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Symbol
Name
ID
Slc35d1
solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1
MGI:2140361
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Malar flattening
Macrocephaly
Short neck
Brachydactyly
Advanced tarsal ossification
Metaphyseal irregularity
Dumbbell-shaped long bone
Flat acetabular roof
Advanced ossification of carpal bones
Limb undergrowth
Short long bone
Snail-like ilia
Lateral clavicle hook
Short ribs
Anterior rib cupping
Hypoplastic scapulae
Thoracic hypoplasia
Narrow chest
Ovoid vertebral bodies
Platyspondyly
Narrow vertebral interpedicular distance
Disease(s) Associated with SLC35D1
schneckenbecken dysplasia

Mouse Phenotypes
abnormal craniofacial bone morphology
abnormal long bone epiphyseal plate proliferative zone
decreased length of long bones
short ilium
platyspondylia
chondrodystrophy
Availability Mouse Genotype
Slc35d1tm1Hko/Slc35d1tm1Hko

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory