About Help FAQ

Symbol
Name
ID

Hnrnph2
heterogeneous nuclear ribonucleoprotein H2
MGI:1201779

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Micrognathia	Secondary microcephaly	Prominent fingertip pads	Arachnodactyly	Joint hypermobility	Pectus carinatum	Hyperlordosis	Scoliosis
Disease(s) Associated with HNRNPH2
syndromic X-linked intellectual developmental disorder bain type

Mouse Phenotypes		decreased cranium height	short mandible	short maxilla	domed cranium
Availability	Mouse Genotype	decreased cranium height	short mandible	short maxilla	domed cranium
	Hnrnph2^em1Jpat/Hnrnph2⁺
	Hnrnph2^em1Jpat/Y
	Hnrnph2^em2Jpat/Y

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 05/14/2024 MGI 6.23