HSPA13 - heat shock protein family A (Hsp70) member 13 Gene

中文名称：热休克蛋白家族 A (Hsp70) 成员 13

种属: Homo sapiens

同用名: STCH

基因 ID: 6782 | 基因类型: protein coding

关于 HSPA13

Cytogenetic location: 21q11.2 Genomic coordinates (GRCh38): 21:14,371,115-14,383,146 (from NCBI)

This gene has 2 transcripts (splice variants), 205 orthologues and 13 paralogues. Ubiquitous expression in brain (RPKM 23.3), thyroid (RPKM 21.7) and 25 other tissues.

功能概要

由该基因编码的蛋白质是热休克蛋白 70 家族的成员，被发现与微粒体相关。该蛋白质家族的成员在细胞溶质和分泌蛋白的加工以及去除变性或错误折叠的蛋白质方面发挥作用。编码的蛋白质包含一个 ATPase 结构域，并已被证明与一种泛素样蛋白质相关。[RefSeq 提供，2008 年 7 月]

The protein encoded by this gene is a member of the heat shock protein 70 family and is found associated with microsomes. Members of this protein family play a role in the processing of cytosolic and secretory proteins, as well as in the removal of denatured or incorrectly-folded proteins. The encoded protein contains an ATPase domain and has been shown to associate with a ubiquitin-like protein. [provided by RefSeq, Jul 2008]

HSPA13 基因产物(1)

mRNA	Protein	Name
NM_006948.5	NP_008879.3	heat shock 70 kDa protein 13 precursor

基因本体论

分子功能

分子功能 GO 注释	逻辑证据	参考文献	来源
enables protein binding	IPI IPI: 通过物理相互作用推断	16189514	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

HSPA13 蛋白结构

HSP70

0
100
200
300
400
471 a.a.

蛋白主名

其他名称

heat shock 70 kDa protein 13

heat shock protein 70kDa family, member 13

HSPA13 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	HSPA13	P48723	UBQLN1	Homo sapiens	Q9UMX0-2	Y2H Prey Pooling	25416956
种属内	HSPA13	P48723	UBQLN1	Homo sapiens	Q9UMX0-2	Validated Y2H	25416956
种属内	HSPA13	P48723	UBQLN1	Homo sapiens	Q9UMX0-2	Y2H Fragment Pooling	35914814
种属内	HSPA13	P48723	UBQLN1	Homo sapiens	Q9UMX0-2	Y2H Array	25416956
种属内	HSPA13	P48723	CRYGA	Homo sapiens	Q24JT5	Y2H Prey Pooling	32296183
种属内	HSPA13	P48723	CRYGA	Homo sapiens	Q24JT5	Validated Y2H	32296183
种属内	HSPA13	P48723	CRYGA	Homo sapiens	Q24JT5	Y2H Array	32296183
种属内	HSPA13	P48723	B4GALT5	Homo sapiens	O43286	Anti Tag CoIP	28514442
种属内	HSPA13	P48723	SGTA	Homo sapiens	O43765	Y2H Array	32296183
种属内	HSPA13	P48723	SGTA	Homo sapiens	O43765	Validated Y2H	25416956
种属内	HSPA13	P48723	SGTA	Homo sapiens	O43765	Y2H Prey Pooling	32296183
种属内	HSPA13	P48723	SGTA	Homo sapiens	O43765	Y2H Array	25416956
种属内	HSPA13	P48723	UBQLN4	Homo sapiens	Q9NRR5	Y2H Array	16713569
种属内	HSPA13	P48723	UBQLN4	Homo sapiens	Q9NRR5	Y2H Fragment Pooling	35914814
种属内	HSPA13	P48723	UBQLN1	Homo sapiens	Q9UMX0	Y2H Prey Pooling	25416956
种属内	HSPA13	P48723	UBQLN1	Homo sapiens	Q9UMX0	Y2H Prey Pooling	32296183
种属内	HSPA13	P48723	UBQLN1	Homo sapiens	Q9UMX0	Validated Y2H	32296183
种属内	HSPA13	P48723	UBQLN1	Homo sapiens	Q9UMX0	Y2H Array	25416956
种属内	HSPA13	P48723	UBQLN1	Homo sapiens	Q9UMX0	Y2H Array	32296183
种属内	HSPA13	P48723	UBQLN1	Homo sapiens	Q9UMX0	Y2H Pooling	16189514
种属内	HSPA13	P48723	SGTB	Homo sapiens	Q96EQ0	Y2H Fragment Pooling	35914814
种属内	HSPA13	P48723	SGTB	Homo sapiens	Q96EQ0	Y2H Prey Pooling	32296183
种属内	HSPA13	P48723	SGTB	Homo sapiens	Q96EQ0	Validated Y2H	32296183
种属内	HSPA13	P48723	SGTB	Homo sapiens	Q96EQ0	Y2H Array	32296183
种属内	HSPA13	P48723	UBQLN2	Homo sapiens	Q9UHD9	Y2H Fragment Pooling	35914814
种属内	HSPA13	P48723	UBQLN2	Homo sapiens	Q9UHD9	Y2H Prey Pooling	32296183
种属内	HSPA13	P48723	UBQLN2	Homo sapiens	Q9UHD9	Validated Y2H	32296183
种属内	HSPA13	P48723	UBQLN2	Homo sapiens	Q9UHD9	Y2H Array	32296183

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

Bartter Syndrome, Type 1, Antenatal

Hyperprostaglandin E Syndrome 1	Bartter Disease Type 1
BARTS1	Bartter Syndrome, Type 1
Bartter Syndrome Type 1	Hypokalemic Alkalosis With Hypercalciuria Antenatal 1
Hypokalemic Alkalosis With Hypercalciuria 1, Antenatal	Bartter Syndrome Type 1 Antenatal
Hypokalemic Alkalosis With Hypercalciuria 1 Antenatal	Bartter Syndrome Antenatal Type 1
Antenatal Bartter Syndrome Type 1	Bartter Syndrome Type I
Bartter Syndrome 1, Antenatal	Abs1
Antenatal Bartter Syndrome 1	Bs1
Bartter Syndrome, Antenatal Type 1	Antley-Bixler Syndrome With Genital Anomalies And Disordered Steroidogenesis

Deafness, Autosomal Dominant 28

DFNA28	Autosomal Dominant Nonsyndromic Deafness 28
Autosomal Dominant Deafness 28	Deafness, Autosomal Dominant, 28
Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 28	Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 28
Deafness, Autosomal Dominant, Type 28

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-RS06422	HSPA13 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	HSPA13	VGNC	VGNC:102758
Bos taurus	HSPA13	VGNC	VGNC:53581
Macaca mulatta	HSPA13	VGNC	VGNC:81327
Rattus norvegicus	HSPA13	RGD	RGD:3775
Mus musculus	HSPA13	MGD	MGI:1309463
Canis familiaris	HSPA13	VGNC	VGNC:53026
Others	HSPA13	NCBI

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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）

HSPA13 - heat shock protein family A (Hsp70) member 13 Gene

关于 HSPA13

功能概要

HSPA13 基因产物(1)

HSPA13 蛋白结构

HSPA13 蛋白互作信息

关联疾病

直系同源

热门区域

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HSPA13 - heat shock protein family A (Hsp70) member 13 Gene

关于 HSPA13

功能概要

HSPA13 基因产物(1)

HSPA13 蛋白结构

HSPA13 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