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  2. LHX5 - LIM homeobox 5 Gene

LHX5 - LIM homeobox 5 Gene

中文名称:LIM 同源框 5

种属: Homo sapiens

基因 ID: 64211 | 基因类型: protein coding

关于 LHX5

Cytogenetic location: 12q24.13 Genomic coordinates (GRCh38): 12:113,462,033-113,471,871 (from NCBI)

This gene has 2 transcripts (splice variants), 128 orthologues and 20 paralogues. Low expression observed in reference dataset.

功能概要

该基因编码属于一个大蛋白质家族的蛋白质,其成员携带 LIM 结构域,这是一个独特的富含半胱氨酸的锌结合结构域。编码的蛋白质可能作为转录调节因子发挥作用,并参与控制前脑的分化和发育。在小鼠中,这种蛋白质对于调节前体细胞增殖和控制海马发育过程中的神经元分化和迁移至关重要。这种蛋白质参与成年小鼠的学习和运动功能。[RefSeq 提供,2008 年 7 月]

This gene encodes a protein belonging to a large protein family, members of which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator and be involved in the control of differentiation and development of the forebrain. In mice, this protein is essential for the regulation of precursor cell proliferation and the control of neuronal differentiation and migration during hippocampal development. This protein is involved in learning and motor functions in adult mice. [provided by RefSeq, Jul 2008]

LHX5 基因产物(1)

mRNA Protein Name
NM_022363.3 NP_071758.1 LIM/homeobox protein Lhx5
基因本体论
  • 分子功能
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
32814053 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: 通过直接分析推断
28473536 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

LHX5 蛋白结构

LIM

LIM: LIM domain (5 - 60)

LIM

LIM: LIM domain (64 - 121)

Homeobox

Homeobox: Homeobox domain (181 - 237)

  • 0
  • 100
  • 200
  • 300
  • 402 a.a.
蛋白主名 其他名称

LIM/homeobox protein Lhx5

LIM homeobox protein 5

LHX5 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
Intra LHX5 Q9H2C1 DMWD Homo sapiens G5E9A7
Y2H Pooling
32814053
Intra LHX5 Q9H2C1 DMWD Homo sapiens G5E9A7
Validated Y2H
32814053
Intra LHX5 Q9H2C1 DMWD Homo sapiens G5E9A7
Y2H Array
32814053
Intra LHX5 Q9H2C1 FGFR3 Homo sapiens P22607
Y2H Array
32814053
Intra LHX5 Q9H2C1 FGFR3 Homo sapiens P22607
Validated Y2H
32814053
Intra LHX5 Q9H2C1 FGFR3 Homo sapiens P22607
Y2H Pooling
32814053
Intra LHX5 Q9H2C1 GSN Homo sapiens P06396
Y2H Array
32814053
Intra LHX5 Q9H2C1 GSN Homo sapiens P06396
Validated Y2H
32814053
Intra LHX5 Q9H2C1 GSN Homo sapiens P06396
Y2H Pooling
32814053
Intra LHX5 Q9H2C1 YWHAG Homo sapiens P61981
Validated Y2H
32814053
Intra LHX5 Q9H2C1 YWHAG Homo sapiens P61981
Y2H Array
32814053
Intra LHX5 Q9H2C1 YWHAG Homo sapiens P61981
Y2H Pooling
32814053
Intra LHX5 Q9H2C1 KAT5 Homo sapiens Q92993
Validated Y2H
32814053
Intra LHX5 Q9H2C1 KAT5 Homo sapiens Q92993
Y2H Pooling
32814053
Intra LHX5 Q9H2C1 KAT5 Homo sapiens Q92993
Y2H Array
32814053
Intra LHX5 Q9H2C1 HIP1 Homo sapiens O00291
Y2H Array
32814053
Intra LHX5 Q9H2C1 HIP1 Homo sapiens O00291
Y2H Pooling
32814053
Intra LHX5 Q9H2C1 HIP1 Homo sapiens O00291
Validated Y2H
32814053
Intra LHX5 Q9H2C1 PMP22 Homo sapiens A0A6Q8PF08
Y2H Array
32814053
Intra LHX5 Q9H2C1 PMP22 Homo sapiens A0A6Q8PF08
Y2H Pooling
32814053
Intra LHX5 Q9H2C1 PMP22 Homo sapiens A0A6Q8PF08
Validated Y2H
32814053
Intra LHX5 Q9H2C1 SPRED1 Homo sapiens Q7Z699
Validated Y2H
32814053
Intra LHX5 Q9H2C1 SPRED1 Homo sapiens Q7Z699
Y2H Array
32814053
Intra LHX5 Q9H2C1 SPRED1 Homo sapiens Q7Z699
Y2H Pooling
32814053
Intra LHX5 Q9H2C1 COQ8A Homo sapiens Q8NI60
Validated Y2H
32814053
Intra LHX5 Q9H2C1 COQ8A Homo sapiens Q8NI60
Y2H Pooling
32814053
Intra LHX5 Q9H2C1 COQ8A Homo sapiens Q8NI60
Y2H Array
32814053
Intra LHX5 Q9H2C1 SETDB1 Homo sapiens Q15047-2
Y2H Pooling
32814053
Intra LHX5 Q9H2C1 SETDB1 Homo sapiens Q15047-2
Validated Y2H
32814053
Intra LHX5 Q9H2C1 SETDB1 Homo sapiens Q15047-2
Y2H Array
32814053
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
Bestiality

Zoophilia

Scapuloperoneal Spinal Muscular Atrophy

SPSMA

Amyotrophy, Neurogenic Scapuloperoneal, New England Type

Neurogenic Scapuloperoneal Amyotrophy, New England Type

Scapuloperoneal Neuronopathy

Spinal Muscular Atrophy, Scapuloperoneal

Amyotrophy Neurogenic Scapuloperoneal New England Type

Muscular Atrophy, Spinal

Scapuloperoneal Form Of Spinal Muscular Atrophy

Scapuloperoneal Myopathy
Kluver-Bucy Syndrome

Bilateral Temporal Lobe Disorder

Klüver-Bucy Syndrome

Klver-Bucy Syndrome

Kluver Bucy Syndrome

Memory Loss, Extreme Sexual Behavior, Placidity, And Visual Distractibility

Post-Encephalitic Kluver Bucy Syndrome

Post-Traumatic Kluver Bucy Syndrome

Developmental And Epileptic Encephalopathy 28

DEE28

Epileptic Encephalopathy, Early Infantile, 28

Eiee28

Developmental And Epileptic Encephalopathy, 28

Early Infantile Epileptic Encephalopathy 28

Encephalopathy, Epileptic, Early Infantile, Type 28

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 LHX5 VGNC VGNC:30875
Mus musculus LHX5 MGD MGI:107792
Canis familiaris LHX5 VGNC VGNC:42666
Felis catus LHX5 VGNC VGNC:80449
Rattus norvegicus LHX5 RGD RGD:71079