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MGI:Rpgrip1l
Contents |
| Species (Taxon ID) | Mus musculus (house mouse) (taxon:10090) | |
| Gene Name(s) | Rpgrip1l ( synonyms: fantom, Ftm ) | |
| Protein Name(s) | Rpgrip1-like, | |
| External Links | ||
| MGI | MGI:1920563 | |
Annotations
| Qualifier | GO ID | GO term name | Reference | Evidence Code | with/from | Aspect | Notes | Status |
|---|---|---|---|---|---|---|---|---|
| GO:0001701 |
in utero embryonic development |
MGI:MGI:3715393 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0001822 |
kidney development |
MGI:MGI:3716248 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0001889 |
liver development |
MGI:MGI:3716248 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0005515 |
protein binding |
MGI:MGI:5013991 |
IPI: Inferred from Physical Interaction |
F |
From MGI |
|||
| GO:0005737 |
cytoplasm |
MGI:MGI:3716248 |
ISA: Inferred from Sequence Alignment |
C |
From MGI |
|||
| GO:0005813 |
centrosome |
MGI:MGI:3716248 |
ISA: Inferred from Sequence Alignment |
C |
From MGI |
|||
| GO:0005813 |
centrosome |
MGI:MGI:4834177 |
ISO: Inferred from Sequence Orthology |
C |
From MGI |
|||
| GO:0005856 |
cytoskeleton |
MGI:MGI:1354194 |
IEA: Inferred from Electronic Annotation |
UniProtKB-KW:KW-0206 |
C |
From MGI |
||
| GO:0005911 |
cell-cell junction |
MGI:MGI:4834177 |
ISO: Inferred from Sequence Orthology |
C |
From MGI |
|||
| GO:0005923 |
tight junction |
MGI:MGI:1354194 |
IEA: Inferred from Electronic Annotation |
UniProtKB-KW:KW-0796 |
C |
From MGI |
||
| GO:0005929 |
cilium |
MGI:MGI:3716248 |
ISA: Inferred from Sequence Alignment |
C |
From MGI |
|||
| GO:0005932 |
microtubule basal body |
MGI:MGI:3715393 |
IDA: Inferred from Direct Assay |
C |
From MGI |
|||
| GO:0005932 |
microtubule basal body |
MGI:MGI:3716248 |
ISA: Inferred from Sequence Alignment |
C |
From MGI |
|||
| GO:0007368 |
determination of left/right symmetry |
MGI:MGI:3715393 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0007420 |
brain development |
MGI:MGI:3715393 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0007420 |
brain development |
MGI:MGI:3716248 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0007420 |
brain development |
MGI:MGI:3716248 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0008589 |
regulation of smoothened signaling pathway |
MGI:MGI:3715393 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0021532 |
neural tube patterning |
MGI:MGI:3715393 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0021537 |
telencephalon development |
MGI:MGI:3716248 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0021549 |
cerebellum development |
MGI:MGI:3716248 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0021670 |
lateral ventricle development |
MGI:MGI:3716248 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0021772 |
olfactory bulb development |
MGI:MGI:3716248 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0022038 |
corpus callosum development |
MGI:MGI:3716248 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0030054 |
cell junction |
MGI:MGI:1354194 |
IEA: Inferred from Electronic Annotation |
UniProtKB-KW:KW-0965 |
C |
From MGI |
||
| GO:0031870 |
thromboxane A2 receptor binding |
MGI:MGI:4834177 |
ISO: Inferred from Sequence Orthology |
F |
From MGI |
|||
| GO:0035085 |
cilium axoneme |
MGI:MGI:3716248 |
ISA: Inferred from Sequence Alignment |
C |
From MGI |
|||
| GO:0035108 |
limb morphogenesis |
MGI:MGI:3716248 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0035115 |
embryonic forelimb morphogenesis |
MGI:MGI:3715393 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0035116 |
embryonic hindlimb morphogenesis |
MGI:MGI:3715393 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0042384 |
cilium assembly |
MGI:MGI:3715393 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0042995 |
cell projection |
MGI:MGI:1354194 |
IEA: Inferred from Electronic Annotation |
UniProtKB-KW:KW-0966 |
C |
From MGI |
||
| GO:0043010 |
camera-type eye development |
MGI:MGI:3715393 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0043010 |
camera-type eye development |
MGI:MGI:3716248 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0043010 |
camera-type eye development |
MGI:MGI:3716248 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0043584 |
nose development |
MGI:MGI:3715393 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0045744 |
negative regulation of G-protein coupled receptor protein signaling pathway |
MGI:MGI:4834177 |
ISO: Inferred from Sequence Orthology |
P |
From MGI |
|||
| GO:0060039 |
pericardium development |
MGI:MGI:3715393 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
||
| GO:0060322 |
head development |
MGI:MGI:3715393 |
IMP: Inferred from Mutant Phenotype |
MGI:MGI:3716208 |
P |
From MGI |
| |
| edit table |
Notes
References
See Help:References for how to manage references in GONUTS.
- ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 Vierkotten J et al. (2007) Ftm is a novel basal body protein of cilia involved in Shh signalling. Development 134: 2569-77 PubMed GONUTS page
- ↑ 2.00 2.01 2.02 2.03 2.04 2.05 2.06 2.07 2.08 2.09 2.10 2.11 2.12 2.13 2.14 2.15 2.16 Delous M et al. (2007) The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome. Nat Genet 39: 875-81 PubMed GONUTS page
- ↑ Sang L et al. (2011) Mapping the NPHP-JBTS-MKS protein network reveals ciliopathy disease genes and pathways. Cell 145: 513-28 PubMed GONUTS page
