| Type | Description |
|---|---|
| Definition | RIKEN cDNA 2700049A03 gene |
| Date | Results | Publications |
|---|---|---|
| 2020-04-18 12:40:00 | Findings in a mouse model reveal a role for Talpid3 in granule precursor cell migration in the cerebellum (either direct or indirect) which together with defective Hedgehog signaling underlies the Joubert syndrome phenotype. | 30924151 |
| 2017-10-14 10:26:00 | Gli2 and Gli3 are dephosphorylated and activated in cilia and that impaired Gli2 and Gli3 processing in Ta3 mutant is at least in part due to a decrease in Gli2 and Gli3 phosphorylation. | 28673820 |
| 2015-06-20 11:20:00 | The loss of Talpid3-binding centrosomal protein Cep120 results in failed centriole duplication and consequently ciliogenesis, which together underlie Cep120 mutant cerebellar hypoplasia. | 25251415 |
| 2011-09-24 11:47:00 | Data show that talpid3-/- mouse embryos lack primary cilia and, like talpid(3) chicken embryos, have face and neural tube defects but also defects in left/right asymmetry. | 21750036 |
| Type | IDs |
|---|---|
| Synonymous | Ta3, Talpid3, mKIAA0586 |
| Gene |
UniProtKB-ID:
TALD3_MOUSE,
E9Q0E2_MOUSE
UniprotKB:
E9PV87,
E9Q0E2
UniParc:
UPI0000429289,
UPI0001B02684
EMBL:
BC150744,
AC159620
Ensembl:
ENSMUSG00000034601
KO:
mmu:76967
|
| Nucleutide sequences |
EMBL-CDS:
AAI50745.1
Ensembl_TRS:
ENSMUST00000149564,
ENSMUST00000045907
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000118956,
ENSMUSP00000044701
RefSeq:
XP_006516429.1,
NP_084094.1,
XP_006516427.1,
NP_001156850.1,
XP_030102838.1,
XP_006516428.1
|
| Others |
UniRef100:
UniRef100_E9PV87,
UniRef100_E9Q0E2
UniRef90:
UniRef90_E9PV87
UniRef50:
UniRef50_Q9BVV6
UniGene:
Mm.87290
CCDS:
CCDS49081.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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