2. Gene
  3. ZG16 - zymogen granule protein 16 Gene

ZG16 - zymogen granule protein 16 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：酶原颗粒蛋白 16

种属: Homo sapiens

同用名: JCLN; JCLN1; ZG16A

基因 ID: 653808 | 基因类型: protein coding

关于 ZG16

Cytogenetic location: 16p11.2 Genomic coordinates (GRCh38): 16:29,778,256-29,782,973 (from NCBI)

This gene has 1 transcript (splice variant) and 128 orthologues. Biased expression in colon (RPKM 333.1), small intestine (RPKM 82.8) and 1 other tissue.

功能概要

预测启用碳水化合物结合活性和肽聚糖结合活性。预计参与蛋白质运输。预计在对革兰氏阳性细菌的防御反应上游或防御反应内起作用，并抑制共生体进入宿主。位于高尔基体腔和含胶原蛋白的细胞外基质中。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable carbohydrate binding activity and peptidoglycan binding activity. Predicted to be involved in protein transport. Predicted to act upstream of or within defense response to Gram-positive bacterium and suppression of symbiont entry into host. Located in Golgi lumen and collagen-containing extracellular matrix. [provided by Alliance of Genome Resources, Apr 2022]

ZG16 基因产物(1)

mRNA Protein Name
NM_152338.4 NP_689551.3 zymogen granule membrane protein 16 precursor

ZG16 蛋白结构

Jacalin

Jacalin: Jacalin-like lectin domain (41 - 158)

  • 0
  • 100
  • 167 a.a.
蛋白主名 其他名称

zymogen granule membrane protein 16

jacalin-like lectin domain containing

重组 ZG16 蛋白

目录号 产品名 蛋白编号 纯度
HY-P71037 ZG16 Protein, Human (HEK293, His) O60844 (N17-C167) ≥95%
HY-P77285 ZG16 Protein, Human (HEK293, Fc) O60844 (M1-C167) ≥95%

关联疾病

疾病名称 别名
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1

Eec Syndrome

Rudiger Syndrome 1

Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome 1

EEC1

Eec Syndrome 1

Eec Syndrome-1

Walker-Clodius Syndrome

Ectrodactyly-Ectodermal Dysplasia-Cleft Lip/Palate Syndrome

Eec

Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome

Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome

Ectrodactyly-Cleft Lip/Palate Syndrome

Ectrodactyly-Ectodermal Dysplasia-Cleft Lip/Cleft Palate

Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome

Ectrodactyly, Ectodermal Dysplasia, Clefting Syndrome

Ectrodactyly-Cleft Lip-Palate Syndrome

Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome
Spondylocostal Dysostosis 5

Spondylothoracic Dysostosis

SCDO5

Jarcho-Levin Syndrome

Scoliosis, Congenital, With Or Without Rib Anomalies

Tacs

Spondylocostal Dysplasia

Costovertebral Segmentation Anomalies

Spondylocostal Dysostosis 1

Spondylocostal Dysostosis

Spondylothoracic Dysplasia

Scdo1

Spondylocostal Dysostosis 1 Autosomal Recessive

Costovertebral Dysplasia

Scdo

Std

Autosomal Dominant Spondylocostal Dysostosis

Autosomal Dominant Spondylocostal Dysplasia

Doid:0112363

Spondylocostal Dysostosis 4, Autosomal Dominant
Colon Mucinous Adenocarcinoma

Colonic Mucinous Adenocarcinoma

Mucinous Adenocarcinoma Of The Colon
Episodic Kinesigenic Dyskinesia 1

Paroxysmal Kinesigenic Choreoathetosis

Paroxysmal Kinesigenic Dyskinesia

Dystonia 10

Familial Paroxysmal Kinesigenic Dyskinesia

Episodic Kinesigenic Dyskinesia

EKD1

Pkc

Pkd

Dyt10

Familial Pkd

Paroxysmal Kinesigenic Choreathetosis

Familial Paroxysmal Dystonia

Dystonia, Familial Paroxysmal

Dyt-Prrt2

Dystonia, Type 10
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

相关产品

Pre-clinical Phase
生物活性分子 (2)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS16063 ZG16 Human Pre-designed siRNA Set A / 否
HY-RS16064 ZG16B Human Pre-designed siRNA Set A / 否

直系同源

种属 基因名 来源 基因 ID
Macaca mulatta ZG16 VGNC VGNC:104766
Bos taurus ZG16 VGNC VGNC:37180
Canis familiaris ZG16 VGNC VGNC:48629
Rattus norvegicus ZG16 RGD RGD:620346
Mus musculus ZG16 MGD MGI:1916286
Others ZG16 NCBI
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