Incidental Mutation 'R7195:Or4c110'
ID 559833
Institutional Source Beutler Lab
Gene Symbol Or4c110
Ensembl Gene ENSMUSG00000100016
Gene Name olfactory receptor family 4 subfamily C member 110
Synonyms MOR233-13, Olfr1215, GA_x6K02T2Q125-50482823-50481885
MMRRC Submission 045336-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.072) question?
Stock # R7195 (G1)
Quality Score 225.009
Status Not validated
Chromosome 2
Chromosomal Location 88831692-88832634 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 88832075 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Phenylalanine at position 186 (L186F)
Ref Sequence ENSEMBL: ENSMUSP00000150030 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000188399] [ENSMUST00000214809] [ENSMUST00000216271]
AlphaFold A3KGY3
Predicted Effect
SMART Domains Protein: ENSMUSP00000141134
Gene: ENSMUSG00000100016
AA Change: L186F

low complexity region 24 34 N/A INTRINSIC
Pfam:7tm_1 39 286 1.9e-25 PFAM
Pfam:7tm_4 138 283 1.7e-38 PFAM
Predicted Effect
Predicted Effect
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.8%
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: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930438A08Rik T C 11: 58,179,242 (GRCm39) probably null Het
Abca2 A G 2: 25,332,088 (GRCm39) D1400G probably benign Het
Actl11 A T 9: 107,806,069 (GRCm39) K131* probably null Het
Adam39 A T 8: 41,277,812 (GRCm39) R68* probably null Het
Akap7 A T 10: 25,147,405 (GRCm39) N108K probably damaging Het
Arhgef10l C A 4: 140,338,721 (GRCm39) A14S probably benign Het
Ccdc141 T G 2: 76,879,927 (GRCm39) N632T probably benign Het
Ccm2 T C 11: 6,546,302 (GRCm39) S435P probably damaging Het
Cd36 A G 5: 18,019,187 (GRCm39) L178P probably damaging Het
Cd7 T C 11: 120,929,075 (GRCm39) I59V probably benign Het
Cds2 T A 2: 132,135,204 (GRCm39) S32T probably benign Het
Cep19 A G 16: 31,925,904 (GRCm39) D104G probably damaging Het
Col1a2 C T 6: 4,510,753 (GRCm39) P68S unknown Het
Col20a1 A G 2: 180,649,024 (GRCm39) H1011R probably damaging Het
Cspg4b A T 13: 113,504,463 (GRCm39) D1864V Het
D7Ertd443e A G 7: 133,896,851 (GRCm39) V513A probably damaging Het
Egfr C T 11: 16,818,162 (GRCm39) P228L probably damaging Het
Fam243 C T 16: 92,118,037 (GRCm39) V84M probably damaging Het
Fam78b A G 1: 166,906,131 (GRCm39) R97G probably damaging Het
Flt1 C T 5: 147,540,386 (GRCm39) V768M probably damaging Het
Gdap1l1 A T 2: 163,288,050 (GRCm39) N96Y probably damaging Het
Gm7168 T A 17: 14,169,622 (GRCm39) Y330N probably benign Het
Hnrnpul1 T C 7: 25,424,203 (GRCm39) N683S unknown Het
Ice2 C T 9: 69,335,782 (GRCm39) P922S possibly damaging Het
Iglv2 A G 16: 19,079,260 (GRCm39) V81A not run Het
Irs1 A G 1: 82,265,177 (GRCm39) I1013T probably benign Het
Itih4 T C 14: 30,621,432 (GRCm39) S832P probably damaging Het
Klhl1 A T 14: 96,517,513 (GRCm39) Y388N probably benign Het
Lrrc37a G A 11: 103,348,601 (GRCm39) S2698L unknown Het
Map4k4 T C 1: 40,058,829 (GRCm39) Y1008H possibly damaging Het
Mdn1 G T 4: 32,701,823 (GRCm39) G1519W probably damaging Het
Mga T A 2: 119,747,809 (GRCm39) D653E probably damaging Het
Npas1 T C 7: 16,208,733 (GRCm39) E48G probably damaging Het
Nup188 G A 2: 30,231,842 (GRCm39) probably null Het
Or1p1b G T 11: 74,130,394 (GRCm39) M1I probably null Het
Or3a4 T A 11: 73,945,223 (GRCm39) M121L probably damaging Het
Or51a39 A G 7: 102,362,873 (GRCm39) V249A possibly damaging Het
Or55b4 A T 7: 102,133,574 (GRCm39) V251D probably damaging Het
Or7h8 A G 9: 20,123,840 (GRCm39) N65S probably damaging Het
Oxct1 T C 15: 4,158,383 (GRCm39) V439A probably damaging Het
Pcdhb22 G T 18: 37,652,341 (GRCm39) G13W probably damaging Het
Pex11g A G 8: 3,509,237 (GRCm39) V230A probably benign Het
Pop1 C T 15: 34,510,525 (GRCm39) S439L probably damaging Het
Ptpn9 T A 9: 56,929,533 (GRCm39) H83Q probably benign Het
Qrfp C T 2: 31,698,704 (GRCm39) R76H probably benign Het
Slc30a3 A G 5: 31,246,139 (GRCm39) V197A probably benign Het
Slc8a3 T C 12: 81,361,047 (GRCm39) N591D possibly damaging Het
Sp4 G T 12: 118,263,807 (GRCm39) Q80K possibly damaging Het
Spock1 C T 13: 58,055,316 (GRCm39) G29D possibly damaging Het
Sprr1a G T 3: 92,391,674 (GRCm39) P109Q probably damaging Het
Suz12 T A 11: 79,904,309 (GRCm39) F239L probably damaging Het
Tbx3 A G 5: 119,813,648 (GRCm39) Y248C probably damaging Het
Trabd2b T C 4: 114,266,637 (GRCm39) L217P probably damaging Het
Ubxn11 A C 4: 133,853,726 (GRCm39) I398L possibly damaging Het
Vmn1r173 T A 7: 23,401,884 (GRCm39) S40T probably damaging Het
Vmn2r2 T C 3: 64,023,900 (GRCm39) S894G probably benign Het
Vmn2r65 A G 7: 84,592,347 (GRCm39) probably null Het
Vps13c G A 9: 67,853,107 (GRCm39) G2400D possibly damaging Het
Vps8 T C 16: 21,275,032 (GRCm39) Y197H probably damaging Het
Wdr91 T C 6: 34,866,209 (GRCm39) N486D possibly damaging Het
Wwp1 A G 4: 19,627,908 (GRCm39) I695T possibly damaging Het
Zc3hc1 T C 6: 30,382,547 (GRCm39) D133G probably benign Het
Zcchc14 T C 8: 122,335,200 (GRCm39) I307V unknown Het
Zfp933 G A 4: 147,910,636 (GRCm39) T320I probably benign Het
Other mutations in Or4c110
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00226:Or4c110 APN 2 88,831,683 (GRCm39) utr 3 prime probably benign
IGL02395:Or4c110 APN 2 88,832,507 (GRCm39) missense probably benign 0.00
IGL02399:Or4c110 APN 2 88,832,507 (GRCm39) missense probably benign 0.00
IGL02409:Or4c110 APN 2 88,832,254 (GRCm39) missense possibly damaging 0.75
IGL02421:Or4c110 APN 2 88,831,688 (GRCm39) splice site probably null
IGL03036:Or4c110 APN 2 88,832,459 (GRCm39) missense possibly damaging 0.94
R2036:Or4c110 UTSW 2 88,831,976 (GRCm39) missense probably damaging 0.97
R2199:Or4c110 UTSW 2 88,831,894 (GRCm39) missense probably damaging 0.98
R3930:Or4c110 UTSW 2 88,832,377 (GRCm39) missense probably benign 0.32
R4990:Or4c110 UTSW 2 88,831,816 (GRCm39) missense probably damaging 0.97
R5199:Or4c110 UTSW 2 88,832,107 (GRCm39) missense possibly damaging 0.70
R5368:Or4c110 UTSW 2 88,832,435 (GRCm39) missense probably damaging 1.00
R5396:Or4c110 UTSW 2 88,832,540 (GRCm39) missense probably benign 0.15
R6881:Or4c110 UTSW 2 88,832,281 (GRCm39) missense probably damaging 1.00
R7425:Or4c110 UTSW 2 88,832,544 (GRCm39) missense
R7804:Or4c110 UTSW 2 88,831,855 (GRCm39) missense unknown
R7976:Or4c110 UTSW 2 88,831,973 (GRCm39) missense probably damaging 0.97
R8094:Or4c110 UTSW 2 88,832,712 (GRCm39) start gained probably benign
R8716:Or4c110 UTSW 2 88,832,060 (GRCm39) missense
R8737:Or4c110 UTSW 2 88,832,351 (GRCm39) nonsense probably null
R9485:Or4c110 UTSW 2 88,831,709 (GRCm39) missense unknown
R9721:Or4c110 UTSW 2 88,832,060 (GRCm39) missense
Z1088:Or4c110 UTSW 2 88,832,182 (GRCm39) missense possibly damaging 0.94
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2019-06-26