CMIP, c-Maf inducing protein, 80790

N. diseases: 54; N. variants: 28
Disease: Language Disorders ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023015
Disease: Language Disorders
Language Disorders 		0.030 GeneticVariation group BEFREE For example, rare protein-coding mutations of the FOXP2 transcription factor cause severe problems with sequencing of speech sounds, while common genetic risk variants of small effect size in genes like CNTNAP2, ATP2C2 and CMIP are associated with typical forms of language impairment. 23228431 2013
CUI: C0023015
Disease: Language Disorders
Language Disorders 		0.030 GeneticVariation group BEFREE We have analyzed common risk variants within RD (MRPL19/C2ORF3, KIAA0319, and DCDC2) and language impairment (CMIP and ATP2C2) candidate loci in the Avon Longitudinal Study of Parents and Children cohort (n = 3725), representing children born in southwest England in the early 1990s. 21457949 2011
CUI: C0023015
Disease: Language Disorders
Language Disorders 		0.030 GeneticVariation group BEFREE We therefore propose that variants in CMIP and ATP2C2 act to modulate phonological short-term memory primarily in the context of language impairment. 19646677 2009