Symbol
Name
ID

Msx2
msh homeobox 2
MGI:97169

Phenotype annotations related to integument

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Low anterior hairline	Single transverse palmar crease	Hyperextensible skin	Minimal subcutaneous fat	Aplasia cutis congenita of scalp
Disease(s) Associated with MSX2	Low anterior hairline	Single transverse palmar crease	Hyperextensible skin	Minimal subcutaneous fat	Aplasia cutis congenita of scalp
craniosynostosis
parietal foramina

Mouse Phenotypes

integument phenotype

abnormal mammary gland embryonic development

alopecia

premature hair loss

abnormal nail morphology

abnormal nail matrix morphology

deformed nails

long nails

long toenails

curly vibrissae

short vibrissae

abnormal hair shedding

delayed hair regrowth

Availability

Mouse Genotype

Msx2^m1Btlr/Msx2^m1Btlr

Msx2^tm1.1Yvla/Msx2^tm1.1Yvla

Msx2^tm1Rilm/Msx2^tm1Rilm

Msx2^tm1Rem/Msx2^tm1Rem
Tg(Msx2-cre)5Rem/0 (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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