Entry |
|
Symbol |
OFD1
|
Name |
oral-facial-digital syndrome 1 protein
|
Disease |
H00454 | Oral-facial-digital syndrome |
H00530 | Joubert syndrome and related disorders |
H01215 | Simpson-Golabi-Behmel syndrome |
|
Brite |
KEGG Orthology (KO) [BR:ko00001]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins
K16480 OFD1; oral-facial-digital syndrome 1 protein
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins
K16480 OFD1; oral-facial-digital syndrome 1 protein
Chromosome and associated proteins [BR:ko03036]
Eukaryotic type
Centrosome formation proteins
Centriole proteins
K16480 OFD1; oral-facial-digital syndrome 1 protein
Pericentriolar materials (PCM)
Centriolar satellite
K16480 OFD1; oral-facial-digital syndrome 1 protein
Centrosome duplication proteins
Centriole replication proteins
K16480 OFD1; oral-facial-digital syndrome 1 protein
Cilium and associated proteins [BR:ko03037]
Primary cilia and associated proteins
Other primary cilia associated proteins
K16480 OFD1; oral-facial-digital syndrome 1 protein
|
Genes |
» show all
|
Reference |
|
Authors |
Romio L, Fry AM, Winyard PJ, Malcolm S, Woolf AS, Feather SA |
Title |
OFD1 is a centrosomal/basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis. |
Journal |
|
Sequence |
|
Reference |
|
Authors |
Singla V, Romaguera-Ros M, Garcia-Verdugo JM, Reiter JF |
Title |
Ofd1, a human disease gene, regulates the length and distal structure of centrioles. |
Journal |
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Sequence |
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LinkDB |
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