BARX1 - BARX homeobox 1 Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 56033

About BARX1

Cytogenetic location: 9q22.32 Genomic coordinates (GRCh38): 9:93,951,627-93,955,355 (from NCBI)

This gene has 2 transcripts (splice variants), 196 orthologues and 3 paralogues. Biased expression in stomach (RPKM 5.0), testis (RPKM 0.6) and 1 other tissue.

Summary

This gene encodes a member of the Bar subclass of homeobox transcription factors. Studies of the mouse and chick homolog suggest the encoded protein may play a role in developing teeth and craniofacial mesenchyme of neural crest origin. The protein may also be associated with differentiation of stomach epithelia. [provided by RefSeq, Jul 2008]

BARX1 Products (1)

mRNA Protein Name
NM_021570.4 NP_067545.3 homeobox protein BarH-like 1

BARX1 Protein Structure

Homeobox

Homeobox: Homeobox domain (143 - 199)

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

homeobox protein BarH-like 1

  • BarH-like homeobox 1

BARX1 Antibodies

Referencia número Nombre del producto Aplicación Reactivity
HY-P82990 BarX1 Antibody (YA2735) WB Human, Rat
HY-P82990A BarX1 Antibody (YA2735)(PBS only) WB, IP Human, Rat, Hamster

Related Diseases

Diseases Alias
Pyloric Stenosis
Hypogonadotropic Hypogonadism 5 With Or Without Anosmia

  • HH5

  • Kallmann Syndrome 5

  • Kal5

  • Hypogonadotropic Hypogonadism 5 Without Anosmia

  • Hypogonadism, Hypogonadotropic, Type 5 With/Without Anosmia
Treacher Collins Syndrome 1

  • Treacher Collins Syndrome

  • Mandibulofacial Dysostosis

  • Treacher Collins-Franceschetti Syndrome

  • Tcof

  • Tcs

  • Mfd1

  • Franceschetti-Klein Syndrome

  • TCS1

  • Franceschetti Syndrome

  • Franceschetti-Zwahlen-Klein Syndrome

  • Zygoauromandibular Dysplasia

  • Treacher-Collins Syndrome

  • Mandibulofacial Dysostosis Without Limb Anomalies

  • Bilateral And Symmetric Oto-Mandibular Dysplasia
Hypertrophic Pyloric Stenosis

  • Congenital Hypertrophic Pyloric Stenosis

  • Pyloric Stenosis, Hypertrophic

  • Congenital Or Infantile Stricture Of Pylorus

  • Achalasia Of The Pylorus

  • Congenital Hypertrophy Of The Pylorus

  • Infantile Hypertrophy Of The Pylorus

  • Infantile Constriction Of The Pylorus

  • Congenital Stenosis Of The Pylorus

  • Congenital Constriction Of The Pylorus

  • Congenital Stricture Of The Pylorus

  • Infantile Hypertrophic Pyloric Stenosis

  • Infantile Stenosis Of The Pylorus

  • Infantile Stricture Of The Pylorus

  • Congenital Or Infantile Constriction Of Pylorus

  • Infantile Pyloric Obstruction

  • Infantile Pyloric Hypertrophy

  • Pylorus Achalasia

  • Pyloric Constriction

  • Infantile Pyloric Stricture

  • Infantile Pyloric Stenosis

  • Congenital Spasm Of Pylorus

  • Congenital Pylorospasm

  • Congenital Pyloric Stricture

  • Congenital Pyloric Spasm

  • Congenital Or Infantile Spasm Of Pylorus

  • Congenital Or Infantile Obstruction Of Pylorus

  • Congenital Pyloric Stenosis
Syngnathia

  • Cleft Palate-Lateral Synechia Syndrome

  • Cpls Syndrome

  • Cleft Palate Lateral Synechia Syndrome
Fraser Syndrome 1

  • Fraser Syndrome

  • Cryptophthalmos With Other Malformations

  • Cryptophthalmos Syndrome

  • FRASRS1

  • Cryptophthalmos-Syndactyly Syndrome

  • Fraser-Francois Syndrome

  • Cyclopism

  • Meyer-Schwickerath'S Syndrome

  • Ulrich-Feichtiger Syndrome

  • Cryptophthalmos Syndactyly Syndrome

  • Fraser'S Syndrome

  • Meyer-Schwickerath Syndrome

  • Ullrich-Feichtiger Syndrome
Hernia, Hiatus

  • Hiatal Hernia

  • Hiatus Hernia

  • Diaphragmatic - Hiatus -Hernia

  • Hernia, Hiatal
Cleft Palate, Isolated

  • Cleft Palate

  • Isolated Cleft Palate

  • CPI

  • Cp

  • Palatoschisis

  • Cleft Palate Isolated

  • Uranostaphyloschisis

  • Congenital Fissure Of Palate

  • Cleft Of Secondary Palate
Microphthalmia, Syndromic 3

  • MCOPS3

  • Aeg Syndrome

  • Microphthalmia And Esophageal Atresia Syndrome

  • Anophthalmia/Microphthalmia-Esophageal Atresia Syndrome

  • Anophthalmia-Esophageal-Genital Syndrome

  • Optic Nerve Hypoplasia And Abnormalities Of The Central Nervous System

  • Syndromic Microphthalmia 3

  • Sox2 Anophthalmia Syndrome

  • Anophthalmia Clinical With Associated Anomalies

  • Anophthalmia Esophageal Genital Syndrome

  • Anophthalmia Microphthalmia Esophageal Atresia

  • Syndromic Microphthalmia Type 3

  • Sox2-Related Eye Disorders

  • Anophthalmia, Clinical, With Associated Anomalies

  • Syndromic Microphthalmia, Type 3

  • Microphthalmia, Syndromic, 3

  • Anophthalmia/Microphthalmia-Esophageal Atresia

  • Microphthalmia Syndromic, Type 3
Ankyloglossia With Or Without Tooth Anomalies

  • Ankyloglossia

  • ANKG

  • 'Tongue-Tie'

  • Tongue-Tie

  • Tongue Tie

  • Aberrant Insertion Of Labial Frenulum

  • Aberrant Insertion Of Frenum Of Tongue

  • Short Frenulum Linguae

  • Short Frenulum Of Tongue
Orofacial Cleft

  • Cleft, Orofacial
Tooth Agenesis

  • Oligodontia

  • Hypodontia

  • Selective Tooth Agenesis

  • Tooth Agenesis, Selective

  • Familial Tooth Agenesis

  • Anodontia

  • Congenital Absence Of One Tooth
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Referencia número Nombre del producto
Efecto
Pureza
Rare Diseases
HY-RS01368 BARX1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Macaca mulatta BARX1 VGNC VGNC:82109
Bos taurus BARX1 VGNC VGNC:26423
Mus musculus BARX1 MGD MGI:103124
Rattus norvegicus BARX1 RGD RGD:1310884
Felis catus BARX1 VGNC VGNC:69114
Canis familiaris BARX1 VGNC VGNC:38382
Others BARX1 NCBI