Incidental Mutation 'R4371:Or5p79'
ID 325997
Institutional Source Beutler Lab
Gene Symbol Or5p79
Ensembl Gene ENSMUSG00000061000
Gene Name olfactory receptor family 5 subfamily P member 79
Synonyms Olfr507, GA_x6K02T2PBJ9-10951546-10952496, MOR204-7
MMRRC Submission 041117-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.139) question?
Stock # R4371 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 108221021-108221971 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 108221096 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Phenylalanine at position 26 (L26F)
Ref Sequence ENSEMBL: ENSMUSP00000078926 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080014]
AlphaFold Q8VG13
Predicted Effect probably benign
Transcript: ENSMUST00000080014
AA Change: L26F

PolyPhen 2 Score 0.266 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000078926
Gene: ENSMUSG00000061000
AA Change: L26F

DomainStartEndE-ValueType
Pfam:7tm_4 34 313 6.1e-52 PFAM
Pfam:7tm_1 44 295 1e-20 PFAM
Meta Mutation Damage Score 0.5410 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.8%
Validation Efficiency 100% (41/41)
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: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alg11 C A 8: 22,558,095 (GRCm39) A469E probably benign Het
Alox12b G A 11: 69,060,442 (GRCm39) R666H possibly damaging Het
Atp9a T C 2: 168,491,535 (GRCm39) T677A probably damaging Het
B4galt3 C A 1: 171,101,613 (GRCm39) H196N probably damaging Het
Bckdk C T 7: 127,505,591 (GRCm39) A238V probably benign Het
Brpf3 C T 17: 29,055,594 (GRCm39) A1181V probably damaging Het
C9 A G 15: 6,520,965 (GRCm39) D470G probably damaging Het
Camsap2 A G 1: 136,215,701 (GRCm39) F337L probably damaging Het
Cep152 G A 2: 125,454,967 (GRCm39) R278W probably damaging Het
Cfb T C 17: 35,079,290 (GRCm39) K287R probably damaging Het
Chfr G A 5: 110,284,034 (GRCm39) R36H probably damaging Het
Cyp4f14 T C 17: 33,128,232 (GRCm39) N261S probably benign Het
Drp2 A T X: 133,335,884 (GRCm39) probably benign Het
Dzip3 A G 16: 48,763,818 (GRCm39) probably null Het
Emb A T 13: 117,405,466 (GRCm39) D296V probably damaging Het
Epha1 T C 6: 42,342,391 (GRCm39) Y319C probably damaging Het
Flcn C T 11: 59,694,610 (GRCm39) V121I possibly damaging Het
Glrp1 GTGCTGCTGCTGCTGCTGCTGCTGCTG GTGCTGCTGCTGCTGCTGCTGCTGCTGCTG 1: 88,430,997 (GRCm39) probably benign Het
Gm6177 A T 1: 160,720,741 (GRCm39) noncoding transcript Het
Hepacam2 A T 6: 3,486,988 (GRCm39) V123E probably damaging Het
Iqsec1 A G 6: 90,671,588 (GRCm39) S194P probably damaging Het
Kat6a T C 8: 23,401,945 (GRCm39) I438T possibly damaging Het
Kcnmb2 A G 3: 32,210,251 (GRCm39) probably null Het
Nbeal1 A T 1: 60,329,105 (GRCm39) K2174N possibly damaging Het
Ncapg G A 5: 45,835,797 (GRCm39) M409I probably benign Het
Ocstamp A G 2: 165,239,233 (GRCm39) S318P possibly damaging Het
Phactr2 A G 10: 13,129,564 (GRCm39) S235P probably damaging Het
Pom121l2 T C 13: 22,166,409 (GRCm39) S227P probably benign Het
Sdf2 C T 11: 78,141,863 (GRCm39) T66I probably damaging Het
Sptbn5 A G 2: 119,896,475 (GRCm39) C729R probably damaging Het
Sys1 T C 2: 164,303,315 (GRCm39) W10R probably damaging Het
Tfap4 A G 16: 4,369,863 (GRCm39) I4T probably damaging Het
Thrb C A 14: 18,030,275 (GRCm38) Q340K probably damaging Het
Tnc T C 4: 63,888,588 (GRCm39) Y1735C probably damaging Het
Ubr1 A T 2: 120,725,547 (GRCm39) probably null Het
Other mutations in Or5p79
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01066:Or5p79 APN 7 108,221,064 (GRCm39) missense probably damaging 1.00
IGL01979:Or5p79 APN 7 108,221,648 (GRCm39) missense probably benign 0.09
IGL02373:Or5p79 APN 7 108,221,310 (GRCm39) missense probably benign 0.11
IGL02754:Or5p79 APN 7 108,221,880 (GRCm39) missense possibly damaging 0.94
IGL03008:Or5p79 APN 7 108,221,490 (GRCm39) missense probably damaging 0.99
R0305:Or5p79 UTSW 7 108,221,792 (GRCm39) missense probably benign 0.01
R0584:Or5p79 UTSW 7 108,221,622 (GRCm39) missense probably benign 0.00
R0611:Or5p79 UTSW 7 108,221,494 (GRCm39) missense possibly damaging 0.72
R0947:Or5p79 UTSW 7 108,221,879 (GRCm39) missense probably benign 0.02
R1488:Or5p79 UTSW 7 108,221,696 (GRCm39) missense probably damaging 1.00
R1808:Or5p79 UTSW 7 108,221,817 (GRCm39) missense possibly damaging 0.87
R3763:Or5p79 UTSW 7 108,221,924 (GRCm39) missense probably damaging 1.00
R4367:Or5p79 UTSW 7 108,221,096 (GRCm39) missense probably benign 0.27
R4369:Or5p79 UTSW 7 108,221,096 (GRCm39) missense probably benign 0.27
R4609:Or5p79 UTSW 7 108,221,711 (GRCm39) missense probably benign 0.35
R5389:Or5p79 UTSW 7 108,221,924 (GRCm39) missense probably damaging 1.00
R6499:Or5p79 UTSW 7 108,221,713 (GRCm39) missense probably benign 0.02
R6684:Or5p79 UTSW 7 108,221,141 (GRCm39) missense probably damaging 0.98
R7531:Or5p79 UTSW 7 108,221,269 (GRCm39) missense probably benign 0.06
R7555:Or5p79 UTSW 7 108,221,933 (GRCm39) missense probably damaging 1.00
R7893:Or5p79 UTSW 7 108,221,844 (GRCm39) missense probably damaging 1.00
R8415:Or5p79 UTSW 7 108,221,163 (GRCm39) missense probably damaging 1.00
R8444:Or5p79 UTSW 7 108,221,027 (GRCm39) missense probably benign 0.00
R8904:Or5p79 UTSW 7 108,221,919 (GRCm39) missense probably damaging 0.98
R9635:Or5p79 UTSW 7 108,221,654 (GRCm39) missense probably benign 0.00
R9795:Or5p79 UTSW 7 108,221,869 (GRCm39) missense probably benign 0.39
Predicted Primers PCR Primer
(F):5'- AGTGAGTGTTTGATGTACTACCC -3'
(R):5'- TGACAAGCATATTGGGTGTGACAG -3'

Sequencing Primer
(F):5'- AGTGTTTGATGTACTACCCAATTATG -3'
(R):5'- TGACAGAAGATGAAATGCCTATGTC -3'
Posted On 2015-07-06