1. Gene
  2. ATL2 - atlastin GTPase 2 Gene

ATL2 - atlastin GTPase 2 Gene

中文名称:阿特拉斯蛋白 GTPase 2

种属: Homo sapiens

同用名: aip-2; ARL3IP2; ARL6IP2; atlastin2

基因 ID: 64225 | 基因类型: protein coding

关于 ATL2

Cytogenetic location: 2p22.2-p22.1 Genomic coordinates (GRCh38): 2:38,293,954-38,378,584 (from NCBI)

This gene has 18 transcripts (splice variants), 297 orthologues and 10 paralogues. Ubiquitous expression in thyroid (RPKM 13.5), skin (RPKM 9.8) and 25 other tissues.

功能概要

实现相同的蛋白质结合活性。参与高尔基组织;内质网管状网络膜组织;和蛋白质同源寡聚化。位于内质网管状网络膜上。是膜的组成部分。 [由基因组资源联盟提供,2022 年 4 月]

Enables identical protein binding activity. Involved in Golgi organization; endoplasmic reticulum tubular network membrane organization; and protein homooligomerization. Located in endoplasmic reticulum tubular network membrane. Is integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

ATL2 基因产物(10)

mRNA Protein Name
NM_001135673.4 NP_001129145.1 atlastin-2 isoform 2
NM_001308076.1 NP_001295005.1 atlastin-2 isoform 3
NM_001330458.2 NP_001317387.1 atlastin-2 isoform 4
NM_001330459.1 NP_001317388.1 atlastin-2 isoform 5
NM_001330460.1 NP_001317389.1 atlastin-2 isoform 6
NM_001330461.2 NP_001317390.1 atlastin-2 isoform 6
NM_001330462.1 NP_001317391.1 atlastin-2 isoform 7
NM_001330463.2 NP_001317392.1 atlastin-2 isoform 8
NM_001330464.2 NP_001317393.1 atlastin-2 isoform 9
NM_022374.5 NP_071769.2 atlastin-2 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 identical protein binding IDA
IDA: 通过直接分析推断
18270207 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
15161933 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in Golgi organization IMP
IMP: 通过突变表型推断
18270207 GOA
involved in endoplasmic reticulum organization IMP
IMP: 通过突变表型推断
18270207 GOA
NOT involved in endoplasmic reticulum to Golgi vesicle-mediated transport IMP
IMP: 通过突变表型推断
18270207 GOA
involved in endoplasmic reticulum tubular network membrane organization IMP
IMP: 通过突变表型推断
27619977 GOA
involved in protein homooligomerization IDA
IDA: 通过直接分析推断
18270207 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in endoplasmic reticulum IDA
IDA: 通过直接分析推断
18270207 GOA
located in endoplasmic reticulum tubular network membrane IDA
IDA: 通过直接分析推断
27619977 GOA
located in membrane IDA
IDA: 通过直接分析推断
18270207 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

ATL2 蛋白结构

GBP

GBP: Guanylate-binding protein, N-terminal domain (70 - 341)

GBP_C

GBP_C: Guanylate-binding protein, C-terminal domain (344 - 464)

  • 0
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  • 200
  • 300
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  • 500
  • 583 a.a.
蛋白主名 其他名称

atlastin-2

ADP-ribosylation factor-like protein 6-interacting protein 2

ATL2 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
种属间
ATL2 Q8NHH9 Rtn3 Mus musculus Q9ES97-3 19665976
种属间
ATL2 Q8NHH9 Reep5 Mus musculus Q60870 19665976
种属内
ATL2 Q8NHH9 YWHAZ Homo sapiens P63104 15161933
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
Spastic Paraplegia 3a

Spg3a

Atl1-Hsp

Spastic Paraplegia Type 3a

Spastic Paraplegia 3

Spastic Paraplegia 3, Autosomal Dominant

Adult T-Cell Leukemia/Lymphoma

Adult T-Cell Leukemia

Atll

Adult T-Cell Leukaemia

Adult T-Cell Leukaemia/Lymphoma

Adult T-Cell Lymphoma

T Cell Leukemia Lymphoma Adult

Leukemia-Lymphoma, Adult T-Cell

Leukemia, T-Cell

Adult T-Cell Lymphoma/Leukemia

Spondylolysis

Acquired Spondylolysis

Hereditary Sensory And Autonomic Neuropathy Type 1

Hereditary Sensory And Autonomic Neuropathy Type I

Hereditary Sensory Neuropathy-Deafness-Dementia Syndrome

Hsan1e

Hsan1

Dnmt1-Related Dementia, Deafness, And Sensory Neuropathy

Hsn1e

Hsnie

Hereditary Sensory Neuropathy Type Ie

Hereditary Sensory Neuropathy-Sensorineural Hearing Loss-Dementia Syndrome

Hereditary Sensory And Autonomic Neuropathy Type Ie

Hereditary Sensory And Autonomic Neuropathy Type 1e

Hereditary Sensory Neuropathy With Hearing Loss And Dementia

Dnmt1-Complex Disorder

Hereditary Sensory And Autonomic Neuropathy Type 1 With Dementia And Hearing Loss

Hsn Ie

Hereditary Sensory Autonomic Neuropathy, Type 1

Hsan1- [Hereditary Sensory And Autonomic Neuropathy Type I]

Hereditary Sensory Neuropathy

Hereditary Sensory And Autonomic Neuropathy

Hereditary Sensory And Autonomic Neuropathies

Familial Dysautonomia, Type Ii

Hsan

Sensory Neuropathy Hereditary

Neuropathy, Sensory And Autonomic, Hereditary

Neuropathy, Sensory, Hereditary

Sensory Neuropathy, Hereditary

Charcot-Marie-Tooth Disease

Cmt - [Charcot-Marie-Tooth Disease]

Hereditary Spastic Paraplegia

Familial Spastic Paraplegia

Hereditary Spastic Paraparesis

Strumpell-Lorrain Disease

Familial Spastic Paraparesis

Hsp

Spg

Strümpell-Lorrain Disease

Spastic Paraplegia, Hereditary

French Settlement Disease

Strumpell-Lorrain Syndrome

Fsp

Spastic Paraplegia, Familial

Spastic Paraplegia Hereditary

Spastic Paraplegia 3, Autosomal Dominant

Spastic Paraparesis

Hereditary Spastic Paralysis

Familial Spastic Paralysis

Hereditary Spastic Ataxia

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 ATL2 VGNC VGNC:26266
Felis catus ATL2 VGNC VGNC:60009
Rattus norvegicus ATL2 RGD RGD:1305125
Mus musculus ATL2 MGD MGI:1929492
Canis familiaris ATL2 VGNC VGNC:38231
Macaca mulatta ATL2 VGNC VGNC:70116
Others ATL2 NCBI