Incidental Mutation 'R9701:Or13j1'
ID 729553
Institutional Source Beutler Lab
Gene Symbol Or13j1
Ensembl Gene ENSMUSG00000046450
Gene Name olfactory receptor family 13 subfamily J member 1
Synonyms MOR262-4, Olfr71, mOR17, GA_x6K02T2N78B-16230286-16231224
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.079) question?
Stock # R9701 (G1)
Quality Score 225.009
Status Not validated
Chromosome 4
Chromosomal Location 43705628-43706566 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 43705793 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Isoleucine at position 258 (M258I)
Ref Sequence ENSEMBL: ENSMUSP00000103494 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055401] [ENSMUST00000055545] [ENSMUST00000107862] [ENSMUST00000217544]
AlphaFold Q9QZ18
Predicted Effect probably benign
Transcript: ENSMUST00000055401
AA Change: M258I

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000060230
Gene: ENSMUSG00000046450
AA Change: M258I

DomainStartEndE-ValueType
Pfam:7tm_1 41 290 2.4e-34 PFAM
Pfam:7tm_4 139 283 4.5e-44 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000055545
SMART Domains Protein: ENSMUSP00000060748
Gene: ENSMUSG00000050215

DomainStartEndE-ValueType
Pfam:7tm_4 30 306 9.6e-51 PFAM
Pfam:7tm_1 41 289 3.4e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000107862
AA Change: M258I

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
SMART Domains Protein: ENSMUSP00000103494
Gene: ENSMUSG00000046450
AA Change: M258I

DomainStartEndE-ValueType
Pfam:7tm_4 30 307 2.2e-52 PFAM
Pfam:7tm_1 41 290 7.5e-25 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000217544
AA Change: M258I

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
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: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc8 T C 7: 45,786,054 (GRCm39) D673G probably benign Het
Alg8 T A 7: 97,027,486 (GRCm39) V118E possibly damaging Het
Ap4e1 T C 2: 126,875,563 (GRCm39) V218A probably benign Het
Armc12 A T 17: 28,751,375 (GRCm39) D123V probably damaging Het
Bltp3b G A 10: 89,615,755 (GRCm39) V133I probably benign Het
Bms1 T A 6: 118,368,147 (GRCm39) K1039I probably damaging Het
Col4a2 A G 8: 11,493,104 (GRCm39) N1299S probably benign Het
Cux1 T C 5: 136,343,169 (GRCm39) D405G probably damaging Het
Cwf19l2 A T 9: 3,430,454 (GRCm39) Q262L probably damaging Het
Dclk3 A G 9: 111,298,244 (GRCm39) D596G probably damaging Het
Dnah7a A T 1: 53,561,388 (GRCm39) C2090S probably benign Het
Dock7 T C 4: 98,846,384 (GRCm39) D1749G unknown Het
Dock9 A T 14: 121,876,983 (GRCm39) C463S probably benign Het
Dyrk1b G A 7: 27,885,838 (GRCm39) R548Q probably damaging Het
Egr1 T C 18: 34,995,674 (GRCm39) F152S probably damaging Het
Eln C A 5: 134,744,559 (GRCm39) A479S unknown Het
Gm973 T A 1: 59,566,032 (GRCm39) W84R possibly damaging Het
Gnpat A G 8: 125,613,678 (GRCm39) K642E probably benign Het
Gpr180 G A 14: 118,391,302 (GRCm39) G235R probably damaging Het
Gpx6 A T 13: 21,501,777 (GRCm39) Q133L probably benign Het
Gzmn T C 14: 56,405,310 (GRCm39) Y58C probably benign Het
Hcfc2 G T 10: 82,574,269 (GRCm39) G148* probably null Het
Hspa5 C T 2: 34,664,649 (GRCm39) R368* probably null Het
Igkv3-10 T C 6: 70,550,001 (GRCm39) V49A probably damaging Het
Inpp5f A C 7: 128,278,515 (GRCm39) D435A possibly damaging Het
Jmjd1c A T 10: 67,060,745 (GRCm39) I852F possibly damaging Het
Lhx5 T A 5: 120,572,663 (GRCm39) V94E possibly damaging Het
Map1s C T 8: 71,369,712 (GRCm39) T928I possibly damaging Het
Mib1 T A 18: 10,798,494 (GRCm39) L785H probably damaging Het
Mrgpra6 C T 7: 46,835,533 (GRCm39) R296K probably benign Het
Mrpl9 A G 3: 94,351,892 (GRCm39) probably null Het
Mutyh A G 4: 116,676,485 (GRCm39) S486G probably benign Het
Naa15 T A 3: 51,349,370 (GRCm39) Y96* probably null Het
Nlrp1a T C 11: 70,987,946 (GRCm39) S1175G probably benign Het
Nup153 A T 13: 46,840,211 (GRCm39) D1132E probably benign Het
Nxf1 G A 19: 8,739,772 (GRCm39) G42D probably damaging Het
Plekhg6 C T 6: 125,347,602 (GRCm39) V451I probably benign Het
Prkab1 T C 5: 116,162,274 (GRCm39) E12G probably benign Het
Ptprd A G 4: 75,916,896 (GRCm39) Y752H probably damaging Het
Rbm12 A G 2: 155,938,166 (GRCm39) I702T probably benign Het
Rnf212 A G 5: 108,922,738 (GRCm39) probably null Het
Sall3 C A 18: 81,017,443 (GRCm39) A162S probably benign Het
Sec24d T C 3: 123,063,321 (GRCm39) S13P probably damaging Het
Serpina16 T C 12: 103,638,873 (GRCm39) Q238R probably benign Het
Shank1 G A 7: 43,962,342 (GRCm39) S71N unknown Het
Skint3 T A 4: 112,111,094 (GRCm39) V73E probably damaging Het
Slc6a20a T A 9: 123,489,585 (GRCm39) T153S probably damaging Het
Slc6a6 T C 6: 91,700,478 (GRCm39) Y69H probably damaging Het
Sorl1 A G 9: 42,003,766 (GRCm39) Y177H probably damaging Het
Srbd1 T C 17: 86,433,559 (GRCm39) Y346C probably damaging Het
Syne2 A G 12: 76,037,197 (GRCm39) E3792G probably damaging Het
Tg C G 15: 66,637,991 (GRCm39) T2268S probably benign Het
Thbs1 A G 2: 117,950,716 (GRCm39) N721S probably benign Het
Treh A G 9: 44,594,648 (GRCm39) Y275C probably damaging Het
Trpv5 G T 6: 41,651,594 (GRCm39) H195N possibly damaging Het
Tshz1 A G 18: 84,032,579 (GRCm39) S610P possibly damaging Het
Ttll4 A G 1: 74,720,482 (GRCm39) N499S probably benign Het
Ttn G T 2: 76,748,927 (GRCm39) H4041N probably benign Het
Ubtf A G 11: 102,199,718 (GRCm39) probably null Het
Urod C T 4: 116,849,778 (GRCm39) V207M probably damaging Het
Vegfa G A 17: 46,342,713 (GRCm39) P35L probably damaging Het
Zc3h7b C T 15: 81,676,505 (GRCm39) P749L probably damaging Het
Other mutations in Or13j1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02317:Or13j1 APN 4 43,706,172 (GRCm39) missense probably damaging 1.00
PIT4453001:Or13j1 UTSW 4 43,706,464 (GRCm39) missense probably damaging 1.00
R0597:Or13j1 UTSW 4 43,706,592 (GRCm39) splice site probably null
R0610:Or13j1 UTSW 4 43,706,400 (GRCm39) missense possibly damaging 0.69
R1588:Or13j1 UTSW 4 43,705,923 (GRCm39) missense probably damaging 0.98
R1619:Or13j1 UTSW 4 43,706,292 (GRCm39) missense probably damaging 1.00
R1779:Or13j1 UTSW 4 43,706,041 (GRCm39) missense probably damaging 1.00
R2871:Or13j1 UTSW 4 43,706,458 (GRCm39) missense probably benign 0.30
R2871:Or13j1 UTSW 4 43,706,458 (GRCm39) missense probably benign 0.30
R4723:Or13j1 UTSW 4 43,705,785 (GRCm39) missense probably damaging 1.00
R4891:Or13j1 UTSW 4 43,706,194 (GRCm39) missense probably damaging 0.99
R5049:Or13j1 UTSW 4 43,706,259 (GRCm39) missense probably damaging 1.00
R5151:Or13j1 UTSW 4 43,706,518 (GRCm39) missense probably damaging 0.99
R5491:Or13j1 UTSW 4 43,705,990 (GRCm39) missense probably damaging 1.00
R5521:Or13j1 UTSW 4 43,705,788 (GRCm39) missense possibly damaging 0.88
R6225:Or13j1 UTSW 4 43,705,698 (GRCm39) missense probably damaging 1.00
R6518:Or13j1 UTSW 4 43,706,334 (GRCm39) missense probably benign 0.05
R6883:Or13j1 UTSW 4 43,705,723 (GRCm39) missense possibly damaging 0.93
R7185:Or13j1 UTSW 4 43,706,082 (GRCm39) missense possibly damaging 0.82
R7339:Or13j1 UTSW 4 43,706,080 (GRCm39) missense probably benign 0.05
R7502:Or13j1 UTSW 4 43,706,316 (GRCm39) missense probably damaging 0.97
R8052:Or13j1 UTSW 4 43,705,884 (GRCm39) missense probably damaging 0.97
R8797:Or13j1 UTSW 4 43,706,455 (GRCm39) missense probably damaging 1.00
X0017:Or13j1 UTSW 4 43,705,990 (GRCm39) missense probably damaging 1.00
X0021:Or13j1 UTSW 4 43,706,326 (GRCm39) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- TAGGCTGATCCACATAACAAGGG -3'
(R):5'- TGAAGCTGACCTGTGGTGAC -3'

Sequencing Primer
(F):5'- TACCCATGCAGAGCCCTG -3'
(R):5'- TGACACCTCAGTCAGCGATG -3'
Posted On 2022-10-06