CIB3 - calcium and integrin binding family member 3 Gene

Homo sapiens

Also known as KIP3

Gene ID: 117286 | Gene type: protein coding

About CIB3

Cytogenetic location: 19p13.11 Genomic coordinates (GRCh38): 19:16,161,368-16,173,525 (from NCBI)

This gene has 4 transcripts (splice variants), 197 orthologues and 8 paralogues. Low expression observed in reference dataset.

Summary

This gene product shares a high degree of sequence similarity with DNA-dependent protein kinase catalytic subunit-interacting protein 2 in human and mouse, and like them may bind the catalytic subunit of DNA-dependent protein kinases. The exact function of this gene is not known. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]

CIB3 Products(2)

mRNA	Protein	Name
NM_001300922.2	NP_001287851.1	calcium and integrin-binding family member 3 isoform 2
NM_054113.4	NP_473454.1	calcium and integrin-binding family member 3 isoform 1

CIB3 Protein Structure

EF-hand_7

0
100
187 a.a.

Protein Preferred Names

Protein Names

calcium and integrin-binding family member 3

DNA-dependent protein kinase catalytic subunit-interacting protein 3

Related Diseases

Diseases

Alias

Usher Syndrome, Type Ij

Usher Syndrome Type 1j	USH1J
Usher Syndrome Type Ij	Usher Syndrome 1j
Usher'S Syndrome Type 1j

Colon Small Cell Carcinoma

Colonic Small Cell Carcinoma

Colon Small Cell Neuroendocrine Carcinoma

Congenital Fibrosis Of The Extraocular Muscles

Congenital Fibrosis Of Extraocular Muscles	Cfeom
Feom	Congenital External Ophthalmoplegia
Congenital Fibrosis Syndrome	General Fibrosis Syndrome

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

Diseases	Alias
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

Related Agents

Pre-clinical Phase

Bioactive Molecules (2)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-147918	Anticancer agent 73	Inhibitor	99.92%	Unkown
HY-RS02708	CIB3 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	CIB3	VGNC	VGNC:39268
Bos taurus	CIB3	VGNC	VGNC:27361
Felis catus	CIB3	VGNC	VGNC:69375
Mus musculus	CIB3	MGD	MGI:2685953
Macaca mulatta	CIB3	VGNC	VGNC:71339
Rattus norvegicus	CIB3	RGD	RGD:1590245

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