SOBP - sine oculis binding protein homolog Gene

中文名称：正弦波结合蛋白同系物

种属: Homo sapiens

同用名: JXC1; MRAMS

基因 ID: 55084 | 基因类型: protein coding

关于 SOBP

Cytogenetic location: 6q21 Genomic coordinates (GRCh38): 6:107,490,117-107,661,306 (from NCBI)

This gene has 4 transcripts (splice variants), 205 orthologues, 1 paralogue and is associated with 3 phenotypes. Broad expression in brain (RPKM 6.2), ovary (RPKM 3.5) and 21 other tissues.

功能概要

该基因编码的蛋白质是一种参与耳蜗发育的核锌指蛋白。该基因的缺陷也与智力障碍有关。[RefSeq 提供，2011 年 3 月]

The protein encoded by this gene is a nuclear zinc finger protein that is involved in development of the cochlea. Defects in this gene have also been linked to intellectual disability. [provided by RefSeq, Mar 2011]

SOBP 基因产物(1)

mRNA	Protein	Name
NM_018013.4	NP_060483.3	sine oculis-binding protein homolog

基因本体论

生物过程

生物过程 GO 注释	逻辑证据	参考文献	来源
involved in cognition	IMP IMP: 通过突变表型推断	21035105	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

SOBP 蛋白结构

SOBP

0
200
400
600
800
873 a.a.

蛋白主名

其他名称

sine oculis-binding protein homolog

jackson circler protein 1

关联疾病

疾病名称

别名

Mental Retardation, Anterior Maxillary Protrusion, And Strabismus

Intellectual Disability, Anterior Maxillary Protrusion, And Strabismus	MRAMS
Anterior Maxillary Protrusion-Strabismus-Intellectual Disability Syndrome	Mrams Syndrome

Deafness, Autosomal Recessive 62

DFNB62	Autosomal Recessive Nonsyndromic Deafness 62
Autosomal Recessive Deafness 62

Esotropia

Convergence In Manifest Squint	Crossed Eyes
Internal Strabismus	Convergent Concomitant Strabismus
Convergent Squint	Convergent Strabismus
Cross-Eye

Amblyopia

Lazy Eye

Spermatocytoma

Spermatocytic Seminoma

Strabismus

Strabismus, Susceptibility To	Strabismus, Susceptibility To, 1
Strabismus 1

Branchiootorenal Syndrome

Branchio-Oto-Renal Syndrome	Bor Syndrome
Branchiootorenal Dysplasia	Melnick-Fraser Syndrome
Branchiootorenal Spectrum Disorders	Branchio-Otorenal Dysplasia
Branchio Oto Renal Syndrome	Branchiootorenal/Branchiootic Syndrome
Bo Syndrome	Bor
Bos	Branchio-Otorenal Syndrome
Branchiootic Syndrome	Branchiootorenal Syndrome
Branchiootic Syndrome 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

Cat. No.	产品名	作用方式 Pre-designed Sets	纯度	是否罕见病否
HY-16776A	(2S,5S)-Censavudine		98.12%	否
HY-RS13551	SOBP Human Pre-designed siRNA Set A	Pre-designed Sets	/	否

直系同源

种属	基因名	来源	基因 ID
Canis familiaris	SOBP	VGNC	VGNC:49867
Mus musculus	SOBP	MGD	MGI:1924427
Rattus norvegicus	SOBP	RGD	RGD:1560479
Macaca mulatta	SOBP	VGNC	VGNC:77790
Bos taurus	SOBP	VGNC	VGNC:35118
Felis catus	SOBP	VGNC	VGNC:102522

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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）

SOBP - sine oculis binding protein homolog Gene

关于 SOBP

功能概要

SOBP 基因产物(1)

SOBP 蛋白结构

关联疾病

直系同源

热门区域

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SOBP - sine oculis binding protein homolog Gene

关于 SOBP

功能概要

SOBP 基因产物(1)

SOBP 蛋白结构

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