Incidental Mutation 'R9494:Or5p75-ps1'
ID 717106
Institutional Source Beutler Lab
Gene Symbol Or5p75-ps1
Ensembl Gene
Gene Name olfactory receptor family 5 subfamily P member 75, pseudogene 1
Synonyms MOR204-27P, GA_x6K02T2PBJ9-10838051-10838996, Olfr501-ps1
MMRRC Submission
Accession Numbers
Essential gene? Not available question?
Stock # R9494 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 108107265-108108207 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 108107800 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Lysine at position 179 (T179K)
Ref Sequence ENSEMBL: ENSMUSP00000148208 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094105]
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000094105
AA Change: T179K
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.6%
  • 20x: 98.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Als2 T C 1: 59,206,664 (GRCm39) D1593G probably damaging Het
Atad2b C A 12: 5,081,852 (GRCm39) P1254T probably benign Het
Brsk2 C T 7: 141,555,955 (GRCm39) R716C possibly damaging Het
Bzw2 T A 12: 36,184,947 (GRCm39) M1L probably benign Het
Cd300ld2 T A 11: 114,901,249 (GRCm39) H277L possibly damaging Het
Col6a5 A T 9: 105,822,732 (GRCm39) D208E unknown Het
Cul3 T A 1: 80,255,169 (GRCm39) S544C probably damaging Het
Enpp1 C A 10: 24,527,234 (GRCm39) R651L probably benign Het
Epha10 C T 4: 124,808,649 (GRCm39) A766V Het
Epor A G 9: 21,870,522 (GRCm39) Y453H probably damaging Het
Fam13a T C 6: 58,930,508 (GRCm39) K468R probably benign Het
Ffar4 C T 19: 38,086,083 (GRCm39) A170V probably benign Het
Fhip1a A T 3: 85,583,565 (GRCm39) Y410* probably null Het
Gm10203 A G 6: 149,031,740 (GRCm39) Y15C unknown Het
Kansl1 T C 11: 104,247,566 (GRCm39) T595A probably benign Het
Lmtk2 A T 5: 144,037,338 (GRCm39) probably benign Het
Mybl2 G A 2: 162,917,843 (GRCm39) V69I possibly damaging Het
Myo1d T C 11: 80,375,093 (GRCm39) K994E probably benign Het
Pcdhga10 A T 18: 37,882,421 (GRCm39) R727S probably benign Het
Pgp T A 17: 24,689,809 (GRCm39) L109Q probably damaging Het
Piwil2 C T 14: 70,660,421 (GRCm39) G68D probably benign Het
Pms2 T A 5: 143,853,214 (GRCm39) I193N probably damaging Het
Pnpla7 T A 2: 24,942,390 (GRCm39) L1236* probably null Het
Pole2 A G 12: 69,249,731 (GRCm39) V489A possibly damaging Het
Rapgef2 G A 3: 79,019,495 (GRCm39) L59F probably damaging Het
Rnf32 T C 5: 29,429,145 (GRCm39) S241P probably damaging Het
Samd9l T A 6: 3,375,830 (GRCm39) K477I possibly damaging Het
Stn1 C T 19: 47,513,125 (GRCm39) probably null Het
Svep1 A G 4: 58,070,577 (GRCm39) V2403A possibly damaging Het
Synrg T C 11: 83,881,747 (GRCm39) M361T probably benign Het
Tbc1d2b A T 9: 90,152,563 (GRCm39) Y68N probably damaging Het
Tbc1d4 A T 14: 101,845,895 (GRCm39) M1K probably null Het
Thsd1 C T 8: 22,733,268 (GRCm39) P105L probably benign Het
Tnxb T C 17: 34,904,796 (GRCm39) L1187P probably damaging Het
Trio T C 15: 27,846,843 (GRCm39) T1057A probably benign Het
Tubg1 T C 11: 101,011,724 (GRCm39) I77T probably damaging Het
Txndc11 A G 16: 10,952,156 (GRCm39) L73P probably damaging Het
Uck1 G A 2: 32,148,179 (GRCm39) R182* probably null Het
Vangl1 T C 3: 102,070,665 (GRCm39) S424G probably damaging Het
Vmn2r69 A G 7: 85,056,084 (GRCm39) W685R probably benign Het
Vmn2r69 G A 7: 85,060,768 (GRCm39) S272L probably damaging Het
Zbtb18 A T 1: 177,275,648 (GRCm39) D327V probably benign Het
Zfp607b T C 7: 27,403,092 (GRCm39) F516S probably damaging Het
Zzz3 A G 3: 152,133,468 (GRCm39) I175M possibly damaging Het
Other mutations in Or5p75-ps1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4982:Or5p75-ps1 UTSW 7 108,107,855 (GRCm39) nonsense probably null
R4993:Or5p75-ps1 UTSW 7 108,107,450 (GRCm39) missense probably damaging 1.00
R7392:Or5p75-ps1 UTSW 7 108,107,291 (GRCm39) missense possibly damaging 0.57
R7395:Or5p75-ps1 UTSW 7 108,107,611 (GRCm39) missense unknown
R7452:Or5p75-ps1 UTSW 7 108,107,800 (GRCm39) missense unknown
R8289:Or5p75-ps1 UTSW 7 108,108,125 (GRCm39) missense unknown
R8442:Or5p75-ps1 UTSW 7 108,107,851 (GRCm39) missense unknown
R8922:Or5p75-ps1 UTSW 7 108,107,957 (GRCm39) missense unknown
R9108:Or5p75-ps1 UTSW 7 108,107,779 (GRCm39) missense unknown
R9422:Or5p75-ps1 UTSW 7 108,108,155 (GRCm39) missense unknown
R9467:Or5p75-ps1 UTSW 7 108,107,790 (GRCm39) makesense probably null
Predicted Primers PCR Primer
(F):5'- GGCATACAGCTCAGCTTTGG -3'
(R):5'- CCGTGGAACGCATCTTTAGG -3'

Sequencing Primer
(F):5'- GCATACAGCTCAGCTTTGGTGATATC -3'
(R):5'- CATCTTTAGGATGGTGATGAGGATG -3'
Posted On 2022-07-18