2. Gene
  3. CLUAP1 - clusterin associated protein 1 Gene

CLUAP1 - clusterin associated protein 1 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：凝聚素相关蛋白 1

种属: Homo sapiens

同用名: FAP22; IFT38; CFAP22

基因 ID: 23059 | 基因类型: protein coding

关于 CLUAP1

Cytogenetic location: 16p13.3 Genomic coordinates (GRCh38): 16:3,495,427-3,539,048 (from NCBI)

This gene has 12 transcripts (splice variants), 211 orthologues and is associated with 2 phenotypes. Broad expression in testis (RPKM 8.8), endometrium (RPKM 6.3) and 25 other tissues.

功能概要

该基因编码的蛋白质包含一个单一的卷曲螺旋区域。可变剪接导致多种转录本变体和蛋白质同种型。[RefSeq 提供，2012 年 7 月]

The protein encoded by this gene contains a single coiled-coil region. Alternative splicing results in multiple transcript variants and protein isoforms. [provided by RefSeq, Jul 2012]

CLUAP1 基因产物(3)

mRNA Protein Name
NM_001330454.2 NP_001317383.1 clusterin-associated protein 1 isoform 3
NM_015041.3 NP_055856.1 clusterin-associated protein 1 isoform 1
NM_024793.3 NP_079069.1 clusterin-associated protein 1 isoform 2
基因本体论
  • 分子功能
  • 细胞组分
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
16189514 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
part of intraciliary transport particle B IPI
IPI: 通过物理相互作用推断
26980730 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

CLUAP1 蛋白结构

Cluap1

Cluap1: Clusterin-associated protein-1 (14 - 285)

  • 0
  • 100
  • 200
  • 300
  • 413 a.a.
蛋白主名 其他名称

clusterin-associated protein 1

cilia and flagella associated protein 22

CLUAP1 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 CLUAP1 Q96AJ1 MAGEA11 Homo sapiens P43364-2
Y2H Array
25416956
Intra CLUAP1 Q96AJ1 MYOG Homo sapiens P15173
Y2H Array
31515488
Intra CLUAP1 Q96AJ1 MYOG Homo sapiens P15173
Y2H Array
25416956
Intra CLUAP1 Q96AJ1 MYOG Homo sapiens P15173
Y2H Array
32296183
Intra CLUAP1 Q96AJ1 MYOG Homo sapiens P15173
Y2H Prey Pooling
32296183
Intra CLUAP1 Q96AJ1 MAGEA11 Homo sapiens P43364
Y2H Prey Pooling
32296183
Intra CLUAP1 Q96AJ1 MAGEA11 Homo sapiens P43364
Pull Down
16189514
Intra CLUAP1 Q96AJ1 MAGEA11 Homo sapiens P43364
Y2H Array
32296183
Intra CLUAP1 Q96AJ1 CRACR2A Homo sapiens Q9BSW2
Anti Tag CoIP
33961781
Intra CLUAP1 Q96AJ1 CRACR2A Homo sapiens Q9BSW2
Anti Tag CoIP
28514442
Intra CLUAP1 Q96AJ1 CINP Homo sapiens Q9BW66
Y2H Pooling
16189514
Intra CLUAP1 Q96AJ1 CINP Homo sapiens Q9BW66
Y2H Array
31515488
Intra CLUAP1 Q96AJ1 CINP Homo sapiens Q9BW66
Validated Y2H
32296183
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
Leber Plus Disease

Leber Congenital Amaurosis

Lca

Leber'S Amaurosis

Leber'S Disease

Amaurosis Congenita Of Leber

Amaurosis Congenita Of Leber, Type 1

Lhon Plus Disease

Congenital Absence Of The Rods And Cones

Congenital Retinal Blindness

Crb

Congenital Amaurosis Of Retinal Origin

Leber'S Congenital Amaurosis

Leber Congenital Amaurosis 1

Leber'S Congenital Tapetoretinal Degeneration

Leber'S Congenital Tapetoretinal Dysplasia

Lca1

Leber Congenital Amaurosis Type 1

Retinal Blindness, Congenital

Amaurosis, Leber Congenital

Dysgenesis Neuroepithelialis Retinae

Hereditary Epithelial Dysplasia Of Retina

Hereditary Retinal Aplasia

Heredoretinopathia Congenitalis

Leber Abiotrophy

Leber Congenital Tapetoretinal Degeneration

Lebers Congenital Amaurosis

Optic Atrophy, Hereditary, Leber
Joubert Syndrome 1

Joubert Syndrome

Jbts

Cerebellooculorenal Syndrome 1

JBTS1

Joubert-Boltshauser Syndrome

Cerebelloparenchymal Disorder Iv

Cpd4

Cors1

Joubert Syndrome And Related Disorders

Jsrd

Familial Aplasia Of The Vermis

Joubert Syndrome Related Disorders

Js

Cerebellar Vermis Agenesis

Cerebelloparenchymal Disorder 4

Agenesis Of Cerebellar Vermis

Cerebello-Oculo-Renal Syndrome

Cors

Joubert-Bolthauser Syndrome

Cpd Iv

Classic Joubert Syndrome

Joubert Syndrome Type A

Pure Joubert Syndrome

Cerebello-Oculo-Renal Syndrome 1

Joubert Syndrome-1

Joubert Syndrome, Type 1

Joubert'S Syndrome
Leber Congenital Amaurosis 15

LCA15

Leber Congenital Amaurosis, Type 15
Cone-Rod Dystrophy 18

CORD18

Dystrophy, Cone-Rod, Type 18
Short-Rib Thoracic Dysplasia 7 With Or Without Polydactyly

SRTD7

Srps5

Short Rib-Polydactyly Syndrome Type V

Short-Rib Thoracic Dysplasia 7/20 With Polydactyly, Digenic

Short Rib-Polydactyly Syndrome, Type V

Short Rib-Polydactyly Syndrome Type 5

Srps Type V

SRTD7/20

Short-Rib Thoracic Dysplasia 7 Without Polydactyly
Bardet-Biedl Syndrome

Bbs

Biedl-Bardet Syndrome
Short-Rib Thoracic Dysplasia 3 With Or Without Polydactyly

Asphyxiating Thoracic Dystrophy 3

Saldino-Noonan Syndrome

SRTD3

Atd3

Srps1

Srps3

Verma-Naumoff Syndrome

Srps2b

Short Rib-Polydactyly Syndrome, Verma-Naumoff Type

Short Rib-Polydactyly Syndrome, Type I

Polydactyly With Neonatal Chondrodystrophy, Type I

Polydactyly With Neonatal Chondrodystrophy, Type Iii

Short Rib-Polydactyly Syndrome, Type Iib

Short Rib-Polydactyly Syndrome Type 3

Polydactyly With Neonatal Chondrodystrophy Type Iii

Short Rib-Polydactyly Syndrome Type Iii

Short Rib-Polydactyly Syndrome Type 1

Short Rib-Polydactyly Syndrome, Saldino-Noonan Type

Majewski Syndrome

Short Rib-Polydactyly Syndrome, Type Iii

Type I Short Rib Polydactyly Syndrome

Srps Type 3

Short Rib Polydactyly Syndrome Verma Naumoff Type

Verma Naumoff Syndrome

Polydactyly With Neonatal Chondrodystrophy Type 1

Srps Type 1

Short Rib-Polydactyly Syndrome Saldino-Noonan Type

Jatd

Jeune Asphyxiating Thoracic Dystrophy

Jeune Syndrome 3

Polydactyly With Neonatal Chondrodystrophy Type I

Short Rib-Polydactyly Syndrome Type I

Short Rib-Polydactyly Syndrome Type Iib

Srps Type Iib

Srps Type Iii
Short-Rib Thoracic Dysplasia 9 With Or Without Polydactyly

Conorenal Syndrome

Saldino-Mainzer Syndrome

SRTD9

Mainzer-Saldino Syndrome

Mzsds

Mainzer-Saldino Disease

Renal Dysplasia, Retinal Pigmentary Dystrophy, Cerebellar Ataxia, And Skeletal Dysplasia

Renal Dysplasia, Retinal Pigmentary Dystrophy, Cerebellar Ataxia And Skeletal Dysplasia

Renal Dysplasia, Retinal Pigmentary Dystrophy, Cerebellar Ataxia And Skeletal Dy

Mainzer Saldino Syndrome

Conorenal Dysplasia

Mainzer-Saldino Chondrodysplasia

Saldino-Mainzer Dysplasia

Short-Rib Thoracic Dysplasia 9

Renal Dysplasia-Retinal Pigmentary Dystrophy-Cerebellar Ataxia-Skeletal Dysplasia Syndrome

Mss

Renal Dysplasia Retinal Pigmentary Dystrophy Cerebellar Ataxia And Skeletal Dysplasia
Senior-Loken Syndrome 1

Senior-Loken Syndrome

Renal Dysplasia And Retinal Aplasia

Renal-Retinal Syndrome

Loken-Senior Syndrome

Juvenile Nephronophthisis With Leber Amaurosis

SLSN1

Senior-Loken Syndrome-1

Loken Senior Syndrome

Senior Loken Syndrome

Renal Dysplasia Retinal Aplasia

Nephronophthisis With Retinal Dystrophy

Renal Dysplasia-Retinal Aplasia Syndrome

Slsn
Primary Ciliary Dyskinesia

Immotile Cilia Syndrome

Kartagener Syndrome

Dextrocardia Bronchiectasis And Sinusitis

Pcd

Ciliary Motility Disorders

Ciliary Motility Disorder

Immotile Ciliary Syndrome

Ciliary Dyskinesia Primary

Ics

Polynesian Bronchiectasis

Dextrocardia-Bronchiectasis-Sinusitis Syndrome

Immotile Cilia Syndrome, Kartagener Type

Primary Ciliary Dyskinesia And Situs Inversus

Primary Ciliary Dyskinesia, Kartagener Type

Siewert Syndrome

Dyskinesia, Ciliary, Primary
Fundus Dystrophy

Retinal Dystrophy

Retinal Dystrophies

Dystrophy, Retinal
Cone-Rod Dystrophy 2

Cone-Rod Dystrophy

CORD2

Cone-Rod Retinal Dystrophy

Rcrd2

Cone-Rod Retinal Dystrophy 2

Crd2

Cord

Crd

Retinal Cone-Rod Dystrophy

Cone-Rod Retinal Dystrophy-2

Retinal Cone-Rod Dystrophy 2

Tapetoretinal Degeneration

Cone-Rod Degeneration

Cone Rod Dystrophy

Dystrophy, Cone-Rod

Dystrophy, Cone-Rod, Type 2

Retinitis Pigmentosa

Retinitis Pigmentosa 2

Progressive Cone-Rod Dystrophy
Retinitis Pigmentosa

RP

Rod-Cone Dystrophy

Autosomal Recessive Retinitis Pigmentosa

Non-Syndromic Retinitis Pigmentosa

Pericentral Pigmentary Retinopathy

Pigmentary Retinopathy

Tapetoretinal Degeneration

Rcd

Retinitis Pigmentosa Autosomal Recessive

ARRP

Retinitis Pigmentosa, Autosomal Recessive

Retinitis Pigmentosa 1
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS02849 CLUAP1 Human Pre-designed siRNA Set A Pre-designed Sets / 否

直系同源

种属 基因名 来源 基因 ID
Macaca mulatta CLUAP1 VGNC VGNC:71211
Canis familiaris CLUAP1 VGNC VGNC:39370
Rattus norvegicus CLUAP1 RGD RGD:1359189
Felis catus CLUAP1 VGNC VGNC:60987
Mus musculus CLUAP1 MGD MGI:1924029
Bos taurus CLUAP1 VGNC VGNC:27472
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