| Gene Symbol |
HMGN2
|
| Entrez Gene |
3151
|
| Alt Symbol |
HMG17
|
| Species |
Human
|
| Gene Type |
protein-coding
|
| Description |
high mobility group nucleosomal binding domain 2
|
| Other Description |
high mobility group nucleosome-binding domain-containing protein 2|high mobility group protein N2|high-mobility group (nonhistone chromosomal) protein 17|high-mobility group nucleosomal binding domain 2|non-histone chromosomal protein HMG-17|nonhistone chromosomal protein HMG-17
|
| Swissprots |
Q6FGI5 Q0VGD5 Q96C64 P05204
|
| Accessions |
CAA31898 EAX07803 P05204 AK026562 AU100588 BC000378 AAH00378 BC003050 AAH03050 BC003689 BC007124 BC014644 AAH14644 BC020307 BC032140 AAH32140 BC061898 BC064347 BC070297 AAH70297 BC071707 AAH71707 BC072010 AAH72010 BC072011 AAH72011 BC075837 AAH75837 BC081567 AAH81567 BC110390 AAI10391 BU074476 CR542122 CAG46919 EU446509 ABZ92038 M12623 AAA52678 NM_005517 NP_005508
|
| Function |
Binds to the inner side of the nucleosomal DNA thus altering the interaction between the DNA and the histone octamer. May be involved in the process which maintains transcribable genes in a unique chromatin conformation (By similarity). {ECO:0000250}.
|
| Subcellular Location |
Nucleus {ECO:0000269|PubMed:10739259}. Cytoplasm {ECO:0000269|PubMed:10739259}. Note=Cytoplasmic enrichment upon phosphorylation.
|
