1. Gene
  2. PIP5K1C - phosphatidylinositol-4-phosphate 5-kinase type 1 gamma Gene

PIP5K1C - phosphatidylinositol-4-phosphate 5-kinase type 1 gamma Gene

中文名称:磷脂酰肌醇 4-磷酸 5-激酶 1 型γ

种属: Homo sapiens

同用名: LCCS3; PIP5Kgamma; PIP5K-GAMMA; PIP5K1-gamma

基因 ID: 23396 | 基因类型: protein coding

关于 PIP5K1C

Cytogenetic location: 19p13.3 Genomic coordinates (GRCh38): 19:3,630,183-3,700,468 (from NCBI)

This gene has 10 transcripts (splice variants), 265 orthologues, 6 paralogues and is associated with 3 phenotypes. Broad expression in testis (RPKM 14.7), brain (RPKM 13.9) and 25 other tissues.

功能概要

该基因座编码 I 型磷脂酰肌醇 4-磷酸 5-激酶。编码的蛋白质催化磷脂酰肌醇 4-磷酸的磷酸化,产生磷脂酰肌醇 4,5-二磷酸。这种酶存在于突触中,并被发现在内吞作用和细胞迁移中发挥作用。该位点的突变与致命的先天性挛缩综合征有关。已经描述了编码不同亚型的选择性剪接转录变体。[RefSeq 提供,2010 年 9 月]

This locus encodes a type I phosphatidylinositol 4-phosphate 5-kinase. The encoded protein catalyzes phosphorylation of phosphatidylinositol 4-phosphate, producing phosphatidylinositol 4,5-bisphosphate. This Enzyme is found at synapses and has been found to play roles in endocytosis and cell migration. Mutations at this locus have been associated with lethal congenital contractural syndrome. Alternatively spliced transcript variants encoding different isoforms have been described.[provided by RefSeq, Sep 2010]

PIP5K1C 基因产物(3)

mRNA Protein Name
NM_001195733.2 NP_001182662.1 phosphatidylinositol 4-phosphate 5-kinase type-1 gamma isoform 1
NM_001300849.2 NP_001287778.1 phosphatidylinositol 4-phosphate 5-kinase type-1 gamma isoform 3
NM_012398.3 NP_036530.1 phosphatidylinositol 4-phosphate 5-kinase type-1 gamma isoform 2

PIP5K1C 蛋白结构

PIP5K

PIP5K: Phosphatidylinositol-4-phosphate 5-Kinase (158 - 442)

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

phosphatidylinositol 4-phosphate 5-kinase type-1 gamma

PIP5K1gamma

关联疾病

疾病名称 别名
Lethal Congenital Contracture Syndrome 3

LCCS3

Lethal Congenital Contractural Syndrome 3

Multiple Contracture Syndrome, Israeli Bedouin Type B

Israeli Bedouin Type B Multiple Contracture Syndrome

Lethal Congenital Contracture Syndrome Type 3

Multiple Contractural Syndrome Israeli Bedouin Type B

Contracture Syndrome, Lethal, Congenital, Type 3

Lethal Congenital Contracture Syndrome

Lccs

Lethal Congenital Contracture Syndrome 1

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

Neurogenic Bladder

Neurogenic Dysfunction Of The Urinary Bladder

Neurogenic Urinary Bladder Disorder

Neuropathic Bladder

Bladder Neurogenic

Urinary Bladder, Neurogenic

Neurogenic Urinary Bladder

Lethal Congenital Contracture Syndrome 1

LCCS1

Multiple Contracture Syndrome, Finnish Type

Lccs

Lethal Autosomal Recessive Syndrome Of Multiple Congenital Contractures

Lethal Congenital Contracture Syndrome Type 1

Herva Disease

Multiple Contracture Syndrome Finnish Type

Contracture Syndrome, Lethal, Congenital, Type 1

Arthrogryposis, Distal, Type 5

Oculomelic Amyoplasia

Distal Arthrogryposis Type 5

Distal Arthrogryposis Type Iib

DA5

Arthrogryposis With Oculomotor Limitation And Electroretinal Abnormalities

Daiib

Distal Arthrogryposis Type 2b

Arthrogryposis-Oculomotor Limitation-Electroretinal Anomalies Syndrome

Distal Arthrogryposis With Ophthalmoplegia

Arthrogryposis- Oculomotor Limitation-Electroretinal Anomalies Syndrome

Arthrogryposis, Distal, Type Iib

Da2b

Freeman-Sheldon Syndrome Variant

Sheldon-Hall Syndrome

Arthogryposis With Oculomotor Limitation And Electroretinal Abnormalities

Arthrogryposis Ophthalmoplegia Retinopathy

Arthrogryposis, Distal, 5

Arthrogryposis, Distal, Type 2b

Cerebellar Ataxia, Cayman Type

Cayman Type Cerebellar Ataxia

Ataxia, Cerebellar, Cayman Type

ATCAY

Cayman Cerebellar Ataxia

Cayman Ataxia

Multiple Pterygium Syndrome, Escobar Variant

Multiple Pterygium Syndrome

Pterygium

Escobar Syndrome

EVMPS

Pterygium Syndrome

Autosomal Recessive Multiple Pterygium Syndrome

Pterygium Colli Syndrome

Pterygium Universale

Autosomal Recessive Non-Lethal Multiple Pterygium Syndrome

Escobar Variant Multiple Pterygium Syndrome

Multiple Pterygium Syndrome, Nonlethal Type

Surfer'S Eye

Multiple Pterygium Syndrome Escobar Type

Multiple Pterygium Syndrome Nonlethal Type

Familial Pterygium Syndrome

Pterygium Colli

Multiple Pterygium Syndrome, Non-Lethal Type

Nonlethal Type Multiple Pterygium Syndrome

Pterygium Syndrome, Multiple, Escobar Type

Pterygium Of Eye

Web Eye

Macrocephaly/Autism Syndrome

Macrocephaly-Autism Syndrome

Macrocephaly-Intellectual Disability-Autism Syndrome

MCEPHAS

Distal Arthrogryposis

Arthrogryposis Multiplex Congenita

Arthrogryposis

Congenital Multiple Arthrogryposis

Congenital Arthromyodysplasia

Fibrous Ankylosis Of Multiple Joints

Guerin-Stern Syndrome

Guérin-Stern Syndrome

Myodystrophia Fetalis Deformans

Otto Syndrome

Rocher-Sheldon Syndrome

Rossi Syndrome

Amc

Multiple Congenital Arthrogryposis

Arthrogryposis Syndrome

Arthrogryposis, Distal

Distal Arthrogryposis Syndrome

Freeman-Sheldon Syndrome

Arthrogryposis, Distal, Type 2b

Congenital Multiplex Arthrogryposis

Amyoplasia Congenita

Congenital Amyoplasia

Amc - [Arthrogryposis Multiplex Congenita]

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

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
Canis familiaris PIP5K1C VGNC VGNC:44576
Felis catus PIP5K1C VGNC VGNC:68863
Mus musculus PIP5K1C MGD MGI:1298224
Rattus norvegicus PIP5K1C RGD RGD:1309938
Bos taurus PIP5K1C VGNC VGNC:32912
Macaca mulatta PIP5K1C VGNC VGNC:76002