Gene: [07q32/MEST] mesoderm specific transcript (mouse) homolog; paternally expressed gene 1 (PEG1); [PEG1 ]
|
COM |
Nishita-1996 mapped a human homolog of the mouse Mest gene to 7q32. The human PEG1/MEST is an imprinted gene expressed from a paternal allele and is located on 7q31-q32, near D7S649 (Kobayashi-1997)." |
|
TIS |
Southern blot analysis showed that the MEST gene is expressed in all major fetal organs and tissues, which does not contradict the mesoderm-specific expression (Nishita-1996)." |
|
ASS |
Nishita et al. suggested that MEST is involved in the causation of Russell Silver syndrome (GEM:00.0/RSS) which is characterized by pre- and postnatal growth retardation (Nishita-1996)." |
|
REL |
GEM:19q134/PEG3 |
|
REF |
LOC,CLO,EXP "Kobayashi S &: Hum Mol Genet, 6, 781-786, 1997 COD,SEQ,EVO,LOC "Nishita Y &: Genomics, 36, N3, 539-542, 1996 |
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KEY |
ont |
|
CLA |
coding, basic |
|
LOC |
07 q32 |
|
MIM |
MIM: 601029 |
|
SYN |
PEG1 |
