1. Gene
  2. GNAZ - G protein subunit alpha z Gene

GNAZ - G protein subunit alpha z Gene

中文名称:G 蛋白亚基αz

种属: Homo sapiens

同用名: HG1H; gz-alpha

基因 ID: 2781 | 基因类型: protein coding

关于 GNAZ

Cytogenetic location: 22q11.22-q11.23 Genomic coordinates (GRCh38): 22:23,070,519-23,125,032 (from NCBI)

This gene has 3 transcripts (splice variants), 211 orthologues and 15 paralogues. Broad expression in brain (RPKM 3.2), gall bladder (RPKM 1.3) and 16 other tissues.

功能概要

由该基因编码的蛋白质是 G 蛋白亚家族的成员,该亚家族在百日咳毒素不敏感系统中介导信号转导。这种编码的蛋白质可能在维持外淋巴和内淋巴耳蜗液的离子平衡方面发挥作用。[RefSeq 提供,2008 年 7 月]

The protein encoded by this gene is a member of a G protein subfamily that mediates signal transduction in pertussis toxin-insensitive systms. This encoded protein may play a role in maintaining the ionic balance of perilymphatic and endolymphatic cochlear fluids. [provided by RefSeq, Jul 2008]

GNAZ 基因产物(1)

mRNA Protein Name
NM_002073.4 NP_002064.1 guanine nucleotide-binding protein G(z) subunit alpha

GNAZ 蛋白结构

G-alpha

G-alpha: G-protein alpha subunit (4 - 344)

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

guanine nucleotide-binding protein G(z) subunit alpha

g(x) alpha chain

重组 GNAZ 蛋白

目录号 产品名 蛋白编号 纯度
HY-P72208 GNAZ Protein, Human (His-SUMO) P19086 (G2-C355) ≥95%

关联疾病

疾病名称 别名
Pertussis

Whooping Cough

Bordetella Infections

Bordetella Infection

Bordetella Pertussis Infection

Wc - Whooping Cough

Whooping Cough Due To Unspecified Organism

Bordetellosis

Tussis Convulsiva

Whooping Cough, Unspecified Organism

Wc - [Whooping Cough]

Whooping Cough Due To B. Parapertussis

Infection Due To Bordetella Parapertussis

Night Blindness

Nyctalopia

Thrombocytopenia-Absent Radius Syndrome

Tar Syndrome

Radial Aplasia-Thrombocytopenia Syndrome

Absent Radii And Thrombocytopenia

TAR

Chromosome 1q21.1 Deletion Syndrome, 200-Kb

Thrombocytopenia Absent Radius Syndrome

Thrombocytopenia Absent Radii

Chromosome 1q21.1 Deletion Syndrome

Thrombocytopenia With Absent Radii Syndrome

Radial Aplasia-Amegakaryocytic Thrombocytopenia

Achromatopsia

Achm

Rod Monochromatism

Total Color Blindness

Rod Monochromacy

Monochromatism

Achromatism

Complete Or Incomplete Color Blindness

Pingelapese Blindness

Achromatopsia 1

Achromatopsia 2

Achromatopsia 3

Ulna And Fibula, Absence Of, With Severe Limb Deficiency

Schinzel Phocomelia Syndrome

Aarrs

Limb/Pelvis-Hypoplasia/Aplasia Syndrome

LPHAS

Schinzel Type Phocomelia

Absence Of Ulna And Fibula With Severe Limb Deficiency

Al-Awadi/Raas-Rothschild Syndrome

Al Awadi-Raas-Rothschild Syndrome

Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome

Aplasia/Hypoplasia Of Limbs And Pelvis

Congenital Absence Of Ulna And Fibula

Severe Limb Deficit

Phocomelia, Schinzel Type

Al-Awadi-Raas-Rothschild Syndrome

Ulna And Fibula Absence Of With Severe Limb Deficiency

Limb Pelvis Hypoplasia Aplasia Syndrome

Limb/Pelvis/Uterus-Hypoplasia/Aplasia Syndrome

Ulna And Fibula, Absence Of, With Sever Limb Deficiency

Pancreas, Annular

Annular Pancreas

Pancreas Annulare

Congenital Annular Pancreas

Usher Syndrome, Type Id

Usher Syndrome Type 1d

USH1D

Usher Syndrome, Type 1d

Usher Syndrome Type Id

Usher Syndrome, Type Id/F, Digenic

Usher Syndrome, Type 1d/F Digenic

Usher Syndrome 1d

Usher'S Syndrome Type 1d

Usher Syndrome 1d/F

USH1DF

Ush1d/F

Usher'S Syndrome Type 1h

Usher Syndrome 1h

Usher Syndrome Type Ih

Usher Syndrome, Type 1d/F

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
Rattus norvegicus GNAZ RGD RGD:2717
Bos taurus GNAZ VGNC VGNC:58379
Canis familiaris GNAZ VGNC VGNC:41310
Felis catus GNAZ VGNC VGNC:62619
Macaca mulatta GNAZ VGNC VGNC:73094
Mus musculus GNAZ MGD MGI:95780
Others GNAZ NCBI