Incidental Mutation 'R7500:Or4a79'
ID 581409
Institutional Source Beutler Lab
Gene Symbol Or4a79
Ensembl Gene ENSMUSG00000110819
Gene Name olfactory receptor family 4 subfamily A member 79
Synonyms GA_x6K02T2Q125-51162884-51161940, Olfr1252, MOR231-22_p
MMRRC Submission 045573-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.334) question?
Stock # R7500 (G1)
Quality Score 225.009
Status Validated
Chromosome 2
Chromosomal Location 89551509-89552453 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 89552281 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 58 (Y58C)
Ref Sequence ENSEMBL: ENSMUSP00000150304 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000186710] [ENSMUST00000213196] [ENSMUST00000216203]
AlphaFold Q7TQZ2
Predicted Effect possibly damaging
Transcript: ENSMUST00000186710
AA Change: Y58C

PolyPhen 2 Score 0.896 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000140045
Gene: ENSMUSG00000110819
AA Change: Y58C

DomainStartEndE-ValueType
Pfam:7tm_1 39 285 5.1e-28 PFAM
Pfam:7tm_4 137 278 1e-37 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000213196
AA Change: Y58C

PolyPhen 2 Score 0.896 (Sensitivity: 0.82; Specificity: 0.94)
Predicted Effect possibly damaging
Transcript: ENSMUST00000216203
AA Change: Y58C

PolyPhen 2 Score 0.896 (Sensitivity: 0.82; Specificity: 0.94)
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency 98% (49/50)
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: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acaa1a A G 9: 119,173,564 (GRCm39) M146V probably benign Het
Adcy1 C T 11: 7,094,762 (GRCm39) R563C probably damaging Het
Ambn A T 5: 88,609,493 (GRCm39) Y67F possibly damaging Het
Ankrd42 T A 7: 92,241,080 (GRCm39) E426D probably benign Het
Ankzf1 A G 1: 75,174,623 (GRCm39) T538A probably benign Het
Arhgap20 A G 9: 51,751,802 (GRCm39) I418V probably benign Het
Arhgef28 A G 13: 98,115,003 (GRCm39) Y616H probably benign Het
B4galt4 T C 16: 38,588,376 (GRCm39) F340S probably damaging Het
Bmp1 C T 14: 70,727,562 (GRCm39) E674K probably benign Het
Ccr9 T A 9: 123,608,534 (GRCm39) V72D probably damaging Het
Chd2 T A 7: 73,101,556 (GRCm39) K1390I probably damaging Het
Col5a3 C T 9: 20,711,585 (GRCm39) R513Q unknown Het
Cracd A G 5: 76,805,905 (GRCm39) R126G unknown Het
Cttnbp2 G T 6: 18,378,419 (GRCm39) N1472K probably benign Het
Edn3 A G 2: 174,621,328 (GRCm39) probably null Het
Eps15l1 A G 8: 73,136,634 (GRCm39) F331L probably damaging Het
Gm45337 CACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCTACAGCCTCC CACAGCCTCC 7: 141,698,021 (GRCm39) probably benign Het
Lrrc56 A G 7: 140,789,443 (GRCm39) S487G probably benign Het
Moxd2 A G 6: 40,868,746 (GRCm39) T93A probably benign Het
Ngp G T 9: 110,248,833 (GRCm39) probably null Het
Npr2 T C 4: 43,650,415 (GRCm39) V970A probably damaging Het
Or5an10 T C 19: 12,276,041 (GRCm39) S152G probably damaging Het
Or8b9 T C 9: 37,766,314 (GRCm39) S67P probably damaging Het
Or8g28 T G 9: 39,169,762 (GRCm39) I69L probably benign Het
Pacc1 A G 1: 191,078,910 (GRCm39) probably null Het
Pdf A T 8: 107,773,781 (GRCm39) F221I probably damaging Het
Plekhn1 A C 4: 156,317,771 (GRCm39) S205R probably benign Het
Ppp6r1 G A 7: 4,639,129 (GRCm39) A606V probably benign Het
Prpf38b C T 3: 108,812,446 (GRCm39) V256I probably benign Het
Rbbp5 T A 1: 132,421,879 (GRCm39) H291Q probably benign Het
Rnf169 T C 7: 99,629,445 (GRCm39) E66G probably damaging Het
Rp1 T A 1: 4,381,501 (GRCm39) N328Y unknown Het
Skint5 A T 4: 113,417,035 (GRCm39) V1138E unknown Het
Slc27a4 T C 2: 29,702,717 (GRCm39) V539A probably damaging Het
Smo G T 6: 29,755,534 (GRCm39) R402L probably benign Het
Srgap2 A T 1: 131,364,569 (GRCm39) L4Q probably damaging Het
Tbxas1 A T 6: 38,959,146 (GRCm39) R110* probably null Het
Thoc7 A C 14: 13,951,204 (GRCm38) probably null Het
Tmub1 G A 5: 24,652,507 (GRCm39) probably benign Het
Tnrc6a A G 7: 122,772,673 (GRCm39) probably null Het
Traj19 T A 14: 54,437,860 (GRCm39) H6Q unknown Het
Trim30c T C 7: 104,036,758 (GRCm39) E200G probably benign Het
Ubqlnl A T 7: 103,798,048 (GRCm39) I483N probably damaging Het
Usp25 G T 16: 76,874,089 (GRCm39) R555L probably damaging Het
Vgll4 A G 6: 114,839,293 (GRCm39) S233P probably damaging Het
Vps13b G A 15: 35,910,670 (GRCm39) C3478Y possibly damaging Het
Vwa8 T A 14: 79,162,686 (GRCm39) probably null Het
Zfp977 A G 7: 42,229,629 (GRCm39) Y299H probably damaging Het
Zmynd11 T A 13: 9,785,434 (GRCm39) H17L probably benign Het
Other mutations in Or4a79
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01481:Or4a79 APN 2 89,551,870 (GRCm39) missense probably damaging 1.00
PIT4151001:Or4a79 UTSW 2 89,552,237 (GRCm39) missense probably benign 0.42
R1838:Or4a79 UTSW 2 89,552,053 (GRCm39) missense probably damaging 0.99
R1866:Or4a79 UTSW 2 89,551,550 (GRCm39) missense probably benign 0.00
R3835:Or4a79 UTSW 2 89,551,799 (GRCm39) missense possibly damaging 0.75
R4577:Or4a79 UTSW 2 89,552,387 (GRCm39) missense possibly damaging 0.80
R4675:Or4a79 UTSW 2 89,551,838 (GRCm39) missense probably benign
R4799:Or4a79 UTSW 2 89,551,706 (GRCm39) missense probably benign 0.24
R4845:Or4a79 UTSW 2 89,552,120 (GRCm39) missense probably benign 0.05
R5076:Or4a79 UTSW 2 89,551,745 (GRCm39) missense probably damaging 1.00
R5160:Or4a79 UTSW 2 89,551,763 (GRCm39) missense probably damaging 0.99
R5384:Or4a79 UTSW 2 89,551,649 (GRCm39) missense possibly damaging 0.94
R5418:Or4a79 UTSW 2 89,552,343 (GRCm39) missense probably benign
R5763:Or4a79 UTSW 2 89,552,372 (GRCm39) missense probably benign 0.00
R6997:Or4a79 UTSW 2 89,552,269 (GRCm39) missense possibly damaging 0.71
R7013:Or4a79 UTSW 2 89,551,730 (GRCm39) missense probably benign 0.20
R7608:Or4a79 UTSW 2 89,551,642 (GRCm39) missense probably benign 0.42
R7671:Or4a79 UTSW 2 89,551,603 (GRCm39) missense probably damaging 1.00
R7781:Or4a79 UTSW 2 89,551,879 (GRCm39) missense probably benign 0.38
R7841:Or4a79 UTSW 2 89,552,309 (GRCm39) missense probably benign 0.06
R7999:Or4a79 UTSW 2 89,552,344 (GRCm39) missense probably benign 0.06
R8147:Or4a79 UTSW 2 89,552,186 (GRCm39) missense probably damaging 1.00
R8882:Or4a79 UTSW 2 89,551,740 (GRCm39) nonsense probably null
X0064:Or4a79 UTSW 2 89,551,700 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGCAGTGGCTTACAGATGG -3'
(R):5'- TCCTCCTTGAAGAGTAAATGGGAC -3'

Sequencing Primer
(F):5'- TGGCTTACAGATGGCCACATAGC -3'
(R):5'- TGGGACAGAAAAACAATGTTACAG -3'
Posted On 2019-10-17