Incidental Mutation 'R5784:Or13g1'
ID 447917
Institutional Source Beutler Lab
Gene Symbol Or13g1
Ensembl Gene ENSMUSG00000054054
Gene Name olfactory receptor family 13 subfamily G member 1
Synonyms MOR251-4P, GA_x6K02T2NHDJ-9801340-9802266, Olfr309
MMRRC Submission 043381-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.071) question?
Stock # R5784 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 85955393-85956319 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 85955743 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Asparagine to Aspartic acid at position 193 (N193D)
Ref Sequence ENSEMBL: ENSMUSP00000134377 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000055690] [ENSMUST00000174158]
AlphaFold Q7TS01
Predicted Effect probably damaging
Transcript: ENSMUST00000055690
AA Change: N193D

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000061929
Gene: ENSMUSG00000054054
AA Change: N193D

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 33 303 4.5e-11 PFAM
Pfam:7tm_1 39 288 1.5e-26 PFAM
Pfam:7tm_4 137 281 7.9e-44 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000174158
AA Change: N193D

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000134377
Gene: ENSMUSG00000054054
AA Change: N193D

DomainStartEndE-ValueType
Pfam:7tm_4 29 305 1.6e-55 PFAM
Pfam:7TM_GPCR_Srsx 33 303 4.5e-11 PFAM
Pfam:7tm_1 39 288 2.4e-18 PFAM
Meta Mutation Damage Score 0.3268 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.8%
  • 10x: 97.5%
  • 20x: 95.8%
Validation Efficiency 98% (51/52)
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: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2610008E11Rik T C 10: 78,903,441 (GRCm39) R292G possibly damaging Het
4932416K20Rik T A 8: 105,524,261 (GRCm39) noncoding transcript Het
Aox3 A G 1: 58,192,658 (GRCm39) D544G probably benign Het
Atg2a C A 19: 6,311,535 (GRCm39) A1830D probably damaging Het
Casp1 T C 9: 5,299,337 (GRCm39) I22T probably damaging Het
Ccdc141 A C 2: 76,859,671 (GRCm39) L990W probably damaging Het
Cnbd2 A G 2: 156,180,577 (GRCm39) T125A probably damaging Het
Cnep1r1 T A 8: 88,857,354 (GRCm39) probably benign Het
Dhx38 G T 8: 110,286,245 (GRCm39) Y348* probably null Het
Dnah7c A T 1: 46,563,228 (GRCm39) I593L possibly damaging Het
Dpep3 T C 8: 106,705,375 (GRCm39) D125G probably benign Het
Eif1ad10 T A 12: 88,216,525 (GRCm39) N116Y probably damaging Het
Epb41l4b A C 4: 57,086,003 (GRCm39) S191A probably damaging Het
Etl4 A G 2: 20,811,016 (GRCm39) Y1033C possibly damaging Het
Fam193a T C 5: 34,623,567 (GRCm39) L32P probably damaging Het
Grin2c T C 11: 115,149,121 (GRCm39) E159G possibly damaging Het
Gtf2h3 C T 5: 124,722,360 (GRCm39) T121I probably benign Het
Hdhd2 A T 18: 77,054,841 (GRCm39) D205V probably damaging Het
Helz T A 11: 107,561,307 (GRCm39) N774K unknown Het
Idh3b A G 2: 130,121,591 (GRCm39) V71A probably damaging Het
Lars1 T C 18: 42,352,964 (GRCm39) M818V probably benign Het
Ltbp2 A G 12: 84,915,513 (GRCm39) V162A probably damaging Het
Ltk G A 2: 119,584,840 (GRCm39) Q136* probably null Het
Mafb A T 2: 160,208,461 (GRCm39) C46S probably damaging Het
Map1s T C 8: 71,367,002 (GRCm39) S636P probably damaging Het
Map3k13 A G 16: 21,717,391 (GRCm39) K209E possibly damaging Het
Mppe1 T C 18: 67,361,098 (GRCm39) N220D probably benign Het
Mydgf T C 17: 56,485,254 (GRCm39) probably benign Het
Myh6 T C 14: 55,190,521 (GRCm39) K999E possibly damaging Het
Nemp1 T A 10: 127,513,067 (GRCm39) V34D possibly damaging Het
Npr2 A G 4: 43,632,801 (GRCm39) E206G probably benign Het
Or10x4 G A 1: 174,218,965 (GRCm39) C110Y probably damaging Het
Or9q2 A T 19: 13,772,710 (GRCm39) H88Q probably benign Het
Papln A G 12: 83,828,754 (GRCm39) N820S probably benign Het
Pcdh10 T G 3: 45,335,075 (GRCm39) F463C probably damaging Het
Pde7a A G 3: 19,319,009 (GRCm39) V12A probably benign Het
Radil G T 5: 142,473,268 (GRCm39) H804Q possibly damaging Het
Rbfox1 A T 16: 7,042,203 (GRCm39) D39V probably damaging Het
Rims2 T G 15: 39,399,383 (GRCm39) probably null Het
Rnf121 A G 7: 101,684,583 (GRCm39) F110S probably benign Het
Saxo2 C T 7: 82,284,082 (GRCm39) V259I probably benign Het
Slc22a30 G A 19: 8,321,757 (GRCm39) Q436* probably null Het
Slc2a3 A T 6: 122,712,376 (GRCm39) probably null Het
Traf2 A T 2: 25,429,049 (GRCm39) V6E probably benign Het
Trim43c A T 9: 88,729,696 (GRCm39) N379I probably benign Het
Ubr4 C G 4: 139,152,529 (GRCm39) C1973W probably damaging Het
Unc13a G T 8: 72,108,310 (GRCm39) D514E possibly damaging Het
Wdr27 T A 17: 15,146,495 (GRCm39) T167S probably damaging Het
Zfp174 A T 16: 3,672,438 (GRCm39) E329V probably benign Het
Zfp422 A T 6: 116,603,771 (GRCm39) I76N probably damaging Het
Other mutations in Or13g1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00886:Or13g1 APN 7 85,956,259 (GRCm39) missense probably damaging 1.00
R0370:Or13g1 UTSW 7 85,956,057 (GRCm39) missense probably benign 0.42
R1869:Or13g1 UTSW 7 85,955,875 (GRCm39) missense possibly damaging 0.96
R2047:Or13g1 UTSW 7 85,956,012 (GRCm39) missense probably damaging 1.00
R3939:Or13g1 UTSW 7 85,955,437 (GRCm39) missense probably benign 0.00
R4562:Or13g1 UTSW 7 85,956,360 (GRCm39) start gained probably benign
R4640:Or13g1 UTSW 7 85,956,274 (GRCm39) missense probably benign 0.01
R4811:Or13g1 UTSW 7 85,956,166 (GRCm39) missense probably benign 0.41
R4867:Or13g1 UTSW 7 85,955,491 (GRCm39) missense probably benign 0.00
R4954:Or13g1 UTSW 7 85,955,809 (GRCm39) missense probably benign 0.01
R6043:Or13g1 UTSW 7 85,955,547 (GRCm39) missense probably damaging 0.97
R6498:Or13g1 UTSW 7 85,956,226 (GRCm39) missense probably benign
R6849:Or13g1 UTSW 7 85,956,248 (GRCm39) missense possibly damaging 0.54
R7238:Or13g1 UTSW 7 85,955,799 (GRCm39) missense probably damaging 1.00
R7811:Or13g1 UTSW 7 85,955,554 (GRCm39) missense probably damaging 1.00
R7917:Or13g1 UTSW 7 85,955,686 (GRCm39) missense probably damaging 1.00
R8010:Or13g1 UTSW 7 85,956,260 (GRCm39) missense probably benign 0.24
R8271:Or13g1 UTSW 7 85,955,962 (GRCm39) missense probably benign 0.13
R9017:Or13g1 UTSW 7 85,955,957 (GRCm39) nonsense probably null
R9150:Or13g1 UTSW 7 85,955,942 (GRCm39) missense probably damaging 0.96
T0975:Or13g1 UTSW 7 85,955,492 (GRCm39) nonsense probably null
Predicted Primers PCR Primer
(F):5'- AGTAAAGGGACACCACCATG -3'
(R):5'- AATGGCCTATGACCGCTATGTG -3'

Sequencing Primer
(F):5'- GTAGAGAAGGCCTTCTTCT -3'
(R):5'- GACCGCTATGTGGCCATTTGC -3'
Posted On 2016-12-15