Protein Cyld

URN urn:agi-llid:1540
Total Entities 0
Connectivity 276
Name Cyld
Description cylindromatosis (turban tumor syndrome)
Notes This gene is encodes a cytoplasmic protein with three cytoskeletal-associated protein-glycine-conserved (CAP-GLY) domains that functions as a deubiquitinating enzyme. Mutations in this gene have been associated with cylindromatosis, multiple familial trichoepithelioma, and Brooke-Spiegler syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

GO Molecular Function proline-rich region binding
protein kinase binding
metal ion binding
zinc ion binding
hydrolase activity
peptidase activity
ubiquitin thiolesterase activity
cysteine-type peptidase activity
ubiquitin-specific protease activity
structural constituent of ribosome

GO Cellular Component membrane
microtubule
cytoplasmic microtubule
extrinsic to internal side of plasma membrane
ribosome
midbody
plasma membrane
cytoplasm
perinuclear region of cytoplasm
cytosol
cytoskeleton

GO Biological Process cell cycle
regulation of microtubule cytoskeleton organization
regulation of mitotic cell cycle
negative regulation of canonical Wnt receptor signaling pathway
positive regulation of extrinsic apoptotic signaling pathway
negative regulation of NF-kappaB import into nucleus
nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway
nucleotide-binding oligomerization domain containing signaling pathway
Wnt receptor signaling pathway
negative regulation of NF-kappaB transcription factor activity
induction of apoptosis
translation
protein K63-linked deubiquitination
ubiquitin-dependent protein catabolic process
innate immune response
negative regulation of type I interferon production
proteolysis

Pathway nuclear factor kappa B signaling pathway
tumor necrosis factor signaling pathway
tumor necrosis factor mediated signaling pathway

Group cell cycle
regulation of microtubule cytoskeleton organization
regulation of mitotic cell cycle
negative regulation of canonical Wnt receptor signaling pathway
positive regulation of extrinsic apoptotic signaling pathway
negative regulation of NF-kappaB import into nucleus
nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway
nucleotide-binding oligomerization domain containing signaling pathway
Wnt receptor signaling pathway
negative regulation of NF-kappaB transcription factor activity
induction of apoptosis
translation
protein K63-linked deubiquitination
ubiquitin-dependent protein catabolic process
innate immune response
negative regulation of type I interferon production
proteolysis
proline-rich region binding
protein kinase binding
metal ion binding
zinc ion binding
hydrolase activity
peptidase activity
ubiquitin thiolesterase activity
cysteine-type peptidase activity
ubiquitin-specific protease activity
structural constituent of ribosome
membrane
microtubule
cytoplasmic microtubule
extrinsic to internal side of plasma membrane
ribosome
midbody
plasma membrane
cytoplasm
perinuclear region of cytoplasm
cytosol
cytoskeleton

MedScan ID 1540
649965

Hugo ID 2584

Human chromosome position 16q12.1

GenBank ID NC_000016
NM_015247
NP_056062
NM_001042355
NP_001035814
NM_001042412
NP_001035877
NG_012061
NC_018927
AC_000148
AC007728
CH471092
EAW82768
EAW82769
EAW82770
EAW82771
EAW82772
EAW82773
CQ834224
CAH05327
AF161542
AAF29029
AJ250014
CAB93533
AK000187
AK024212
BAG51271
AK024348
BAG51293
AK056226
AK225202
AK292975
BAF85664
AK310832
AL050166
BC012342
AAH12342
BI458962
BX642061
DA157717
DA785459
DA940312
DB119480
FN823255
CBL94217
Q9NQC7
NC_000074
NM_001128171
NP_001121643
NM_001128170
NP_001121642
NM_173369
NP_775545
NM_001128169
NP_001121641
AC_000030
AC138025
AC156937
CH466525
EDL11060
AK008239
AK013508
AK039054
BAC30222
AK041535
AK042764
BAC31357
AK048183
AK122389
BAC65671
AK133479
BAE21677
AK134926
BAE22340
AK147204
AK147426
AK167424
BAE39512
BC023702
BC024596
BC028885
BC042438
AAH42438
BC049879
AAH49879
Q80TQ2
NC_005118
NM_001017380
NP_001017380
AC_000087
CH474037
EDL87530
AY383658
AAQ96216
BC082001
AAH82001
Q66H62

LocusLink ID 1540
74256
312937
100360670

Alias EAC
MFT
SBS
TEM
BRSS
CDMT
MFT1
CYLD1
CYLDI
USPL2
HSPC057
ubiquitin carboxyl-terminal hydrolase CYLD
ubiquitin thioesterase CYLD
deubiquitinating enzyme CYLD
ubiquitin thiolesterase CYLD
ubiquitin specific peptidase like 2
ubiquitin-specific-processing protease CYLD
probable ubiquitin carboxyl-terminal hydrolase CYLD
mKIAA0849
2010013M14Rik
2900009M21Rik
C130039D01Rik
Rp1
Rp1h
LRRGT00003
retinitis pigmentosa 1 homolog
Kiaa0849
FLJ78684
Spiegler-Brooke syndrome gene
multiple familial trichoepithelioma gene
Spiegler-Brooke syndrome protein
turban tumour syndrome protein
turban tumor syndrome gene
FLJ31664
turban tumour syndrome gene
cylindromatosis I
ubiquitin-specific-processing proteinase CYLD
turban tumor syndrome protein
2010013M14
2900009M21
C130039D01
Cyld
CYLD I
FLJ20180
cylindromatosis (turban tumor syndrome) gene
cylindromatosis (turban tumor syndrome) protein
cylindromatosis (turban tumour syndrome) gene
cylindromatosis (turban tumour syndrome) protein
cylindromatosis 1
cylindromatosis gene
cylindromatosis protein
LOC100360670
probable ubiquitin carboxyl-terminal hydrolase CYLD-like

Organism Homo sapiens
Mus musculus
Rattus norvegicus

OMIM ID 605018
132700
601606
605041

Unigene ID Hs.578973
Mm.490395
Rn.128760
Rn.168938

KEGG ID hsa:1540
mmu:74256
rno:312937

Swiss-Prot Accession Q9NQC7
Q3V028
Q80TQ2
Q66H62
Q80VB3
Q8BXZ3
Q8BYL9
Q8CGB0
O94934
Q7L3N6
Q96EH0
Q9NZX9

EC Number 3.4.19.12

GO ID 0070064
0019901
0004221
0004843
0008270
0016055
0007049
0006917
0045087
0042347
0032088
0090090
0032480
0035872
0070423
2001238
0070536
0070507
0007346
0006511
0005881
0005829
0031234
0030496
0048471
0008234
0016787
0046872
0008233
0006508
0005737
0005856
0016020
0005874
0005886
0003735
0006412
0005840

Swiss-Prot ID CYLD_MOUSE
CYLD_RAT
CYLD_HUMAN

Cell Localization Cytoplasm
perinuclear region
cytoskeleton
Cell membrane

IPI ID IPI00277703
IPI00463126
IPI00875098
IPI00951730
IPI00106663
IPI00456609

Mouse chromosome position 8

Rat chromosome position 19p11

Homologene ID 9069

MGI ID 1921506

RGD ID 1308346