Incidental Mutation 'IGL02468:Or7g32'
ID 294611
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or7g32
Ensembl Gene ENSMUSG00000052625
Gene Name olfactory receptor family 7 subfamily G member 32
Synonyms MOR155-1, GA_x6K02T2PVTD-13234278-13235216, Olfr851
Accession Numbers
Essential gene? Probably non essential (E-score: 0.127) question?
Stock # IGL02468
Quality Score
Status
Chromosome 9
Chromosomal Location 19404591-19414111 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 19408473 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Phenylalanine at position 143 (C143F)
Ref Sequence ENSEMBL: ENSMUSP00000149033 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000064582] [ENSMUST00000214130]
AlphaFold Q7TRG0
Predicted Effect probably benign
Transcript: ENSMUST00000064582
AA Change: C143F

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000066500
Gene: ENSMUSG00000052625
AA Change: C143F

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 2.1e-54 PFAM
Pfam:7tm_1 41 290 1e-23 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000214130
AA Change: C143F

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Coding Region Coverage
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: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrl2 A T 3: 148,596,116 (GRCm39) D73E probably damaging Het
Aspm A G 1: 139,408,688 (GRCm39) Y2525C probably damaging Het
Cdc45 C T 16: 18,617,479 (GRCm39) M200I probably benign Het
Cep89 T G 7: 35,102,577 (GRCm39) S97A probably benign Het
Clec16a T A 16: 10,559,742 (GRCm39) I1005N probably benign Het
Cog5 T C 12: 31,887,357 (GRCm39) probably null Het
Crybg2 T C 4: 133,809,898 (GRCm39) S1217P probably damaging Het
Csgalnact1 C A 8: 68,854,144 (GRCm39) G219V probably damaging Het
Cytip A T 2: 58,024,025 (GRCm39) M265K probably benign Het
Ddx60 T G 8: 62,411,676 (GRCm39) S509R probably damaging Het
Fat4 T C 3: 39,037,195 (GRCm39) S3616P probably benign Het
Galnt9 T C 5: 110,762,089 (GRCm39) F409S possibly damaging Het
Hrh2 T C 13: 54,368,828 (GRCm39) V268A probably benign Het
Ifi47 T A 11: 48,986,810 (GRCm39) S192R probably damaging Het
Igdcc4 T C 9: 65,034,114 (GRCm39) Y596H probably damaging Het
Lamb2 T C 9: 108,364,348 (GRCm39) C1096R probably damaging Het
Marchf1 A G 8: 66,871,563 (GRCm39) Q109R probably damaging Het
Or2y1d A T 11: 49,321,941 (GRCm39) I213F probably damaging Het
Or7d9 T C 9: 20,197,574 (GRCm39) L201P probably damaging Het
Patl1 T A 19: 11,909,574 (GRCm39) V500D probably damaging Het
Pbx3 A T 2: 34,114,589 (GRCm39) L57H probably damaging Het
Pcdhb1 T C 18: 37,399,231 (GRCm39) V394A probably benign Het
Pogz A G 3: 94,786,394 (GRCm39) N994S probably damaging Het
Prom1 T A 5: 44,187,040 (GRCm39) M406L probably benign Het
Psg26 T C 7: 18,212,387 (GRCm39) S323G probably damaging Het
Ptprm T C 17: 67,121,504 (GRCm39) T854A probably benign Het
Puf60 A C 15: 75,947,685 (GRCm39) probably benign Het
Six2 C T 17: 85,992,931 (GRCm39) E191K possibly damaging Het
Tbc1d17 A G 7: 44,497,753 (GRCm39) F40L probably benign Het
Tektip1 G T 10: 81,201,563 (GRCm39) L20I possibly damaging Het
Thsd7a A G 6: 12,318,170 (GRCm39) V1600A probably damaging Het
Tm4sf19 C A 16: 32,226,533 (GRCm39) probably benign Het
Tnfrsf1a A G 6: 125,334,824 (GRCm39) T33A probably benign Het
Troap A T 15: 98,973,242 (GRCm39) T3S possibly damaging Het
Wdfy4 T A 14: 32,688,389 (GRCm39) I3074L probably benign Het
Zfp13 C T 17: 23,795,072 (GRCm39) A493T probably benign Het
Other mutations in Or7g32
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00094:Or7g32 APN 9 19,408,155 (GRCm39) missense probably damaging 1.00
IGL01992:Or7g32 APN 9 19,408,070 (GRCm39) missense probably benign 0.00
IGL02455:Or7g32 APN 9 19,408,559 (GRCm39) nonsense probably null
IGL02685:Or7g32 APN 9 19,408,098 (GRCm39) missense probably benign
IGL02723:Or7g32 APN 9 19,388,805 (GRCm39) missense probably damaging 1.00
IGL03294:Or7g32 APN 9 19,389,285 (GRCm39) missense possibly damaging 0.95
PIT4305001:Or7g32 UTSW 9 19,389,357 (GRCm39) missense probably damaging 1.00
R0153:Or7g32 UTSW 9 19,408,233 (GRCm39) missense probably damaging 1.00
R0364:Or7g32 UTSW 9 19,389,268 (GRCm39) nonsense probably null
R0379:Or7g32 UTSW 9 19,388,776 (GRCm39) missense possibly damaging 0.75
R0449:Or7g32 UTSW 9 19,389,388 (GRCm39) missense possibly damaging 0.89
R0682:Or7g32 UTSW 9 19,388,645 (GRCm39) missense probably benign 0.03
R0693:Or7g32 UTSW 9 19,389,268 (GRCm39) nonsense probably null
R0789:Or7g32 UTSW 9 19,408,458 (GRCm39) missense possibly damaging 0.68
R1484:Or7g32 UTSW 9 19,389,423 (GRCm39) missense probably damaging 1.00
R1599:Or7g32 UTSW 9 19,389,517 (GRCm39) missense probably damaging 0.97
R1626:Or7g32 UTSW 9 19,389,495 (GRCm39) missense probably damaging 1.00
R1742:Or7g32 UTSW 9 19,389,337 (GRCm39) missense probably damaging 1.00
R2041:Or7g32 UTSW 9 19,408,131 (GRCm39) missense probably benign
R2060:Or7g32 UTSW 9 19,408,533 (GRCm39) missense possibly damaging 0.88
R4232:Or7g32 UTSW 9 19,389,022 (GRCm39) missense probably damaging 0.98
R4237:Or7g32 UTSW 9 19,388,893 (GRCm39) missense probably benign 0.00
R4474:Or7g32 UTSW 9 19,408,173 (GRCm39) missense probably damaging 1.00
R5081:Or7g32 UTSW 9 19,408,557 (GRCm39) missense probably benign 0.05
R5116:Or7g32 UTSW 9 19,389,094 (GRCm39) missense possibly damaging 0.67
R5643:Or7g32 UTSW 9 19,388,853 (GRCm39) missense probably benign 0.22
R6271:Or7g32 UTSW 9 19,389,337 (GRCm39) missense probably damaging 1.00
R6815:Or7g32 UTSW 9 19,389,061 (GRCm39) missense probably benign 0.20
R6853:Or7g32 UTSW 9 19,408,102 (GRCm39) nonsense probably null
R7150:Or7g32 UTSW 9 19,408,145 (GRCm39) missense probably benign 0.44
R7222:Or7g32 UTSW 9 19,388,763 (GRCm39) missense probably damaging 1.00
R7378:Or7g32 UTSW 9 19,408,398 (GRCm39) missense probably damaging 1.00
R7456:Or7g32 UTSW 9 19,408,844 (GRCm39) missense probably damaging 1.00
R7527:Or7g32 UTSW 9 19,408,685 (GRCm39) missense probably damaging 0.98
R7587:Or7g32 UTSW 9 19,408,818 (GRCm39) missense probably damaging 1.00
R7592:Or7g32 UTSW 9 19,389,128 (GRCm39) missense possibly damaging 0.52
R8155:Or7g32 UTSW 9 19,389,453 (GRCm39) missense probably benign 0.17
R8215:Or7g32 UTSW 9 19,408,796 (GRCm39) missense probably damaging 1.00
R8220:Or7g32 UTSW 9 19,408,317 (GRCm39) missense probably damaging 0.97
R8296:Or7g32 UTSW 9 19,408,377 (GRCm39) missense probably damaging 1.00
R8732:Or7g32 UTSW 9 19,408,098 (GRCm39) missense probably benign
R8813:Or7g32 UTSW 9 19,389,477 (GRCm39) missense possibly damaging 0.75
R9152:Or7g32 UTSW 9 19,408,448 (GRCm39) missense probably damaging 1.00
R9187:Or7g32 UTSW 9 19,389,166 (GRCm39) missense probably benign
R9528:Or7g32 UTSW 9 19,389,444 (GRCm39) missense probably damaging 1.00
R9789:Or7g32 UTSW 9 19,389,382 (GRCm39) missense probably benign 0.35
R9795:Or7g32 UTSW 9 19,408,412 (GRCm39) missense probably damaging 1.00
RF034:Or7g32 UTSW 9 19,388,928 (GRCm39) missense possibly damaging 0.46
X0058:Or7g32 UTSW 9 19,389,519 (GRCm39) missense probably benign 0.10
Z1177:Or7g32 UTSW 9 19,388,633 (GRCm39) frame shift probably null
Posted On 2015-04-16