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RPGRIP1L
HPA
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  • RPGRIP1L
PROTEIN SUMMARY GENE INFORMATION RNA DATA ANTIBODY DATA
GENERAL INFORMATIONi

General description of the gene and the encoded protein(s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project.

Gene namei

Official gene symbol, which is typically a short form of the gene name, according to HGNC.

RPGRIP1L
Synonyms CORS3, FTM, JBTS7, KIAA1005, MKS5, NPHP8, PPP1R134
Gene descriptioni

Full gene name according to HGNC.

RPGRIP1 like
Protein classi

Assigned HPA protein class(es) for the encoded protein(s).

Disease related genes
Human disease related genes
Predicted locationi

All transcripts of all genes have been analyzed regarding the location(s) of corresponding protein based on prediction methods for signal peptides and transmembrane regions.

  • Genes with at least one transcript predicted to encode a secreted protein, according to prediction methods or to UniProt location data, have been further annotated and classified with the aim to determine if the corresponding protein(s) are secreted or actually retained in intracellular locations or membrane-attached.

  • Remaining genes, with no transcript predicted to encode a secreted protein, will be assigned the prediction-based location(s).

The annotated location overrules the predicted location, so that a gene encoding a predicted secreted protein that has been annotated as intracellular will have intracellular as the final location.

Intracellular
Protein evidence Evidence at protein level (all genes)
GENE INFORMATIONi

Gene information from Ensembl and Entrez, as well as links to available gene identifiers are displayed here. Information was retrieved from Ensembl if not indicated otherwise.

Chromosome 16
Cytoband q12.2
Chromosome location (bp) 53598153 - 53703938
Number of transcriptsi

Number of protein-coding transcripts from the gene as defined by Ensembl.

10
Ensembl ENSG00000103494 (version 109)
Entrez gene 23322
HGNC HGNC:29168
UniProt Q68CZ1 (UniProt - Evidence at protein level)
neXtProt NX_Q68CZ1
GeneCards RPGRIP1L
Antibodypedia RPGRIP1L antibodies


PROTEIN FUNCTION
Protein function (UniProt)i

Useful information about the protein provided by UniProt.

Negatively regulates signaling through the G-protein coupled thromboxane A2 receptor (TBXA2R) 1. May be involved in mechanisms like programmed cell death, craniofacial development, patterning of the limbs, and formation of the left-right axis (By similarity). Involved in the organization of apical junctions; the function is proposed to implicate a NPHP1-4-8 module. Does not seem to be strictly required for ciliogenesis 2. Involved in establishment of planar cell polarity such as in cochlear sensory epithelium and is proposed to implicate stabilization of disheveled proteins (By similarity). Involved in regulation of proteasomal activity at the primary cilium probably implicating association with PSDM2 (By similarity).... show less
Gene summary (Entrez)i

Useful information about the gene from Entrez

The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). [provided by RefSeq, Jun 2016]... show less
PROTEIN INFORMATIONi

The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.

The Splice variant identifier links to the Ensembl website protein summary for the selected splice variant. The data in the Swissprot and TrEMBL columns links to corresponding pages in the UniProt database.

The protein classes assigned to this protein are shown if expanding the data in the protein class column. Parent protein classes are in bold font and subclasses are listed under the parent class.

The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide and number of predicted transmembrane region(s) according to in-house majority decision methods based on sets of predictors are also reported.
Splice variant SwissProt TrEMBL Protein class Gene ontology Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
RPGRIP1L-201
ENSP00000262135
ENST00000262135
Q68CZ1
[Direct mapping] Protein fantom
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the urinary system
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001736 [establishment of planar polarity]
GO:0005515 [protein binding]
GO:0005654 [nucleoplasm]
GO:0005737 [cytoplasm]
GO:0005813 [centrosome]
GO:0005815 [microtubule organizing center]
GO:0005829 [cytosol]
GO:0005856 [cytoskeleton]
GO:0005886 [plasma membrane]
GO:0005911 [cell-cell junction]
GO:0005923 [bicellular tight junction]
GO:0005929 [cilium]
GO:0005930 [axoneme]
GO:0031870 [thromboxane A2 receptor binding]
GO:0032391 [photoreceptor connecting cilium]
GO:0032502 [developmental process]
GO:0035869 [ciliary transition zone]
GO:0036064 [ciliary basal body]
GO:0042995 [cell projection]
GO:0045744 [negative regulation of G protein-coupled receptor signaling pathway]
GO:0046548 [retinal rod cell development]
GO:0070161 [anchoring junction]
GO:1905515 [non-motile cilium assembly]
Show all
1235 aa
142.8 kDa
No 0
RPGRIP1L-202
ENSP00000455295
ENST00000562230
H3BPF5
[Direct mapping] Protein fantom
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the urinary system
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001736 [establishment of planar polarity]
GO:0005654 [nucleoplasm]
GO:0005829 [cytosol]
GO:0005886 [plasma membrane]
GO:0032502 [developmental process]
Show all
354 aa
41.3 kDa
No 0
RPGRIP1L-203
ENSP00000459817
ENST00000562588
I3L2P2
[Direct mapping] Protein fantom
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the urinary system
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001736 [establishment of planar polarity]
GO:0032502 [developmental process]
Show all
122 aa
14.1 kDa
No 0
RPGRIP1L-204
ENSP00000457889
ENST00000563746
H3BV03
[Direct mapping] Protein fantom
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the urinary system
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001736 [establishment of planar polarity]
GO:0005654 [nucleoplasm]
GO:0005829 [cytosol]
GO:0005886 [plasma membrane]
GO:0005929 [cilium]
GO:0032502 [developmental process]
GO:0042995 [cell projection]
Show all
1281 aa
147.3 kDa
No 0
RPGRIP1L-205
ENSP00000456534
ENST00000564374
H3BS47
[Direct mapping] Protein fantom
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the urinary system
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001736 [establishment of planar polarity]
GO:0005654 [nucleoplasm]
GO:0005829 [cytosol]
GO:0005886 [plasma membrane]
GO:0005929 [cilium]
GO:0032502 [developmental process]
GO:0042995 [cell projection]
Show all
1253 aa
144.8 kDa
No 0
RPGRIP1L-207
ENSP00000458705
ENST00000566096
I3L1B5
[Direct mapping] Protein fantom
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the urinary system
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001736 [establishment of planar polarity]
GO:0032502 [developmental process]
Show all
78 aa
8.9 kDa
No 0
RPGRIP1L-209
ENSP00000455451
ENST00000568653
H3BPS4
[Direct mapping] Protein fantom
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the urinary system
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001736 [establishment of planar polarity]
GO:0032502 [developmental process]
Show all
125 aa
14.3 kDa
No 0
RPGRIP1L-210
ENSP00000463678
ENST00000569716
J3QLR9
[Direct mapping] Protein fantom
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the urinary system
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001736 [establishment of planar polarity]
GO:0032502 [developmental process]
Show all
56 aa
6.2 kDa
No 0
RPGRIP1L-211
ENSP00000480698
ENST00000621565
A0A087WX34
[Direct mapping] Protein fantom
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the urinary system
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001736 [establishment of planar polarity]
GO:0005654 [nucleoplasm]
GO:0005829 [cytosol]
GO:0005886 [plasma membrane]
GO:0005929 [cilium]
GO:0032502 [developmental process]
GO:0042995 [cell projection]
Show all
1269 aa
146.7 kDa
No 0
RPGRIP1L-212
ENSP00000493946
ENST00000647211
Q68CZ1
[Direct mapping] Protein fantom
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Disease related genes
Human disease related genes
   Congenital malformations
   Congenital malformations of the nervous system
   Congenital malformations of the urinary system
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Kim et al 2014)
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0001701 [in utero embryonic development]
GO:0001736 [establishment of planar polarity]
GO:0001822 [kidney development]
GO:0001889 [liver development]
GO:0005515 [protein binding]
GO:0005654 [nucleoplasm]
GO:0005737 [cytoplasm]
GO:0005813 [centrosome]
GO:0005815 [microtubule organizing center]
GO:0005829 [cytosol]
GO:0005856 [cytoskeleton]
GO:0005879 [axonemal microtubule]
GO:0005886 [plasma membrane]
GO:0005911 [cell-cell junction]
GO:0005923 [bicellular tight junction]
GO:0005929 [cilium]
GO:0005930 [axoneme]
GO:0007163 [establishment or maintenance of cell polarity]
GO:0007368 [determination of left/right symmetry]
GO:0007420 [brain development]
GO:0008589 [regulation of smoothened signaling pathway]
GO:0021532 [neural tube patterning]
GO:0021537 [telencephalon development]
GO:0021549 [cerebellum development]
GO:0021670 [lateral ventricle development]
GO:0021772 [olfactory bulb development]
GO:0022038 [corpus callosum development]
GO:0031870 [thromboxane A2 receptor binding]
GO:0032391 [photoreceptor connecting cilium]
GO:0032502 [developmental process]
GO:0035108 [limb morphogenesis]
GO:0035115 [embryonic forelimb morphogenesis]
GO:0035116 [embryonic hindlimb morphogenesis]
GO:0035253 [ciliary rootlet]
GO:0035869 [ciliary transition zone]
GO:0036064 [ciliary basal body]
GO:0042995 [cell projection]
GO:0043010 [camera-type eye development]
GO:0043584 [nose development]
GO:0045744 [negative regulation of G protein-coupled receptor signaling pathway]
GO:0046548 [retinal rod cell development]
GO:0060039 [pericardium development]
GO:0060271 [cilium assembly]
GO:0060322 [head development]
GO:0070161 [anchoring junction]
GO:0090102 [cochlea development]
GO:1905515 [non-motile cilium assembly]
Show all
1315 aa
151.2 kDa
No 0

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