Synonyms:ENTREZ:5108, HGNC:8727, MIM:600299, NM_001315507, NM_001315508, NM_001352632, NM_001352633, NM_001352634, NM_001352635, NM_001352636, NM_001352637, NM_001352638, NM_001352639, NM_001352640, NM_001352641, NM_001352642, NM_001352643, NM_001352644, NM_001352645, NM_001352646, NM_001352647, NM_001352648, NM_001352649, NM_001352650, NM_001352651, NM_001352652, NM_001352653, NM_001352654, NM_001352655, NM_001352656, NM_001352657, NM_001352658, NM_001352659, NM_001352660, NM_006197, NP_001302436, NP_001302437, NP_001339561, NP_001339562, NP_001339563, NP_001339564, NP_001339565, NP_001339566, NP_001339567, NP_001339568, NP_001339569, NP_001339570, NP_001339571, NP_001339572, NP_001339573, NP_001339574, NP_001339575, NP_001339576, NP_001339577, NP_001339578, NP_001339579, NP_001339580, NP_001339581, NP_001339582, NP_001339583, NP_001339584, NP_001339585, NP_001339586, NP_001339587, NP_001339588, NP_001339589, NP_006188, NR_148032, PCM1, PTC4, RET/PCM-1, XM_006716336, XM_006716340, XM_011544528, XM_011544529, XM_011544530, XM_011544532, XM_011544534, XM_017013472, XM_017013473, XM_017013478, XM_017013480, XM_017013481, XM_017013486, XM_017013489, XM_017013490, XM_017013491, XM_017013493, XM_017013496, XM_017013501, XM_024447167, XM_024447168, XM_024447169, XM_024447170, XM_024447171, XP_006716399, XP_006716403, XP_011542830, XP_011542831, XP_011542832, XP_011542834, XP_011542836, XP_016868961, XP_016868962, XP_016868967, XP_016868969, XP_016868970, XP_016868975, XP_016868978, XP_016868979, XP_016868980, XP_016868982, XP_016868985, XP_016868990, XP_024302935, XP_024302936, XP_024302937, XP_024302938, XP_024302939, pericentriolar material 1
Omim:OMIM:600299
Id:a7b9a0d3-fa95-5c70-85c7-d1e7e0dce6c5
Hgnc:HGNC:8727
Description:pericentriolar material 1
The protein encoded by this gene is a component of centriolar satellites, which are electron dense granules scattered around centrosomes. Inhibition studies show that this protein is essential for the correct localization of several centrosomal proteins, and for anchoring microtubules to the centrosome. Chromosomal aberrations involving this gene are associated with papillary thyroid carcinomas and a variety of hematological malignancies, including atypical chronic myeloid leukemia and T-cell lymphoma. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015]
