1. Gene
  2. HYPK - huntingtin interacting protein K Gene

HYPK - huntingtin interacting protein K Gene

中文名称:亨廷顿相互作用蛋白 K

种属: Homo sapiens

同用名: HSPC136; C15orf63

基因 ID: 25764 | 基因类型: protein coding

关于 HYPK

Cytogenetic location: 15q15.3 Genomic coordinates (GRCh38): 15:43,800,421-43,804,427 (from NCBI)

This gene has 5 transcripts (splice variants) and 202 orthologues. Ubiquitous expression in fat (RPKM 18.1), prostate (RPKM 18.1) and 25 other tissues.

功能概要

启用蛋白质 N 末端结合活性。参与细胞凋亡过程和蛋白质稳定的负调节。位于细胞质中;微管细胞骨架;和核质。部分含蛋白质复合物。 [由基因组资源联盟提供,2022 年 4 月]

Enables protein N-terminus binding activity. Involved in negative regulation of apoptotic process and protein stabilization. Located in cytoplasm; microtubule cytoskeleton; and nucleoplasm. Part of protein-containing complex. [provided by Alliance of Genome Resources, Apr 2022]

HYPK 基因产物(2)

mRNA Protein Name
NM_001199885.1 NP_001186814.1 huntingtin-interacting protein K isoform 2
NM_016400.4 NP_057484.4 huntingtin-interacting protein K 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
17500595 GOA
enables protein folding chaperone EXP
EXP: 通过实验结果推断
18076027 GOA
enables protein folding chaperone IDA
IDA: 通过直接分析推断
18076027 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in negative regulation of apoptotic process IDA
IDA: 通过直接分析推断
17947297 GOA
involved in protein stabilization IDA
IDA: 通过直接分析推断
17947297 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
17947297 GOA
located in nucleus IDA
IDA: 通过直接分析推断
17947297 GOA
part of protein-containing complex IDA
IDA: 通过直接分析推断
17947297 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
蛋白主名 其他名称

huntingtin-interacting protein K

huntingtin yeast partner K

HYPK 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
HYPK Q9NX55 NAA15 Homo sapiens Q9BXJ9
Anti Tag CoIP
33961781
种属内
HYPK Q9NX55 NAA15 Homo sapiens Q9BXJ9
TAP
24981860
种属内
HYPK Q9NX55 TXLNA Homo sapiens P40222
Y2H Array
32296183
种属内
HYPK Q9NX55 TXLNA Homo sapiens P40222
Y2H Prey Pooling
25416956
种属内
HYPK Q9NX55 TXLNA Homo sapiens P40222
Validated Y2H
25416956
种属内
HYPK Q9NX55 TXLNA Homo sapiens P40222
Y2H Prey Pooling
32296183
种属内
HYPK Q9NX55 HTT Homo sapiens P42858
Y2H
17500595
种属内
HYPK Q9NX55 MAGEA1 Homo sapiens P43355
Validated Y2H
25416956
种属内
HYPK Q9NX55 MAGEA1 Homo sapiens P43355
Y2H Array
25416956
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
Microphthalmia, Syndromic 1

MCOPS1

Lenz Microphthalmia Syndrome

Lenz Dysplasia

Mcops4

Syndromic Microphthalmia 1

Lenz Microphthalmia

Maa

Microphthalmia Or Anophthalmos With Associated Anomalies

Syndromic Microphthalmia Type 4

Microphthalmia, Syndromic 4

Microphthalmia, Syndromic 4, Formerly

Mcops4, Formerly

Anop1, Formerly

Maa, Formerly

Lenz Type Microphthalmia

Syndromic Microphthalmia 4

Microphthalmia Lenz Type

Microphthalmia Syndromic 1

Syndromic Microphthalmia Type 1

Microphthalmia Syndromic 4

Microphthalmia With Ankyloblepharon And Intellectual Disability

Microphthalmia, Lenz Type

Microphthalmia-Ankyloblepharon-Intellectual Disability Syndrome

Microphthalmia, Syndromic, 1

Anop1

Microphthalmia, Syndromic, Type 1

46,Xx Sex Reversal 3

SRXX3

Chromosome Xq26 Duplication Syndrome

46,Xx Sex Reversal, Sox3-Related

46xx Sex Reversal 3

46,Xx Male Sex Reversal Sox3-Related

Ogden Syndrome

OGDNS

N-Terminal Acetyltransferase Deficiency

NATD

N-Alpha-Acetyltransferase

X-Linked Malformation And Infantile Lethality Syndrome

Premature Aging Appearance-Developmental Delay-Cardiac Arrhythmia Syndrome

Syndromic Microphthalmia

Microphthalmia, Syndromic

Dysgraphia

Agraphia

Developmental And Epileptic Encephalopathy 1

Epileptic Encephalopathy, Early Infantile, 1

Infantile Epileptic-Dyskinetic Encephalopathy

DEE1

Eiee1

Issx1

Xmesid

X-Linked Infantile Spasm Syndrome 1

X-Linked Infantile Spasm Syndrome

X-Linked Spasticity-Intellectual Disability-Epilepsy Syndrome

Developmental And Epileptic Encephalopathy, 1

Infantile Epileptic Dyskinetic Encephalopathy

Infantile Spasm Syndrome, X-Linked 1

West Syndrome, X-Linked

Ohtahara Syndrome, X-Linked

Early Infantile Epileptic Encephalopathy 1

Early Infantile Epileptic Encephalopathy-1

Issx

X-Linked Ohtahara Syndrome

X-Linked West Syndrome

Infantile Spasm Syndrome X-Linked 1

Myoclonic Epilepsy X-Linked With Intellectual Disability And Spasticity

Ohtahara Syndrome X-Linked

West Syndrome X-Linked

Encephalopathy, Epileptic, Early Infantile, Type 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
Macaca mulatta HYPK VGNC VGNC:84350
Felis catus HYPK VGNC VGNC:62862
Bos taurus HYPK VGNC VGNC:30015
Rattus norvegicus HYPK RGD RGD:1311457
Mus musculus HYPK MGD MGI:1914943