Incidental Mutation 'R1846:Or4c10'
ID 207701
Institutional Source Beutler Lab
Gene Symbol Or4c10
Ensembl Gene ENSMUSG00000049149
Gene Name olfactory receptor family 4 subfamily C member 10
Synonyms GA_x6K02T2Q125-51361752-51362687, MOR232-3, Olfr1258
MMRRC Submission 039871-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.059) question?
Stock # R1846 (G1)
Quality Score 225
Status Validated
Chromosome 2
Chromosomal Location 89752288-89761090 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 89761010 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 286 (T286A)
Ref Sequence ENSEMBL: ENSMUSP00000149547 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000102609] [ENSMUST00000111516] [ENSMUST00000213720]
AlphaFold Q8VGN6
Predicted Effect possibly damaging
Transcript: ENSMUST00000102609
AA Change: T286A

PolyPhen 2 Score 0.454 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000099669
Gene: ENSMUSG00000049149
AA Change: T286A

DomainStartEndE-ValueType
Pfam:7tm_4 29 303 2.6e-52 PFAM
Pfam:7TM_GPCR_Srsx 33 299 3.4e-5 PFAM
Pfam:7tm_1 39 285 6.4e-20 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000111516
AA Change: T286A

PolyPhen 2 Score 0.454 (Sensitivity: 0.89; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000107141
Gene: ENSMUSG00000049149
AA Change: T286A

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 33 299 3.4e-5 PFAM
Pfam:7tm_1 39 285 4.9e-32 PFAM
Pfam:7tm_4 137 278 2.7e-43 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000213720
AA Change: T286A

PolyPhen 2 Score 0.454 (Sensitivity: 0.89; Specificity: 0.90)
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 97.5%
  • 3x: 96.9%
  • 10x: 95.4%
  • 20x: 92.6%
Validation Efficiency 99% (75/76)
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: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2900092C05Rik G A 7: 12,246,809 (GRCm39) R63Q probably benign Het
Adamts20 A T 15: 94,243,871 (GRCm39) C619S probably damaging Het
Alx1 T C 10: 102,861,165 (GRCm39) D121G possibly damaging Het
Anks3 A C 16: 4,771,748 (GRCm39) M215R probably benign Het
Anxa4 T A 6: 86,718,893 (GRCm39) probably null Het
Arhgef25 A G 10: 127,021,733 (GRCm39) V222A probably damaging Het
Bglap2 A G 3: 88,285,932 (GRCm39) probably benign Het
Cars2 A G 8: 11,564,674 (GRCm39) V22A probably benign Het
Ccdc198 G T 14: 49,473,420 (GRCm39) L102I probably damaging Het
Cenpe T A 3: 134,945,606 (GRCm39) I1040N probably damaging Het
Cep170 C T 1: 176,583,335 (GRCm39) D1015N probably damaging Het
Chia1 T A 3: 106,038,181 (GRCm39) I359N probably damaging Het
Crot A T 5: 9,038,248 (GRCm39) V93E probably benign Het
Dab1 C T 4: 104,588,948 (GRCm39) A524V probably benign Het
Dnmbp T C 19: 43,891,186 (GRCm39) I194V probably damaging Het
Dock4 T A 12: 40,783,267 (GRCm39) C734S probably benign Het
Eif4e3 T C 6: 99,617,662 (GRCm39) S70G probably benign Het
Entpd3 G A 9: 120,387,441 (GRCm39) D213N probably benign Het
Ern2 T G 7: 121,775,759 (GRCm39) Y445S probably benign Het
Fasn A G 11: 120,704,133 (GRCm39) S1429P probably benign Het
Fat4 A G 3: 39,036,532 (GRCm39) I3395V probably benign Het
Fbln2 C A 6: 91,233,399 (GRCm39) Q628K possibly damaging Het
Fbxo28 T C 1: 182,153,845 (GRCm39) N164D probably benign Het
Fez1 T C 9: 36,779,063 (GRCm39) S247P probably damaging Het
Gars1 A G 6: 55,040,153 (GRCm39) D360G probably benign Het
Gcfc2 A T 6: 81,933,873 (GRCm39) Q710L probably damaging Het
Ggt5 A G 10: 75,446,376 (GRCm39) probably null Het
Glp1r A G 17: 31,148,909 (GRCm39) probably null Het
Hspa14 T C 2: 3,492,697 (GRCm39) D356G possibly damaging Het
Htt T A 5: 35,006,288 (GRCm39) I1399N probably damaging Het
Kmt2e G A 5: 23,704,484 (GRCm39) probably benign Het
Krt36 C A 11: 99,996,374 (GRCm39) G17C probably damaging Het
Lama2 T C 10: 27,088,092 (GRCm39) E895G probably damaging Het
Lamb2 G A 9: 108,364,586 (GRCm39) R1142H probably benign Het
Lhcgr C T 17: 89,072,575 (GRCm39) probably null Het
Lpin2 A G 17: 71,532,064 (GRCm39) T140A probably benign Het
Metap1 A G 3: 138,186,443 (GRCm39) probably benign Het
Mpeg1 T C 19: 12,440,486 (GRCm39) V648A probably benign Het
Mroh2a A G 1: 88,186,386 (GRCm39) S64G probably benign Het
Muc4 T A 16: 32,752,369 (GRCm38) I749N probably benign Het
N4bp2 T C 5: 65,965,862 (GRCm39) F1304L probably damaging Het
Nup85 A G 11: 115,459,239 (GRCm39) E114G probably benign Het
Or2a5 A G 6: 42,874,254 (GRCm39) S290G probably damaging Het
Or6b2b A T 1: 92,418,822 (GRCm39) Y218* probably null Het
Pafah2 GCCCC GCCCCC 4: 134,152,852 (GRCm39) probably null Het
Parp2 T A 14: 51,052,843 (GRCm39) C145* probably null Het
Plpp6 T C 19: 28,941,680 (GRCm39) S94P probably benign Het
Polr1a T C 6: 71,953,172 (GRCm39) I1580T probably damaging Het
Polrmt A T 10: 79,574,043 (GRCm39) V860E probably damaging Het
Ppp1r17 A G 6: 55,999,412 (GRCm39) E15G possibly damaging Het
Prl7b1 A T 13: 27,786,831 (GRCm39) W133R probably damaging Het
Ptk7 A G 17: 46,887,416 (GRCm39) probably null Het
Rad23b C T 4: 55,383,637 (GRCm39) Q290* probably null Het
Rorb C T 19: 18,932,445 (GRCm39) E369K probably damaging Het
Rusc1 T C 3: 88,999,452 (GRCm39) D110G probably damaging Het
Smg7 A G 1: 152,724,601 (GRCm39) S527P probably damaging Het
Ssbp2 C T 13: 91,812,268 (GRCm39) P105L probably damaging Het
Stt3a C T 9: 36,674,681 (GRCm39) R34H probably damaging Het
Sufu T A 19: 46,439,386 (GRCm39) I202N possibly damaging Het
Thsd7b G A 1: 129,540,993 (GRCm39) R289Q probably damaging Het
Tph1 A T 7: 46,309,863 (GRCm39) S130T probably damaging Het
Ttn A G 2: 76,776,030 (GRCm39) S1671P probably damaging Het
Usp4 A G 9: 108,249,935 (GRCm39) I441V probably benign Het
Vmn1r8 A G 6: 57,013,413 (GRCm39) N155D probably benign Het
Vmn2r115 A C 17: 23,578,357 (GRCm39) K610T probably damaging Het
Vmn2r62 G A 7: 42,438,546 (GRCm39) P97S probably damaging Het
Zbtb40 T C 4: 136,735,150 (GRCm39) D297G probably benign Het
Zfp174 C A 16: 3,672,599 (GRCm39) Q383K probably benign Het
Zfp318 T A 17: 46,724,592 (GRCm39) D2198E probably benign Het
Zfp628 C T 7: 4,923,866 (GRCm39) P696L possibly damaging Het
Zgrf1 T A 3: 127,409,112 (GRCm39) N1695K probably damaging Het
Other mutations in Or4c10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02386:Or4c10 APN 2 89,760,888 (GRCm39) missense probably damaging 0.96
IGL02552:Or4c10 APN 2 89,760,903 (GRCm39) missense probably benign 0.01
IGL03300:Or4c10 APN 2 89,760,571 (GRCm39) nonsense probably null
R0081:Or4c10 UTSW 2 89,760,423 (GRCm39) missense possibly damaging 0.90
R0197:Or4c10 UTSW 2 89,760,545 (GRCm39) missense probably benign 0.00
R0701:Or4c10 UTSW 2 89,760,545 (GRCm39) missense probably benign 0.00
R0883:Or4c10 UTSW 2 89,760,545 (GRCm39) missense probably benign 0.00
R1163:Or4c10 UTSW 2 89,760,449 (GRCm39) missense possibly damaging 0.78
R1833:Or4c10 UTSW 2 89,760,645 (GRCm39) nonsense probably null
R4504:Or4c10 UTSW 2 89,760,695 (GRCm39) missense possibly damaging 0.89
R4507:Or4c10 UTSW 2 89,760,695 (GRCm39) missense possibly damaging 0.89
R4679:Or4c10 UTSW 2 89,761,008 (GRCm39) missense possibly damaging 0.63
R4908:Or4c10 UTSW 2 89,760,923 (GRCm39) missense probably benign 0.00
R5430:Or4c10 UTSW 2 89,760,257 (GRCm39) missense probably benign 0.00
R6836:Or4c10 UTSW 2 89,760,683 (GRCm39) missense probably damaging 1.00
R7552:Or4c10 UTSW 2 89,761,064 (GRCm39) missense probably benign 0.06
R7709:Or4c10 UTSW 2 89,760,225 (GRCm39) missense probably benign 0.00
R8060:Or4c10 UTSW 2 89,760,693 (GRCm39) missense probably benign 0.04
R8349:Or4c10 UTSW 2 89,760,878 (GRCm39) missense possibly damaging 0.48
R8449:Or4c10 UTSW 2 89,760,878 (GRCm39) missense possibly damaging 0.48
Z1177:Or4c10 UTSW 2 89,760,942 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- CCACATTCTGGGGCTCTTTG -3'
(R):5'- CTGGGTAACATTCTTGCTGGC -3'

Sequencing Primer
(F):5'- GTTCATTAAGAAACCACAGTGCAG -3'
(R):5'- CTTGCTGGCTTCAAATACAATGTC -3'
Posted On 2014-06-23