CIB4 - calcium and integrin binding family member 4 Gene

中文名称：钙和整合素结合家族成员 4

种属: Homo sapiens

同用名: KIP4

基因 ID: 130106 | 基因类型: protein coding

关于 CIB4

Cytogenetic location: 2p23.3 Genomic coordinates (GRCh38): 2:26,581,205-26,641,366 (from NCBI)

This gene has 3 transcripts (splice variants), 112 orthologues and 8 paralogues. Low expression observed in reference dataset.

启用钙离子结合活性和镁离子结合活性。 [由基因组资源联盟提供，2022 年 4 月]

Enables calcium ion binding activity and magnesium ion binding activity. [provided by Alliance of Genome Resources, Apr 2022]

mRNA	Protein	Name
NM_001029881.3	NP_001025052.1	calcium and integrin-binding family member 4

基因本体论

分子功能 GO 注释	逻辑证据	参考文献	来源
enables calcium ion binding	IDA IDA: 通过直接分析推断	22779914	GOA
enables magnesium ion binding	IDA IDA: 通过直接分析推断	22779914	GOA
enables protein binding	IPI IPI: 通过物理相互作用推断	22779914	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

EF-hand_7

蛋白主名

其他名称

calcium and integrin-binding family member 4

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
Intra	CIB4	A0PJX0	CREB5	Homo sapiens	Q02930-3	Validated Y2H	32296183
Intra	CIB4	A0PJX0	VASN	Homo sapiens	Q6EMK4	Validated Y2H	32296183
Intra	CIB4	A0PJX0	ATG9A	Homo sapiens	Q7Z3C6-3	Validated Y2H	32296183
Intra	CIB4	A0PJX0	MYPOP	Homo sapiens	Q86VE0	Validated Y2H	32296183
Intra	CIB4	A0PJX0	TXN2	Homo sapiens	Q99757	Validated Y2H	32296183
Intra	CIB4	A0PJX0	ZBTB9	Homo sapiens	Q96C00	Validated Y2H	32296183
Intra	CIB4	A0PJX0	UBB	Homo sapiens	P0CG47	Anti Tag CoIP	28514442
Intra	CIB4	A0PJX0	UBB	Homo sapiens	P0CG47	Anti Tag CoIP	33961781
Intra	CIB4	A0PJX0	TACO1	Homo sapiens	Q9BSH4	Validated Y2H	32296183

种属间: 跨种属相互作用 种属内: 同种属相互作用

疾病名称

别名

Usher Syndrome, Type Ij

Gingival Hypertrophy

Hypertrophy Of Gingivae

Gingival Fibromatosis

Hereditary Gingival Fibromatosis	Hereditary Gingival Hyperplasia
Autosomal Dominant Gingival Fibromatosis	Autosomal Dominant Gingival Hyperplasia
Fibromatosis, Gingival, Hereditary	Fibromatosis, Gingival

Usher Syndrome, Type I

USH1	Usher Syndrome Type 1
Us1	Usher Syndrome, Type 1b
Usher Syndrome Type 1e	Retinitis Pigmentosa And Congenital Deafness
Usher Syndrome, Type Ie	USH1E
Usher Syndrome, Type 1e	Usher Syndrome, Type 1a
Usher Syndrome, Type Ib	Usher Syndrome Type 1b
Usher Syndrome Type Ie	Usher Syndrome Type I
Usher 1	Usher Syndrome, Type 1
Ush1a	Usher Syndrome, Type I, French Variety
Usher Syndrome, Type Ia	Usher Syndrome 1b
USH1B	Usher'S Syndrome Type 1b
Usher Syndrome Type Ib	Ushib

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-RS02709	CIB4 Human Pre-designed siRNA Set A	Pre-designed Sets	/	否

种属	基因名	来源	基因 ID
Bos taurus	CIB4	VGNC	VGNC:27362
Rattus norvegicus	CIB4	RGD	RGD:1584147
Mus musculus	CIB4	MGD	MGI:1920509
Macaca mulatta	CIB4	VGNC	VGNC:71379
Canis familiaris	CIB4	VGNC	VGNC:39269
Felis catus	CIB4	VGNC	VGNC:60899

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