2. Gene
  3. VCX2 - variable charge X-linked 2 Gene

VCX2 - variable charge X-linked 2 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品

中文名称：可变电荷 X 连锁 2

种属: Homo sapiens

同用名: VCXB; VCX2R; VCX-2r

基因 ID: 51480 | 基因类型: protein coding

关于 VCX2

Cytogenetic location: Xp22.31 Genomic coordinates (GRCh38): X:8,169,944-8,171,267 (from NCBI)

This gene has 1 transcript (splice variant), 34 orthologues and 5 paralogues. Restricted expression toward testis (RPKM 16.4).

功能概要

该基因属于 VCX/Y 基因家族，该家族在 X 和 Y 染色体上都有多个成员，这些成员仅在雄性生殖细胞中表达。 VCX 基因簇在拷贝数方面具有多态性；不同的个体可能有不同数量的 VCX 基因。该基因包含两个 30 nt 串联重复拷贝。这个家族附近成员的缺失与认知障碍有关。[RefSeq 提供，2015 年 2 月]

This gene belongs to the VCX/Y gene family, which has multiple members on both X and Y chromosomes that are expressed exclusively in male germ cells. The VCX gene cluster is polymorphic in terms of copy number; different individuals may have a different number of VCX genes. This gene contains two copies of a 30 nt tandem repeat. Deletion of a nearby member of this family was implicated in cognitive disability. [provided by RefSeq, Feb 2015]

VCX2 基因产物(1)

mRNA Protein Name
NM_016378.3 NP_057462.2 variable charge X-linked protein 2

VCX2 蛋白结构

VCX_VCY

VCX_VCY: Variable charge X/Y family (1 - 126)

  • 0
  • 100
  • 139 a.a.
蛋白主名 其他名称

variable charge X-linked protein 2

variable charge protein on X with two repeats

关联疾病

疾病名称 别名
Ichthyosis, X-Linked

X-Linked Ichthyosis

Steroid Sulfatase Deficiency

Placental Steroid Sulfatase Deficiency

Steroid Sulfatase Deficiency Disease

XLI

Sts Deficiency

Ssdd

X-Linked Recessive Ichthyosis

X-Linked Ichthyosis With Steryl-Sulphatase Deficiency

X-Linked Placental Steryl-Sulphatase Deficiency

Ssd

X Linked Ichthyosis

Recessive X-Linked Ichthyosis

Rxli

Syndromic Recessive X-Linked Ichthyosis

Recessive X-Linked Ichthyosis With Extracutaneous Manifestations

Syndromic Rxli

X-Linked Ichthyosis Syndrome

IXL

Ichthyosis X-Linked

Sex-Linked Ichthyosis

X-Linked Ichthyosis With Steryl-Sulfatase Deficiency
Ichthyosis

Ichthyoses

Non-Syndromic Ichthyosis

Congenital Ichthyosis
Kallmann Syndrome

Hypogonadism With Anosmia

Kallman'S Syndrome

Anosmic Hypogonadism

Anosmic Idiopathic Hypogonadotropic Hypogonadism

Hypogonadotropic Hypogonadism And Anosmia

Hypogonadotropic Hypogonadism-Anosmia Syndrome

Olfacto-Genital Pathological Sequence

Familial Hypogonadism With Anosmia

Kallman Syndrome

Dysplasia Olfactogenitalis Of De Morsier

Kallmann'S Syndrome

Congenital Hypogonadotropic Hypogonadism With Anosmia
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS15626 VCX2 Human Pre-designed siRNA Set A Pre-designed Set / 否
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