FAM167A - family with sequence similarity 167 member A Gene

中文名称：具有序列相似性的家族 167 成员 A

种属: Homo sapiens

同用名: D8S265; C8orf13; DIORA-1

基因 ID: 83648 | 基因类型: protein coding

关于 FAM167A

Cytogenetic location: 8p23.1 Genomic coordinates (GRCh38): 8:11,421,476-11,475,908 (from NCBI)

This gene has 8 transcripts (splice variants), 214 orthologues and 3 paralogues. Biased expression in thyroid (RPKM 28.9), brain (RPKM 11.5) and 4 other tissues.

FAM167A 基因产物(1)

mRNA	Protein	Name
NM_053279.3	NP_444509.2	protein FAM167A

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	25416956	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

FAM167A 蛋白结构

FAM167

0
100
200
214 a.a.

蛋白主名

其他名称

protein FAM167A

disordered autoimmunity 1

FAM167A 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	FAM167A	Q96KS9	FLJ13057	Homo sapiens	Q53SE7	Y2H Array	25416956
种属内	FAM167A	Q96KS9	PPP3CA	Homo sapiens	Q08209-2	Y2H Array	32296183
种属内	FAM167A	Q96KS9	PPP3CA	Homo sapiens	Q08209-2	Y2H Prey Pooling	32296183
种属内	FAM167A	Q96KS9	GMCL1	Homo sapiens	Q96IK5	Anti Tag CoIP	33961781
种属内	FAM167A	Q96KS9	GMCL1	Homo sapiens	Q96IK5	Anti Tag CoIP	28514442
种属内	FAM167A	Q96KS9	GMCL1	Homo sapiens	Q96IK5	Y2H Array	31515488
种属内	FAM167A	Q96KS9	GMCL1	Homo sapiens	Q96IK5	Y2H Prey Pooling	32296183
种属内	FAM167A	Q96KS9	GMCL1	Homo sapiens	Q96IK5	Y2H Array	32296183
种属内	FAM167A	Q96KS9	HIP1	Homo sapiens	O00291	Validated Y2H	32814053
种属内	FAM167A	Q96KS9	HIP1	Homo sapiens	O00291	Y2H Pooling	32814053
种属内	FAM167A	Q96KS9	HIP1	Homo sapiens	O00291	Y2H Array	32814053
种属内	FAM167A	Q96KS9	COQ8A	Homo sapiens	Q8NI60	Y2H Array	32814053
种属内	FAM167A	Q96KS9	COQ8A	Homo sapiens	Q8NI60	Y2H Pooling	32814053
种属内	FAM167A	Q96KS9	COQ8A	Homo sapiens	Q8NI60	Validated Y2H	32814053
种属内	FAM167A	Q96KS9	PRPH	Homo sapiens	P41219	Anti Tag CoIP	33961781
种属内	FAM167A	Q96KS9	PRPH	Homo sapiens	P41219	Validated Y2H	32814053
种属内	FAM167A	Q96KS9	PRPH	Homo sapiens	P41219	Y2H Pooling	32814053
种属内	FAM167A	Q96KS9	PRPH	Homo sapiens	P41219	Y2H Array	32814053
种属内	FAM167A	Q96KS9	PRKCG	Homo sapiens	P05129	Y2H Pooling	32814053
种属内	FAM167A	Q96KS9	PRKCG	Homo sapiens	P05129	Validated Y2H	32814053
种属内	FAM167A	Q96KS9	PRKCG	Homo sapiens	P05129	Y2H Array	32814053

种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 FAM167A 蛋白

目录号	产品名	蛋白编号	纯度
HY-P71678	FAM167A Protein, Human (HEK293, Myc, His)	Q96KS9 (M1-C214)	≥95%

关联疾病

疾病名称

别名

Maturity-Onset Diabetes Of The Young, Type 11

Maturity-Onset Diabetes Of The Young Type 11	MODY11
Maturity-Onset Diabetes Of The Young 11	Mody-11
Mody Type 11	Diabetes Of The Young, Maturity-Onset, Type 11

Keratolytic Winter Erythema

KWE	Oudtshoorn Skin Disease
Erythrokeratolysis Hiemalis Ichthyosis	Erythrokeratolysis Hiemalis
Oudtshoorn Skin	Oudtshoorn Disease

Kawasaki Disease

Mucocutaneous Lymph Node Syndrome	Acute Febrile Mucocutaneous Lymph Node Syndrome
Kawasaki Syndrome	Kd
Infantile Polyarteritis	Kawasaki Disease, Susceptibility To
Acute Febrile Mcls	Kawasaki'S Disease
Mlns	KWD

Bacterial Conjunctivitis

Purulent Conjunctivitis

Conjunctivitis, Bacterial

Potocki-Shaffer Syndrome

Proximal 11p Deletion Syndrome	Chromosome 11p11.2 Deletion Syndrome
Pss	11p11.2 Deletion
P11pds	Defect11 Syndrome
Deletion Of Chromosome 11p11.2	POSHS

Systemic Lupus Erythematosus

Lupus Nephritis	SLE
Disseminated Lupus Erythematosus	Systemic Lupus Erythematosus, Susceptibility To
Lupus Erythematosus, Systemic	Lupus Nephritis, Susceptibility To
Libman-Sacks Disease	Systemic Lupus Erythematosus Susceptibility To
Sle - Lupus Erythematosus, Systemic	Le Syndrome
Lupus	Lupus Erythematosus Systemic
Lupus Erythematosus, Systemic, Susceptibility To	Lupus Vulgaris
Lupus Erythematosus, Discoid	Lupus Erythematosus
Systemic Lupus Erythematosus Nos	Sle - [Systemic Lupus Erythematosus]

Limited Scleroderma

Limited Cutaneous Systemic Sclerosis	Limited Systemic Sclerosis
Systemic Sclerosis Sine Scleroderma	Crest Syndrome
Limited Cutaneous Systemic Scleroderma	Scleroderma, Limited
Systemic Sclerosis, Limited	Progressive Systemic Sclerosis Sine Scleroderma
Scleroderma, Sine	Crest - [Calcinosis, Raynaud Phenomenon, Oesophageal Dysmotility, Sclerodactyly, And Telangiectasia] Syndrome
Crst - [Calcinosis, Raynaud Phenomenon, Sclerodactyly And Telangiectasia] Syndrome

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-RS04690	FAM167A Human Pre-designed siRNA Set A	Pre-designed Sets	/	否

直系同源

种属	基因名	来源	基因 ID
Bos taurus	FAM167A	VGNC	VGNC:28750
Mus musculus	FAM167A	MGD	MGI:3606565
Canis familiaris	FAM167A	VGNC	VGNC:40617
Rattus norvegicus	FAM167A	RGD	RGD:1561302
Macaca mulatta	FAM167A	VGNC	VGNC:83998
Felis catus	FAM167A	VGNC	VGNC:78491
Others	FAM167A	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）

FAM167A - family with sequence similarity 167 member A Gene

关于 FAM167A

FAM167A 基因产物(1)

FAM167A 蛋白结构

FAM167A 蛋白互作信息

重组 FAM167A 蛋白

关联疾病

直系同源

热门区域

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FAM167A - family with sequence similarity 167 member A Gene

关于 FAM167A

FAM167A 基因产物(1)

FAM167A 蛋白结构

FAM167A 蛋白互作信息

重组 FAM167A 蛋白

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