctacactgaccaggcatacttttgttgttttcttccgtgtgatgatggct
gaactagagaagacggtgaaaaaaattgagcctggcacagcagcagactcgcagcagatt
catgaagagaaactcctctactggaacatggctgttcgagacttcagtatcctcatcaac
ttgataaaggtatttgatagtcatcctgttctgcatgtatgtttgaagtatgggcgtctc
tttgtggaagcatttctgaagcaatgtatgccgctcctagacttcagttttagaaaacac
cgggaagatgttctgagcttactggaaaccttccagttggacacaaggctgcttcatcac
ctgtgtgggcattccaagattcaccaggacacgagactcacccaacatgtgcctctgctc
aaaaagaccctggaacttttagtttgcagagtcaaagctatgctcactctcaacaattgt
agagaggctttctggctgggcaatctaaaaaaccgggacttgcagggtgaagagattaag
tcccaaaattcccaggagagcacagcagatgagagtgaggatgacatgtcatcccaggcc
tccaagagcaaagccactgaggatggtgaagaagacgaagtaagtgctggagaaaaggag
caagatagtgatgagagttatgatgactctgattag

Homo sapiens (human): 55215

Entry

55215             CDS       T01001

Symbol

FANCI, KIAA1794

Name

(RefSeq) FA complementation group I

K10895

fanconi anemia group I protein

Organism

hsa Homo sapiens (human)

Pathway

hsa03460

Fanconi anemia pathway

Network

nt06508 Interstrand crosslink repair

Element

N01464

Fanconi anemia pathway

N01465

Lesion bypass by TLS and DSB formation

N01466

Homologous recombination in ICLR

Disease

H00238

Fanconi anemia

Brite

KEGG Orthology (KO) [BR:hsa00001]
09120 Genetic Information Processing
  09124 Replication and repair
   03460 Fanconi anemia pathway
    55215 (FANCI)
09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03400 DNA repair and recombination proteins [BR:hsa03400]
    55215 (FANCI)
DNA repair and recombination proteins [BR:hsa03400]
Eukaryotic type
  DSBR (double strand breaks repair)
   FA (Fanconi anemia) pathway
    FANCD2-I complex
     55215 (FANCI)

SSDB

Motif

Pfam:

FANCI_S4 FANCI_HD2 FANCI_S1 FANCI_S3 FANCI_S2 FANCI_HD1 FANCI_S1-cap DUF3894 Ribul_P_3_epim DUF3972

Other DBs

NCBI-GeneID:

NCBI-ProteinID:

OMIM:

HGNC:

Ensembl:

UniProt:

Structure

LinkDB

Position

15:89243979..89317259

AA seq 1328 aa
MDQKILSLAAEKTADKLQEFLQTLREGDLTNLLQNQAVKGKVAGALLRAIFKGSPCSEEA
GTLRRRKIYTCCIQLVESGDLQKEIASEIIGLLMLEAHHFPGPLLVELANEFISAVREGS
LVNGKSLELLPIILTALATKKENLAYGKGVLSGEECKKQLINTLCSGRWDQQYVIQLTSM
FKDVPLTAEEVEFVVEKALSMFSKMNLQEIPPLVYQLLVLSSKGSRKSVLEGIIAFFSAL
DKQHNEEQSGDELLDVVTVPSGELRHVEGTIILHIVFAIKLDYELGRELVKHLKVGQQGD
SNNNLSPFSIALLLSVTRIQRFQDQVLDLLKTSVVKSFKDLQLLQGSKFLQNLVPHRSYV
STMILEVVKNSVHSWDHVTQGLVELGFILMDSYGPKKVLDGKTIETSPSLSRMPNQHACK
LGANILLETFKIHEMIRQEILEQVLNRVVTRASSPISHFLDLLSNIVMYAPLVLQSCSSK
VTEAFDYLSFLPLQTVQRLLKAVQPLLKVSMSMRDCLILVLRKAMFANQLDARKSAVAGF
LLLLKNFKVLGSLSSSQCSQSLSVSQVHVDVHSHYNSVANETFCLEIMDSLRRCLSQQAD
VRLMLYEGFYDVLRRNSQLANSVMQTLLSQLKQFYEPKPDLLPPLKLEACILTQGDKISL
QEPLDYLLCCIQHCLAWYKNTVIPLQQGEEEEEEEEAFYEDLDDILESITNRMIKSELED
FELDKSADFSQSTSIGIKNNICAFLVMGVCEVLIEYNFSISSFSKNRFEDILSLFMCYKK
LSDILNEKAGKAKTKMANKTSDSLLSMKFVSSLLTALFRDSIQSHQESLSVLRSSNEFMR
YAVNVALQKVQQLKETGHVSGPDGQNPEKIFQNLCDITRVLLWRYTSIPTSVEESGKKEK
GKSISLLCLEGLQKIFSAVQQFYQPKIQQFLRALDVTDKEGEEREDADVSVTQRTAFQIR
QFQRSLLNLLSSQEEDFNSKEALLLVTVLTSLSKLLEPSSPQFVQMLSWTSKICKENSRE
DALFCKSLMNLLFSLHVSYKSPVILLRDLSQDIHGHLGDIDQDVEVEKTNHFAIVNLRTA
APTVCLLVLSQAEKVLEEVDWLITKLKGQVSQETLSEEASSQATLPNQPVEKAIIMQLGT
LLTFFHELVQTALPSGSCVDTLLKDLCKMYTTLTALVRYYLQVCQSSGGIPKNMEKLVKL
SGSHLTPLCYSFISYVQNKSKSLNYTGEKKEKPAAVATAMARVLRETKPIPNLIFAIEQY
EKFLIHLSKKSKVNLMQHMKLSTSRDFKIKGNILDMVLREDGEDENEEGTASEHGGQNKE
PAKKKRKK

NT seq 3987 nt +upstreamnt +downstreamnt
atggaccagaagattttatctctagcagcagaaaaaacagcagacaaactgcaagaattt
cttcaaaccctgagagaaggtgatttgactaatctccttcagaatcaagcagtgaaagga
aaagttgctggagcactcctgagagccatcttcaaaggttccccctgctctgaggaagct
ggaacacttaggagacgtaagatatacacttgttgtatccagttggtggaatcgggggat
ttgcagaaagaaatagcgtctgagatcataggattactgatgctggaggctcaccatttt
ccaggaccattattggttgaattagccaatgagtttattagtgctgtcagagaaggcagc
ctagtgaatggaaaatctttggagttactacctatcattctcactgccctggctacgaaa
aaggaaaatctggcttatggaaaaggtgtactgagtggggaagaatgtaagaaacagttg
attaacaccctgtgttctggcaggtgggatcagcaatatgtaatccaactcacctccatg
ttcaaggatgtccctctgactgcagaagaggtggaatttgtggtggaaaaagcattgagc
atgttctccaagatgaatcttcaagaaataccacctttggtctatcagcttctggttctc
tcctccaagggaagcagaaagagtgttttggaaggaatcatagccttcttcagtgcacta
gataagcagcacaatgaggaacagagtggtgacgagctattggatgttgtcactgtgcca
tcaggtgaacttcgtcatgtggaaggcaccattattctacacattgtgtttgccatcaaa
ttggactatgaactaggcagagaactcgtgaaacacttaaaggtaggacagcaaggagat
tccaataataacttaagtcccttcagcattgctcttcttctgtctgtaacaagaatacaa
agatttcaggaccaggtgcttgatcttttaaagacttcggttgtaaagagctttaaggat
cttcaactcctccaaggctcaaaatttcttcagaatctagttcctcatagatcttatgtt
tcaaccatgatcttggaagtagtgaagaatagcgttcatagctgggaccatgttactcag
ggcctcgtagaacttggtttcattttgatggattcatatgggccaaagaaggttcttgat
ggaaaaactattgaaaccagcccaagtctttctagaatgccaaaccagcatgcatgtaag
ctcggagctaatatcctgttggaaacttttaagatccatgagatgatcagacaagaaatt
ttggagcaggtcctcaacagggttgttaccagagcatcttctcccatcagtcatttctta
gacctgctttcaaatatcgtcatgtatgcacccttagttcttcaaagttgttcttctaaa
gtcacagaagcttttgactatttgtcctttctgccccttcagactgtacaaaggctgctt
aaggcagtgcagccccttctcaaagtcagcatgtcaatgagagactgcttgatacttgtc
cttcggaaagctatgtttgccaaccagcttgatgcccgaaaatctgcagttgctgggttt
ttgctgctcctgaagaactttaaagttttaggcagcctgtcatcctctcagtgcagtcag
tctctcagtgtcagtcaggttcatgtggatgttcacagccattacaattctgtcgccaat
gaaactttttgccttgagatcatggatagtttgaggagatgcttaagccagcaagctgat
gttcgactcatgctttatgaggggttttatgatgttcttcgaaggaactctcagctggct
aattcagtcatgcaaactctgctctcacagttaaaacagttctatgagccaaaacctgat
ctgctgcctcctctgaaattagaagcttgtattctgacccaaggagataagatctctcta
caagaaccactggattatctgctgtgttgtattcagcattgtttggcctggtataagaat
acagtcatacccttacagcagggagaggaggaagaggaggaggaagaggcattctacgaa
gacctagatgatatattggagtccattactaatagaatgattaagagtgagctggaagac
tttgaactggataaatcagcagatttttctcagagcaccagtattggcataaaaaataat
atctgtgcttttcttgtgatgggagtttgtgaggttttaatagaatacaatttctccata
agtagtttcagtaagaataggtttgaggacattctgagcttatttatgtgttacaaaaaa
ctctctgacattcttaatgaaaaagcgggtaaagccaaaactaaaatggccaacaagaca
agtgatagtcttttgtccatgaaatttgtgtccagtcttctcactgctcttttcagggat
agtatccaaagccaccaagaaagcctttctgttctcaggtccagcaatgagtttatgcgc
tatgcagtgaatgtagctctgcagaaagtacagcagctaaaggaaacagggcatgtgagt
ggccctgatggccaaaacccagaaaagatctttcagaacctctgtgacataactcgagtc
ttgctatggagatacacttcaattcctacttcagtggaagagtcgggaaagaaagagaaa
ggaaagagcatctcactgctgtgcttggagggtttacagaaaatattcagtgctgtgcaa
cagttctatcagcccaagattcagcagtttctcagagctctggatgtcacagataaggaa
ggagaagagagagaagatgcagatgtcagtgtcactcagagaacagcattccagatccgg
caatttcagaggtccttgttgaatttacttagcagtcaagaggaagattttaatagcaaa
gaagccctcctgctagtcacggttcttaccagtttgtccaagttactggagccctcctct
cctcagtttgtgcagatgttatcctggacatcaaagatttgcaaggaaaacagccgggag
gatgccttgttttgcaagagcttgatgaacttgctcttcagcctgcatgtttcgtataag
agtcctgtcattctgctgcgtgacttgtcccaggatatccacgggcatctgggagatata
gaccaggatgtagaggtggagaaaacaaaccactttgcaatagtgaatttgagaacggct
gcccccactgtctgtttacttgttctgagtcaggccgagaaggttctagaagaagtggac
tggctaatcaccaagcttaagggacaagtgagccaagaaaccttatcagaagaggcctct
tctcaggcaaccctaccaaatcagcctgttgagaaagctatcatcatgcaactgggaact
ctgcttacatttttccacgagctggtgcagacagctctgccatcaggcagctgtgtggac
accttgttaaaggacttgtgcaaaatgtacaccacacttacagcccttgtcagatattat
ctccaggtgtgtcagagctccggaggaattccaaaaaatatggaaaagctggtgaagctg
tctggttctcatctgacccccctgtgttattctttcatttcttacgtacagaataagagt
aagagcctgaactatacgggagagaaaaaggagaaacctgctgccgttgccacagccatg
gccagagttcttcgggaaaccaagccaatccctaacctcatctttgccatagaacagtat
gaaaaatttctcatccacctttctaagaagtccaaggtgaacctgatgcagcacatgaag
ctcagcacctcacgagacttcaagatcaaaggaaacatcctagacatggttcttcgagag
gatggtgaagatgaaaatgaagagggcactgcatcagagcatgggggacagaacaaagaa
ccagccaagaagaaaaggaaaaaataa

Homo sapiens (human): 7314

Entry

7314              CDS       T01001

Symbol

UBB, HEL-S-50

Name

(RefSeq) ubiquitin B

K04551

ubiquitin B

Organism

hsa Homo sapiens (human)

Pathway

hsa04120

Ubiquitin mediated proteolysis

hsa04137

Mitophagy - animal

hsa04140

Autophagy - animal

hsa05012

Parkinson disease

hsa05022

Pathways of neurodegeneration - multiple diseases

hsa05131

Shigellosis

hsa05167

Kaposi sarcoma-associated herpesvirus infection

Network

nt06460  Alzheimer disease
nt06461  Huntington disease
nt06463  Parkinson disease
nt06464  Amyotrophic lateral sclerosis
nt06465  Prion disease
nt06466  Pathways of neurodegeneration
nt06506  Double-strand break repair
nt06508  Interstrand crosslink repair
nt06509  DNA replication
nt06523  Epigenetic regulation by Polycomb complexes
nt06532  Autophagy

Element

N01027

UCHL1-mediated hydrolysis

N01028

Mutation-inactivated UCHL1 to UCHL1-mediated hydrolysis

N01029

26S proteasome-mediated protein degradation

N01144

Mutation-caused aberrant SOD1 to 26S proteasome-mediated protein degradation

N01145

Mutation-inactivated VCP to 26S proteasome-mediated protein degradation

N01146

Mutation-inactivated UBQLN2 to 26S proteasome-mediated protein degradation

N01464

Fanconi anemia pathway

N01465

Lesion bypass by TLS and DSB formation

N01466

Homologous recombination in ICLR

N01473

DNA replication termination

N01474

TRAIP-dependent replisome disassembly

N01577

Gene silencing by methylation of H3K27 and ubiquitination of H2AK119

N01586

Activation of PRC2.2 by ubiquitination of H2AK119

N01614

Activation of PRC2.2 by ubiquitination of H2AK119 in germline genes

N01636

Loading of the SMC5-SMC6 complex

N01716

Autophagy-vesicle nucleation/elongation/maturation, sequestosome-1-like receptor

Brite

KEGG Orthology (KO) [BR:hsa00001]
09120 Genetic Information Processing
  09123 Folding, sorting and degradation
   04120 Ubiquitin mediated proteolysis
    7314 (UBB)
09140 Cellular Processes
  09141 Transport and catabolism
   04140 Autophagy - animal
    7314 (UBB)
   04137 Mitophagy - animal
    7314 (UBB)
09160 Human Diseases
  09172 Infectious disease: viral
   05167 Kaposi sarcoma-associated herpesvirus infection
    7314 (UBB)
  09171 Infectious disease: bacterial
   05131 Shigellosis
    7314 (UBB)
  09164 Neurodegenerative disease
   05012 Parkinson disease
    7314 (UBB)
   05022 Pathways of neurodegeneration - multiple diseases
    7314 (UBB)
09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04121 Ubiquitin system [BR:hsa04121]
    7314 (UBB)
  09183 Protein families: signaling and cellular processes
   04147 Exosome [BR:hsa04147]
    7314 (UBB)
Ubiquitin system [BR:hsa04121]
Ubiquitins and ubiquitin-like proteins
  Ubiquitins
   7314 (UBB)
Exosome [BR:hsa04147]
Exosomal proteins
  Exosomal proteins of breast milk
   7314 (UBB)
  Exosomal proteins of other body fluids (saliva and urine)
   7314 (UBB)
  Exosomal proteins of colorectal cancer cells
   7314 (UBB)
  Exosomal proteins of bladder cancer cells
   7314 (UBB)

SSDB

Motif

Pfam:

ubiquitin Rad60-SLD Ubiquitin_2 DUF2604 Rad60-SLD_2 TBK1_ULD Ubiquitin_5 Dsc3_N OTU1_UBXL

Other DBs

NCBI-GeneID:

NCBI-ProteinID:

OMIM:

HGNC:

Ensembl:

UniProt:

Structure

LinkDB

Position

17:16380779..16382745

AA seq 229 aa
MQIFVKTLTGKTITLEVEPSDTIENVKAKIQDKEGIPPDQQRLIFAGKQLEDGRTLSDYN
IQKESTLHLVLRLRGGMQIFVKTLTGKTITLEVEPSDTIENVKAKIQDKEGIPPDQQRLI
FAGKQLEDGRTLSDYNIQKESTLHLVLRLRGGMQIFVKTLTGKTITLEVEPSDTIENVKA
KIQDKEGIPPDQQRLIFAGKQLEDGRTLSDYNIQKESTLHLVLRLRGGC

NT seq 690 nt +upstreamnt +downstreamnt
atgcagatcttcgtgaaaacccttaccggcaagaccatcacccttgaggtggagcccagt
gacaccatcgaaaatgtgaaggccaagatccaggataaggaaggcattccccccgaccag
cagaggctcatctttgcaggcaagcagctggaagatggccgtactctttctgactacaac
atccagaaggagtcgaccctgcacctggtcctgcgtctgagaggtggtatgcagatcttc
gtgaagaccctgaccggcaagaccatcaccctggaagtggagcccagtgacaccatcgaa
aatgtgaaggccaagatccaggataaagaaggcatccctcccgaccagcagaggctcatc
tttgcaggcaagcagctggaagatggccgcactctttctgactacaacatccagaaggag
tcgaccctgcacctggtcctgcgtctgagaggtggtatgcagatcttcgtgaagaccctg
accggcaagaccatcactctggaggtggagcccagtgacaccatcgaaaatgtgaaggcc
aagatccaagataaagaaggcatcccccccgaccagcagaggctcatctttgcaggcaag
cagctggaagatggccgcactctttctgactacaacatccagaaagagtcgaccctgcac
ctggtcctgcgcctgaggggtggctgttaa

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