1. Gene
  2. SEBOX - SEBOX homeobox Gene

SEBOX - SEBOX homeobox Gene

Homo sapiens

Also known as OG9; OG-9; OG9X

Gene ID: 645832 | Gene type: protein coding

About SEBOX

Cytogenetic location: 17q11.2 Genomic coordinates (GRCh38): 17:28,363,506-28,365,199 (from NCBI)

This gene has 1 transcript (splice variant), 192 orthologues and 50 paralogues. Low expression observed in reference dataset.

Summary

Homeodomain proteins, such as SEBOX, play a key role in coordinating gene expression during development (Cinquanta et al., 2000 [PubMed 10922053]).[supplied by OMIM, Mar 2008]

SEBOX Products(1)

mRNA Protein Name
NM_001080837.4 NP_001074306.3 homeobox protein SEBOX

SEBOX Protein Structure

Homeobox

Homeobox: Homeobox domain (45 - 98)

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

homeobox protein SEBOX

homeobox OG-9

Related Diseases

Diseases Alias
Deafness, Autosomal Recessive 84a

DFNB84A

Deafness, Autosomal Recessive 84

Autosomal Recessive Nonsyndromic Deafness 84a

Dfnb84

Deafness, Autosomal Recessive 84a, With Vestibular Dysfunction

Autosomal Recessive Deafness 84a

Autosomal Recessive Deafness 84a With Vestibular Dysfunction

Deafness, Autosomal Recessive, 84a

Deafness Autosomal Recessive 84

Deafness Autosomal Recessive 84a With Vestibular Dysfunction

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 84

Deafness, Autosomal Recessive, Type 84a

Cleft Palate With Or Without Ankyloglossia, X-Linked

Cleft Palate With Ankyloglossia

CPX

X-Linked Cleft Palate And Ankyloglossia

X-Linked Cleft Palate With Or Without Ankyloglossia

X-Linked Cleft Palate

X-Linked Cleft Palate With Ankyloglossia

Cleft Palate, With/Without Ankyloglossia, X-Linked

Arthrogryposis, Distal, Type 7

Hecht Syndrome

Trismus-Pseudocamptodactyly Syndrome

Distal Arthrogryposis Type 7

Dutch-Kentucky Syndrome

DA7

Hecht-Beals Syndrome

Mouth, Inability To Open Completely, And Short Finger-Flexor Tendons

Mouth, Inability To Completely Open, And Short Finger-Flexor Tendons

Arthrogryposis Distal Type 7

Trismus Pseudocamptodactyly Syndrome

Arthrogryposis, Distal, 7

Alopecia, Neurologic Defects, And Endocrinopathy Syndrome

Ane Syndrome

ANES

Alopecia-Progressive Neurological Defect-Endocrinopathy Syndrome

Alopecia-Progressive Neurological Defect-Endocrinopathy

Endocrine System Diseases

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
Rattus norvegicus SEBOX RGD RGD:62077
Bos taurus SEBOX VGNC VGNC:34401
Felis catus SEBOX VGNC VGNC:64959
Canis familiaris SEBOX VGNC VGNC:45960
Mus musculus SEBOX MGD MGI:108012