Incidental Mutation 'R5701:Or5m11'
ID 450877
Institutional Source Beutler Lab
Gene Symbol Or5m11
Ensembl Gene ENSMUSG00000057207
Gene Name olfactory receptor family 5 subfamily M member 11
Synonyms Olfr1028, GA_x6K02T2Q125-47430129-47431103, MOR198-3P, MOR198-4, MOR198-3P, MOR198-6_p, Olfr1534-ps1
MMRRC Submission 043181-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.062) question?
Stock # R5701 (G1)
Quality Score 225
Status Not validated
Chromosome 2
Chromosomal Location 85781409-85782383 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 85782168 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 254 (T254A)
Ref Sequence ENSEMBL: ENSMUSP00000079522 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080698]
AlphaFold Q7TR89
Predicted Effect possibly damaging
Transcript: ENSMUST00000080698
AA Change: T254A

PolyPhen 2 Score 0.867 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000079522
Gene: ENSMUSG00000057207
AA Change: T254A

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 3.1e-55 PFAM
Pfam:7tm_1 41 290 1.5e-24 PFAM
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.9%
Validation Efficiency
MGI Phenotype FUNCTION: Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. The nomenclature assigned to the olfactory receptor genes and proteins for this organism is independent of other organisms. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Armc8 A G 9: 99,378,202 (GRCm39) probably null Het
Asxl1 A G 2: 153,241,409 (GRCm39) E653G probably damaging Het
AW551984 G A 9: 39,504,118 (GRCm39) A616V probably benign Het
Birc6 T C 17: 75,004,420 (GRCm39) M4763T possibly damaging Het
Bltp1 T A 3: 36,975,509 (GRCm39) M727K probably benign Het
Cand2 T G 6: 115,774,893 (GRCm39) F1034V probably damaging Het
Ccdc80 T C 16: 44,936,741 (GRCm39) V722A possibly damaging Het
Cd109 CATTTATTTATTTATTTATTTATTTATTTATTTAT CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT 9: 78,619,782 (GRCm39) probably benign Het
Chrnd G A 1: 87,125,380 (GRCm39) V340I possibly damaging Het
Clip1 T C 5: 123,751,366 (GRCm39) probably benign Het
Csmd3 T C 15: 47,513,617 (GRCm39) E1920G probably damaging Het
Csmd3 A T 15: 48,403,729 (GRCm39) F194I probably damaging Het
D930048N14Rik T A 11: 51,544,556 (GRCm39) probably null Het
Defa28 T C 8: 22,073,863 (GRCm39) Y89H probably benign Het
Dnah1 C T 14: 30,996,001 (GRCm39) G2705E probably damaging Het
Eci2 A T 13: 35,174,250 (GRCm39) S104T possibly damaging Het
Ep300 T C 15: 81,485,696 (GRCm39) S228P unknown Het
Gabrb2 T A 11: 42,378,201 (GRCm39) M139K probably damaging Het
Gbp4 T A 5: 105,266,265 (GRCm39) N592I possibly damaging Het
Gpr158 C T 2: 21,751,520 (GRCm39) R480C probably damaging Het
Gps1 A G 11: 120,676,008 (GRCm39) D71G probably benign Het
Hoxc9 T C 15: 102,890,313 (GRCm39) Y77H possibly damaging Het
Il9r T A 11: 32,143,263 (GRCm39) Y231F probably benign Het
Klhl1 A G 14: 96,438,816 (GRCm39) M494T probably benign Het
Kmt2c A G 5: 25,519,015 (GRCm39) V2365A probably benign Het
Kri1 T A 9: 21,192,425 (GRCm39) K241M possibly damaging Het
Macf1 A T 4: 123,397,018 (GRCm39) C928S probably damaging Het
Mcm2 T C 6: 88,870,073 (GRCm39) D32G probably damaging Het
Mex3d T C 10: 80,217,379 (GRCm39) T613A probably benign Het
Mptx2 G A 1: 173,102,414 (GRCm39) L92F probably benign Het
Myh9 T C 15: 77,675,964 (GRCm39) I241V probably benign Het
Myo6 C T 9: 80,165,809 (GRCm39) T398I probably damaging Het
Nckap1l G A 15: 103,381,195 (GRCm39) A366T probably benign Het
Plscr5 A T 9: 92,087,564 (GRCm39) K178* probably null Het
Rapgef6 T C 11: 54,567,220 (GRCm39) W857R possibly damaging Het
Raxos1 G A 18: 66,071,059 (GRCm39) probably benign Het
Rnf145 G A 11: 44,422,120 (GRCm39) V68M possibly damaging Het
Slc66a2 T A 18: 80,315,693 (GRCm39) D118E possibly damaging Het
Synpo2 C G 3: 122,873,879 (GRCm39) G1029A probably damaging Het
Tbc1d5 TTGCTGCTGCTGCTGCTGCTGGTGCTGCTGCTGCTG TTGCTGCTGCTGCTGCTGGTGCTGCTGCTGCTG 17: 51,106,983 (GRCm39) probably benign Het
Vmn2r14 T C 5: 109,367,816 (GRCm39) Y392C probably damaging Het
Vmn2r55 A G 7: 12,404,492 (GRCm39) F304L probably benign Het
Zfp316 C T 5: 143,240,132 (GRCm39) G629D probably benign Het
Other mutations in Or5m11
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02155:Or5m11 APN 2 85,782,352 (GRCm39) missense probably benign
R0386:Or5m11 UTSW 2 85,782,217 (GRCm39) missense probably damaging 0.97
R0483:Or5m11 UTSW 2 85,781,587 (GRCm39) missense probably damaging 0.98
R0539:Or5m11 UTSW 2 85,782,353 (GRCm39) missense probably benign
R6459:Or5m11 UTSW 2 85,781,862 (GRCm39) missense probably damaging 1.00
R7124:Or5m11 UTSW 2 85,781,817 (GRCm39) missense possibly damaging 0.57
R7631:Or5m11 UTSW 2 85,782,218 (GRCm39) missense probably benign 0.06
R7943:Or5m11 UTSW 2 85,782,342 (GRCm39) missense probably benign 0.01
R8025:Or5m11 UTSW 2 85,781,856 (GRCm39) missense probably benign
R9221:Or5m11 UTSW 2 85,782,185 (GRCm39) nonsense probably null
R9312:Or5m11 UTSW 2 85,781,509 (GRCm39) missense possibly damaging 0.90
Z1177:Or5m11 UTSW 2 85,781,826 (GRCm39) missense not run
Predicted Primers PCR Primer
(F):5'- TGTGCTGACCCACCACTTATTAAG -3'
(R):5'- TCCTGATGACGTTTTGCCTG -3'

Sequencing Primer
(F):5'- GACCCACCACTTATTAAGCTATCTTG -3'
(R):5'- GCCTGAGTATTGTCTTCAAGGCC -3'
Posted On 2017-01-03