1. Gene
  2. KATNAL2 - katanin catalytic subunit A1 like 2 Gene

KATNAL2 - katanin catalytic subunit A1 like 2 Gene

中文名称:katanin 催化亚基 A1 样 2

种属: Homo sapiens

基因 ID: 83473 | 基因类型: protein coding

关于 KATNAL2

Cytogenetic location: 18q21.1 Genomic coordinates (GRCh38): 18:46,917,594-47,102,243 (from NCBI)

This gene has 25 transcripts (splice variants), 202 orthologues and 9 paralogues. Broad expression in testis (RPKM 2.3), thyroid (RPKM 1.9) and 23 other tissues.

功能概要

预计会启用微管切断 ATP 酶活性。预计参与细胞质微管组织。位于细胞质中;微管;和主轴杆。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to enable microtubule-severing ATPase activity. Predicted to be involved in cytoplasmic microtubule organization. Located in cytoplasm; microtubule; and spindle pole. [provided by Alliance of Genome Resources, Apr 2022]

KATNAL2 基因产物(14)

mRNA Protein Name
NM_001353899.1 NP_001340828.1 katanin p60 ATPase-containing subunit A-like 2 isoform 1
NM_001353900.1 NP_001340829.1 katanin p60 ATPase-containing subunit A-like 2 isoform 2
NM_001353901.1 NP_001340830.1 katanin p60 ATPase-containing subunit A-like 2 isoform 3
NM_001353902.1 NP_001340831.1 katanin p60 ATPase-containing subunit A-like 2 isoform 4
NM_001353903.1 NP_001340832.1 katanin p60 ATPase-containing subunit A-like 2 isoform 6
NM_001353904.1 NP_001340833.1 katanin p60 ATPase-containing subunit A-like 2 isoform 7
NM_001353905.1 NP_001340834.1 katanin p60 ATPase-containing subunit A-like 2 isoform 8
NM_001353906.1 NP_001340835.1 katanin p60 ATPase-containing subunit A-like 2 isoform 8
NM_001353907.1 NP_001340836.1 katanin p60 ATPase-containing subunit A-like 2 isoform 9
NM_001353908.1 NP_001340837.1 katanin p60 ATPase-containing subunit A-like 2 isoform 10
NM_001353909.1 NP_001340838.1 katanin p60 ATPase-containing subunit A-like 2 isoform 11
NM_001367621.1 NP_001354550.1 katanin p60 ATPase-containing subunit A-like 2 isoform 13
NM_001387690.1 NP_001374619.1 katanin p60 ATPase-containing subunit A-like 2 isoform 13
NM_031303.3 NP_112593.2 katanin p60 ATPase-containing subunit A-like 2 isoform 5
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
25910212 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
26929214 GOA
located in microtubule IDA
IDA: 通过直接分析推断
26929214 GOA
located in spindle IDA
IDA: 通过直接分析推断
26929214 GOA
located in spindle pole IDA
IDA: 通过直接分析推断
26929214 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

KATNAL2 蛋白结构

LisH

LisH: LisH (27 - 53)

AAA

AAA: ATPase family associated with various cellular activities (AAA) (290 - 421)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 538 a.a.
蛋白主名 其他名称

katanin p60 ATPase-containing subunit A-like 2

katanin catalytic subunit A like 2

KATNAL2 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
KATNAL2 Q8IYT4 LNX1 Homo sapiens Q8TBB1 32296183
种属内
KATNAL2 Q8IYT4 LNX1 Homo sapiens Q8TBB1 32296183
种属内
KATNAL2 Q8IYT4 LNX1 Homo sapiens Q8TBB1 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
Schizophrenia

SCZD

Schizophrenia With Or Without An Affective Disorder

Schizophrenia 12

Schizophrenia, Susceptibility To

Schizophrenia-1

Dementia Praecox

Schizophrenia 1

Fraser Syndrome 2

FRASRS2

Ceroid Lipofuscinosis, Neuronal, 8

Neuronal Ceroid Lipofuscinosis 8

CLN8

Cln8 Disease

Epilepsy Mental Deterioration Finnish Type

Northern Epilepsy

Cln8 Disease, Epmr

Cln8 Disease, Northern Epilepsy Variant

Cln8 Disease, Late Infantile

Ceroid Lipofuscinosis Neuronal 8

Ncl, Northern Epilepsy Variant

Neuronal Ceroid Lipofuscinosis, Northern Epilepsy Variant

Progressive Epilepsy - Intellectual Disability, Finnish Type

Progressive Epilepsy-Intellectual Disability Syndrome, Finnish Type

Turkish Variant Late Infantile Ncl

Ceroid Lipofuscinosis, Neuronal 8

Lipofuscinosis, Ceroid, Neuronal, Type 8

Northern Epilepsy Syndrome

Bainbridge-Ropers Syndrome

BRPS

Severe Feeding Difficulties-Failure To Thrive-Microcephaly Due To Asxl3 Deficiency Syndrome

Asxl3-Related Disorder

Meningioma, Familial

Meningioma

Familial Meningioma

Meningioma, Familial, Susceptibility To

Meningeal Neoplasm

Meningeal Neoplasms

Meningiomas

Meningioma, Nf2-Related, Somatic

Meningioma, Sis-Related

Meningothelial Cell Tumor

Neoplasm Of The Meninges

Primary Meningeal Tumor

Familial Multiple Meningioma

MNGMA

Meningioma, Benign, No Icd-O Subtype

Intracranial Meningioma

Meningothelial Cell Neoplasm

Supratentorial Meningioma

Primary Neoplasm Of Spinal Meninges

Benign Intracranial Meningioma

Benign Meningioma

Meningeal Tumours

Meningeal Sarcoma Of Unspecified Site

Meningothelial Sarcoma Of Unspecified Site

Coffin-Siris Syndrome 1

Coffin-Siris Syndrome

Fifth Digit Syndrome

Css

CSS1

Mrd12

Mental Retardation, Autosomal Dominant 12

Hhid

Dwarfism-Onychodysplasia

Hypertrichosis, Hyperkeratosis, Mental Retardation, And Distinctive Facial Features

Autosomal Dominant Mental Retardation 12

Short Stature-Onychodysplasia.

Intellectual Disability With Absent Fifth Fingernail And Terminal Phalanx

Mental Retardation With Hypoplastic Fifth Fingernails And Toenails

Short Stature-Onychodysplasia

Coffin-Siris Syndrome, Type 1

Mental Retardation, Autosomal Dominant, Type 12

Autism

Autistic Disorder

Autism Susceptibility 1

Childhood Autism

Autistic Disorder Of Childhood Onset

Infantile Autism

Kanner'S Syndrome

Autistic

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
Macaca mulatta KATNAL2 VGNC VGNC:73904
Bos taurus KATNAL2 VGNC VGNC:30407
Mus musculus KATNAL2 MGD MGI:1924234
Rattus norvegicus KATNAL2 RGD RGD:1564708
Felis catus KATNAL2 VGNC VGNC:63029
Canis familiaris KATNAL2 VGNC VGNC:42218