1. Gene
  2. CDX4 - caudal type homeobox 4 Gene

CDX4 - caudal type homeobox 4 Gene

Homo sapiens
Gene ID: 1046 | Gene type: protein coding

About CDX4

Cytogenetic location: Xq13.2 Genomic coordinates (GRCh38): X:73,447,053-73,455,171 (from NCBI)

This gene has 1 transcript (splice variant), 96 orthologues and 2 paralogues. Low expression observed in reference dataset.

Summary

This gene encodes a member of a small subfamily of homeobox containing transcription factors. The encoded protein may regulate homeobox gene expression during anteroposterior patterning and hematopoiesis. [provided by RefSeq, Aug 2012]

CDX4 Products(1)

mRNA Protein Name
NM_005193.2 NP_005184.1 homeobox protein CDX-4

CDX4 Protein Structure

Caudal_act

Caudal_act: Caudal like protein activation region (13 - 171)

Homeobox

Homeobox: Homeobox domain (175 - 230)

  • 0
  • 100
  • 200
  • 284 a.a.
Protein Preferred Names Protein Names

homeobox protein CDX-4

caudal type homeobox transcription factor 4

Related Diseases

Diseases Alias
Renpenning Syndrome 1

Renpenning Syndrome

Golabi-Ito-Hall Syndrome

Mrxs3

Mrxs8

X-Linked Intellectual Disability Due To Pqbp1 Mutations

RENS1

Sutherland-Haan X-Linked Mental Retardation Syndrome

Shs

Mrx55

X-Linked Intellectual Disability, Renpenning Type

Sutherland-Haan Syndrome

Mental Retardation, X-Linked, Renpenning Type

Mental Retardation, X-Linked, With Spastic Diplegia

Mental Retardation, X-Linked, Syndromic 3

Mental Retardation, X-Linked, Syndromic 8

Mental Retardation, X-Linked 55

Syndromic X-Linked Mental Retardation 8

X-Linked Mental Retardation Renpenning Type

X-Linked Mental Retardation With Spastic Diplegia

Sutherland-Haan X-Linked Intellectual Disability Syndrome

X-Linked Intellectual Disability With Spastic Diplegia

Hamel Cerebropalatocardiac Syndrome

Porteous Syndrome

X-Linked Intellectual Deficit Due To Pqbp1 Mutations

X-Linked Intellectual Deficit, Renpenning Type

X-Linked Intellectual Disability, Sutherland-Haan Type

Hamel Cerebro-Palato-Cardiac Syndrome

Renpenning Syndrome, Type 1

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

Orthologs Information

Species Symbol Source ID
Bos taurus CDX4 VGNC VGNC:27159
Mus musculus CDX4 MGD MGI:88362
Macaca mulatta CDX4 VGNC VGNC:70997
Canis familiaris CDX4 VGNC VGNC:39086
Rattus norvegicus CDX4 RGD RGD:1561529