|
Symbol Name ID |
Slc26a2
solute carrier family 26 (sulfate transporter), member 2 MGI:892977 |
| Darker colors indicate more annotations |
| Human Phenotypes | Short neck |
Rhizomelia |
Abdominal distention |
Protuberant abdomen |
Inguinal hernia |
Umbilical hernia |
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 | abnormal facial morphology |
protruding tongue |
postnatal growth retardation |
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| Availability | Mouse Genotype | |||
| Slc26a2em1(IMPC)Bay/Slc26a2em1(IMPC)Bay | ||||
| Slc26a2tm1Aros/Slc26a2tm1Aros | ||||
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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last database update 04/23/2024 MGI 6.23 |
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