Incidental Mutation 'R5219:Or7s1a-ps1'
ID 402226
Institutional Source Beutler Lab
Gene Symbol Or7s1a-ps1
Ensembl Gene ENSMUSG00000066914
Gene Name olfactory receptor family 7 subfamily S member 1A, pseudogene 1
Synonyms Olfr831-ps1, GA_x6K02T2PVTD-12676123-12675082
MMRRC Submission 042792-MU
Accession Numbers
Essential gene? Not available question?
Stock # R5219 (G1)
Quality Score 225
Status Validated
Chromosome 9
Chromosomal Location 18843224-18844265 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 18843990 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000151834 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000218385]
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000086496
SMART Domains Protein: ENSMUSP00000136442
Gene: ENSMUSG00000066914

DomainStartEndE-ValueType
transmembrane domain 10 32 N/A INTRINSIC
transmembrane domain 39 61 N/A INTRINSIC
transmembrane domain 66 88 N/A INTRINSIC
transmembrane domain 109 131 N/A INTRINSIC
low complexity region 137 146 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000218385
Meta Mutation Damage Score 0.3303 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.7%
Validation Efficiency 97% (68/70)
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700063H04Rik A G 6: 122,369,299 (GRCm39) noncoding transcript Het
4933428M09Rik G T X: 138,080,282 (GRCm39) G16* probably null Het
A2m A G 6: 121,653,909 (GRCm39) H1414R possibly damaging Het
A530064D06Rik G T 17: 48,470,518 (GRCm39) D154E possibly damaging Het
Adam34 C T 8: 44,104,461 (GRCm39) D395N probably benign Het
Agl A G 3: 116,572,370 (GRCm39) V195A possibly damaging Het
Aip T C 19: 4,165,180 (GRCm39) I230V probably benign Het
Akap10 A C 11: 61,813,617 (GRCm39) S43A probably benign Het
Ap3d1 T C 10: 80,545,651 (GRCm39) E1026G probably benign Het
Arid5b T A 10: 68,113,940 (GRCm39) K32N probably benign Het
Atp6v0a2 C A 5: 124,790,249 (GRCm39) N477K probably damaging Het
Atr A C 9: 95,763,291 (GRCm39) I1062L probably damaging Het
Ces2h T C 8: 105,743,278 (GRCm39) V171A probably damaging Het
Cnot2 A G 10: 116,342,215 (GRCm39) probably null Het
Cpne3 A T 4: 19,526,366 (GRCm39) L391H probably damaging Het
Ctdp1 A G 18: 80,490,675 (GRCm39) L715P probably damaging Het
Dcxr T C 11: 120,616,314 (GRCm39) probably benign Het
Dhtkd1 C T 2: 5,919,627 (GRCm39) A585T probably benign Het
Elapor2 G T 5: 9,511,486 (GRCm39) W949C probably damaging Het
Fcgbp G A 7: 27,803,510 (GRCm39) A1705T probably damaging Het
Galr1 A T 18: 82,412,110 (GRCm39) V252D probably damaging Het
Gm11677 A G 11: 111,616,225 (GRCm39) noncoding transcript Het
Gp6 A G 7: 4,371,998 (GRCm39) V252A possibly damaging Het
Inpp4b T C 8: 82,610,785 (GRCm39) V176A probably benign Het
Irx2 G C 13: 72,779,420 (GRCm39) A235P probably damaging Het
Klk1b11 G A 7: 43,649,120 (GRCm39) C219Y probably damaging Het
Lamc1 C A 1: 153,103,442 (GRCm39) V1375L probably damaging Het
Lars1 A T 18: 42,367,785 (GRCm39) V431E probably benign Het
Lmntd2 T C 7: 140,791,387 (GRCm39) probably null Het
Ltbp4 A T 7: 27,026,746 (GRCm39) W500R probably benign Het
Ltbp4 AATTCAGGCCAAGGCTGGGATTCAGGCCGAGGCCGGGATTCAGGCCTAGGCTGGGATTCAGGC AATTCAGGCCTAGGCTGGGATTCAGGC 7: 27,026,736 (GRCm39) probably benign Het
Mdn1 C T 4: 32,723,690 (GRCm39) P2542L probably damaging Het
Nadk A G 4: 155,668,711 (GRCm39) I127M probably benign Het
Nxph1 T A 6: 9,247,765 (GRCm39) Y245* probably null Het
Or4a73 C T 2: 89,421,046 (GRCm39) V138I probably benign Het
Or8g34 G T 9: 39,373,563 (GRCm39) V276L probably benign Het
Or9k7 T A 10: 130,046,793 (GRCm39) T69S possibly damaging Het
Orc1 T C 4: 108,447,966 (GRCm39) F71S probably damaging Het
Pccb A T 9: 100,867,262 (GRCm39) Y404* probably null Het
Pde2a A C 7: 101,153,811 (GRCm39) I460L probably damaging Het
Ppp3cb G T 14: 20,578,263 (GRCm39) C162* probably null Het
Prickle2 T C 6: 92,353,511 (GRCm39) S652G probably benign Het
Prss38 A G 11: 59,266,309 (GRCm39) probably benign Het
Rcor3 T A 1: 191,821,813 (GRCm39) probably benign Het
Rgp1 C T 4: 43,579,440 (GRCm39) A16V probably damaging Het
Rptor G A 11: 119,734,539 (GRCm39) G514D probably damaging Het
Scnn1g T A 7: 121,365,489 (GRCm39) Y514N probably damaging Het
Sephs1 A G 2: 4,896,501 (GRCm39) D134G probably benign Het
Slc38a3 A G 9: 107,529,111 (GRCm39) probably benign Het
Slc6a1 A T 6: 114,287,182 (GRCm39) M388L probably benign Het
Ssbp3 A T 4: 106,904,655 (GRCm39) N350I probably damaging Het
Stam2 G A 2: 52,626,305 (GRCm39) probably benign Het
Sult1e1 A T 5: 87,726,445 (GRCm39) I223N probably damaging Het
Tcf20 C A 15: 82,740,582 (GRCm39) G290C probably damaging Het
Tekt2 G T 4: 126,216,057 (GRCm39) T412K possibly damaging Het
Trabd2b A G 4: 114,460,007 (GRCm39) T382A probably damaging Het
Ttn A T 2: 76,641,587 (GRCm39) L5176Q possibly damaging Het
Ubr4 C A 4: 139,204,543 (GRCm39) Y4818* probably null Het
Vmn1r204 A T 13: 22,741,069 (GRCm39) R233S probably damaging Het
Vmn1r86 A G 7: 12,836,382 (GRCm39) Y165H probably damaging Het
Yaf2 A C 15: 93,183,355 (GRCm39) C152G probably benign Het
Zfp804b A T 5: 6,820,703 (GRCm39) F751I probably benign Het
Other mutations in Or7s1a-ps1
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1760:Or7s1a-ps1 UTSW 9 18,843,791 (GRCm39) unclassified probably benign
Predicted Primers PCR Primer
(F):5'- TAGCAACCCTAGTGCACAGAG -3'
(R):5'- CTGACAAATGATCCAGACTTCAG -3'

Sequencing Primer
(F):5'- TAGTGCACAGAGCTAATAATACCAG -3'
(R):5'- AGACCATCATAATCACTCTTTACCTG -3'
Posted On 2016-07-22