| Gene Symbol |
CECR2
|
| Entrez Gene |
27443
|
| Alt Symbol |
-
|
| Species |
Human
|
| Gene Type |
protein-coding
|
| Description |
cat eye syndrome chromosome region, candidate 2
|
| Other Description |
cat eye syndrome critical region protein 2
|
| Swissprots |
Q658Z4 Q9BXF3 A8MX16 A8MS90 Q9C0C3 Q96P58
|
| Accessions |
CCQ43745 Q9BXF3 AB051527 BAB21831 AF336133 AAK15343 AF411609 AAL07393 AK055696 AK091754 AK308330 AL832377 CAH56212 BC166664 AAI66664 BX647449 CAH56122 XM_006724078 XP_006724141 XM_006724079 XP_006724142 XM_011546128 XP_011544430 XM_011546129 XP_011544431 XM_011546130 XP_011544432 XM_011546131 XP_011544433 XM_011546132 XP_011544434 XR_951200 XR_951201 NM_001290046 NP_001276975 NM_001290047 NP_001276976 NM_031413
|
| Function |
Part of the CERF (CECR2-containing-remodeling factor) complex, which facilitates the perturbation of chromatin structure in an ATP-dependent manner. May be involved through its interaction with LRPPRC in the integration of cytoskeletal network with vesicular trafficking, nucleocytosolic shuttling, transcription, chromosome remodeling and cytokinesis. {ECO:0000269|PubMed:15640247}.
|
| Tissue Specificity |
Highly expressed in skeletal muscle, thymus, placenta and lung. Expressed at lower level in brain, heart, colon, spleen, kidney.
|