1. Gene
  2. ANTXR1 - ANTXR cell adhesion molecule 1 Gene

ANTXR1 - ANTXR cell adhesion molecule 1 Gene

中文名称:ANTXR 细胞粘附分子 1

种属: Homo sapiens

同用名: ATR; GAPO; TEM8

基因 ID: 84168 | 基因类型: protein coding

关于 ANTXR1

Cytogenetic location: 2p13.3 Genomic coordinates (GRCh38): 2:69,013,144-69,249,327 (from NCBI)

This gene has 11 transcripts (splice variants), 268 orthologues, 2 paralogues and is associated with 5 phenotypes. Broad expression in gall bladder (RPKM 37.4), ovary (RPKM 30.6) and 21 other tissues.

功能概要

该基因编码 I 型跨膜蛋白,是一种与结直肠癌有关的肿瘤特异性内皮标记物。编码的蛋白质已被证明也是炭疽杆菌毒素的停靠蛋白或受体,炭疽杆菌毒素是炭疽病的病原体。三联炭疽毒素的保护性抗原 (PA) 成分与该受体蛋白的结合介导毒素成分向细胞胞质溶胶的递送。一旦进入细胞,炭疽毒素的另外两种成分水肿因子 (EF) 和致死因子 (LF) 就会破坏正常的细胞过程。已经描述了编码不同蛋白质同种型的三种可变剪接变体。[RefSeq 提供,2008 年 10 月]

This gene encodes a type I transmembrane protein and is a tumor-specific endothelial marker that has been implicated in colorectal Cancer. The encoded protein has been shown to also be a docking protein or receptor for Bacillus anthracis toxin, the causative agent of the disease, anthrax. The binding of the protective antigen (PA) component, of the tripartite anthrax toxin, to this receptor protein mediates delivery of toxin components to the cytosol of cells. Once inside the cell, the Other two components of anthrax toxin, edema factor (EF) and lethal factor (LF) disrupt normal cellular processes. Three alternatively spliced variants that encode different protein isoforms have been described. [provided by RefSeq, Oct 2008]

ANTXR1 基因产物(4)

mRNA Protein Name
NM_001410840.1 NP_001397769.1 anthrax toxin receptor 1 isoform 4 precursor
NM_018153.3 NP_060623.2 anthrax toxin receptor 1 isoform 3 precursor
NM_032208.3 NP_115584.1 anthrax toxin receptor 1 isoform 1 precursor
NM_053034.2 NP_444262.1 anthrax toxin receptor 1 isoform 2 precursor
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables actin filament binding IDA
IDA: 通过直接分析推断
16762926 GOA
enables collagen binding IDA
IDA: 通过直接分析推断
16762926 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
14507921 GOA
enables transmembrane signaling receptor activity IDA
IDA: 通过直接分析推断
16762926 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in actin cytoskeleton organization IDA
IDA: 通过直接分析推断
16762926 GOA
involved in substrate adhesion-dependent cell spreading IDA
IDA: 通过直接分析推断
16762926 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cell surface IDA
IDA: 通过直接分析推断
21129411 GOA
located in external side of plasma membrane IDA
IDA: 通过直接分析推断
21129411 GOA
located in filopodium membrane IDA
IDA: 通过直接分析推断
16762926 GOA
located in lamellipodium membrane IDA
IDA: 通过直接分析推断
16762926 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

ANTXR1 蛋白结构

VWA

VWA: von Willebrand factor type A domain (44 - 203)

Anth_Ig

Anth_Ig: Anthrax receptor extracellular domain (216 - 320)

Ant_C

Ant_C: Anthrax receptor C-terminus region (396 - 489)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 564 a.a.
蛋白主名 其他名称

anthrax toxin receptor 1

2310008J16Rik

重组 ANTXR1 蛋白

目录号 产品名 蛋白编号 纯度
HY-P7521 TEM8/ANTXR1 Protein, Human Q9H6X2-4 (E33-K321) ≥95%
HY-P77226 TEM8/ANTXR1 Protein, Human (HEK293, Fc) Q9H6X2-1 (E33-S321) ≥95%

关联疾病

疾病名称 别名
Gapo Syndrome

GAPOS

Growth Retardation, Alopecia, Pseudoanodontia, And Optic Atrophy

Growth Delay-Alopecia-Pseudoanodontia-Optic Atrophy Syndrome

Growth Retardation, Alopecia, Pseudoanodontia And Optic Atrophy

Hemangioma, Capillary Infantile

HCI

Capillary Infantile Hemangioma

Hemangioma, Hereditary Capillary

Hemangioma, Capillary Infantile, Susceptibility To

Hemangioma, Capillary Infantile, Somatic

Hemangioma Hereditary Capillary

Anthrax Disease

Anthrax

Ragpicker'S Disease

Black Baine

Malignant Edema

Malignant Pustule

Siberian Plague

Wool Sorter'S Disease

Gas Gangrene

Cutaneous Anthrax

Anthrax Infection

Splenic Fever

Hemangioma

Hemangiomas

Hyaline Fibromatosis Syndrome

Juvenile Hyaline Fibromatosis

Inherited Systemic Hyalinosis

Puretic Syndrome

Infantile Systemic Hyalinosis

HFS

Hyalinosis, Systemic

Systemic Hyalinosis

Molluscum Fibrosum

Murray Syndrome

Murray-Puretic-Drescher Syndrome

Ish

Jhf

Fibromatosis, Juvenile Hyaline

Hyalinosis, Systemic Infantile

Fibromatosis, Hyaline Syndrome

Neurofibromatosis 1

Cutaneous Anthrax

Anthrax, Skin Type

Skin Anthrax

Inhalation Anthrax

Pulmonary Anthrax

Respiratory Anthrax

Inhalational Anthrax

Wool-Sorters' Disease

Woolsorters' Disease

Inhalation Anthrax Disease

Respiratory Anthrax Disease

Gastrointestinal Anthrax
Oropharyngeal Anthrax
Gingival Hypertrophy

Hypertrophy Of Gingivae

Capillary Hemangioma

Infantile Hemangioma

Strawberry Nevus Of Skin

Cellular Hemangioma Of Infancy

Congenital Vascular Hamartoma

Congenital Vascular Naevus

Juvenile Hemangioma

Strawberry Haemangioma

Strawberry Nevus

Hemangioma Capillary

Hemangioma, Capillary

Hemangioma, Cavernous

Bardet-Biedl Syndrome 2

BBS2

Bardet-Biedl Syndrome

Bardet-Biedl Syndrome, Type 2

Bbs

Colorectal Cancer

Colon Cancer

Colorectal Carcinoma

Colon Carcinoma

Colorectal Cancer, Susceptibility To

Carcinoma Of Colon

CRC

Colorectal Cancer With Chromosomal Instability, Somatic

Colon Cancer, Somatic

Colon Cancer, Susceptibility To

Colonic Neoplasms

Colorectal Neoplasms

Colorectal Cancer, Somatic

Colon Cancer, Advanced, Somatic

Colonic Carcinoma

Colorectal Carcinomas

Colon Cancers

Colorectal Cancers

Cancer, Colorectal, Somatic

Cancer, Colon

Cancer, Colorectal, Susceptibility To

Colorectal Neoplasm

Colonic Neoplasm

Malignant Tumor Of Colon

Capillary Disease

Disease Of Capillaries

Robinow Syndrome, Autosomal Recessive 1

Robinow Syndrome, Autosomal Recessive

Autosomal Recessive Robinow Syndrome

Covesdem Syndrome

RRS1

Costovertebral Segmentation Defect-Mesomelia Syndrome

Rrs

Costovertebral Segmentation Defect With Mesomelia, Formerly

Covesdem Syndrome, Formerly

Costovertebral Segmentation Defect With Mesomelia

Robinow Syndrome Autosomal Recessive With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals

Robinow Syndrome Autosomal Recessive With Brachy-Syn-Polydactyly

Robinow Syndrome, Autosomal Recessive, With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals

Robinow Syndrome, Autosomal Recessive, With Brachy-Syn-Polydactyly

Robinow, Autosomal Recessive Syndrome, Type 1

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
Canis familiaris ANTXR1 VGNC VGNC:37935
Rattus norvegicus ANTXR1 RGD RGD:1307144
Macaca mulatta ANTXR1 VGNC VGNC:69873
Felis catus ANTXR1 VGNC VGNC:59837
Bos taurus ANTXR1 VGNC VGNC:25961
Mus musculus ANTXR1 MGD MGI:1916788
Others ANTXR1 NCBI