1. Gene
  2. UBXN6 - UBX domain protein 6 Gene

UBXN6 - UBX domain protein 6 Gene

中文名称:UBX 结构域蛋白 6

种属: Homo sapiens

同用名: UBXD1; UBXDC2

基因 ID: 80700 | 基因类型: protein coding

关于 UBXN6

Cytogenetic location: 19p13.3 Genomic coordinates (GRCh38): 19:4,445,006-4,457,879 (from NCBI)

This gene has 10 transcripts (splice variants), 204 orthologues and 1 paralogue. Ubiquitous expression in testis (RPKM 49.0), kidney (RPKM 36.6) and 25 other tissues.

功能概要

参与 ERAD 通路;通过多泡体分选途径将核内体转运至溶酶体;和巨自噬。位于细胞器和细胞质的边界膜上。是膜的外在成分。内体和含蛋白质复合物的一部分。 [由基因组资源联盟提供,2022 年 4 月]

Involved in ERAD pathway; endosome to lysosome transport via multivesicular body sorting pathway; and macroautophagy. Located in bounding membrane of organelle and cytosol. Is extrinsic component of membrane. Part of endosome and protein-containing complex. [provided by Alliance of Genome Resources, Apr 2022]

UBXN6 基因产物(2)

mRNA Protein Name
NM_001171091.2 NP_001164562.1 UBX domain-containing protein 6 isoform 2
NM_025241.3 NP_079517.1 UBX domain-containing protein 6 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 protein binding IPI
IPI: 通过物理相互作用推断
18656546 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in ERAD pathway IMP
IMP: 通过突变表型推断
19275885 GOA
involved in endosome to lysosome transport via multivesicular body sorting pathway IMP
IMP: 通过突变表型推断
21822278 GOA
involved in macroautophagy IMP
IMP: 通过突变表型推断
27753622 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cytoplasm IDA
IDA: 通过直接分析推断
27753622 GOA
located in cytosol IDA
IDA: 通过直接分析推断
19275885 GOA
located in early endosome membrane IDA
IDA: 通过直接分析推断
21822278 GOA
located in endosome IDA
IDA: 通过直接分析推断
26475856 GOA
located in late endosome membrane IDA
IDA: 通过直接分析推断
21822278 GOA
located in lysosomal membrane IDA
IDA: 通过直接分析推断
21822278 GOA
located in membrane IDA
IDA: 通过直接分析推断
19275885 GOA
part of protein-containing complex IDA
IDA: 通过直接分析推断
21822278 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

UBXN6 蛋白结构

PUB

PUB: PUB domain (166 - 260)

UBX

UBX: UBX domain (333 - 409)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 441 a.a.
蛋白主名 其他名称

UBX domain-containing protein 6

CTB-50L17.16

UBXN6 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
种属内
UBXN6 Q9BZV1 MAGEA4 Homo sapiens Q1RN33 25416956
种属内
UBXN6 Q9BZV1 MAGEA4 Homo sapiens Q1RN33 25416956
种属内
UBXN6 Q9BZV1 MAGEA4 Homo sapiens Q1RN33 25416956
种属内
UBXN6 Q9BZV1 TRIM39 Homo sapiens Q9HCM9-2 32296183
种属内
UBXN6 Q9BZV1 TRIM39 Homo sapiens Q9HCM9-2 32296183
种属内
UBXN6 Q9BZV1 TRIM39 Homo sapiens Q9HCM9-2 32296183
种属内
UBXN6 Q9BZV1 FAM168A Homo sapiens Q92567-2 32296183
种属内
UBXN6 Q9BZV1 FAM168A Homo sapiens Q92567-2 32296183
种属内
UBXN6 Q9BZV1 UBXN2A Homo sapiens P68543 32296183
种属内
UBXN6 Q9BZV1 UBXN2A Homo sapiens P68543 32296183
种属内
UBXN6 Q9BZV1 UBXN2A Homo sapiens P68543 33961781
种属内
UBXN6 Q9BZV1 SVIP Homo sapiens Q8NHG7 32296183
种属内
UBXN6 Q9BZV1 SVIP Homo sapiens Q8NHG7 32296183
种属内
UBXN6 Q9BZV1 SUSD6 Homo sapiens Q92537 32296183
种属内
UBXN6 Q9BZV1 SUSD6 Homo sapiens Q92537 32296183
种属内
UBXN6 Q9BZV1 VCP Homo sapiens P55072 32814053
种属内
UBXN6 Q9BZV1 VCP Homo sapiens P55072 18656546
种属内
UBXN6 Q9BZV1 VCP Homo sapiens P55072 33961781
种属内
UBXN6 Q9BZV1 VCP Homo sapiens P55072 32814053
种属内
UBXN6 Q9BZV1 VCP Homo sapiens P55072 29997244
种属内
UBXN6 Q9BZV1 VCP Homo sapiens P55072 32814053
种属内
UBXN6 Q9BZV1 VCP Homo sapiens P55072 18656546
种属内
UBXN6 Q9BZV1 VCP Homo sapiens P55072 29997244
种属内
UBXN6 Q9BZV1 VCP Homo sapiens P55072 18775313
种属内
UBXN6 Q9BZV1 PLEKHB2 Homo sapiens Q96CS7 32296183
种属内
UBXN6 Q9BZV1 PLEKHB2 Homo sapiens Q96CS7 32296183
种属内
UBXN6 Q9BZV1 DAZAP2 Homo sapiens Q15038 32296183
种属内
UBXN6 Q9BZV1 DAZAP2 Homo sapiens Q15038 32296183
种属内
UBXN6 Q9BZV1 TRIM39 Homo sapiens Q9HCM9 25416956
种属内
UBXN6 Q9BZV1 MAGEA4 Homo sapiens P43358 32296183
种属内
UBXN6 Q9BZV1 MAGEA4 Homo sapiens P43358 32296183
种属内
UBXN6 Q9BZV1 MAGEA4 Homo sapiens P43358 31515488
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
Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia

Ibmpfd

Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia

Pagetoid Amyotrophic Lateral Sclerosis

Pagetoid Neuroskeletal Syndrome

Inclusion Body Myopathy With Paget Disease Of Bone And/Or Frontotemporal Dementia

Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone And/Or Frontotemporal Dementia

Multisystem Proteinopathy

Limb-Girdle Muscular Dystrophy With Paget Disease Of Bone

Inclusion Body Myopathy With Paget'S Disease Of Bone And Frontotemporal Dementia

Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dement

Lower Motor Neuron Degeneration With Paget-Like Bone Disease

Muscular Dystrophy, Limb-Girdle, With Paget Disease Of Bone

Myopathy, Inclusion Body, With Early-Onset Paget Disease And Frontotemporal Dementia

Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 1

Ibmpfd1

Msp1

Multisystem Proteinopathy 1

Multisystem Proteinopathy
Mammary Paget'S Disease

Paget'S Disease

Mammary Paget Disease

Paget'S Disease Of The Breast

Paget Disease Of The Breast

Paget'S Disease Of The Nipple

Paget'S Disease, Mammary

Paget Cell Neoplasm

Paget Disease Of The Nipple

Pagets Disease Mammary

Osteitis Deformans

Paget'S Disease Of Bone

Osteitis Deformans

Paget Disease Of Bone

Osseous Paget'S Disease

Paget Disease Of Bone, Familial

Bone Paget Disease

Familial Paget'S Disease Of Bone

Paget'S Bone Disease

Familial Paget Disease Of Bone

Paget Disease, Bone

Pdb

Pagets Bone Disease

Charcot-Marie-Tooth Disease, Axonal, Type 2e

Charcot-Marie-Tooth Disease Type 2

CMT2E

CMT2S

CMT2Y

Charcot-Marie-Tooth Disease Type 2e

Charcot-Marie-Tooth Disease Type 2y

Charcot-Marie-Tooth Disease Axonal Type 2s

Charcot-Marie-Tooth Disease, Axonal, Type 2s

Charcot-Marie-Tooth Disease, Type 2e

Hereditary Motor And Sensory Neuropathy Type 2

Charcot-Marie-Tooth Neuropathy, Type 2s

Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2s

Charcot-Marie-Tooth Disease, Axonal, Type 2y

Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2y

Charcot-Marie-Tooth Neuropathy, Type 2y

Charcot-Marie-Tooth Disease, Type 2y

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2e

Charcot-Marie-Tooth Neuropathy Type 2e

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Vcp Mutation

Cmt2 Due To Vcp Mutation

Charcot-Marie-Tooth Disease Type 2s

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2

Autosomal Dominant Axonal Charcot-Marie-Tooth Disease

Cmt2

Charcot-Marie-Tooth Neuropathy, Type 2e

Hereditary Motor And Sensory Neuropathy Guadalajara Neuronal Type

Hereditary Motor And Sensory Neuropathy Okinawa Type

Autosomal Dominant Axonal Charcot-Marie-Tooth Type 2y

Charcot-Marie-Tooth Neuropathy Type 2y

Autosomal Recessive Axonal Charcot-Marie-Tooth Type 2s

Charcot-Marie-Tooth Neuropathy Type 2s

Charcot-Marie-Tooth Type 2

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2y

Charcot-Marie-Tooth Disease 2e

Charcot-Marie-Tooth Disease Axonal Type 2e

Charcot-Marie-Tooth Disease Neuronal Type 2e

Charcot-Marie-Tooth Disease 2s

Charcot-Marie-Tooth Neuropathy Axonal Type 2s

Charcot-Marie-Tooth Disease 2y

Charcot-Marie-Tooth Disease, Type 2

Hereditary Motor And Sensory-Neuropathy Type Ii

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
Bos taurus UBXN6 VGNC VGNC:36628
Macaca mulatta UBXN6 VGNC VGNC:78971
Canis familiaris UBXN6 VGNC VGNC:48101
Rattus norvegicus UBXN6 RGD RGD:1590866
Felis catus UBXN6 VGNC VGNC:80752
Mus musculus UBXN6 MGD MGI:1913780