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Cellular Component
Molecular Function
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![]() Biological Process Term | Qualifier | Evidence | With | Reference | Notes | Source | Original Reference(s) | detection of chemical stimulus involved in sensory perception of smell | | IEA | GO:0004984 | 2290271 | | GOC | GO_REF:0000108 | G protein-coupled receptor signaling pathway | | IBA | PANTHER:PTN001239295, UniProtKB:P34982 | 2290271 | (PMID:21873635) | GO_Central | PMID:21873635 | |
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1. | RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations |
2. | RGD automated import pipeline for gene-chemical interactions |
OR2A25 (Homo sapiens - human) |
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Olfr447 (Mus musculus - house mouse) |
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Olr813 (Rattus norvegicus - Norway rat) |
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OR2A25 (Canis lupus familiaris - dog) |
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The detailed report is available here: | ![]() | Full Report | ![]() | CSV | ![]() | TAB | ![]() | Printer |
miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/). For more information about miRGate, see PMID:25858286 or access the full paper here. |
RefSeq Transcripts | NM_001004488 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
GenBank Nucleotide | AC091768 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
AC245175 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC136814 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
BC136829 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH236959 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
CH878732 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
KP290416 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
KP290619 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
KP290620 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
KP290621 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles | |
KP290622 | (Get FASTA) | NCBI Sequence Viewer | Search GEO for Microarray Profiles |
RefSeq Acc Id: | NM_001004488 ⟹ NP_001004488 | |||||||||||||||||||||||||||||||||||||||
RefSeq Status: | PROVISIONAL | |||||||||||||||||||||||||||||||||||||||
Type: | CODING | |||||||||||||||||||||||||||||||||||||||
Position: |
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Sequence: |
ATGGGGGGAAATCAGACTTCCATCACAGAGTTCCTCCTACTGGGATTTCCCATTGGCCCAAGGAhide sequence |
Protein RefSeqs | NP_001004488 | (Get FASTA) | NCBI Sequence Viewer |
GenBank Protein | A4D2G3 | (Get FASTA) | NCBI Sequence Viewer |
AAI36815 | (Get FASTA) | NCBI Sequence Viewer | |
AAI36830 | (Get FASTA) | NCBI Sequence Viewer | |
ALI87583 | (Get FASTA) | NCBI Sequence Viewer | |
ALI87777 | (Get FASTA) | NCBI Sequence Viewer | |
ALI87778 | (Get FASTA) | NCBI Sequence Viewer | |
ALI87779 | (Get FASTA) | NCBI Sequence Viewer | |
ALI87780 | (Get FASTA) | NCBI Sequence Viewer | |
EAL23797 | (Get FASTA) | NCBI Sequence Viewer | |
EAW55630 | (Get FASTA) | NCBI Sequence Viewer |
RefSeq Acc Id: | NP_001004488 ⟸ NM_001004488 |
- UniProtKB: | A4D2G3 (UniProtKB/Swiss-Prot), A0A126GVV5 (UniProtKB/TrEMBL) |
- Sequence: |
MGGNQTSITEFLLLGFPIGPRIQMLLFGLFSLFYIFILLGNGTILGLISLDSRLHTPMYFFLSHhide sequence |
Name | Type | Condition(s) | Position(s) | Clinical significance |
GRCh38/hg38 7q32.1-36.3(chr7:129310166-159282390)x3 | copy number gain | Cleft palate, isolated [RCV000050876]|See cases [RCV000050876] | Chr7:129310166..159282390 [GRCh38] Chr7:128950007..159075079 [GRCh37] Chr7:128737243..158767840 [NCBI36] Chr7:7q32.1-36.3 |
pathogenic |
GRCh38/hg38 7q34-35(chr7:142578948-144254897)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050639]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050639]|See cases [RCV000050639] | Chr7:142578948..144254897 [GRCh38] Chr7:142528609..143951990 [GRCh37] Chr7:141967554..143582923 [NCBI36] Chr7:7q34-35 |
pathogenic |
GRCh38/hg38 7q35-36.1(chr7:143884559-152674271)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050750]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000050750]|See cases [RCV000050750] | Chr7:143884559..152674271 [GRCh38] Chr7:143581652..152371356 [GRCh37] Chr7:143212585..152002289 [NCBI36] Chr7:7q35-36.1 |
pathogenic |
GRCh38/hg38 7q32.3-36.3(chr7:132850196-159325876)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051101]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051101]|See cases [RCV000051101] | Chr7:132850196..159325876 [GRCh38] Chr7:132534956..159118566 [GRCh37] Chr7:132185496..158811327 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh38/hg38 7p22.3-q36.3(chr7:53985-159282531)x1 | copy number loss | Ambiguous genitalia [RCV000052250]|See cases [RCV000052250] | Chr7:53985..159282531 [GRCh38] Chr7:53985..159075220 [GRCh37] Chr7:149068..158767981 [NCBI36] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh38/hg38 7q33-36.3(chr7:136309982-159307523)x3 | copy number gain | Global developmental delay [RCV000053576]|See cases [RCV000053576] | Chr7:136309982..159307523 [GRCh38] Chr7:135994730..159100212 [GRCh37] Chr7:135645270..158792973 [NCBI36] Chr7:7q33-36.3 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:142021716-159325876)x3 | copy number gain | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053577]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053577]|See cases [RCV000053577] | Chr7:142021716..159325876 [GRCh38] Chr7:142528609..159118566 [GRCh37] Chr7:141367985..158811327 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:142358524-159282531)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054177]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054177]|See cases [RCV000054177] | Chr7:142358524..159282531 [GRCh38] Chr7:142528609..159075220 [GRCh37] Chr7:141726947..158767981 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
GRCh38/hg38 7q35-36.3(chr7:143884559-159282390)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054178]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054178]|See cases [RCV000054178] | Chr7:143884559..159282390 [GRCh38] Chr7:143581652..159075079 [GRCh37] Chr7:143212585..158767840 [NCBI36] Chr7:7q35-36.3 |
pathogenic |
GRCh38/hg38 7q32.3-36.1(chr7:132023155-149309794)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054172]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054172]|See cases [RCV000054172] | Chr7:132023155..149309794 [GRCh38] Chr7:131707914..149006885 [GRCh37] Chr7:131358454..148637818 [NCBI36] Chr7:7q32.3-36.1 |
pathogenic |
GRCh38/hg38 7q33-35(chr7:135414108-144140219)x1 | copy number loss | Obesity [RCV000054173]|See cases [RCV000054173] | Chr7:135414108..144140219 [GRCh38] Chr7:135098857..143837312 [GRCh37] Chr7:134749397..143468245 [NCBI36] Chr7:7q33-35 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:139365967-159282531)x1 | copy number loss | Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054175]|See cases [RCV000054175] | Chr7:139365967..159282531 [GRCh38] Chr7:139050713..159075220 [GRCh37] Chr7:138701253..158767981 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:140754198-159307523)x1 | copy number loss | Corpus callosum agenesis [RCV000054176]|See cases [RCV000054176] | Chr7:140754198..159307523 [GRCh38] Chr7:140453998..159100212 [GRCh37] Chr7:140100467..158792973 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
NM_001004488.1(OR2A25):c.120G>A (p.Gly40=) | single nucleotide variant | Malignant melanoma [RCV000067729] | Chr7:144074339 [GRCh38] Chr7:143771432 [GRCh37] Chr7:143402365 [NCBI36] Chr7:7q35 |
not provided |
GRCh38/hg38 7q34-35(chr7:141126407-145652221)x3 | copy number gain | See cases [RCV000133645] | Chr7:141126407..145652221 [GRCh38] Chr7:140826207..145349314 [GRCh37] Chr7:140472676..144980247 [NCBI36] Chr7:7q34-35 |
pathogenic |
GRCh38/hg38 7q35(chr7:143735739-144254897)x3 | copy number gain | See cases [RCV000133872] | Chr7:143735739..144254897 [GRCh38] Chr7:143432832..143951990 [GRCh37] Chr7:143063765..143582923 [NCBI36] Chr7:7q35 |
benign |
GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1 | copy number loss | See cases [RCV000135401] | Chr7:54185..159282390 [GRCh38] Chr7:54185..159075079 [GRCh37] Chr7:149268..158767840 [NCBI36] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh38/hg38 7q35(chr7:143735739-144155939)x3 | copy number gain | See cases [RCV000135478] | Chr7:143735739..144155939 [GRCh38] Chr7:143432832..143853032 [GRCh37] Chr7:143063765..143483965 [NCBI36] Chr7:7q35 |
benign |
GRCh38/hg38 7q35(chr7:143735880-144409525)x3 | copy number gain | See cases [RCV000136107] | Chr7:143735880..144409525 [GRCh38] Chr7:143432973..144106618 [GRCh37] Chr7:143063906..143737551 [NCBI36] Chr7:7q35 |
likely benign |
GRCh38/hg38 7q33-36.2(chr7:137751200-154815582)x3 | copy number gain | See cases [RCV000136592] | Chr7:137751200..154815582 [GRCh38] Chr7:137435946..154607292 [GRCh37] Chr7:137086486..154238225 [NCBI36] Chr7:7q33-36.2 |
pathogenic |
GRCh38/hg38 7q21.3-36.3(chr7:97419852-158923762)x3 | copy number gain | See cases [RCV000136717] | Chr7:97419852..158923762 [GRCh38] Chr7:97049164..158716453 [GRCh37] Chr7:96887100..158409214 [NCBI36] Chr7:7q21.3-36.3 |
pathogenic |
GRCh38/hg38 7q34-36.3(chr7:141960861-159335866)x1 | copy number loss | See cases [RCV000137256] | Chr7:141960861..159335866 [GRCh38] Chr7:142528609..159128556 [GRCh37] Chr7:141307130..158821317 [NCBI36] Chr7:7q34-36.3 |
pathogenic |
GRCh38/hg38 7q33-36.3(chr7:134666829-158591882)x1 | copy number loss | See cases [RCV000138120] | Chr7:134666829..158591882 [GRCh38] Chr7:134351581..158384574 [GRCh37] Chr7:134002121..158077335 [NCBI36] Chr7:7q33-36.3 |
pathogenic |
GRCh38/hg38 7q31.32-36.3(chr7:121863759-159335865)x3 | copy number gain | See cases [RCV000138847] | Chr7:121863759..159335865 [GRCh38] Chr7:121503813..159128555 [GRCh37] Chr7:121291049..158821316 [NCBI36] Chr7:7q31.32-36.3 |
pathogenic |
GRCh38/hg38 7q35-36.1(chr7:143596735-150089125)x4 | copy number gain | See cases [RCV000138555] | Chr7:143596735..150089125 [GRCh38] Chr7:143293828..149786214 [GRCh37] Chr7:143003950..149417147 [NCBI36] Chr7:7q35-36.1 |
likely pathogenic |
GRCh38/hg38 7q35(chr7:143560424-144169056)x3 | copy number gain | See cases [RCV000138272] | Chr7:143560424..144169056 [GRCh38] Chr7:143257517..143866149 [GRCh37] Chr7:142967639..143497082 [NCBI36] Chr7:7q35 |
likely benign |
GRCh38/hg38 7q33-36.1(chr7:135017687-148807400)x1 | copy number loss | See cases [RCV000138903] | Chr7:135017687..148807400 [GRCh38] Chr7:134702438..148504492 [GRCh37] Chr7:134352978..148135425 [NCBI36] Chr7:7q33-36.1 |
pathogenic |
GRCh38/hg38 7q35(chr7:143735880-144155736)x3 | copy number gain | See cases [RCV000139760] | Chr7:143735880..144155736 [GRCh38] Chr7:143432973..143852829 [GRCh37] Chr7:143063906..143483762 [NCBI36] Chr7:7q35 |
likely benign |
GRCh38/hg38 7q32.3-36.3(chr7:132444095-159335866)x3 | copy number gain | See cases [RCV000139654] | Chr7:132444095..159335866 [GRCh38] Chr7:132128854..159128556 [GRCh37] Chr7:131779394..158821317 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh38/hg38 7q31.2-36.3(chr7:115459015-159325817)x3 | copy number gain | See cases [RCV000141413] | Chr7:115459015..159325817 [GRCh38] Chr7:115099069..159118507 [GRCh37] Chr7:114886305..158811268 [NCBI36] Chr7:7q31.2-36.3 |
pathogenic |
GRCh38/hg38 7q35(chr7:143728625-144176869)x1 | copy number loss | See cases [RCV000142117] | Chr7:143728625..144176869 [GRCh38] Chr7:143425718..143873962 [GRCh37] Chr7:143056651..143504895 [NCBI36] Chr7:7q35 |
conflicting data from submitters |
GRCh38/hg38 7q32.3-36.3(chr7:131228764-159335866)x3 | copy number gain | See cases [RCV000142802] | Chr7:131228764..159335866 [GRCh38] Chr7:130913523..159128556 [GRCh37] Chr7:130564063..158821317 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh38/hg38 7q35(chr7:143733925-144255312)x3 | copy number gain | See cases [RCV000143240] | Chr7:143733925..144255312 [GRCh38] Chr7:143431018..143952405 [GRCh37] Chr7:143061951..143583338 [NCBI36] Chr7:7q35 |
uncertain significance |
GRCh38/hg38 7q32.3-36.3(chr7:131171478-159327017)x3 | copy number gain | See cases [RCV000143754] | Chr7:131171478..159327017 [GRCh38] Chr7:130856237..159119707 [GRCh37] Chr7:130506777..158812468 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh38/hg38 7q34-35(chr7:140061285-144622893)x3 | copy number gain | See cases [RCV000143724] | Chr7:140061285..144622893 [GRCh38] Chr7:139761085..144319986 [GRCh37] Chr7:139407554..143950919 [NCBI36] Chr7:7q34-35 |
uncertain significance |
GRCh38/hg38 7q32.3-36.3(chr7:132438072-159327017)x3 | copy number gain | See cases [RCV000143707] | Chr7:132438072..159327017 [GRCh38] Chr7:132122831..159119707 [GRCh37] Chr7:131773371..158812468 [NCBI36] Chr7:7q32.3-36.3 |
pathogenic |
GRCh37/hg19 7q33-36.3(chr7:137589621-159119707)x3 | copy number gain | See cases [RCV000449264] | Chr7:137589621..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
GRCh37/hg19 7p22.3-q36.3(chr7:43360-159119707)x1 | copy number loss | See cases [RCV000446044] | Chr7:43360..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh37/hg19 7q35(chr7:143342375-143913713) | copy number gain | Abnormality of esophagus morphology [RCV000416661]|Abnormality of the esophagus [RCV000416661] | Chr7:143342375..143913713 [GRCh37] Chr7:7q35 |
benign |
GRCh37/hg19 7q33-36.3(chr7:133799185-159119707)x1 | copy number loss | See cases [RCV000448836] | Chr7:133799185..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
GRCh37/hg19 7q22.1-36.3(chr7:98969247-159119707)x3 | copy number gain | See cases [RCV000447709] | Chr7:98969247..159119707 [GRCh37] Chr7:7q22.1-36.3 |
pathogenic |
GRCh37/hg19 7q32.1-36.3(chr7:128276078-159119707)x3 | copy number gain | See cases [RCV000447956] | Chr7:128276078..159119707 [GRCh37] Chr7:7q32.1-36.3 |
pathogenic |
GRCh37/hg19 7q34-36.3(chr7:140636858-159119707)x1 | copy number loss | See cases [RCV000510250] | Chr7:140636858..159119707 [GRCh37] Chr7:7q34-36.3 |
pathogenic |
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707) | copy number gain | See cases [RCV000510686] | Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh37/hg19 7q33-36.3(chr7:136758593-159119707)x3 | copy number gain | See cases [RCV000510490] | Chr7:136758593..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
GRCh37/hg19 7q33-36.3(chr7:137917376-159119707)x1 | copy number loss | See cases [RCV000511889] | Chr7:137917376..159119707 [GRCh37] Chr7:7q33-36.3 |
pathogenic |
GRCh37/hg19 7p22.3-q36.3(chr7:43361-159119707)x3 | copy number gain | See cases [RCV000511549] | Chr7:43361..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh37/hg19 7q34-36.3(chr7:140133025-158982771)x1 | copy number loss | not provided [RCV000682910] | Chr7:140133025..158982771 [GRCh37] Chr7:7q34-36.3 |
pathogenic |
GRCh37/hg19 7q22.1-36.3(chr7:98693388-159119707)x3 | copy number gain | not provided [RCV000682911] | Chr7:98693388..159119707 [GRCh37] Chr7:7q22.1-36.3 |
pathogenic |
GRCh37/hg19 7p22.3-q36.3(chr7:10704-159122532)x3 | copy number gain | not provided [RCV000746278] | Chr7:10704..159122532 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh37/hg19 7p22.3-q36.3(chr7:44935-159126310)x3 | copy number gain | not provided [RCV000746280] | Chr7:44935..159126310 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh37/hg19 7q34-36.3(chr7:139623170-158329903)x3 | copy number gain | not provided [RCV000747070] | Chr7:139623170..158329903 [GRCh37] Chr7:7q34-36.3 |
pathogenic |
GRCh37/hg19 7q34-36.3(chr7:141938235-159126310)x1 | copy number loss | not provided [RCV000747083] | Chr7:141938235..159126310 [GRCh37] Chr7:7q34-36.3 |
pathogenic |
GRCh37/hg19 7q35-36.1(chr7:143711059-152573935)x3 | copy number gain | not provided [RCV000747094] | Chr7:143711059..152573935 [GRCh37] Chr7:7q35-36.1 |
benign |
GRCh37/hg19 7p22.3-q36.3(chr7:10365-159119707)x3 | copy number gain | not provided [RCV000848126] | Chr7:10365..159119707 [GRCh37] Chr7:7p22.3-q36.3 |
pathogenic |
GRCh37/hg19 7q32.1-36.3(chr7:128312450-159119220) | copy number gain | not provided [RCV000767558] | Chr7:128312450..159119220 [GRCh37] Chr7:7q32.1-36.3 |
pathogenic |
GRCh37/hg19 7q34-35(chr7:141751875-147105208)x3 | copy number gain | not provided [RCV000848670] | Chr7:141751875..147105208 [GRCh37] Chr7:7q34-35 |
uncertain significance |
GRCh37/hg19 7q35(chr7:143572320-144474990)x3 | copy number gain | not provided [RCV000848430] | Chr7:143572320..144474990 [GRCh37] Chr7:7q35 |
uncertain significance |
GRCh37/hg19 7q32.3-36.3(chr7:130592554-159119707)x3 | copy number gain | not provided [RCV000849569] | Chr7:130592554..159119707 [GRCh37] Chr7:7q32.3-36.3 |
pathogenic |
Database | Acc Id | Source(s) |
AGR Gene | HGNC:19562 | AgrOrtholog |
COSMIC | OR2A25 | COSMIC |
Ensembl Genes | ENSG00000221933 | ENTREZGENE, UniProtKB/Swiss-Prot |
Ensembl Protein | ENSP00000386167 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENSP00000493159 | UniProtKB/Swiss-Prot | |
ENSP00000493343 | UniProtKB/Swiss-Prot | |
Ensembl Transcript | ENST00000408898 | ENTREZGENE, UniProtKB/Swiss-Prot |
ENST00000641441 | UniProtKB/Swiss-Prot | |
ENST00000641663 | UniProtKB/Swiss-Prot | |
GTEx | ENSG00000221933 | GTEx |
HGNC ID | HGNC:19562 | ENTREZGENE |
Human Proteome Map | OR2A25 | Human Proteome Map |
InterPro | GPCR_Rhodpsn | UniProtKB/Swiss-Prot |
GPCR_Rhodpsn_7TM | UniProtKB/Swiss-Prot | |
Olfact_rcpt | UniProtKB/Swiss-Prot | |
KEGG Report | hsa:392138 | UniProtKB/Swiss-Prot |
NCBI Gene | 392138 | ENTREZGENE |
Pfam | 7tm_4 | UniProtKB/Swiss-Prot |
PharmGKB | PA134892120 | PharmGKB |
PRINTS | GPCRRHODOPSN | UniProtKB/Swiss-Prot |
OLFACTORYR | UniProtKB/Swiss-Prot | |
PROSITE | G_PROTEIN_RECEP_F1_1 | UniProtKB/Swiss-Prot |
G_PROTEIN_RECEP_F1_2 | UniProtKB/Swiss-Prot | |
UniGene | Hs.553787 | ENTREZGENE |
UniProt | A0A126GVV5 | ENTREZGENE, UniProtKB/TrEMBL |
A0A126GWG1_HUMAN | UniProtKB/TrEMBL | |
A0A126GWJ6_HUMAN | UniProtKB/TrEMBL | |
A0A126GWK2_HUMAN | UniProtKB/TrEMBL | |
A4D2G3 | ENTREZGENE, UniProtKB/Swiss-Prot | |
UniProt Secondary | B2RNC9 | UniProtKB/Swiss-Prot |
Date | Current Symbol | Current Name | Previous Symbol | Previous Name | Description | Reference | Status |
---|---|---|---|---|---|---|---|
2015-12-15 | OR2A25 | olfactory receptor family 2 subfamily A member 25 | olfactory receptor, family 2, subfamily A, member 25 | Symbol and/or name change | 5135510 | APPROVED | |
2011-09-01 | OR2A25 | olfactory receptor, family 2, subfamily A, member 25 | OR2A25 | olfactory receptor, family 2, subfamily A, member 25 | Symbol and/or name change | 5135510 | APPROVED |
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More on OR2A25 | |
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Alliance Gene |
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NCBI Gene |
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Ensembl Gene |
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JBrowse: hg19 hg38 |
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HGNC Report |
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NCBI Genome Data Viewer |
CRRD Object Information | |
CRRD ID: | 1343005 |
Created: | 2005-03-08 |
Species: | Homo sapiens |
Last Modified: | 2019-11-26 |
Status: | ACTIVE |
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.