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Symbol
Name
ID

Slc26a2
solute carrier family 26 (sulfate transporter), member 2
MGI:892977

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

Human Phenotypes

Short neck

Rhizomelia

Inguinal hernia

Umbilical hernia

Abdominal distention

Protuberant abdomen

Short stature

Disproportionate short stature

Disproportionate short-limb short stature

Neonatal short-limb short stature

Moderately short stature

Small for gestational age

Disease(s) Associated with SLC26A2

achondrogenesis type IB

atelosteogenesis

diastrophic dysplasia

multiple epiphyseal dysplasia 4

Mouse Phenotypes		mandibular hyperostosis	abnormal facial morphology	protruding tongue	postnatal growth retardation
Availability	Mouse Genotype	mandibular hyperostosis	abnormal facial morphology	protruding tongue	postnatal growth retardation
	Slc26a2^em1(IMPC)Bay/Slc26a2^em1(IMPC)Bay
	Slc26a2^tm1Aros/Slc26a2^tm1Aros

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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