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Symbol
Name
ID

Kcnq1ot1
KCNQ1 overlapping transcript 1
MGI:1926855

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

Human Phenotypes

Hemihypertrophy

Splenomegaly

Visceromegaly

Hepatomegaly

Inguinal hernia

Omphalocele

Umbilical hernia

Diastasis recti

Congenital diaphragmatic hernia

Tall stature

Overgrowth

Large for gestational age

Obesity

Asymmetric growth

Disease(s) Associated with KCNQ1OT1

Beckwith-Wiedemann syndrome

Mouse Phenotypes		decreased embryo size	decreased body weight	weight loss	decreased body size	postnatal growth retardation
Availability	Mouse Genotype	decreased embryo size	decreased body weight	weight loss	decreased body size	postnatal growth retardation
	Kcnq1ot1^tm1.1Mjh/Kcnq1ot1⁺
	Kcnq1ot1^tm1Tilg/Kcnq1ot1⁺
	Kcnq1ot1^tm2Mjh/Kcnq1ot1⁺
	Kcnq1ot1^tm2.1Ckan/Kcnq1ot1⁺ Meox2^tm1(cre)Sor/Meox2⁺ (conditional)

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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