1. Gene
  2. CYLD - CYLD lysine 63 deubiquitinase Gene

CYLD - CYLD lysine 63 deubiquitinase Gene

中文名称:CYLD 赖氨酸 63 去泛素化酶

种属: Homo sapiens

同用名: EAC; MFT; SBS; TEM; BRSS; CDMT; MFT1; CYLD1; CYLDI; USPL2; FTDALS8

基因 ID: 1540 | 基因类型: protein coding

关于 CYLD

Cytogenetic location: 16q12.1 Genomic coordinates (GRCh38): 16:50,742,086-50,801,935 (from NCBI)

This gene has 15 transcripts (splice variants), 212 orthologues and is associated with 82 phenotypes. Ubiquitous expression in bone marrow (RPKM 13.0), lymph node (RPKM 10.5) and 25 other tissues.

功能概要

该基因编码具有三个细胞骨架相关蛋白-甘氨酸保守 (CAP-GLY) 结构域的细胞质蛋白,该结构域起着去泛素化酶的作用。该基因的突变与圆柱瘤病、多发性家族性毛发上皮瘤和 Brooke-Spiegler 综合征有关。已经表征了编码不同亚型的替代转录剪接变体。[RefSeq 提供,2008 年 7 月]

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]

CYLD 基因产物(16)

mRNA Protein Name
NM_001042355.2 NP_001035814.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 2
NM_001042412.3 NP_001035877.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 2
NM_001378743.1 NP_001365672.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 1
NM_001378744.1 NP_001365673.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 2
NM_001378745.1 NP_001365674.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 2
NM_001378746.1 NP_001365675.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 2
NM_001378747.1 NP_001365676.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 2
NM_001378748.1 NP_001365677.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 2
NM_001378749.1 NP_001365678.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 2
NM_001378750.1 NP_001365679.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 2
NM_001378751.1 NP_001365680.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 3
NM_001378752.1 NP_001365681.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 3
NM_001378753.1 NP_001365682.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 3
NM_001378754.1 NP_001365683.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 4
NM_001378755.1 NP_001365684.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 4
NM_015247.3 NP_056062.1 ubiquitin carboxyl-terminal hydrolase CYLD isoform 1
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables K63-linked deubiquitinase activity EXP
EXP: 通过实验结果推断
26997266 GOA
enables K63-linked deubiquitinase activity IDA
IDA: 通过直接分析推断
18313383 GOA
enables Met1-linked polyubiquitin deubiquitinase activity EXP
EXP: 通过实验结果推断
26997266 GOA
enables cysteine-type deubiquitinase activity IDA
IDA: 通过直接分析推断
18313383 GOA
enables proline-rich region binding IPI
IPI: 通过物理相互作用推断
15341735 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
18636086 GOA
enables protein kinase binding IPI
IPI: 通过物理相互作用推断
17495026 GOA
enables zinc ion binding IDA
IDA: 通过直接分析推断
18313383 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in innate immune response IDA
IDA: 通过直接分析推断
26997266 GOA
involved in negative regulation of JNK cascade IDA
IDA: 通过直接分析推断
29291351 GOA
involved in negative regulation of NF-kappaB transcription factor activity IDA
IDA: 通过直接分析推断
18313383 GOA
involved in negative regulation of canonical Wnt signaling pathway IMP
IMP: 通过突变表型推断
20227366 GOA
involved in negative regulation of non-canonical NF-kappaB signal transduction IDA
IDA: 通过直接分析推断
18313383 GOA
involved in negative regulation of p38MAPK cascade IDA
IDA: 通过直接分析推断
29291351 GOA
involved in positive regulation of extrinsic apoptotic signaling pathway IMP
IMP: 通过突变表型推断
21525013 GOA
involved in protein deubiquitination IDA
IDA: 通过直接分析推断
29291351 GOA
involved in protein linear deubiquitination IDA
IDA: 通过直接分析推断
26997266 GOA
involved in regulation of inflammatory response IDA
IDA: 通过直接分析推断
27591049 GOA
involved in regulation of intrinsic apoptotic signaling pathway IMP
IMP: 通过突变表型推断
21525013 GOA
involved in regulation of microtubule cytoskeleton organization IMP
IMP: 通过突变表型推断
20194890 GOA
involved in regulation of mitotic cell cycle IMP
IMP: 通过突变表型推断
17495026 GOA
involved in regulation of necroptotic process IDA
IDA: 通过直接分析推断
27458237 GOA
involved in regulation of tumor necrosis factor-mediated signaling pathway IDA
IDA: 通过直接分析推断
26997266 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in centrosome IDA
IDA: 通过直接分析推断
25134987 GOA
colocalizes with cytoplasmic microtubule IDA
IDA: 通过直接分析推断
17495026 GOA
colocalizes with cytoplasmic side of plasma membrane IDA
IDA: 通过直接分析推断
20194890 GOA
located in cytosol IDA
IDA: 通过直接分析推断
18313383 GOA
colocalizes with midbody IDA
IDA: 通过直接分析推断
17495026 GOA
located in spindle IDA
IDA: 通过直接分析推断
25134987 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

CYLD 蛋白结构

CAP_GLY

CAP_GLY: CAP-Gly domain (127 - 202)

CAP_GLY

CAP_GLY: CAP-Gly domain (232 - 290)

CAP_GLY

CAP_GLY: CAP-Gly domain (469 - 536)

UCH

UCH: Ubiquitin carboxyl-terminal hydrolase (590 - 886)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 953 a.a.
蛋白主名 其他名称

ubiquitin carboxyl-terminal hydrolase CYLD

cylindromatosis (turban tumor syndrome)

CYLD 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
Intra CYLD Q9NQC7 ITCH Homo sapiens Q96J02
Anti Tag CoIP
22057290
Intra CYLD Q9NQC7 HDAC6 Homo sapiens Q9UBN7
Anti Bait CoIP
19893491
Intra CYLD Q9NQC7 TUBA1A Homo sapiens Q71U36
Fluorescence
19893491
Intra CYLD Q9NQC7 TUBA1A Homo sapiens Q71U36
Anti Bait CoIP
19893491
Intra CYLD Q9NQC7 ITCH Homo sapiens Q96J02-2
Pull Down
22057290
Intra CYLD Q9NQC7 SPATA2 Homo sapiens Q9UM82
Anti Tag CoIP
19615732
Intra CYLD Q9NQC7 SPATA2 Homo sapiens Q9UM82
TAP
24981860
Intra CYLD Q9NQC7 RIGI Homo sapiens O95786
Anti Tag CoIP
18636086
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Brooke-Spiegler Syndrome

Cyld Cutaneous Syndrome

Spiegler-Brooke Syndrome

Familial Cylindromatosis

BRSS

Bss

Sbs

Multiple Familial Trichoepithelioma

Ancell-Spiegler Cylindromas

Familial Multiple Trichoepithelioma

Trichoepithelioma

Fc

Mft

Multiple Familial Trichoepitheliomas

Ccs

Turban Tumor Syndrome

Schilbach-Rott Syndrome

Eccrine Dermal Cylindroma

Familial Multiple Trichoepitheliomata

Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 8

FTDALS8

Trichoepithelioma, Multiple Familial, 1

Epithelioma Adenoides Cysticum Of Brooke

MFT1

Eac

Brooke-Fordyce Trichoepitheliomas

Epithelioma, Hereditary Multiple Benign Cystic

Multiple Familial Trichoepithelioma 1

Hereditary Multiple Benign Cystic Epithelioma

Familial Multiple Trichoepitheliomata

Cylindromatosis, Familial

Ancell-Spiegler Cylindromas

'Turban Tumor' Syndrome

Cylindromas, Dermal Eccrine

Dermal Eccrine Cylindroma

FCYL

Dermal Eccrine Cylindromatosis

Turban Tumor Syndrome

Eccrine Dermal Cylindroma

Spiradenoma

Eccrine Spiradenoma

Benign Eccrine Spiradenoma

Eccrine Spiradenoma Of Skin

Es

Eccrine Spiradenoma, Benign

Apocrine Sweat Gland Neoplasm

Apocrine Tumor

Apocrine Neoplasm

Plasma Cell Neoplasm

Plasma Cell Dyscrasia

Paraproteinemias

Plasma Cell Tumour

Plasmacytic Tumor

Multiple Myeloma

Plasmacytoma

Plasma Cell Tumours

Plasma Cells Dyscrasia

Epidermal Appendage Tumor

Neoplasm Of Skin With Adnexal Differentiation

Neoplasm Of The Skin Appendage

Skin Appendage Tumour

Anus Basaloid Carcinoma

Basaloid Carcinoma Of The Anus

Anal Basaloid Carcinoma

Amyotrophic Lateral Sclerosis 8

Amyotrophic Lateral Sclerosis Type 8

ALS8

Sclerosis, Lateral, Amyotrophic, Type Type 8

Salivary Gland Carcinoma

Salivary Gland Cancer

Malignant Neoplasm Of Salivary Gland

Salivary Gland Neoplasms

Malignant Spiradenoma

Malignant Eccrine Spiradenoma

Eccrine Spiradenoma, Malignant

Mes

Basal Cell Carcinoma

Basal Cell Cancer

Basal Cell Neoplasm

Basal Cell Carcinoma Of Skin

Malignant Basal Cell Tumor

Basal Cell Tumor

Epithelioma Basal Cell

Malignant Basal Cell Neoplasm

Rodent Ulcer

Carcinoma Basal Cell

Neoplasms, Basal Cell

Basal Cell Carcinomas

Experimental Organism Basal Cell Carcinoma

Nodulo-Ulcerative Basal Cell Carcinoma

Basalioma

Basal Cell Epithelioma Of Skin

Bcc - [Basal Cell Carcinoma] Of Skin

Rodent Ulcer Of Skin

Rodent Ulcer Of Unspecified Site

Basal Cell Epithelioma Of Unspecified Site

Salivary Gland Adenoid Cystic Carcinoma

Cylindroma

Myeloma, Multiple

Multiple Myeloma

Plasma Cell Myeloma

Kahler Disease

Myelomatosis

Medullary Plasmacytoma

Multiple Myeloma, Resistance To

Myeloma

Plasma Cell Dyscrasia

Kahler'S Disease

Multiple Myeloma, Susceptibility To

Myeloma - Multiple

Kahler-Bozzolo Disease

Plasma Cell Myelomas

MM

Plasma Cell Neoplasm

Primary Systemic Amyloidosis

Primary Amyloidosis

Immunoglobulin Deposition Disease

Plasmacytic Myeloma

Multiple Myelomata

Multiple Myeloma Nos

Multiple Myeloma Without Mention Of Remission

Monostotic Plasma Cell Myeloma

Mm - [Multiple Myeloma]

Sweat Gland Benign Neoplasm

Neoplasm Of Sweat Gland

Sweat Gland Tumor

Tumor Of The Sweat Gland

Sweat Gland Neoplasms

Sweat Gland Neoplasm

Osteonecrosis Of The Jaw
Frontotemporal Dementia

Pallidopontonigral Degeneration

Frontotemporal Lobar Degeneration

Semantic Dementia

FTD

Frontotemporal Lobe Dementia

Multiple System Tauopathy With Presenile Dementia

Dementia, Frontotemporal

Frontotemporal Dementia With Parkinsonism

Mstd

Frontotemporal Lobar Degeneration With Tau Inclusions

Ftld With Tau Inclusions

Dementia, Frontotemporal, With Parkinsonism

Fldem

Ftdp17

Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex

Ddpac

Wilhelmsen-Lynch Disease

Wld

Ppnd

Dementia, Frontotemporal, With Or Without Parkinsonism

Semantic Primary Progressive Aphasia

Semantic Variant Ppa

Wilhemsen-Lynch Disease

Frontotemporal Dementia-Amyotrophic Lateral Sclerosis

Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17

Ftd-Als

Ftld

Pick Complex

Pick Disease Of The Brain

Frontotemporal Dementia With Parkinsonism-17

Grn-Related Frontotemporal Dementia

Frontotemporal Dementia With Motor Neuron Disease

Dementia In Fronto-Temporal Lobar Degeneration

Ftd - [Frontotemporal Dementia]

Temple Dementia

Frontal Lobe Dementia

Adenoid Cystic Carcinoma

Adenocystic Carcinoma

Cribriform Carcinoma

Cylindroma

Carcinoma Adenoid Cystic

Carcinoma, Adenoid Cystic

Adenoid Cystic Carcinoma Of Salivary Gland

Eccrine Dermal Cylindroma

Carcinoma, Cribriform

Salivary Gland Disease

Salivary Gland Disorders

Salivary Gland Diseases

Non-Neoplastic Salivary Gland Disease

Non-Neoplastic Salivary Gland Disorder

Disorder Of Salivary Gland

Lesion Of Salivary Gland Nos

Dementia

Dementias

Presenile Dementia

Alzheimer Type Dementia

Alzheimer Sclerosis

Alzheimer Disease Dementia

Alzheimer Dementia

Primary Degenerative Alzheimer Type Dementia

End Stage Alzheimer'S Dementia

Alzheimer'S Type Atypical Dementia

Alzheimer Type Presenile Dementia

Early Onset Alzheimer Dementia

Dementia In Alzheimer Disease Type 2

Dementia In Alzheimer Disease With Early Onset

Early Onset Alzheimer Type Dementia, Uncomplicated

Primary Degenerative Alzheimer Type Dementia, Early Onset

Primary Degenerative Alzheimer Type Dementia, Presenile Onset, Uncomplicated

Alzheimer Disease Dementia With Early Onset

Presenile Sclerosis

Presenile Brain Sclerosis

Presenile Alzheimer Brain Sclerosis

Late Onset Alzheimer Dementia

Dementia In Alzheimer Disease Type 1

Dementia In Alzheimer Disease With Late Onset

Primary Degenerative Alzheimer Type Dementia, Late Onset

Sdat - [Senile Dementia, Alzheimer Type]

Alzheimer Disease Dementia With Late Onset

Late Onset Alzheimer Brain Sclerosis

Senile Alzheimer Brain Disease

Senile Alzheimer Brain Sclerosis

Senile Primary Degenerative Alzheimer Type Dementia

Senile Dementia Of The Alzheimer Type

Arteriosclerotic Dementia

Strategic-Infarct Dementia

Post Stroke Dementia

Vascular Cognitive Impairment

Vascular Dementia

Dementia Of The Lewy Body Type

Dementia With Lewy Bodies

Sdlt - [Senile Dementia Of The Lewy Body Type]

Senile Dementia Of The Lewy Body Type

Alcohol-Related Dementia

Alcoholic Dementia Nos

Alcohol-Induced Dementia

Alcoholic Brain Syndrome

Chronic Alcoholic Brain Syndrome

Alcohol Dementia

Late Onset Alcoholic Psychosis

Residual And Late-Onset Alcohol-Induced Psychotic Disorder

Mental And Behavioural Disorders Due To Use Of Sedatives Or Hypnotics, Residual And Late-Onset Psychotic Disorder

Late-Onset Psychoactive Substance-Induced Psychotic Disorder

Inhalant Dementia

Volatile Solvents Dementia

Dementia In Paralysis Agitans

Pdd - [Parkinson Disease Dementia]

Dementia Syndrome Of Parkinson Disease

Dementia In Parkinson Disease

Parkinson Related Dementia

Dementia In Huntington Chorea

Hiv - [Human Immunodeficiency Virus] Dementia

Hiv- [Human Immunodeficiency Virus] Associated Cognitive Motor Complex

Hiv- [Human Immunodeficiency Virus] Associated Dementia Complex

Aids - [Acquired Immunodeficiency Syndrome] Dementia Complex

Aids Related Dementia

Dementia Due To Niacin Deficiency

Autoinflammation, Panniculitis, And Dermatosis Syndrome

Otulipenia

Otulin-Related Autoinflammatory Syndrome

AIPDS

Oras

Infantile-Onset Periodic Fever-Panniculitis-Dermatosis Syndrome

Autoinflammation, Panniculitis And Dermatosis Syndrome

Otulin Deficiency

Sweat Gland Disease

Sweat Gland Diseases

Bartholin'S Gland Adenoid Cystic Carcinoma

Bartholin Gland Adenoid Cystic Carcinoma

Eccrine Adenocarcinoma
Glycogen Storage Disease Iv

Gsd Iv

Glycogen Branching Enzyme Deficiency

Andersen Disease

Amylopectinosis

Glycogen Storage Disease Type Iv

GSD4

Brancher Deficiency

Glycogen Storage Disease, Type Iv

Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Congenital Neuromuscular Form

Gbe1 Deficiency

Glycogenosis Iv

Cirrhosis, Familial, With Deposition Of Abnormal Glycogen

Glycogen Storage Disease Type 4

Glycogenosis 4

Potassium-Sensitive Periodic Paralysis, Ventricular Ectopy, And Dysmorphic Features

Andersen'S Disease

Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Childhood Neuromuscular Form

Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Fatal Perinatal Neuromuscular Form

Brancher Deficiency Glycogenosis

Branching-Transferase Deficiency Glycogenosis

Deficiency Of 1,4-Alpha-Glucan Branching Enzyme

Andersen-Tawil Syndrome

Gsd 4

Andersen Cardiodysrhythmic Periodic Paralysis

Lqt7

Long Qt Syndrome 7

Periodic Paralysis, Potassium-Sensitive Cardiodysrhythmic Type

Andersen Glycogenosis

Branching Enzyme Deficiency

Glycogenosis, Type Iv

Gsd Type Iv

Type Iv Glycogenosis

Gbe Deficiency, Childhood Neuromuscular Form

Gsd Due To Glycogen Branching Enzyme Deficiency, Childhood Neuromuscular Form

Gsd Type 4, Childhood Neuromuscular Form

Gsdiv, Childhood Neuromuscular Form

Glycogen Storage Disease Type 4, Childhood Neuromuscular Form

Glycogen Storage Disease Type Iv, Childhood Neuromuscular Form

Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Childhood Neuromuscular Form

Glycogenosis Type 4, Childhood Neuromuscular Form

Glycogenosis Type Iv, Childhood Neuromuscular Form

Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Adult Neuromuscular Form

Gbe Deficiency, Adult Neuromuscular Form

Gsd Due To Glycogen Branching Enzyme Deficiency, Adult Neuromuscular Form

Gsd Type 4, Adult Neuromuscular Form

Gsdiv, Adult Neuromuscular Form

Glycogen Storage Disease Type 4, Adult Neuromuscular Form

Glycogen Storage Disease Type Iv, Adult Neuromuscular Form

Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Adult Neuromuscular Form

Glycogenosis Type 4, Adult Neuromuscular Form

Glycogenosis Type Iv, Adult Neuromuscular Form

Gbe Deficiency, Congenital Neuromuscular Form

Gsd Due To Glycogen Branching Enzyme Deficiency, Congenital Neuromuscular Form

Gsd Type 4, Congenital Neuromuscular Form

Gsdiv, Congenital Neuromuscular Form

Glycogen Storage Disease Type 4, Congenital Neuromuscular Form

Glycogen Storage Disease Type Iv, Congenital Neuromuscular Form

Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Congenital Neuromuscular Form

Glycogenosis Type 4, Congenital Neuromuscular Form

Glycogenosis Type Iv, Congenital Neuromuscular Form

Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Childhood Combined Hepatic And Myopathic Form

Gbe Deficiency, Childhood Combined Hepatic And Myopathic Form

Gsd Due To Glycogen Branching Enzyme Deficiency, Childhood Combined Hepatic And Myopathic Form

Gsd Type 4, Childhood Combined Hepatic And Myopathic Form

Gsdiv, Childhood Combined Hepatic And Myopathic Form

Glycogen Storage Disease Type 4, Childhood Combined Hepatic And Myopathic Form

Glycogen Storage Disease Type Iv, Childhood Combined Hepatic And Myopathic Form

Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Childhood Combined Hepatic And Myopathic Form

Glycogenosis Type 4, Childhood Combined Hepatic And Myopathic Form

Glycogenosis Type Iv, Childhood Combined Hepatic And Myopathic Form

Gbe Deficiency, Fatal Perinatal Neuromuscular Form

Gsd Due To Glycogen Branching Enzyme Deficiency, Fatal Perinatal Neuromuscular Form

Gsd Type 4, Fatal Perinatal Neuromuscular Form

Gsdiv, Fatal Perinatal Neuromuscular Form

Glycogen Storage Disease Type 4, Fatal Perinatal Neuromuscular Form

Glycogen Storage Disease Type Iv, Fatal Perinatal Neuromuscular Form

Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Fatal Perinatal Neuromuscular Form

Glycogenosis Type 4, Fatal Perinatal Neuromuscular Form

Glycogenosis Type Iv, Fatal Perinatal Neuromuscular Form

Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Non Progressive Hepatic Form

Gbe Deficiency, Non Progressive Hepatic Form

Gsd Due To Glycogen Branching Enzyme Deficiency, Non Progressive Hepatic Form

Gsd Type 4, Non Progressive Hepatic Form

Gsdiv, Non Progressive Hepatic Form

Glycogen Storage Disease Type 4, Non Progressive Hepatic Form

Glycogen Storage Disease Type Iv, Non Progressive Hepatic Form

Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Non Progressive Hepatic Form

Glycogenosis Type 4, Non Progressive Hepatic Form

Glycogenosis Type Iv, Non Progressive Hepatic Form

Glycogen Storage Disease Due To Glycogen Branching Enzyme Deficiency, Progressive Hepatic Form

Gbe Deficiency, Progressive Hepatic Form

Gsd Due To Glycogen Branching Enzyme Deficiency, Progressive Hepatic Form

Gsd Type 4, Progressive Hepatic Form

Gsdiv, Progressive Hepatic Form

Glycogen Storage Disease Type 4, Progressive Hepatic Form

Glycogen Storage Disease Type Iv, Progressive Hepatic Form

Glycogenosis Due To Glycogen Branching Enzyme Deficiency, Progressive Hepatic Form

Glycogenosis Type 4, Progressive Hepatic Form

Glycogenosis Type Iv, Progressive Hepatic Form

Glycogen Storage Disease 4

Gsd-Iv

Storage Disease, Glycogen, Type Iv

Skin Benign Neoplasm

Neoplasm Of Skin By Site

Tumor Of The Skin

Skin Tumor

Benign Neoplasm Of Skin

Skin Neoplasms

Inflammatory Bowel Disease

Inflammatory Bowel Diseases

Bowel Disease, Inflammatory

Lymphoma, Mucosa-Associated Lymphoid Type

Malt Lymphoma

Gastric Lymphoma, Primary

Lymphoma, Malt, Somatic

Mucosa-Associated Lymphoid Tissue Lymphoma

Extranodal Marginal Zone B-Cell Lymphoma

MALTOMA

Marginal Zone B-Cell Lymphoma

Mucosa-Associated Lymphatic Tissue Lymphoma

Primary Gastric Lymphoma

Gastric Lymphoma

Familial Primary Gastric Lymphoma

疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus CYLD RGD RGD:1308346
Canis familiaris CYLD VGNC VGNC:50293
Macaca mulatta CYLD VGNC VGNC:71581
Bos taurus CYLD VGNC VGNC:49141
Mus musculus CYLD MGD MGI:1921506
Felis catus CYLD VGNC VGNC:61320
Others CYLD NCBI