Incidental Mutation 'R4198:Or51h7'
ID 318629
Institutional Source Beutler Lab
Gene Symbol Or51h7
Ensembl Gene ENSMUSG00000052785
Gene Name olfactory receptor family 51 subfamily H member 7
Synonyms Olfr573, MOR10-3P, MOR10-4, GA_x6K02T2PBJ9-5653743-5652872
MMRRC Submission 041640-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.070) question?
Stock # R4198 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 102590889-102591782 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 102591004 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Serine at position 260 (F260S)
Ref Sequence ENSEMBL: ENSMUSP00000146786 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000064830] [ENSMUST00000210571]
AlphaFold A0A1B0GRU2
Predicted Effect probably damaging
Transcript: ENSMUST00000064830
AA Change: F260S

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000065147
Gene: ENSMUSG00000052785
AA Change: F260S

DomainStartEndE-ValueType
Pfam:7tm_4 33 296 9.3e-109 PFAM
Pfam:7tm_1 43 288 4.6e-17 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000064830
AA Change: F260S

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
Predicted Effect probably damaging
Transcript: ENSMUST00000210571
AA Change: F260S

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 95.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aox1 G A 1: 58,124,766 (GRCm39) M1002I probably benign Het
Ap2b1 C A 11: 83,233,429 (GRCm39) Q481K probably damaging Het
Arhgap31 G A 16: 38,444,275 (GRCm39) A194V probably damaging Het
Atp10a A G 7: 58,463,434 (GRCm39) D989G probably damaging Het
Ccny G A 18: 9,332,928 (GRCm39) T201I probably damaging Het
Cdca5 T C 19: 6,140,382 (GRCm39) V181A possibly damaging Het
Ces1g A G 8: 94,032,496 (GRCm39) I488T probably benign Het
Csmd2 A G 4: 128,404,717 (GRCm39) T2368A probably benign Het
Cux1 T A 5: 136,315,702 (GRCm39) I1113F probably damaging Het
Dnah3 C T 7: 119,522,061 (GRCm39) G4033D probably damaging Het
Foxg1 T A 12: 49,432,082 (GRCm39) S272T possibly damaging Het
Fyco1 T C 9: 123,655,699 (GRCm39) N1020D probably benign Het
Gprc5c T G 11: 114,754,686 (GRCm39) L121R probably damaging Het
Hyou1 G A 9: 44,300,156 (GRCm39) R815H probably damaging Het
Kera T C 10: 97,448,835 (GRCm39) *352Q probably null Het
Kirrel1 C T 3: 86,996,458 (GRCm39) M380I probably null Het
Lnpk T C 2: 74,399,453 (GRCm39) E30G probably damaging Het
Map2 C T 1: 66,464,457 (GRCm39) R128C probably damaging Het
Or1i2 A T 10: 78,447,901 (GRCm39) D191E possibly damaging Het
Or1o2 T A 17: 37,543,025 (GRCm39) M79L probably benign Het
Or2y11 G A 11: 49,443,461 (GRCm39) V296M possibly damaging Het
Pabir3 G A X: 52,382,376 (GRCm39) R94H possibly damaging Het
Ror2 A G 13: 53,264,680 (GRCm39) M792T probably benign Het
Serpinb9d A G 13: 33,386,948 (GRCm39) I339V probably benign Het
Serpinb9d A G 13: 33,386,657 (GRCm39) probably null Het
Slc1a1 A G 19: 28,878,852 (GRCm39) K197R probably benign Het
Snx20 A G 8: 89,354,226 (GRCm39) V168A possibly damaging Het
Sowaha T C 11: 53,369,395 (GRCm39) E447G possibly damaging Het
Stard8 AGAGGAGGAGGAGGAGGAGGA AGAGGAGGAGGAGGAGGA X: 98,110,114 (GRCm39) probably benign Het
Stx19 G T 16: 62,643,039 (GRCm39) C285F possibly damaging Het
Syp A G X: 7,506,166 (GRCm39) probably null Het
Tbkbp1 C T 11: 97,039,894 (GRCm39) probably null Het
Trim29 G T 9: 43,222,677 (GRCm39) E169* probably null Het
Ttll12 T C 15: 83,461,214 (GRCm39) N602D probably damaging Het
Zfp26 T C 9: 20,348,012 (GRCm39) T851A probably benign Het
Zfp316 T C 5: 143,240,226 (GRCm39) M598V probably benign Het
Zhx2 A G 15: 57,685,125 (GRCm39) I165V probably benign Het
Other mutations in Or51h7
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0472:Or51h7 UTSW 7 102,591,258 (GRCm39) nonsense probably null
R1537:Or51h7 UTSW 7 102,591,547 (GRCm39) missense probably damaging 1.00
R2168:Or51h7 UTSW 7 102,591,678 (GRCm39) missense probably benign 0.00
R3781:Or51h7 UTSW 7 102,591,278 (GRCm39) missense probably benign
R4200:Or51h7 UTSW 7 102,591,004 (GRCm39) missense probably damaging 1.00
R4333:Or51h7 UTSW 7 102,591,176 (GRCm39) missense possibly damaging 0.50
R4838:Or51h7 UTSW 7 102,591,453 (GRCm39) missense probably damaging 1.00
R5041:Or51h7 UTSW 7 102,591,785 (GRCm39) splice site probably null
R5371:Or51h7 UTSW 7 102,591,719 (GRCm39) missense probably benign
R5668:Or51h7 UTSW 7 102,591,128 (GRCm39) missense probably benign 0.44
R7836:Or51h7 UTSW 7 102,591,125 (GRCm39) missense possibly damaging 0.94
R7887:Or51h7 UTSW 7 102,591,358 (GRCm39) missense possibly damaging 0.94
R7991:Or51h7 UTSW 7 102,591,760 (GRCm39) missense probably benign 0.12
R9660:Or51h7 UTSW 7 102,591,259 (GRCm39) missense probably damaging 1.00
R9717:Or51h7 UTSW 7 102,591,165 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CATGCGATTTCATTTGACTAGGC -3'
(R):5'- ACCAAGATATGATGCGCCTAG -3'

Sequencing Primer
(F):5'- GCGATTTCATTTGACTAGGCTCTGC -3'
(R):5'- CGTGTCAACAGCCTCTATGG -3'
Posted On 2015-06-10