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The row for this annotation cannot be found. This might be due to a row or page getting deleted.

GO:0008385IkappaB kinase complexPMID:25473891IMP: Inferred from Mutant Phenotype C
This annotation made on page:
By: Hzuniga (group Team Hot Tamales) on 2015-02-10 17:36:18 CST.

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Entry TypeChallenging User,GroupTime/DateChallenge ReasonPoints/Assessment
Team Mic Drop
2015-02-17 15:33:04 CST

Need IDA at least the description of phenotypes as stated in the experimental results in Figure 1. Phenotype of patients with infantile-onset multisystem neurologic, endocrine, and pancreatic disease (IMNEPD). (A) The index patients (II.1, II.4) are children of healthy, consanguineous Yazidian parents from Turkey. (B) Both patients displayed facial dysmorphism with midface hypoplasia, hypertelorism, exotropia, and thin upper lip (II.1: 13 years, II.4: 5 years) and deformities of (C) fingers and (D) toes (II.1). (E) Cranial MRI revealed progressive cerebellar atrophy (II.1: left at 2 and right at 12 years of age). (F) Abnormal rhythmic alpha-beta-waves with high amplitudes on EEG recording (II.1). (G) High echo intensity of the pancreas (arrow) of the affected female patient II.1 (top) compared to that of a healthy, age-matched control (bottom) in an abdominal ultrasound indicates organ fibrosis and/or increase in fatty tissue.

Team Bio Bois
2015-02-16 22:01:47 CST

Needs to be IDA.

Team Designated Drinkers
2015-02-16 21:18:50 CST

The PubMed ID does not exist and there are no notes mentioned that provide necessary information about the annotation.

Team Dos Juanitas
2015-02-16 16:48:49 CST

no notes or figured mentioned and PMID does not exist.

Suzialeksander2015-02-20 14:59:23 CSTYou need to be an instructor to view these notes.Unacceptable