OR4V1P Olfactory Receptor
Gene Symbol | OR4V1P1 (View this gene in GeneCards) |
Family | 4 |
Subfamily | V |
Pseudogene | Yes |
CORP pseudogene probability score | |
Aliases | OR11-131, OR11-133, ORL3483 |
External Ids | HGNC: 14736 GeneBank: BK004690, BK004704, NG_002270 ORDB: ORL3483 |
Build #39 labels | OR4V1P |
Chromosomal location | 11:55,673,592-55,674,555 (+) |
Cluster | 11@56 |
Synteny | CLIC#26 |
Remarks |
Most Similar ORs in Humans (Paralogs)
Symbol | Percent | Length |
---|---|---|
OR4C3 | 47.33% | 300 |
OR4P4 | 53.42% | 307 |
OR4S2 | 50.49% | 309 |
Most Similar ORs in other species (Orthologs)
Specie | Symbol | Percent | Length |
---|---|---|---|
Dog | OR4P10 | 66% | 302 |
Mouse | Or4p22 | 65% | 310 |
Rat | Or4p22c | 62% | 311 |
Cow | OR4P36P | 56% | 308 |
Orang | OR4H12P | 46% | 311 |
Horse | OR4P76P | 65% | 310 |
Chimp | OR4P4 | 53% | 307 |
Sequence information
Nucleotide sequence |
ATTCATTTTTCCCTAGATACTTTATTTTTGCATAGCACACAACATATGGAAAGTCAAAGG AACATATAAAAATTCATACTCATGAGCCTTTCCTCTATCCAGAACATACAAATATTTGTT TTTGTGTTCTTATTTTGTAATGTTGCCATCTTGGTGGGAAACTTTCTGATCCTTATCTCT ATTTGATGTAGTCCTCTTTTTAACCAACCAATGCACTATTTCTTCAGGCTATATGAATAT CTACTATACCTCCTGTGTCACACCCAAAATAATTGGTGATCTAGTAGTGGGAAGAATAAA CATCTCCTATGATAGGAGTCTTTCCCATGCACTTCTTTGGAATCATTGAAATCTTCATCC TTACAGTCATGGCTTTTGATCACTATGTTGCCATCTGCAAACCTCCCCGCTACCTAATTA TCATGAATAGGACAAAATACAATACTCTAATCTCGGTTGCTTGGCTGTTGGGGCTTTCCA TTCTTTGTTTCAGTTTTCTATGAAAATCTGGTTGCCTTTCTGTGGCTCCAACAAAATTGA TGACTAATATTAAGATATTTTTCCTTTACTGAAAGTCGCTTGTACTGATACCTGCATCAC TGGTGTCCTCGTGGTTGCCAATTCTGGAATGTTTGCCTTGGTAACCTTGTTCTGTCGTTT GGCTCTTATGTCATTATACTATTCCCCTTAAAAAATCATTCAGTAGAGGGAAGATGCAAA GCCCTCTCTACCTGTGGATCTCATATCACCATGGTAATCTTTTTCTTCGAACCTTCAATC TTTGCCTACCTTAGACCTTCTCACTTTTCCTGAGGACAAAATATCTGCTCTGTTTTACAC TATTATTGCTCCAATGTTCAACCACCTAATCTATAACCTGAGAAATACAGAGATGAAAAA GGCCATGAGAAAAGTTTGGTACCAAATATCATTTTCAGAAGAAAAACAGCTGATTTGTCC TACT |
Conceptual translation |
IHFSLDTLFLHSTQHMESQRNIXFILMSLSS/P/TYKYLF/VFLFCNVAILVGNFL ILISIXSPLFNQPMHYFFRLY\IYYTSCVTPKIIGDLVVGRINISYDRSLS\HFFGI IEIFILTVMAFDHYVAICKPPRYLIIMNRTKYNTLISVAWLLGL/HSLFQFSMKIWLPF CGSNKIDDXXIFPLLKVACTDTCITGVLVVANSGM/CLGNLVLSFGSYVIILFPLKN HSVEGRCKALSTCGSHITMVIFFFEPSIFAYLRP//TFPEDKISALFYTIIAPMFNHL IYNLRNTEMKKAMRKVWYQISFSEEKQLICPT Protein domains and features |
Variations - SNPs
Chr | Start | End | Type | Variation | AA Change | SNP IDs |
---|---|---|---|---|---|---|
11 | 55,441,969 | 55,441,969 | SNP | A/G | rs57303593 (DbSNP) | |
11 | 55,441,603 | 55,441,603 | SNP | A/G | rs295630 (DbSNP) | |
11 | 55,441,070 | 55,441,070 | SNP | A/T | rs57197484 (DbSNP) | |
11 | 55,441,256 | 55,441,256 | SNP | C/T | rs73471428 (DbSNP) | |
11 | 55,441,470 | 55,441,470 | SNP | C/T | rs57625794 (DbSNP) | |
11 | 55,441,896 | 55,441,896 | SNP | G/T | rs11601087 (DbSNP) | |
11 | 55,674,420 | 55,674,420 | SNP | T/G | 1000GP (CEU, CHBJPT) | |
11 | 100 | -100 | SNP | T/C | 1000GP (YRI, YRI, YRI, YRI) |
Variations - CNVs
Chr | Start | End | Type | Sources |
---|---|---|---|---|
11 | 55,153,930 | 55,816,828 | CopyNumber | Variation_0308 (DGV) |
11 | 55,359,025 | 55,470,359 | CopyNumber | Variation_0419 (DGV), Variation_34977 (DGV) |
11 | 55,339,702 | 55,638,112 | CopyNumber | Variation_2926 (DGV) |
11 | 55,222,420 | 55,621,884 | CopyNumber | Variation_3852 (DGV) |
11 | 55,382,681 | 55,548,038 | CopyNumber | Variation_4743 (DGV) |
11 | 55,367,167 | 55,452,993 | CopyNumber | Variation_6923 (DGV) |
11 | 54,835,623 | 55,879,426 | CopyNumber | Variation_8690 (DGV) |
11 | 55,377,006 | 55,620,699 | CopyNumber | Variation_9188 (DGV) |
11 | 55,360,213 | 55,447,427 | CopyNumber | Variation_9663 (DGV), Variation_48827 (DGV) |
11 | 55,371,021 | 55,447,427 | CopyNumber | Variation_10359 (DGV), Variation_48834 (DGV), Variation_48835 (DGV) |
11 | 55,422,586 | 55,596,313 | CopyNumber | Variation_10360 (DGV) |
11 | 55,360,213 | 55,447,426 | CopyNumber | Variation_29606 (DGV) |
11 | 55,371,020 | 55,460,788 | CopyNumber | Variation_29910 (DGV) |
11 | 55,422,585 | 55,596,313 | CopyNumber | Variation_29911 (DGV) |
11 | 55,367,884 | 55,459,183 | CopyNumber | Variation_31823 (DGV) |
11 | 55,362,651 | 55,460,561 | CopyNumber | Variation_34978 (DGV) |
11 | 55,432,955 | 55,495,323 | Inversion | Variation_37124 (DGV) |
11 | 55,374,032 | 55,453,009 | CopyNumber | Variation_38079 (DGV) |
11 | 55,368,154 | 55,450,788 | CopyNumber | Variation_38972 (DGV) |
11 | 55,434,499 | 55,444,020 | CopyNumber | Variation_41254 (DGV) |
11 | 55,335,878 | 55,453,486 | CopyNumber | Variation_48051 (DGV) |
11 | 55,381,588 | 55,474,194 | CopyNumber | Variation_48053 (DGV) |
11 | 55,437,126 | 55,483,713 | CopyNumber | Variation_48054 (DGV) |
11 | 55,422,490 | 55,475,200 | CopyNumber | Variation_48055 (DGV) |
11 | 55,360,213 | 55,442,368 | CopyNumber | Variation_48826 (DGV) |
11 | 55,360,213 | 55,470,003 | CopyNumber | Variation_48828 (DGV) |
11 | 55,371,021 | 55,442,368 | CopyNumber | Variation_48833 (DGV) |
11 | 55,371,021 | 55,460,095 | CopyNumber | Variation_48836 (DGV) |
11 | 55,383,157 | 55,447,427 | CopyNumber | Variation_48837 (DGV), Variation_53573 (DGV) |
11 | 55,396,041 | 55,442,368 | CopyNumber | Variation_48839 (DGV) |
11 | 55,437,126 | 55,596,313 | CopyNumber | Variation_48840 (DGV) |
11 | 55,339,829 | 55,447,427 | CopyNumber | Variation_53140 (DGV) |
11 | 55,408,664 | 55,447,427 | CopyNumber | Variation_53178 (DGV) |
11 | 55,360,213 | 55,490,377 | CopyNumber | Variation_53507 (DGV) |
11 | 55,360,213 | 55,460,788 | CopyNumber | Variation_53994 (DGV) |
11 | 55,360,213 | 55,470,994 | CopyNumber | Variation_54018 (DGV) |
11 | 55,364,677 | 55,453,061 | CopyNumber | Variation_65955 (DGV) |
11 | 55,422,345 | 55,603,590 | CopyNumber | Variation_65956 (DGV) |
11 | 55,366,131 | 55,452,023 | CopyNumber | Variation_75644 (DGV) |
11 | 55,421,049 | 55,452,023 | CopyNumber | Variation_75645 (DGV) |
11 | 55,422,701 | 55,509,962 | CopyNumber | Variation_85778 (DGV) |
11 | 55,365,707 | 55,452,023 | CopyNumber | Variation_85779 (DGV) |
Deletion | 256 (Hasin) | |||
11 | 55,440,968 | 55,444,031 | Deletion | #16 (Waszak) |
Haplotypes
Protein haplotypes were calculated using the 1000 genomes project as described in Olender T. et. al. BMC Genomics 2012.