1. Gene
  2. BARX1 - BARX homeobox 1 Gene

BARX1 - BARX homeobox 1 Gene

中文名称:BARX 同源框 1

种属: Homo sapiens

基因 ID: 56033 | 基因类型: protein coding

关于 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.

功能概要

该基因编码同源盒转录因子 Bar 亚类的成员。对小鼠和小鸡同系物的研究表明,编码的蛋白质可能在发育牙齿和神经嵴起源的颅面间充质中发挥作用。该蛋白质还可能与胃上皮细胞的分化有关。[RefSeq 提供,2008 年 7 月]

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 基因产物(1)

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

BARX1 蛋白结构

Homeobox

Homeobox: Homeobox domain (143 - 199)

  • 0
  • 100
  • 200
  • 254 a.a.
蛋白主名 其他名称

homeobox protein BarH-like 1

BarH-like homeobox 1

BARX1 抗体

目录号 产品名 应用 反应物种
HY-P82990 BarX1 Antibody (YA2735) WB Human, Rat
HY-P82990A BarX1 Antibody (YA2735)(PBS only) WB, IP Human, Rat, Hamster

关联疾病

疾病名称 别名
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

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

直系同源

种属 基因名 来源 基因 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