129555535 - GEO Profiles - NCBI

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LOC100862433 - Double-knockout p53/PRKDC model of B cell acute lymphoblastic leukemia: leukemic blasts

Annotation:: LOC100862433, 40S ribosomal protein S16 (multiple annotations exist)

Organism:: Mus musculus

Reporter:: GPL1261, 1416404_s_at (ID_REF), GDS5640, 20055 (Gene ID), 100039355 (Gene ID), 100862433 (Gene ID), NM_013647

DataSet type:: Expression profiling by array, count, 9 samples

ID:: 129555535

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Joubert syndrome 16
Joubert syndrome 16

MedGen
C3280906[conceptid] (1)
MedGen
Hypothyroidism, Congenital, Nongoitrous, 1 [Supplementary Concept]
Hypothyroidism, Congenital, Nongoitrous, 1 [Supplementary Concept]
also known as CHNG 1; associated with mutations oITSHR<br/>Date introduced: October 24, 2013<br/>

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