LUZP1 - leucine zipper protein 1 Gene

中文名称：亮氨酸拉链蛋白 1

种属: Homo sapiens

同用名: LUZP

基因 ID: 7798 | 基因类型: protein coding

关于 LUZP1

Cytogenetic location: 1p36.12 Genomic coordinates (GRCh38): 1:23,083,642-23,178,122 (from NCBI)

This gene has 4 transcripts (splice variants), 201 orthologues, 3 paralogues and is associated with 1 phenotype. Ubiquitous expression in small intestine (RPKM 10.5), duodenum (RPKM 8.9) and 25 other tissues.

功能概要

该基因编码一种含有亮氨酸拉链基序的蛋白质。编码蛋白质的确切功能尚不清楚。在小鼠中，该基因影响神经管闭合。可变剪接导致多个转录本变体。[RefSeq 提供，2008 年 12 月]

This gene encodes a protein that contains a leucine zipper motif. The exact function of the encoded protein is not known. In mice this gene affects neural tube closure. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2008]

LUZP1 基因产物(4)

mRNA	Protein	Name
NM_001142546.4	NP_001136018.1	leucine zipper protein 1
NM_001395461.1	NP_001382390.1	leucine zipper protein 1
NM_001395462.2	NP_001382391.1	leucine zipper protein 1
NM_033631.5	NP_361013.3	leucine zipper protein 1

蛋白主名

其他名称

leucine zipper protein 1

LUZP1 蛋白互作信息

分类	蛋白名称	蛋白编号	互作蛋白	互作蛋白种属	互作蛋白编号	实验方法	参考文献
种属内	LUZP1	Q86V48	YWHAE	Homo sapiens	P62258	Crosslink	36931259
种属内	LUZP1	Q86V48	DAPK3	Homo sapiens	O43293	Anti Tag CoIP	33961781

种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称

别名

Chromosome 1p36 Deletion Syndrome

1p36 Deletion Syndrome	Deletion 1p36
Monosomy 1p36	Subtelomeric 1p36 Deletion
Monosomy 1p36 Syndrome	Distal Monosomy 1p36
Del(1)(P36)	Deletion 1pter
Monosomy 1pter

Townes-Brocks Syndrome

Townes Syndrome	Renal-Ear-Anal-Radial Syndrome
Anus, Imperforate, With Hand, Foot And Ear Anomalies	Imperforate Anus-Hand, Foot And Ear Anomalies Syndrome
Rear Syndrome	Sensorineural Deafness With Imperforate Anus And Hypoplastic Thumbs
Tbs	Deafness, Sensorineural, With Imperforate Anus And Hypoplastic Thumbs
Imperforate Anus With Hand, Foot And Ear Anomalies	Anal-Ear-Renal-Radial Malformation Syndrome
Deafness-Imperforate Anus-Hypoplastic Thumbs Syndrome	Imperforate Anus-Hand And Foot Anomalies Syndrome
Sensorineural Deafness-Imperforate Anus-Hypoplastic Thumbs Syndrome	Sensorineural Hearing Loss With Imperforate Anus And Hypoplastic Thumbs

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

Cat. No.	产品名	作用方式	纯度	是否罕见病
HY-RS07892	LUZP1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	否

直系同源

种属	基因名	来源	基因 ID
Felis catus	LUZP1	VGNC	VGNC:63330
Bos taurus	LUZP1	VGNC	VGNC:31084
Mus musculus	LUZP1	MGD	MGI:107629
Canis familiaris	LUZP1	VGNC	VGNC:42868
Macaca mulatta	LUZP1	VGNC	VGNC:100004
Rattus norvegicus	LUZP1	RGD	RGD:61839

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MedChemExpress (MCE) 只为有资质的科研机构、医药企业基于科学研究或药证申报的用途提供医药研发服务，不为任何个人或者非科研性质的、非用于药证申报使用等其他用途提供服务。

站点地图隐私声明

沪ICP备15051369号-4

上海工商

沪公网安备31011502019417

沪(浦)应急管危经许[2021]201709(QFYS)

营业执照（三证合一）

LUZP1 - leucine zipper protein 1 Gene

关于 LUZP1

功能概要

LUZP1 基因产物(4)

LUZP1 蛋白互作信息

关联疾病

直系同源

热门区域

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LUZP1 - leucine zipper protein 1 Gene

关于 LUZP1

功能概要

LUZP1 基因产物(4)

LUZP1 蛋白互作信息

关联疾病

相关产品

直系同源

热门区域

A

B

C

F

G

H

J

L

N

Q

S

T

X

Y

Z