1. Gene
  2. ZFHX2 - zinc finger homeobox 2 Gene

ZFHX2 - zinc finger homeobox 2 Gene

中文名称:锌指同源盒 2

种属: Homo sapiens

同用名: ZFH5; ZFH-5; MARSIS; ZNF409

基因 ID: 85446 | 基因类型: protein coding

关于 ZFHX2

Cytogenetic location: 14q11.2 Genomic coordinates (GRCh38): 14:23,520,857-23,555,952 (from NCBI)

This gene has 4 transcripts (splice variants), 169 orthologues, 20 paralogues and is associated with 1 phenotype. Biased expression in testis (RPKM 3.0), brain (RPKM 0.7) and 5 other tissues.

功能概要

预测可实现 DNA 结合转录因子活性、RNA 聚合酶 II 特异性和 RNA 聚合酶 II 顺式调节区序列特异性 DNA 结合活性。参与调节疼痛的感官知觉。位于核内。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Involved in regulation of sensory perception of pain. Located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

ZFHX2 基因产物(1)

mRNA Protein Name
NM_033400.3 NP_207646.2 zinc finger homeobox protein 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
32814053 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in regulation of sensory perception of pain IMP
IMP: 通过突变表型推断
29253101 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in nucleus IDA
IDA: 通过直接分析推断
29253101 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

ZFHX2 蛋白结构

zf-C2H2_2

zf-C2H2_2: C2H2 type zinc-finger (2 copies) (566 - 595)

zf-C2H2_2

zf-C2H2_2: C2H2 type zinc-finger (2 copies) (1247 - 1280)

Homeobox

Homeobox: Homeobox domain (1598 - 1652)

Homeobox

Homeobox: Homeobox domain (1858 - 1914)

Homeobox

Homeobox: Homeobox domain (2066 - 2122)

  • 0
  • 400
  • 800
  • 1200
  • 1600
  • 2000
  • 2400
  • 2572 a.a.
蛋白主名 其他名称

zinc finger homeobox protein 2

ZFH-2

ZFHX2 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
ZFHX2 Q9C0A1 MAPT Homo sapiens P10636 32814053
种属内
ZFHX2 Q9C0A1 MAPT Homo sapiens P10636 32814053
种属内
ZFHX2 Q9C0A1 MAPT Homo sapiens P10636 32814053
种属内
ZFHX2 Q9C0A1 PMP22 Homo sapiens A0A6Q8PF08 32814053
种属内
ZFHX2 Q9C0A1 PMP22 Homo sapiens A0A6Q8PF08 32814053
种属内
ZFHX2 Q9C0A1 PMP22 Homo sapiens A0A6Q8PF08 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
Marsili Syndrome

Congenital Insensitivity To Pain

Congenital Analgesia, Autosomal Dominant

MARSIS

Insensitivity To Pain, Congenital, Autosomal Dominant

Congenital Analgesia

Congenital Indifference To Pain

Hereditary Sensory And Autonomic Neuropathy Type V

Hereditary Sensory And Autonomic Neuropathy

Channelopathy-Associated Cip

Channelopathy-Associated Congenital Insensitivity To Pain

Congenital Insensitivity To Pain And Thermal Analgesia

Hsan V

Hsan5

Hereditary Sensory And Autonomic Neuropathy Type 5

Insensitivity To Pain, Congenital

Neuropathy, Hereditary Sensory And Autonomic, Type V

Hsan

Hereditary Sensory Autonomic Neuropathy

Asymbolia For Pain

Channelopathy-Associated Insensitivity To Pain

Cip

Congenital Pain Indifference

Indifference To Pain, Congenital, Autosomal Recessive

Pain Insensitivity, Congenital

Chromosome 8q21.11 Deletion Syndrome

8q21.11 Microdeletion Syndrome

Del(8)(Q21.11)

Deletion 8q21.11

Monosomy 8q21.11

Congenital Ptosis

Congenital Blepharoptosis

Congenital Eyelid Ptosis

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
Mus musculus ZFHX2 MGD MGI:2686934
Macaca mulatta ZFHX2 VGNC VGNC:99346
Bos taurus ZFHX2 VGNC VGNC:37156
Canis familiaris ZFHX2 VGNC VGNC:48606
Felis catus ZFHX2 VGNC VGNC:80786
Rattus norvegicus ZFHX2 RGD RGD:735143