Q8WXG9 (GPR98_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
May 1, 2013.
Version 92.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Web links·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Web links·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: G-protein coupled receptor 98 Alternative name(s): Monogenic audiogenic seizure susceptibility protein 1 homolog Usher syndrome type-2C protein Very large G-protein coupled receptor 1 | ||||
| Gene names |
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| Organism | Homo sapiens (Human) [Reference proteome] | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo![]() |
Protein attributes
| Sequence length | 6306 AA. |
| Sequence status | Complete. |
| Sequence processing | The displayed sequence is further processed into a mature form. |
| Protein existence | Evidence at protein level |
General annotation (Comments)
| Function | Receptor that may have an important role in the development of the central nervous system. |
| Subunit structure | |
| Subcellular location | |
| Tissue specificity | Expressed at low levels in adult tissues. Ref.1 |
| Developmental stage | Isoform 1 is 4 times more abundant than isoform 2 in most tissues tested, despite wide variations in absolute levels of expression. Isoform 3 is expressed at about 1.5 times isoform 1 levels in most tissues examined. In fetal testis, isoform 3 is expressed almost exclusively. Ref.2 |
| Involvement in disease | Usher syndrome 2C (USH2C) [MIM:605472]: USH is a genetically heterogeneous condition characterized by the association of retinitis pigmentosa with sensorineural deafness. Age at onset and differences in auditory and vestibular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome type 3 (USH3). USH2 is characterized by congenital mild hearing impairment with normal vestibular responses. Familial febrile convulsions 4 (FEB4) [MIM:604352]: Seizures associated with febrile episodes in childhood without any evidence of intracranial infection or defined pathologic or traumatic cause. It is a common condition, affecting 2-5% of children aged 3 months to 5 years. The majority are simple febrile seizures (generally defined as generalized onset, single seizures with a duration of less than 30 minutes). Complex febrile seizures are characterized by focal onset, duration greater than 30 minutes, and/or more than one seizure in a 24 hour period. The likelihood of developing epilepsy following simple febrile seizures is low. Complex febrile seizures are associated with a moderately increased incidence of epilepsy. |
| Miscellaneous | By far is the largest known cell surface protein. |
| Sequence similarities | Belongs to the G-protein coupled receptor 2 family. LN-TM7 subfamily. Contains 35 Calx-beta domains. Contains 6 EAR repeats. Contains 1 GPS domain. |
| Sequence caution | The sequence AAL30811.1 differs from that shown. Reason: Frameshift at positions 3524 and 3532. The sequence CAB66476.2 differs from that shown. Reason: Erroneous translation. Wrong genetic code use for translating the sequence. |
Ontologies
Alternative products
| This entry describes 4 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: Q8WXG9-1) Also known as: VLGR1b; This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Isoform 2 (identifier: Q8WXG9-2) Also known as: VLGR1a; The sequence of this isoform differs from the canonical sequence as follows: 1-4339: Missing. 4340-4359: DDYPEGPEEFSLTITKVELQ → MQLCIFCCCCILFYFDLYDF | ||||||
| Isoform 3 (identifier: Q8WXG9-3) Also known as: VLGR1c; The sequence of this isoform differs from the canonical sequence as follows: 2296-2306: PGETIQTLLLE → RVVSGYPSATN 2307-6306: Missing. | ||||||
| Isoform 4 (identifier: Q8WXG9-4) The sequence of this isoform differs from the canonical sequence as follows: 1461-1466: PGILRI → EGHHHN 1467-6306: Missing. | ||||||
| Note: No experimental confirmation available. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Signal peptide | 1 – 29 | 29 | Potential | ||||||
| Chain | 30 – 6306 | 6277 | G-protein coupled receptor 98 | PRO_0000232735 | |||||
Regions | |||||||||
| Topological domain | 30 – 5908 | 5879 | Extracellular Potential | ||||||
| Transmembrane | 5909 – 5929 | 21 | Helical; Potential | ||||||
| Topological domain | 5930 – 5939 | 10 | Cytoplasmic Potential | ||||||
| Transmembrane | 5940 – 5960 | 21 | Helical; Potential | ||||||
| Topological domain | 5961 – 5979 | 19 | Extracellular Potential | ||||||
| Transmembrane | 5980 – 6000 | 21 | Helical; Potential | ||||||
| Topological domain | 6001 – 6010 | 10 | Cytoplasmic Potential | ||||||
| Transmembrane | 6011 – 6031 | 21 | Helical; Potential | ||||||
| Topological domain | 6032 – 6059 | 28 | Extracellular Potential | ||||||
| Transmembrane | 6060 – 6080 | 21 | Helical; Potential | ||||||
| Topological domain | 6081 – 6104 | 24 | Cytoplasmic Potential | ||||||
| Transmembrane | 6105 – 6125 | 21 | Helical; Potential | ||||||
| Topological domain | 6126 – 6133 | 8 | Extracellular Potential | ||||||
| Transmembrane | 6134 – 6154 | 21 | Helical; Potential | ||||||
| Topological domain | 6155 – 6306 | 152 | Cytoplasmic Potential | ||||||
| Domain | 77 – 116 | 40 | Calx-beta 1 | ||||||
| Domain | 195 – 235 | 41 | Calx-beta 2 | ||||||
| Domain | 321 – 362 | 42 | Calx-beta 3 | ||||||
| Domain | 447 – 488 | 42 | Calx-beta 4 | ||||||
| Domain | 706 – 745 | 40 | Calx-beta 5 | ||||||
| Domain | 821 – 861 | 41 | Calx-beta 6 | ||||||
| Domain | 938 – 979 | 42 | Calx-beta 7 | ||||||
| Domain | 1051 – 1092 | 42 | Calx-beta 8 | ||||||
| Domain | 1167 – 1208 | 42 | Calx-beta 9 | ||||||
| Domain | 1504 – 1544 | 41 | Calx-beta 10 | ||||||
| Domain | 1626 – 1666 | 41 | Calx-beta 11 | ||||||
| Domain | 1767 – 1808 | 42 | Calx-beta 12 | ||||||
| Domain | 1911 – 1941 | 31 | Calx-beta 13 | ||||||
| Domain | 2038 – 2078 | 41 | Calx-beta 14 | ||||||
| Domain | 2165 – 2205 | 41 | Calx-beta 15 | ||||||
| Domain | 2283 – 2323 | 41 | Calx-beta 16 | ||||||
| Domain | 2501 – 2541 | 41 | Calx-beta 17 | ||||||
| Domain | 2635 – 2675 | 41 | Calx-beta 18 | ||||||
| Domain | 2749 – 2789 | 41 | Calx-beta 19 | ||||||
| Domain | 2884 – 2924 | 41 | Calx-beta 20 | ||||||
| Domain | 3007 – 3047 | 41 | Calx-beta 21 | ||||||
| Domain | 3131 – 3171 | 41 | Calx-beta 22 | ||||||
| Repeat | 3189 – 3241 | 53 | EAR 1 | ||||||
| Repeat | 3296 – 3345 | 50 | EAR 2 | ||||||
| Repeat | 3347 – 3393 | 47 | EAR 3 | ||||||
| Repeat | 3394 – 3439 | 46 | EAR 4 | ||||||
| Repeat | 3440 – 3488 | 49 | EAR 5 | ||||||
| Repeat | 3491 – 3534 | 44 | EAR 6 | ||||||
| Domain | 3584 – 3625 | 42 | Calx-beta 23 | ||||||
| Domain | 3700 – 3739 | 40 | Calx-beta 24 | ||||||
| Domain | 3834 – 3875 | 42 | Calx-beta 25 | ||||||
| Domain | 3965 – 4005 | 41 | Calx-beta 26 | ||||||
| Domain | 4082 – 4122 | 41 | Calx-beta 27 | ||||||
| Domain | 4199 – 4239 | 41 | Calx-beta 28 | ||||||
| Domain | 4313 – 4353 | 41 | Calx-beta 29 | ||||||
| Domain | 4448 – 4488 | 41 | Calx-beta 30 | ||||||
| Domain | 4570 – 4612 | 43 | Calx-beta 31 | ||||||
| Domain | 4693 – 4734 | 42 | Calx-beta 32 | ||||||
| Domain | 5053 – 5094 | 42 | Calx-beta 33 | ||||||
| Domain | 5291 – 5333 | 43 | Calx-beta 34 | ||||||
| Domain | 5427 – 5468 | 42 | Calx-beta 35 | ||||||
| Domain | 5853 – 5902 | 50 | GPS | ||||||
Natural variations | |||||||||
| Alternative sequence | 1 – 4339 | 4339 | Missing in isoform 2. | VSP_017947 | |||||
| Alternative sequence | 1461 – 1466 | 6 | PGILRI → EGHHHN in isoform 4. | VSP_035313 | |||||
| Alternative sequence | 1467 – 6306 | 4840 | Missing in isoform 4. | VSP_035314 | |||||
| Alternative sequence | 2296 – 2306 | 11 | PGETIQTLLLE → RVVSGYPSATN in isoform 3. | VSP_017948 | |||||
| Alternative sequence | 2307 – 6306 | 4000 | Missing in isoform 3. | VSP_017949 | |||||
| Alternative sequence | 4340 – 4359 | 20 | DDYPE…KVELQ → MQLCIFCCCCILFYFDLYDF in isoform 2. | VSP_017950 | |||||
| Natural variant | 127 | 1 | L → R. Ref.10 Corresponds to variant rs41311333 [ dbSNP | Ensembl ]. | VAR_025995 | |||||
| Natural variant | 249 | 1 | R → K. Ref.10 Corresponds to variant rs41303344 [ dbSNP | Ensembl ]. | VAR_025996 | |||||
| Natural variant | 551 | 1 | V → A. Corresponds to variant rs6889939 [ dbSNP | Ensembl ]. | VAR_046346 | |||||
| Natural variant | 1093 | 1 | L → F. Ref.4 Ref.10 Corresponds to variant rs2366777 [ dbSNP | Ensembl ]. | VAR_025997 | |||||
| Natural variant | 1187 | 1 | I → V. Corresponds to variant rs16868935 [ dbSNP | Ensembl ]. | VAR_046347 | |||||
| Natural variant | 1916 | 1 | T → I. Corresponds to variant rs35791889 [ dbSNP | Ensembl ]. | VAR_046348 | |||||
| Natural variant | 1927 | 1 | T → M. Ref.10 Corresponds to variant rs17544552 [ dbSNP | Ensembl ]. | VAR_025998 | |||||
| Natural variant | 1951 | 1 | V → I. Ref.10 Corresponds to variant rs4916684 [ dbSNP | Ensembl ]. | VAR_025999 | |||||
| Natural variant | 1985 | 1 | N → D. Ref.10 Corresponds to variant rs41303352 [ dbSNP | Ensembl ]. | VAR_026000 | |||||
| Natural variant | 1987 | 1 | P → L. Ref.10 Corresponds to variant rs4916685 [ dbSNP | Ensembl ]. | VAR_026001 | |||||
| Natural variant | 2004 | 1 | L → F. Ref.10 Corresponds to variant rs16868972 [ dbSNP | Ensembl ]. | VAR_026002 | |||||
| Natural variant | 2097 | 1 | R → C. Corresponds to variant rs16868974 [ dbSNP | Ensembl ]. | VAR_046349 | |||||
| Natural variant | 2232 | 1 | Y → C. Ref.10 Corresponds to variant rs10037067 [ dbSNP | Ensembl ]. | VAR_026003 | |||||
| Natural variant | 2345 | 1 | N → S. Ref.10 Corresponds to variant rs2366926 [ dbSNP | Ensembl ]. | VAR_026004 | |||||
| Natural variant | 2379 | 1 | G → A. Ref.10 | VAR_026005 | |||||
| Natural variant | 2584 | 1 | N → S. Ref.5 Ref.10 Corresponds to variant rs1878878 [ dbSNP | Ensembl ]. | VAR_026006 | |||||
| Natural variant | 2764 | 1 | S → L. Ref.10 Corresponds to variant rs16869016 [ dbSNP | Ensembl ]. | VAR_026007 | |||||
| Natural variant | 2803 | 1 | A → T. Ref.10 | VAR_026008 | |||||
| Natural variant | 3094 | 1 | V → I. Corresponds to variant rs13157270 [ dbSNP | Ensembl ]. | VAR_046350 | |||||
| Natural variant | 3217 | 1 | A → V. Ref.10 | VAR_026009 | |||||
| Natural variant | 3248 | 1 | G → D. Ref.10 Corresponds to variant rs16869032 [ dbSNP | Ensembl ]. | VAR_026010 | |||||
| Natural variant | 3347 | 1 | F → L. Corresponds to variant rs10067636 [ dbSNP | Ensembl ]. | VAR_046351 | |||||
| Natural variant | 3471 | 1 | E → K. Ref.5 Ref.10 Corresponds to variant rs2366928 [ dbSNP | Ensembl ]. | VAR_026011 | |||||
| Natural variant | 3867 | 1 | E → A. Corresponds to variant rs16869088 [ dbSNP | Ensembl ]. | VAR_046352 | |||||
| Natural variant | 3868 | 1 | E → A. Corresponds to variant rs16869088 [ dbSNP | Ensembl ]. | VAR_055933 | |||||
| Natural variant | 4789 | 1 | R → W in USH2C. Ref.12 | VAR_068032 | |||||
| Natural variant | 5344 | 1 | E → G. Ref.1 Ref.2 Ref.6 Ref.10 | VAR_026012 | |||||
| Natural variant | 5437 | 1 | T → A. | VAR_026013 | |||||
| Natural variant | 5978 | 1 | H → R in USH2C. Ref.12 | VAR_068033 | |||||
Experimental info | |||||||||
| Sequence conflict | 107 | 1 | E → G in AAL30811. Ref.2 | ||||||
| Sequence conflict | 219 | 1 | T → A in AAL30811. Ref.2 | ||||||
| Sequence conflict | 257 | 1 | K → E in AAL30811. Ref.2 | ||||||
| Sequence conflict | 435 – 437 | 3 | LTR → VTP in AAL30811. Ref.2 | ||||||
| Sequence conflict | 471 – 472 | 2 | VV → GG in AAL30811. Ref.2 | ||||||
| Sequence conflict | 534 | 1 | E → G in AAL30811. Ref.2 | ||||||
| Sequence conflict | 747 | 1 | R → W in AAL30811. Ref.2 | ||||||
| Sequence conflict | 1096 | 1 | T → P in AAL30811. Ref.2 | ||||||
| Sequence conflict | 1099 | 1 | T → P in AAL30811. Ref.2 | ||||||
| Sequence conflict | 1232 | 1 | V → A in AAL30811. Ref.2 | ||||||
| Sequence conflict | 1320 | 1 | R → G in AAL30811. Ref.2 | ||||||
| Sequence conflict | 1340 – 1342 | 3 | VNP → GNS in AAL30811. Ref.2 | ||||||
| Sequence conflict | 1347 | 1 | S → F in AAL30811. Ref.2 | ||||||
| Sequence conflict | 3230 | 1 | G → D in AAL30811. Ref.2 | ||||||
| Sequence conflict | 3528 | 1 | A → T in AAL30811. Ref.2 | ||||||
| Sequence conflict | 3552 | 1 | A → V in AAL30811. Ref.2 | ||||||
| Sequence conflict | 4244 | 1 | E → G in AAL30811. Ref.2 | ||||||
| Sequence conflict | 5427 | 1 | V → M in AAD55586. Ref.1 | ||||||
| Sequence conflict | 5427 | 1 | V → M in AAL30811. Ref.2 | ||||||
| Sequence conflict | 5427 | 1 | V → M in BAA31661. Ref.6 | ||||||
| Sequence conflict | 5876 | 1 | V → I in AAD55586. Ref.1 | ||||||
| Sequence conflict | 5876 | 1 | V → I in AAL30811. Ref.2 | ||||||
| Sequence conflict | 5876 | 1 | V → I in BAA31661. Ref.6 | ||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Sequence similarities between a novel putative G protein-coupled receptor and Na+/Ca2+ exchangers define a cation binding domain." Nikkila H., McMillan D.R., Nunez B.S., Pascoe L., Curnow K.M., White P.C. Mol. Endocrinol. 14:1351-1364(2000) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 2), VARIANT GLY-5344, TISSUE SPECIFICITY. |
| [2] | "Very large G protein-coupled receptor-1, the largest known cell surface protein, is highly expressed in the developing central nervous system." McMillan D.R., Kayes-Wandover K.M., Richardson J.A., White P.C. J. Biol. Chem. 277:785-792(2002) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS 1; 2 AND 3), VARIANT GLY-5344, DEVELOPMENTAL STAGE. |
| [3] | "The DNA sequence and comparative analysis of human chromosome 5." Schmutz J., Martin J., Terry A., Couronne O., Grimwood J., Lowry S., Gordon L.A., Scott D., Xie G., Huang W., Hellsten U., Tran-Gyamfi M., She X., Prabhakar S., Aerts A., Altherr M., Bajorek E., Black S. Rubin E.M.Nature 431:268-274(2004) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [4] | "Prediction of the coding sequences of unidentified human genes. XXII. The complete sequences of 50 new cDNA clones which code for large proteins." Nagase T., Kikuno R., Ohara O. DNA Res. 8:319-327(2001) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 413-6306 (ISOFORM 4), VARIANT PHE-1093. Tissue: Brain. |
| [5] | "Towards a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs." Wiemann S., Weil B., Wellenreuther R., Gassenhuber J., Glassl S., Ansorge W., Boecher M., Bloecker H., Bauersachs S., Blum H., Lauber J., Duesterhoeft A., Beyer A., Koehrer K., Strack N., Mewes H.-W., Ottenwaelder B., Obermaier B. Poustka A.Genome Res. 11:422-435(2001) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 2436-4042 (ISOFORM 1), VARIANTS SER-2584 AND LYS-3471. Tissue: Amygdala. |
| [6] | "Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro." Ishikawa K., Nagase T., Suyama M., Miyajima N., Tanaka A., Kotani H., Nomura N., Ohara O. DNA Res. 5:169-176(1998) [PubMed] [Europe PMC] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 5107-6306 (ISOFORMS 1/2), VARIANT GLY-5344. Tissue: Brain. |
| [7] | "Construction of expression-ready cDNA clones for KIAA genes: manual curation of 330 KIAA cDNA clones." Nakajima D., Okazaki N., Yamakawa H., Kikuno R., Ohara O., Nagase T. DNA Res. 9:99-106(2002) [PubMed] [Europe PMC] [Abstract] Cited for: SEQUENCE REVISION. |
| [8] | "The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1." van Wijk E., van der Zwaag B., Peters T., Zimmermann U., Te Brinke H., Kersten F.F.J., Maerker T., Aller E., Hoefsloot L.H., Cremers C.W.R.J., Cremers F.P.M., Wolfrum U., Knipper M., Roepman R., Kremer H. Hum. Mol. Genet. 15:751-765(2006) [PubMed] [Europe PMC] [Abstract] Cited for: INTERACTION WITH WHRN. |
| [9] | "A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures." Nakayama J., Fu Y.H., Clark A.M., Nakahara S., Hamano K., Iwasaki N., Matsui A., Arinami T., Ptacek L.J. Ann. Neurol. 52:654-657(2002) [PubMed] [Europe PMC] [Abstract] Cited for: POSSIBLE INVOLVEMENT IN FAMILIAL FEBRILE CONVULSIONS 4. |
| [10] | "Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II." Weston M.D., Luijendijk M.W.J., Humphrey K.D., Moeller C., Kimberling W.J. Am. J. Hum. Genet. 74:357-366(2004) [PubMed] [Europe PMC] [Abstract] Cited for: INVOLVEMENT IN USH2C, VARIANTS ARG-127; LYS-249; PHE-1093; MET-1927; ILE-1951; ASP-1985; LEU-1987; PHE-2004; CYS-2232; SER-2345; ALA-2379; SER-2584; LEU-2764; THR-2803; VAL-3217; ASP-3248; LYS-3471 AND GLY-5344. |
| [11] | "PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome." Ebermann I., Phillips J.B., Liebau M.C., Koenekoop R.K., Schermer B., Lopez I., Schafer E., Roux A.F., Dafinger C., Bernd A., Zrenner E., Claustres M., Blanco B., Nurnberg G., Nurnberg P., Ruland R., Westerfield M., Benzing T., Bolz H.J. J. Clin. Invest. 120:1812-1823(2010) [PubMed] [Europe PMC] [Abstract] Cited for: INTERACTION WITH PDZD7. |
| [12] | "Non-USH2A mutations in USH2 patients." Besnard T., Vache C., Baux D., Larrieu L., Abadie C., Blanchet C., Odent S., Blanchet P., Calvas P., Hamel C., Dollfus H., Lina-Granade G., Lespinasse J., David A., Isidor B., Morin G., Malcolm S., Tuffery-Giraud S., Claustres M., Roux A.F. Hum. Mutat. 33:504-510(2012) [PubMed] [Europe PMC] [Abstract] Cited for: VARIANTS USH2C TRP-4789 AND ARG-5978. |
| + | Additional computationally mapped references. |
Web resources
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AF055084 mRNA. Translation: AAD55586.1. AF435925 mRNA. Translation: AAL30811.1. Frameshift. AC027323 Genomic DNA. No translation available. AC034215 Genomic DNA. No translation available. AC074132 Genomic DNA. No translation available. AC093281 Genomic DNA. No translation available. AC093529 Genomic DNA. No translation available. AC094109 Genomic DNA. No translation available. AC099512 Genomic DNA. No translation available. AB075823 mRNA. Translation: BAB85529.1. AL136541 mRNA. Translation: CAB66476.2. Sequence problems. AB014586 mRNA. Translation: BAA31661.2. |
| IPI | IPI00165934. IPI00743628. IPI00749231. IPI00902954. |
| RefSeq | NP_115495.3. NM_032119.3. |
| UniGene | Hs.591777. |
3D structure databases | |
| ProteinModelPortal | Q8WXG9. |
| ModBase | Search... |
Protein-protein interaction databases | |
| STRING | 9606.ENSP00000384582. |
Protein family/group databases | |
| GPCRDB | Search... |
PTM databases | |
| PhosphoSite | Q8WXG9. |
Polymorphism databases | |
| DMDM | 74716281. |
Proteomic databases | |
| PaxDb | Q8WXG9. |
| PRIDE | Q8WXG9. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000405460; ENSP00000384582; ENSG00000164199. ENST00000425867; ENSP00000392618; ENSG00000164199. |
| GeneID | 84059. |
| KEGG | hsa:84059. |
| UCSC | uc003kjt.3. human. |
Organism-specific databases | |
| CTD | 84059. |
| GeneCards | GC05P089891. |
| H-InvDB | HIX0005029. |
| HGNC | HGNC:17416. GPR98. |
| MIM | 602851. gene. 604352. phenotype. 605472. phenotype. |
| neXtProt | NX_Q8WXG9. |
| Orphanet | 231178. Usher syndrome type 2. |
| HUGE | Search... Search... |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | NOG12793. |
| HOGENOM | HOG000088618. |
| HOVERGEN | HBG081572. |
| InParanoid | Q8WXG9. |
| OMA | PANDNPY. |
| OrthoDB | EOG4Q58NG. |
Gene expression databases | |
| ArrayExpress | Q8WXG9. |
| Bgee | Q8WXG9. |
| CleanEx | HS_GPR98. |
| Genevestigator | Q8WXG9. |
| GermOnline | ENSG00000164199. Homo sapiens. |
Family and domain databases | |
| Gene3D | 2.60.120.200. 1 hit. |
| InterPro | IPR003644. Calx_beta. IPR008985. ConA-like_lec_gl_sf. IPR013320. ConA-like_subgrp. IPR009039. EAR. IPR005492. EPTP. IPR017981. GPCR_2-like. IPR000832. GPCR_2_secretin-like. IPR026919. GPR98. IPR000203. GPS_dom. [Graphical view] |
| PANTHER | PTHR11878:SF10. PTHR11878:SF10. 1 hit. |
| Pfam | PF00002. 7tm_2. 1 hit. PF03160. Calx-beta. 16 hits. PF03736. EPTP. 1 hit. PF01825. GPS. 1 hit. [Graphical view] |
| SMART | SM00237. Calx_beta. 19 hits. SM00303. GPS. 1 hit. [Graphical view] |
| SUPFAM | SSF49899. ConA_like_lec_gl. 1 hit. |
| PROSITE | PS50912. EAR. 5 hits. PS00649. G_PROTEIN_RECEP_F2_1. False negative. PS00650. G_PROTEIN_RECEP_F2_2. False negative. PS50227. G_PROTEIN_RECEP_F2_3. False negative. PS50261. G_PROTEIN_RECEP_F2_4. 1 hit. PS50221. GPS. 1 hit. [Graphical view] |
| ProtoNet | Search... |
Other | |
| ChiTaRS | GPR98. human. |
| GenomeRNAi | 84059. |
| NextBio | 73207. |
| SOURCE | Search... |
Entry information
| Entry name | GPR98_HUMAN | ||||||||
| Accession | Primary (citable) accession number: Q8WXG9 Secondary accession number(s): O75171 Q9UL61 | ||||||||
| Entry history |
| ||||||||
| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care. | ||||||||
Relevant documents
| 7-transmembrane G-linked receptors List of 7-transmembrane G-linked receptor entries |
| Human chromosome 5 Human chromosome 5: entries, gene names and cross-references to MIM |
| Human entries with polymorphisms or disease mutations List of human entries with polymorphisms or disease mutations |
| Human polymorphisms and disease mutations Index of human polymorphisms and disease mutations |
| MIM cross-references Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot |
| SIMILARITY comments Index of protein domains and families |

Clusters with
