1. Gene
  2. DPYSL5 - dihydropyrimidinase like 5 Gene

DPYSL5 - dihydropyrimidinase like 5 Gene

中文名称:二氢嘧啶酶 5

种属: Homo sapiens

同用名: CV2; CRAM; CRMP5; RTSC4; Ulip6; CRMP-5

基因 ID: 56896 | 基因类型: protein coding

关于 DPYSL5

Cytogenetic location: 2p23.3 Genomic coordinates (GRCh38): 2:26,847,995-26,950,351 (from NCBI)

This gene has 7 transcripts (splice variants), 255 orthologues, 5 paralogues and is associated with 3 phenotypes. Biased expression in brain (RPKM 10.7), testis (RPKM 2.0) and 1 other tissue.

功能概要

该基因编码被认为参与神经发育的 CRMP (塌陷反应介体蛋白) 家族成员。在一些患有副肿瘤综合征的神经系统症状患者中发现了编码蛋白的抗体。在 11 号染色体上发现了该基因的假基因。已鉴定出编码相同蛋白质的多个可变剪接变体。[RefSeq 提供,2011 年 12 月]

This gene encodes a member of the CRMP (collapsing response mediator protein) family thought to be involved in neural development. Antibodies to the encoded protein were found in some patients with neurologic symptoms who had paraneoplastic syndrome. A pseudogene of this gene is found on chromosome 11. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Dec 2011]

DPYSL5 基因产物(3)

mRNA Protein Name
NM_001253723.2 NP_001240652.1 dihydropyrimidinase-related protein 5
NM_001253724.2 NP_001240653.1 dihydropyrimidinase-related protein 5
NM_020134.4 NP_064519.2 dihydropyrimidinase-related protein 5
基因本体论
  • 分子功能
  • 生物过程
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
25416956 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in negative regulation of dendrite morphogenesis IMP
IMP: 通过突变表型推断
33894126 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

DPYSL5 蛋白结构

Amidohydro_1

Amidohydro_1: Amidohydrolase family (58 - 406)

  • 0
  • 100
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  • 400
  • 500
  • 564 a.a.
蛋白主名 其他名称

dihydropyrimidinase-related protein 5

CRMP3-associated molecule

DPYSL5 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 DPYSL5 Q9BPU6 KIF1B Homo sapiens O60333-2
Validated Y2H
32814053
Intra DPYSL5 Q9BPU6 KIF1B Homo sapiens O60333-2
Y2H Array
32814053
Intra DPYSL5 Q9BPU6 KIF1B Homo sapiens O60333-2
Y2H Pooling
32814053
Intra DPYSL5 Q9BPU6 DPYSL2 Homo sapiens Q16555
Anti Tag CoIP
33961781
Intra DPYSL5 Q9BPU6 DPYSL2 Homo sapiens Q16555
Anti Tag CoIP
28514442
Intra DPYSL5 Q9BPU6 DPYSL2 Homo sapiens Q16555
Y2H Array
25416956
Intra DPYSL5 Q9BPU6 DPYSL2 Homo sapiens Q16555
Y2H Array
32296183
Intra DPYSL5 Q9BPU6 DPYSL2 Homo sapiens Q16555
Y2H Array
29892012
Intra DPYSL5 Q9BPU6 DPYSL2 Homo sapiens Q16555
Y2H Prey Pooling
32296183
Intra DPYSL5 Q9BPU6 DPYSL2 Homo sapiens Q16555
Y2H Array
31515488
Intra DPYSL5 Q9BPU6 CFAP161 Homo sapiens Q6P656
Y2H Array
32296183
Intra DPYSL5 Q9BPU6 CFAP161 Homo sapiens Q6P656
Y2H Prey Pooling
32296183
Intra DPYSL5 Q9BPU6 q9y649_human Homo sapiens Q9Y649
Validated Y2H
32814053
Intra DPYSL5 Q9BPU6 q9y649_human Homo sapiens Q9Y649
Y2H Array
32814053
Intra DPYSL5 Q9BPU6 q9y649_human Homo sapiens Q9Y649
Y2H Pooling
32814053
Intra DPYSL5 Q9BPU6 FGFR3 Homo sapiens P22607
Y2H Pooling
32814053
Intra DPYSL5 Q9BPU6 FGFR3 Homo sapiens P22607
Validated Y2H
32814053
Intra DPYSL5 Q9BPU6 FGFR3 Homo sapiens P22607
Y2H Array
32814053
Intra DPYSL5 Q9BPU6 GSN Homo sapiens P06396
Validated Y2H
32814053
Intra DPYSL5 Q9BPU6 GSN Homo sapiens P06396
Y2H Array
32814053
Intra DPYSL5 Q9BPU6 GSN Homo sapiens P06396
Y2H Pooling
32814053
Intra DPYSL5 Q9BPU6 HSPB1 Homo sapiens P04792
Y2H Array
32814053
Intra DPYSL5 Q9BPU6 HSPB1 Homo sapiens P04792
Validated Y2H
32814053
Intra DPYSL5 Q9BPU6 HSPB1 Homo sapiens P04792
Y2H Pooling
32814053
Intra DPYSL5 Q9BPU6 RNF11 Homo sapiens Q9Y3C5
Validated Y2H
32814053
Intra DPYSL5 Q9BPU6 RNF11 Homo sapiens Q9Y3C5
Y2H Array
32814053
Intra DPYSL5 Q9BPU6 RNF11 Homo sapiens Q9Y3C5
Y2H Pooling
32814053
Intra DPYSL5 Q9BPU6 HIP1 Homo sapiens O00291
Validated Y2H
32814053
Intra DPYSL5 Q9BPU6 HIP1 Homo sapiens O00291
Y2H Array
32814053
Intra DPYSL5 Q9BPU6 HIP1 Homo sapiens O00291
Y2H Pooling
32814053
Intra DPYSL5 Q9BPU6 WFS1 Homo sapiens O76024
Validated Y2H
32814053
Intra DPYSL5 Q9BPU6 WFS1 Homo sapiens O76024
Y2H Array
32814053
Intra DPYSL5 Q9BPU6 WFS1 Homo sapiens O76024
Y2H Pooling
32814053
Intra DPYSL5 Q9BPU6 COQ8A Homo sapiens Q8NI60
Y2H Array
32814053
Intra DPYSL5 Q9BPU6 COQ8A Homo sapiens Q8NI60
Validated Y2H
32814053
Intra DPYSL5 Q9BPU6 COQ8A Homo sapiens Q8NI60
Y2H Pooling
32814053
Intra DPYSL5 Q9BPU6 PEX1 Homo sapiens O43933
Y2H Array
32814053
Intra DPYSL5 Q9BPU6 PEX1 Homo sapiens O43933
Validated Y2H
32814053
Intra DPYSL5 Q9BPU6 PEX1 Homo sapiens O43933
Y2H Pooling
32814053
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
Ritscher-Schinzel Syndrome 4

RTSC4

Non-Specific Syndromic Intellectual Disability

Complex Neurodevelopmental Disorder

Thymoma

Primary Thymic Epithelial Neoplasm

Primary Thymic Epithelial Tumor

Thymus Neoplasms

Ritscher-Schinzel Syndrome

3c Syndrome

Ccc Dysplasia

Craniocerebellocardiac Dysplasia

Cranio-Cerebello-Cardiac Dysplasia

Optic Neuritis

Inflammatory Optic Neuropathy

Chorea Gravidarum
Anal Spasm

Proctospasm

Anorectal Spasm

Rectal Spasm

Vascular Myelopathy

Vascular Myelopathies

Choroid Plexus Meningioma

Choroid Meningioma

Meningioma Of The Choroid Plexus

Neuroretinitis

Juxtapapillary Focal Retinitis And Retinochoroiditis

Retinitis

Focal Retinitis And Retinochoroiditis, Juxtapapillary

Papilloretinitis

Autoimmune Optic Neuritis
Autoimmune Epilepsy
Transverse Myelitis

Myelitis Transverse

Myelitis, Transverse

Nutritional Optic Neuropathy
Cerebellopontine Angle Meningioma

Meningioma Of The Cerebellar Pontine Angle

Polyradiculopathy
La Crosse Encephalitis

California Encephalitis

California Virus Encephalitis

Neuroinvasive California Encephalitis Virus Infection

Californian Encephalitis

Encephalitis, California

California Meningoencephalitis

California Encephalitis Virus Infection

California Encephalitis Virus Infection Neuroinvasive Disease

California Meningoencephalitis Virus Disease

California Serogroup Virus Neuroinvasive Disease

California Viral Encephalitis

Ce - [California Encephalitis]

Lac - [La Crosse Encephalitis]

Autoimmune Disease Of Peripheral Nervous System
Thymus Gland Disease

Disease Of Thymus Gland

Neuritis

Peripheral Neuritis

Limbic Encephalitis
Thymus Cancer

Thymic Neoplasm

Thymic Tumor

Thymus Neoplasm

Thymus Neoplasms

Malignant Neoplasm Of Thymus

Neoplasm Of Thymus

Thymic Neoplasms

Thymoma, Familial

Thymic Carcinoma

Thymoma, Type C

Cancer Of Thymus

Malignant Tumour Of Thymus

Primary Malignant Neoplasm Of Thymus

Thymic Glandular Cancer

Thymus Gland Cancer

Choreatic Disease

Chorea

Hereditary Chorea

Lung Cancer

Lung Carcinoma

Non-Small Cell Lung Carcinoma

Lung Cancer, Susceptibility To

Lung Cancer, Protection Against

Adenocarcinoma Of Lung, Somatic

Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer

Lung Neoplasm

Carcinoma Of Lung

Lung Non-Small Cell Carcinoma

Non-Small Cell Lung Cancer

Nsclc

Lung Neoplasms

Malignant Neoplasm Of Lung

Alveolar Cell Carcinoma

Nonsmall Cell Lung Cancer, Somatic

Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer, Susceptibility To

Lung Cancer, Somatic

Lung Cancer, Resistance To

Cancer Of Lung

Cancer Of Bronchus

Cancer Of The Lung

Lung Malignancies

Lung Malignant Tumors

Malignant Lung Tumor

Malignant Tumor Of Lung

Pulmonary Cancer

Pulmonary Carcinoma

Pulmonary Neoplasms

Respiratory Carcinoma

LNCR

Adenocarcinoma Of Lung

Neoplasm Of Lung

Cancer Lung

Carcinoma Non-Small Cell Lung

Carcinoma, Non-Small-Cell Lung

Lung Cancers

Lung Carcinomas

Cancer, Lung

Cancer, Lung, Non-Small Cell

Primary Malignant Neoplasm Of Lung

Bronchioloalveolar Adenocarcinoma

Neurosarcoidosis

Cerebral Sarcoidosis

Plexopathy
Stiff-Person Syndrome

SPS

Stiff-Man Syndrome

Stiff Man Syndrome

Stiff Person Syndrome

Moersch-Woltman Syndrome

Sms

Stiff-Trunk Syndrome

Morsch Woltman Syndrome

Stiff Person Syndrome And Related Disorders

Stiff Person Spectrum Disorder

Classic Stiff Person Syndrome

Classic Sps

Focal Stiff Limb Syndrome

Focal Stiff-Person Syndrome

Stiff Leg Syndrome

Progressive Encephalomyelitis With Rigidity

Acute Disseminated Encephalomyelitis

Acute Disseminated Encephalitis

Adem

Ade

Encephalomyelitis Acute Disseminated

Encephalomyelitis, Acute Disseminated

Adem - [Acute Disseminated Encephalomyelitis]

Optic Papillitis

Papillitis

Papilledema

Anterograde Amnesia

Amnesia, Anterograde

Ritscher-Schinzel Syndrome 2

RTSC2

Brain Meningioma

Intracranial Meningioma

Mononeuritis Multiplex
Lingual-Facial-Buccal Dyskinesia

Orofacial Dyskinesia

Oro-Facial Dyskinesia

Dyskinesias

Neuromuscular Junction Disease

Neuromuscular Junction Diseases

Mononeuritis Of Upper Limb And Mononeuritis Multiplex
Myelitis

Spinal Cord Inflammation Nos

Radiculomyelitis Nos

Myeloradiculitis

Autoimmune Neuropathy
Whipple Disease

Intestinal Lipodystrophy

Whipple'S Disease

Intestinal Lipophagic Granulomatosis

Secondary Non-Tropical Sprue

Tropheryma Whippelii Infection

Whipples Disease

Cranial Nerve Disease

Cranial Nerve Disorder

Disorder Of Cranial Nerve

Cranial Nerve Diseases

Optic Nerve Disease

Optic Neuropathy

Disorder Of The Second Nerve

Optic Nerve Disorder

Optic Nerve

Abnormality Of The Optic Nerve

Optic Nerve Disorders

Neuropathy, Optic

Disorder Of The Optic Nerve

Mutism
Hyperekplexia

Hereditary Hyperekplexia

Kok Disease

Congenital Stiff Man Syndrome

Familial Startle Disease

Sthe

Stiff-Baby Syndrome

Hereditary Hyperexplexia

Startle Disease

Exaggerated Startle Reaction

Hyperexplexia Hereditary

Startle Disease, Familial

Startle Reaction, Exaggerated

Stiff-Man Syndrome, Congenital

Stiff-Person Syndrome, Congenital

Congenital Stiff-Man Syndrome

Congenital Stiff-Person Syndrome

Familial Hyperekplexia

Startle Syndrome

Stiff Baby Syndrome

Hyperekplexia, Hereditary

Stiff-Person Syndrome

Spinal Cord Disease

Spinal Cord Diseases

Myelopathy

Bone Marrow Diseases

Cerebellar Disease

Cerebellar Diseases

Cerebellar Dysfunction

Cerebellar Abnormality

Cerebellar Disorders

Movement Disease

Movement Disorders

Movement Disorder

Peripheral Nervous System Disease

Peripheral Neuropathy

Peripheral Nerve Disease

Peripheral Nerve Disorders

Neuropathy, Peripheral

Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation

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
Mus musculus DPYSL5 MGD MGI:1929772
Rattus norvegicus DPYSL5 RGD RGD:620467
Canis familiaris DPYSL5 VGNC VGNC:40085
Bos taurus DPYSL5 VGNC VGNC:28198
Macaca mulatta DPYSL5 VGNC VGNC:71872
Felis catus DPYSL5 VGNC VGNC:61618