VCX - variable charge X-linked Gene

Also Known as VCX1; VCXB1; VCX-B1; VCX10R; VCX-10r

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 26609

About VCX

Cytogenetic location: Xp22.31 Genomic coordinates (GRCh38): X:7,842,262-7,844,143 (from NCBI)

This gene has 5 transcripts (splice variants), 34 orthologues and 5 paralogues. Restricted expression toward testis (RPKM 23.7).

Summary

This gene belongs to the VCX/Y gene family, which has multiple members on both X and Y chromosomes, and all are expressed exclusively in male germ cells. The X-linked members are clustered on chromosome Xp22 and Y-linked members are two identical copies of the gene within a palindromic region on Yq11. The family members share a high degree of sequence identity, with the exception that a 30-bp unit is tandemly repeated in X-linked members but occurs only once in Y-linked members. The VCX gene cluster is polymorphic in terms of copy number; different individuals may have a different number of VCX genes. VCX/Y genes encode small and highly charged proteins of unknown function. The presence of a putative bipartite nuclear localization signal suggests that VCX/Y members are nuclear proteins. This gene contains 10 repeats of the 30-bp unit. [provided by RefSeq, Jul 2008]

VCX Products (2)

mRNA Protein Name
NM_001393662.1 NP_001380591.1 variable charge X-linked protein 1
NM_013452.3 NP_038480.2 variable charge X-linked protein 1
Cellular Component GO Annotation Evidence References Source
located in nucleolus IDA
IDA: Inferred from direct assay
12862317 GOA
located in nucleus IDA
IDA: Inferred from direct assay
12862317 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

VCX Protein Structure

VCX_VCY

VCX_VCY: Variable charge X/Y family (1 - 142)

VCX_VCY

VCX_VCY: Variable charge X/Y family (122 - 162)

VCX_VCY

VCX_VCY: Variable charge X/Y family (132 - 172)

VCX_VCY

VCX_VCY: Variable charge X/Y family (142 - 182)

VCX_VCY

VCX_VCY: Variable charge X/Y family (162 - 202)

  • 0
  • 100
  • 206 a.a.
Protein Preferred Names Protein Names

variable charge X-linked protein 1

  • variable charge protein on X with ten repeats

Related Diseases

Diseases Alias
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

Vertical Talus, Congenital
  • Congenital Vertical Talus

  • CVT

  • Congenital Convex Pes Valgus

  • Rocker-Bottom Foot Deformity

  • Vertical Talus

  • Pes Valgus, Congenital Convex

  • Congenital Convex Foot

  • Congenital Rocker-Bottom Foot

  • Rocker Bottom Foot

  • Flatfoot

  • Rocker-Bottom Foot

  • Charcot-Marie-Tooth Disease, Foot Deformity Of

Hemophagocytic Lymphohistiocytosis, Familial, 1
  • Familial Hemophagocytic Lymphohistiocytosis

  • Fhl

  • Familial Erythrophagocytic Lymphohistiocytosis

  • Hemophagocytic Syndrome

  • FHL1

  • Hplh1

  • Hlh1

  • Fel

  • Familial Hemophagocytic Lymphohistiocytosis 1

  • Primary Hemophagocytic Lymphohistiocytosis

  • Familial Hlh

  • Hlh

  • Familial Hemophagocytic Lymphocytosis

  • Hemophagocytic Lymphohistiocytosis, Familial

  • Reticulosis, Familial Histiocytic

  • Hemophagocytic Reticulosis, Familial

  • Erythrophagocytic Lymphohistiocytosis, Familial

  • Familial Histiocytic Reticulosis

  • Familial Hemophagocytic Histiocytosis

  • Familial Hemophagocytic Reticulosis

  • Fhlh

  • Hplh

  • Primary Hemophagocytic Hymphohistiocytosis

  • Genetic Hemophagocytic Lymphohistiocytosis

  • Hemophagocytic Lymphohistiocytosis

  • Familial Hemophagocytic Lymphohistiocytosis Type 1

Male Infertility
  • Infertility, Male

  • Infertility Male

  • Male Sterility

  • Absolute Infertility

Diseases Alias
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