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  2. NEK9 - NIMA related kinase 9 Gene

NEK9 - NIMA related kinase 9 Gene

中文名称:NIMA 相关激酶 9

种属: Homo sapiens

同用名: NC; APUG; NERCC; LCCS10; NERCC1

基因 ID: 91754 | 基因类型: protein coding

关于 NEK9

Cytogenetic location: 14q24.3 Genomic coordinates (GRCh38): 14:75,079,353-75,127,202 (from NCBI)

This gene has 18 transcripts (splice variants), 200 orthologues, 8 paralogues and is associated with 5 phenotypes. Ubiquitous expression in ovary (RPKM 24.4), testis (RPKM 21.8) and 25 other tissues.

功能概要

该基因编码 NimA (从未在有丝分裂 A 中) 丝氨酸/苏氨酸蛋白激酶家族的成员。编码的蛋白质在有丝分裂中被激活,进而在有丝分裂期间激活其他家族成员。这种蛋白质还介导对间期进展至关重要的细胞过程。[RefSeq 提供,2016 年 7 月]

This gene encodes a member of the NimA (never in mitosis A) family of serine/threonine protein kinases. The encoded protein is activated in mitosis and, in turn, activates Other family members during mitosis. This protein also mediates cellular processes that are essential for interphase progression. [provided by RefSeq, Jul 2016]

NEK9 基因产物(3)

mRNA Protein Name
NM_001329237.2 NP_001316166.1 serine/threonine-protein kinase Nek9 isoform 1
NM_001329238.2 NP_001316167.1 serine/threonine-protein kinase Nek9 isoform 3
NM_033116.6 NP_149107.4 serine/threonine-protein kinase Nek9 isoform 2
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
20562859 GOA
enables protein kinase activator activity IDA
IDA: 通过直接分析推断
12840024 GOA
enables protein kinase binding IPI
IPI: 通过物理相互作用推断
19001501 GOA
enables protein serine/threonine kinase activity IDA
IDA: 通过直接分析推断
12840024 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in mitotic cell cycle IDA
IDA: 通过直接分析推断
12840024 GOA
involved in regulation of mitotic cell cycle IDA
IDA: 通过直接分析推断
19941817 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
colocalizes with centrosome IDA
IDA: 通过直接分析推断
20873783 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

NEK9 蛋白结构

Pkinase

Pkinase: Protein kinase domain (55 - 307)

RCC1

RCC1: Regulator of chromosome condensation (RCC1) repeat (403 - 441)

RCC1

RCC1: Regulator of chromosome condensation (RCC1) repeat (444 - 495)

RCC1

RCC1: Regulator of chromosome condensation (RCC1) repeat (500 - 547)

RCC1

RCC1: Regulator of chromosome condensation (RCC1) repeat (616 - 664)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 979 a.a.
蛋白主名 其他名称

serine/threonine-protein kinase Nek9

NIMA (never in mitosis gene a)- related kinase 9

NEK9 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
NEK9 Q8TD19 MAP1LC3C Homo sapiens Q9BXW4 20562859
种属内
NEK9 Q8TD19 DYNLL1 Homo sapiens P63167 35271311
种属内
NEK9 Q8TD19 DYNLL1 Homo sapiens P63167 25852190
种属内
NEK9 Q8TD19 DYNLL1 Homo sapiens P63167 20562859
种属内
NEK9 Q8TD19 HSP90AB1 Homo sapiens P08238 22939624
种属内
NEK9 Q8TD19 HSP90AB1 Homo sapiens P08238 22939624
种属内
NEK9 Q8TD19 YWHAE Homo sapiens P62258 36931259
种属内
NEK9 Q8TD19 MAP1LC3B Homo sapiens Q9GZQ8 20562859
种属内
NEK9 Q8TD19 PLK1 Homo sapiens P53350
Y2H
21642957
种属内
NEK9 Q8TD19 PLK1 Homo sapiens P53350 21642957
种属内
NEK9 Q8TD19 GABARAP Homo sapiens O95166 20562859
种属内
NEK9 Q8TD19 GABARAPL2 Homo sapiens P60520 20562859
种属内
NEK9 Q8TD19 GABARAPL1 Homo sapiens Q9H0R8 20562859
种属间: 跨种属相互作用 种属内: 同种属相互作用

NEK9 抗体

目录号 产品名 应用 反应物种
HY-P81617 NEK9 Antibody (YA1362) WB, IHC-F, IHC-P, ICC/IF Human, Rat

关联疾病

疾病名称 别名
Nevus Comedonicus

Nevus Comedonicus Syndrome

NC

Nevus Comedonicus, Somatic

Arthrogryposis, Perthes Disease, And Upward Gaze Palsy

APUG

Lethal Congenital Contracture Syndrome 10

Nek9-Related Lethal Skeletal Dysplasia

LCCS10

Lethal Skeletal Dysplasia-Fetal Akinesia-Contractures-Thoracic Dysplasia-Pulmonary Hypoplasia Syndrome

Goldberg-Shprintzen Syndrome

Goldberg-Shprintzen Megacolon Syndrome

GOSHS

Megacolon-Microcephaly Syndrome

Avascular Necrosis

Avn

Nephronophthisis 9

NPHP9

Nephronophthisis, Type 9

Lethal Congenital Contracture Syndrome

Lccs

Lethal Congenital Contracture Syndrome 1

Combined Oxidative Phosphorylation Deficiency 16

COXPD16

Infantile Hypertrophic Cardiomyopathy Due To Mrpl44 Deficiency

Combined Oxidative Phosphorylation Defect Type 16

Combined Oxidative Phosphorylation Deficiency, Type 16

Nephronophthisis 16

NPHP16

Nephronophthisis, Type 16

Nephronophthisis 20

NPHP20

Nephronophthisis 7

NPHP7

Nephronophthisis, Type 7

Nephronophthisis 14

Joubert Syndrome 19

NPHP14

JBTS19

Nephronophthisis, Type 14

Uterine Adnexa Cancer
Lethal Congenital Contracture Syndrome 2

LCCS2

Lethal Congenital Contractural Syndrome 2

Multiple Contracture Syndrome, Israeli-Bedouin Type

Multiple Contracture Syndrome, Israeli Bedouin Type A

Multiple Contracture Syndrome, Israeli Bedouin Type

Lethal Congenital Contracture Syndrome Type 2

Israeli Bedouin Multiple Contracture Syndrome Type A

Contracture Syndrome, Lethal, Congenital, Type 2

Nephronophthisis 2

NPHP2

Nph2

Nephronophthisis 2, Infantile

Infantile Nephronophthisis 2

Infantile Nephronophthisis

Nephronophthisis, Type 2

Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease

Autosomal Recessive Polycystic Kidney Disease

Arpkd

Polycystic Kidney Disease, Autosomal Recessive

Polycystic Kidney And Hepatic Disease 1

Pkhd1

PKD4

Polycystic Kidney Disease 4 With Or Without Hepatic Disease

Polycystic Kidney Disease, Infantile, Type I

Polycystic Kidney Disease, Infantile Type

Polycystic Kidney, Autosomal Recessive

Pkd3, Formerly

Polycystic Kidney Disease 4, With Or Without Hepatic Disease

Arpkd/Chf

Ar-Pkd

Polycystic Kidney Disease 4, With Or Without Polycystic Liver Disease

Infantile Polycystic Kidney Disease Type I

Pkd3

Kidney, Polycystic, Disease, Type 4, With/Without Hepatic Disease

Polycystic Kidney Disease 3, Autosomal Dominant

Meckel Syndrome, Type 1

Meckel-Gruber Syndrome

Meckel Syndrome

Dysencephalia Splanchnocystica

Meckel Syndrome 1

MKS1

Mks

Gruber Syndrome

Meckel-Gruber Syndrome, Type 1

Mes

Dysencephalia Splachnocystica

Meckel Gruber Syndrome

Meckel Syndrome Type 1

Renal-Hepatic-Pancreatic Dysplasia

Ivemark'S Syndrome

Ivemark Ii Syndrome

Renohepaticopancreatic Dysplasia

Cystic Kidney Disease

Renal Cyst

Simple Renal Cyst

Kidney Cysts

Kidney Diseases, Cystic

Renal Cysts

Kidney Cyst

Cystic Kidney

Congenital Cystic Kidney Disease

Cystic Kidney Diseases

Bosniak 1 Cyst

Nephronophthisis

Medullary Cystic Disease

Medullary Cystic Kidney

Nph

Nphp

Kidney Disease, Cystic, Medullary

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

Visceral Heterotaxy

Situs Ambiguus

Heterotaxia

Heterotaxy Syndrome

Heterotaxy

Lateralization Defect

Situs Ambiguous

Left Isomerism

Htx

Ivemark Syndrome

Right Isomerism

Situs Ambiguus Viscerum

Incomplete Situs Inversus

Partial Situs Inversus

Heterotaxy, Visceral

Asplenia Syndrome

Bilateral Left-Sidedness

Polysplenia Syndrome

Moller Syndrome

Situs Inversus

Situs Inversus Viscerum

Laterality Sequence

Complete Transposition

Siv

Polycystic Kidney Disease

Polycystic Kidney Diseases

Pkd

Polycystic Renal Disease

Kidney Disease, Polycystic

Polycystic Kidney, Autosomal Dominant

Autosomal Dominant Polycystic Kidney Disease

Polycystic Kidney Disease, Adult Type

Adpkd

Polycystic Kidney Diseases

Polycystic Kidney, Autosomal Dominant

Congenital Biliary Ectasias

Polycystic Kidney And Hepatic Disease 1

Polycystic Kidney Disease, Autosomal Dominant

Kidney, Polycystic, Disease, Autosomal Dominant

Adult Polycystic Kidney Disease

Polycystic Kidney, Adult Type

Apckd - [Autosomal Polycystic Kidney Disease]

Asphyxiating Thoracic Dystrophy

Jeune Thoracic Dystrophy

Jeune Syndrome

Asphyxiating Thoracic Dysplasia

Short-Rib Thoracic Dysplasia With Or Without Polydactyly

Thoracic Pelvic Phalangeal Dystrophy

Asphyxiating Thoracic Chondrodystrophy

Atd

Chondroectodermal Dysplasia-Like Syndrome

Infantile Thoracic Dystrophy

Jeune Thoracic Dysplasia

Thoracic Asphyxiant Dystrophy

Thoracic-Pelvic-Phalangeal Dystrophy

Short-Rib Thoracic Dysplasia Without Polydactyly

Asphyxiating Thoracic Dystrophy Of The Newborn

Asphyxiating Thorax Dystrophy

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

Cakut

Renal Or Urinary Tract Malformation

Congenital Anomalies Of Kidney And Urinary Tract

Congenital Anomaly Of Kidney And Urinary Tract

Congenital Anomalies Of The Kidney And Urinary Tract

Kidney And Urinary Tract, Anomalies, Congenital

Renal Hypodysplasia, Nonsyndromic, 1

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

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

Fundus Dystrophy

Retinal Dystrophy

Retinal Dystrophies

Dystrophy, Retinal

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

直系同源

种属 基因名 来源 基因 ID
Bos taurus NEK9 VGNC VGNC:31999
Mus musculus NEK9 MGD MGI:2387995
Canis familiaris NEK9 VGNC VGNC:43735
Macaca mulatta NEK9 VGNC VGNC:75209
Felis catus NEK9 VGNC VGNC:63770
Rattus norvegicus NEK9 RGD RGD:1307187
Others NEK9 NCBI