about
P688
Biophysical and structural studies of the human calcium- and integrin-binding protein family: understanding their functional similarities and differencesAlterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48.Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cellsA Novel C-Terminal CIB2 (Calcium and Integrin Binding Protein 2) Mutation Associated with Non-Syndromic Hearing Loss in a Hispanic Family
P921
description
humanes Protein
@de
mammalian protein found in Homo sapiens
@en
menselijk eiwit
@nl
protein
@id
protein
@sv
proteinë
@sq
protèin
@ace
protéine humaine
@fr
بروتين بشري
@ar
name
Calcium and integrin binding family member 2
@en
Calcium and integrin binding family member 2
@nl
type
label
Calcium and integrin binding family member 2
@en
Calcium and integrin binding family member 2
@nl
altLabel
CIB2
@en
DNA-dependent protein kinase catalytic subunit-interacting protein 2
@en
KIP 2
@en
Kinase-interacting protein 2
@en
calcium and integrin-binding family member 2
@en
prefLabel
Calcium and integrin binding family member 2
@en
Calcium and integrin binding family member 2
@nl
P637
P680
P681
P682
P705
P352
P31
P352
P637
NP_001258817
NP_001258818
NP_001288153
XP_005254183
XP_006720437
XP_011519463
P680
P681
P682
P702
P703
P705
ENSP00000258930
ENSP00000442459
ENSP00000452752
ENSP00000452980
ENSP00000453256
ENSP00000453377
ENSP00000453488
ENSP00000453654
ENSP00000453963
ENSP00000494155