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GRIPAP1
HPA
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  • SUMMARY

  • TISSUE

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  • SUBCELL

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  • BLOOD

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  • GRIPAP1
STRUCTURE STRUCTURE
Protein structures
Structure methods
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.

GRIPAP1
Synonyms DKFZp434P0630, GRASP-1, GRASP1, KIAA1167, MPMGp800B12492Q3
Gene descriptioni

Full gene name according to HGNC.

GRIP1 associated protein 1
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)

HUMAN PROTEIN ATLAS INFORMATIONi

Summary of RNA expression analysis and annotation data generated within the Human Protein Atlas project.

Single cell type
expression clusteri

The RNA data was used to cluster genes according to their expression across single cell types. Clusters contain genes that have similar expression patterns, and each cluster has been manually annotated to describe common features in terms of function and specificity.

Photoreceptor cells - Phototransduction (mainly)
Single cell type specificityi

The RNA specificity category is based on mRNA expression levels in the analyzed cell types based on scRNA-seq data from normal tissues. The categories include: cell type enriched, group enriched, cell type enhanced, low cell type specificity and not detected.

Cell type enhanced (Cone photoreceptor cells, Rod photoreceptor cells)
Tissue expression
cluster (RNA)i

The RNA data was used to cluster genes according to their expression across tissues. Clusters contain genes that have similar expression patterns, and each cluster has been manually annotated to describe common features in terms of function and specificity.

Non-specific - Transcription (mainly)
Tissue specificity (RNA)i

The RNA specificity category is based on mRNA expression levels in the consensus dataset which is calculated from the RNA expression levels in samples from HPA and GTEX. The categories include: tissue enriched, group enriched, tissue enhanced, low tissue specificity and not detected.

Low tissue specificity
Subcellular locationi

Main subcellular location based on data generated in the subcellular section of the Human Protein Atlas.

Localized to the Vesicles, Cytosol
Secretome annotationi

All genes with at least one predicted secreted isoform have been annotated and classified with the aim to determine if the corresponding protein(s) are:

  • secreted into blood
  • locally secreted
  • or actually being attached to membrane or retained in intracellular locations like mitochondria, endoplasmatic reticulum (ER), Golgi apparatus or lysosomes.
Not available
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 X
Cytoband p11.23
Chromosome location (bp) 48973720 - 49002265
Number of transcriptsi

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

44
Ensembl ENSG00000068400 (version 109)
Entrez gene 56850
HGNC HGNC:18706
UniProt Q4V328
GeneCards GRIPAP1
PROTEIN BROWSERi

The Structure section provides in-house generated structures, predicted using the Alphafold source code, for the majority of the proteins and their related isoforms.

Displaying protein features on the AlphaFold structures

Individual splice variants can be selected in the top part of the Protein Browser (see below) and different transcript-related features such as transmembrane regions, InterPro domains and antigen sequences for antibodies can be displayed in the structure by clicking on the respective features in the Protein Browser.

Clinical and population-based amino acid variants based on data from the Ensembl variation database and AlphaMissense (AM) predictions can be highlighted using the sliders to the right of the structure. These can also be used to colour the entire structure by residue index or make the structure autorotate.The structures are displayed using the NGL Viewer and can also be zoomed-in and rotated manually.

The Protein Browser

The ProteinBrowser displays the antigen location on the target protein(s) and the features of the target protein. Transcript names and schematic transcript structures including exons, introns and UTRs for the different isoforms are shown on top, and can be used to switch between the structures for the different splice variants.

At the top of the view, the position of the antigen (identified by the corresponding HPA identifier) is shown as a green bar. A yellow triangle on the bar indicates a <100% sequence identity to the protein target.

Below the antigens, the maximum percent sequence identity of the protein to all other proteins from other human genes is displayed, using a sliding window of 10 aa residues (HsID 10) or 50 aa residues (HsID 50). The region with the lowest possible identity is always selected for antigen design, with a maximum identity of 60% allowed for designing a single-target antigen (read more).

The curve in blue displays the predicted antigenicity i.e. the tendency for different regions of the protein to generate an immune response, with peak regions being predicted to be more antigenic.The curve shows average values based on a sliding window approach using an in-house propensity scale. (read more).

Signal peptides (turquoise) and membrane regions (orange) based on predictions using the majority decision methods MDM and MDSEC are also displayed.

Low complexity regions are shown in yellow and InterPro regions in green. Common (purple) and unique (grey) regions between different splice variants of the gene are also displayed (read more), and at the bottom of the protein view is the protein scale.

«
GRIPAP1-201
GRIPAP1-207
GRIPAP1-208
GRIPAP1-209
GRIPAP1-210
GRIPAP1-211
GRIPAP1-214
GRIPAP1-215
GRIPAP1-216
GRIPAP1-217
GRIPAP1-218
GRIPAP1-219
GRIPAP1-223
GRIPAP1-228
GRIPAP1-229
GRIPAP1-230
GRIPAP1-231
GRIPAP1-235
GRIPAP1-236
GRIPAP1-238
GRIPAP1-239
GRIPAP1-240
GRIPAP1-242
GRIPAP1-244
GRIPAP1-252
GRIPAP1-255
GRIPAP1-256
GRIPAP1-257
GRIPAP1-264
GRIPAP1-266
GRIPAP1-269
GRIPAP1-275
GRIPAP1-281
GRIPAP1-282
GRIPAP1-283
GRIPAP1-286
GRIPAP1-289
GRIPAP1-290
GRIPAP1-291
GRIPAP1-292
GRIPAP1-293
GRIPAP1-294
GRIPAP1-298
GRIPAP1-300
»

Description:

Color scheme:
Confidence
Residue index
Your selection
Variants:
Off
Population
Clinical
Alphamissense variants:
Off
Benign
Pathogenic
Autorotate:
Off
On
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 Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
GRIPAP1-201 Q4V328
Predicted intracellular proteins
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
841 aa
96 kDa
No 0
GRIPAP1-207 Q4V328
Predicted intracellular proteins
Mapped to neXtProt
Protein evidence (Ezkurdia et al 2014)
810 aa
92.8 kDa
No 0
GRIPAP1-208 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
26 aa
3.1 kDa
No 0
GRIPAP1-209 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
625 aa
71.9 kDa
No 0
GRIPAP1-210 A0A087WW92
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
765 aa
87.2 kDa
No 0
GRIPAP1-211 A0A087WXA6
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
815 aa
92.9 kDa
No 0
GRIPAP1-214 A0A087WT45
Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
796 aa
90.9 kDa
No 0
GRIPAP1-215 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
667 aa
76.7 kDa
No 0
GRIPAP1-216 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
124 aa
14.4 kDa
No 0
GRIPAP1-217 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
805 aa
91.8 kDa
No 0
GRIPAP1-218 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
765 aa
87.2 kDa
No 0
GRIPAP1-219 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
832 aa
95.1 kDa
No 0
GRIPAP1-223 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
866 aa
98.7 kDa
No 0
GRIPAP1-228 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
788 aa
90.4 kDa
No 0
GRIPAP1-229 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
739 aa
84.1 kDa
No 0
GRIPAP1-230 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
466 aa
54.2 kDa
No 0
GRIPAP1-231 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
704 aa
80.5 kDa
No 0
GRIPAP1-235 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
790 aa
89.9 kDa
No 0
GRIPAP1-236 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
517 aa
59.3 kDa
No 0
GRIPAP1-238 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
739 aa
84.1 kDa
No 0
GRIPAP1-239 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
851 aa
97.1 kDa
No 0
GRIPAP1-240 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
764 aa
86.8 kDa
No 0
GRIPAP1-242 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
729 aa
83.9 kDa
No 0
GRIPAP1-244 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
873 aa
99.2 kDa
No 0
GRIPAP1-252 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
884 aa
100.8 kDa
No 0
GRIPAP1-255 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
835 aa
95.5 kDa
No 0
GRIPAP1-256 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
707 aa
81.6 kDa
No 0
GRIPAP1-257 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
799 aa
91.3 kDa
No 0
GRIPAP1-264 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
674 aa
77 kDa
No 0
GRIPAP1-266 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
876 aa
99.8 kDa
No 0
GRIPAP1-269 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
673 aa
76.9 kDa
No 0
GRIPAP1-275 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
713 aa
82.1 kDa
No 0
GRIPAP1-281 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
836 aa
95.4 kDa
No 0
GRIPAP1-282 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
862 aa
98.2 kDa
No 0
GRIPAP1-283 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
837 aa
95.5 kDa
No 0
GRIPAP1-286 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
872 aa
99.1 kDa
No 0
GRIPAP1-289 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
154 aa
17.2 kDa
No 0
GRIPAP1-290 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
839 aa
95.8 kDa
No 0
GRIPAP1-291 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
834 aa
95.3 kDa
No 0
GRIPAP1-292 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
830 aa
94.6 kDa
No 0
GRIPAP1-293 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
840 aa
95.9 kDa
No 0
GRIPAP1-294 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
764 aa
87.1 kDa
No 0
GRIPAP1-298 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
782 aa
89.2 kDa
No 0
GRIPAP1-300 Predicted intracellular proteins
Protein evidence (Ezkurdia et al 2014)
851 aa
96.9 kDa
No 0
Show allShow less

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