background:
It is able to complement the radiosensitivity defect of an ataxia telangiectasia (AT) fibroblast cell line.
Function:
It is able to complement the radiosensitivity defect of an ataxia telangiectasia (AT) fibroblast cell line.
Subunit:
Interacts with VIM and HINT1.
Subcellular Location:
Cytoplasm. Note=Colocalizes with intermediate filaments.
Tissue Specificity:
Expressed in placenta, prostate and thymus.
Similarity:
Contains 1 B box-type zinc finger.
Database links:
UniProtKB/Swiss-Prot: Q14134.2
Entrez Gene: 23650 Human
Entrez Gene: 72169 Mouse
Entrez Gene: 300656 Rat
Omim: 610658 Human
SwissProt: Q14134 Human
SwissProt: Q8R2Q0 Mouse
Unigene: 504115 Human
Unigene: 273277 Mouse
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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