# Calcium and integrin binding family member 2

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21115663](https://www.wikidata.org/wiki/Q21115663)  
**Source**: https://4ort.xyz/entity/calcium-and-integrin-binding-family-member-2-q21115663


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/O75838)
3. Q20641742
4. [Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75838)
5. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=O75838&geneProductId=UniProtKB:O75838)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75838)
7. [Biophysical and structural studies of the human calcium- and integrin-binding protein family: understanding their functional similarities and differences](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75838)
8. [Proteomic analysis of microvesicles from plasma of healthy donors reveals high individual variability](http://www.ebi.ac.uk/QuickGO/annotations?protein=O75838&geneProductId=UniProtKB:O75838)
9. [Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cells](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75838)
10. [A Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75838)
11. [Proteomic analysis of microvesicles from plasma of healthy donors reveals high individual variability](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:O75838)
12. Ensembl Release 99