Incidental Mutation 'R1978:Olfr1355'
ID 222038
Institutional Source Beutler Lab
Gene Symbol Olfr1355
Ensembl Gene ENSMUSG00000062873
Gene Name olfactory receptor 1355
Synonyms GA_x6K02T2QGN0-2932609-2931677, MOR139-6
MMRRC Submission 039991-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.073) question?
Stock # R1978 (G1)
Quality Score 225
Status Not validated
Chromosome 10
Chromosomal Location 78875540-78882266 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 78879280 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Cysteine at position 36 (Y36C)
Ref Sequence ENSEMBL: ENSMUSP00000077517 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078414]
AlphaFold Q7TQU9
Predicted Effect probably damaging
Transcript: ENSMUST00000078414
AA Change: Y36C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000077517
Gene: ENSMUSG00000062873
AA Change: Y36C

DomainStartEndE-ValueType
Pfam:7tm_4 32 309 3.1e-48 PFAM
Pfam:7tm_1 42 291 1.1e-20 PFAM
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.7%
  • 20x: 93.9%
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: 74 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610040J01Rik T A 5: 63,898,537 C205* probably null Het
2810474O19Rik T A 6: 149,326,432 N325K probably benign Het
4921539E11Rik T A 4: 103,270,764 T55S possibly damaging Het
Akap12 A G 10: 4,313,855 D88G probably benign Het
Ankrd53 C A 6: 83,763,203 F84L probably damaging Het
Apol7b A C 15: 77,423,339 F319V probably damaging Het
Bsn A G 9: 108,114,549 S1335P probably benign Het
Cep192 T C 18: 67,803,158 probably null Het
Cfap57 A G 4: 118,593,132 S598P probably benign Het
Commd8 T C 5: 72,165,499 H25R probably damaging Het
Crisp4 T C 1: 18,128,665 I143V probably benign Het
Cyp4a12b A T 4: 115,438,145 T483S probably benign Het
Dbx2 C T 15: 95,632,353 M244I probably damaging Het
Dnah6 T G 6: 73,121,970 H1982P possibly damaging Het
Fam220a C A 5: 143,563,127 P98Q probably damaging Het
Ggnbp1 A G 17: 27,029,543 K29E possibly damaging Het
Gm14569 A C X: 36,432,128 M976R probably benign Het
Gm9573 T A 17: 35,622,965 probably benign Het
Hck G T 2: 153,129,856 W112C probably damaging Het
Heatr5a A T 12: 51,939,658 S591T possibly damaging Het
Hhat A G 1: 192,717,107 S242P probably benign Het
Hnrnpll A G 17: 80,044,518 S333P probably benign Het
Hoxc6 T C 15: 103,010,007 probably null Het
Inpp5j G A 11: 3,502,150 P367S probably damaging Het
Lamc2 A G 1: 153,133,597 probably null Het
Loxhd1 T A 18: 77,321,642 I194N possibly damaging Het
Miga1 CCAGGGCAG CCAG 3: 152,335,304 probably null Het
Mkln1 C T 6: 31,490,530 Q60* probably null Het
Mybph C A 1: 134,196,996 H185N probably benign Het
Myo1g T C 11: 6,520,829 D9G possibly damaging Het
Myo6 A T 9: 80,228,925 D110V probably damaging Het
Ncoa7 A G 10: 30,691,299 V412A probably benign Het
Neb T C 2: 52,287,345 K1328R probably damaging Het
Olfm5 T A 7: 104,164,741 Q22L unknown Het
Olfr1106 C T 2: 87,048,835 V134M possibly damaging Het
Olfr1328 A T 4: 118,934,184 Y221* probably null Het
Olfr1414 C A 1: 92,511,777 G84C probably damaging Het
Olfr1423 T C 19: 12,036,341 T134A probably benign Het
Olfr414 T A 1: 174,431,091 I221N probably damaging Het
P3h1 A T 4: 119,247,976 Q717L probably null Het
Pclo T C 5: 14,713,795 I4094T unknown Het
Pfdn6 G A 17: 33,939,077 R73W probably benign Het
Phyhipl A C 10: 70,559,761 M205R possibly damaging Het
Pitpnm1 C T 19: 4,107,973 probably null Het
Plcg1 A G 2: 160,752,578 probably null Het
Pnldc1 A G 17: 12,906,505 S81P possibly damaging Het
Pno1 T C 11: 17,204,519 I221V possibly damaging Het
Porcn A G X: 8,204,301 V75A probably damaging Het
Prkcg T A 7: 3,305,346 C69S probably damaging Het
Rbbp6 G T 7: 122,999,488 probably benign Het
Rif1 GCCACCA GCCA 2: 52,110,324 probably benign Het
Scly A G 1: 91,320,169 D413G probably damaging Het
Scn11a G A 9: 119,780,795 R996* probably null Het
Slc6a13 A T 6: 121,332,373 D281V probably damaging Het
Slfn5 T C 11: 82,956,616 V109A probably benign Het
Smyd1 A T 6: 71,312,719 probably null Het
Snx29 T A 16: 11,367,724 M57K probably benign Het
Stag1 T G 9: 100,888,086 I603S probably benign Het
Svep1 C A 4: 58,097,292 C1417F possibly damaging Het
Tbc1d23 T C 16: 57,189,351 I392V probably benign Het
Tchh T C 3: 93,446,799 L1182P unknown Het
Tle3 T A 9: 61,394,633 V108E probably damaging Het
Tmem144 T C 3: 79,825,400 probably null Het
Tpr T G 1: 150,419,907 L894V possibly damaging Het
Trappc9 A T 15: 73,000,025 V472E probably damaging Het
Trim38 T C 13: 23,791,098 V340A probably damaging Het
Ttc37 T C 13: 76,134,815 V752A probably benign Het
Ttn A T 2: 76,811,243 L5176Q possibly damaging Het
Vmn1r12 T A 6: 57,159,509 I197N possibly damaging Het
Vmn1r26 T C 6: 58,009,126 Y26C possibly damaging Het
Vwa3a A G 7: 120,758,954 I83V probably null Het
Xirp1 C T 9: 120,018,591 E409K probably benign Het
Zc3h14 T G 12: 98,763,922 I46R probably damaging Het
Zfp976 A G 7: 42,613,841 C191R probably damaging Het
Other mutations in Olfr1355
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01571:Olfr1355 APN 10 78879837 missense possibly damaging 0.95
IGL01773:Olfr1355 APN 10 78879936 missense possibly damaging 0.86
IGL02707:Olfr1355 APN 10 78879925 missense probably damaging 1.00
IGL03233:Olfr1355 APN 10 78879572 nonsense probably null
R1067:Olfr1355 UTSW 10 78879683 nonsense probably null
R1201:Olfr1355 UTSW 10 78879477 missense probably benign 0.12
R1956:Olfr1355 UTSW 10 78879433 missense probably benign 0.28
R2014:Olfr1355 UTSW 10 78879388 missense possibly damaging 0.94
R2015:Olfr1355 UTSW 10 78879388 missense possibly damaging 0.94
R2245:Olfr1355 UTSW 10 78879931 missense probably damaging 0.98
R3725:Olfr1355 UTSW 10 78879932 nonsense probably null
R4899:Olfr1355 UTSW 10 78879207 missense probably benign 0.32
R5696:Olfr1355 UTSW 10 78880085 missense probably benign 0.02
R5982:Olfr1355 UTSW 10 78879953 nonsense probably null
R6448:Olfr1355 UTSW 10 78879682 missense possibly damaging 0.78
R7126:Olfr1355 UTSW 10 78879577 missense possibly damaging 0.50
R7385:Olfr1355 UTSW 10 78879454 missense probably damaging 0.97
R7807:Olfr1355 UTSW 10 78879209 missense probably benign
R7886:Olfr1355 UTSW 10 78879823 missense possibly damaging 0.59
R8313:Olfr1355 UTSW 10 78879336 missense probably benign 0.00
R8747:Olfr1355 UTSW 10 78879321 missense probably benign 0.14
R9507:Olfr1355 UTSW 10 78879763 missense probably benign 0.30
Z1177:Olfr1355 UTSW 10 78879156 critical splice acceptor site probably null
Z1177:Olfr1355 UTSW 10 78879559 missense possibly damaging 0.56
Predicted Primers PCR Primer
(F):5'- TCAGTGTGAGAATTGTCCCG -3'
(R):5'- CAGGAGAAAGTTGTCCAGTTCTCC -3'

Sequencing Primer
(F):5'- CAGTGTGAGAATTGTCCCGTTATC -3'
(R):5'- GACATCTGGCTAATACAGTCTGC -3'
Posted On 2014-08-25