Incidental Mutation 'IGL01401:Or13c7d'
ID 79628
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or13c7d
Ensembl Gene ENSMUSG00000044801
Gene Name olfactory receptor family 13 subfamily C member 7D
Synonyms mOR37e, MOR262-5, Olfr37e, GA_x6K02T2N78B-16165641-16166600, Olfr159
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # IGL01401
Quality Score
Status
Chromosome 4
Chromosomal Location 43770050-43771009 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 43770112 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Glycine at position 300 (R300G)
Ref Sequence ENSEMBL: ENSMUSP00000060784 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053931]
AlphaFold Q9QZ19
Predicted Effect probably damaging
Transcript: ENSMUST00000053931
AA Change: R300G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000060784
Gene: ENSMUSG00000044801
AA Change: R300G

DomainStartEndE-ValueType
Pfam:7tm_4 32 315 6.9e-60 PFAM
Pfam:7tm_1 42 297 2.4e-25 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000120783
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: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrl3 T C 5: 81,836,516 (GRCm39) V758A possibly damaging Het
Arf4 T C 14: 26,359,609 (GRCm39) L12P probably damaging Het
Bltp1 A G 3: 36,996,441 (GRCm39) N1051S probably benign Het
C4bp A T 1: 130,575,801 (GRCm39) V230E possibly damaging Het
Carm1 T A 9: 21,480,878 (GRCm39) probably null Het
Cd4 G A 6: 124,856,341 (GRCm39) T50I probably benign Het
Ceacam16 T C 7: 19,595,054 (GRCm39) Y8C probably benign Het
Ckap2l A T 2: 129,111,136 (GRCm39) V687E probably damaging Het
Dcaf4 A G 12: 83,588,148 (GRCm39) D449G probably damaging Het
Dhx38 T C 8: 110,278,746 (GRCm39) Y1113C probably benign Het
Fry A G 5: 150,362,253 (GRCm39) I161V probably benign Het
Gm17093 A C 14: 44,758,984 (GRCm39) M169L unknown Het
Gm20721 A G 2: 174,187,295 (GRCm39) D999G probably damaging Het
Grin2b T C 6: 135,713,361 (GRCm39) H840R probably damaging Het
Hoxc12 C A 15: 102,845,755 (GRCm39) H156Q probably benign Het
Htr3b T C 9: 48,858,934 (GRCm39) D68G probably damaging Het
Inpp5b T C 4: 124,639,880 (GRCm39) V99A probably damaging Het
Klhl42 C T 6: 147,009,241 (GRCm39) T360M probably benign Het
Lmo7 C T 14: 102,031,713 (GRCm39) R36* probably null Het
Lmod3 T G 6: 97,229,513 (GRCm39) N7T probably damaging Het
Malrd1 G A 2: 16,106,768 (GRCm39) probably null Het
Mthfd2l T A 5: 91,148,425 (GRCm39) I284K possibly damaging Het
Myo1e T A 9: 70,234,448 (GRCm39) I267N probably damaging Het
Or2y1g T A 11: 49,171,314 (GRCm39) V113E possibly damaging Het
Prkce T C 17: 86,476,268 (GRCm39) V83A probably damaging Het
Pxdn G T 12: 30,051,983 (GRCm39) C540F probably damaging Het
Resf1 A G 6: 149,228,394 (GRCm39) E480G probably damaging Het
Ryr2 T A 13: 11,606,238 (GRCm39) E4448V possibly damaging Het
Scn1a A T 2: 66,119,455 (GRCm39) N1349K probably damaging Het
Smarcc1 T C 9: 109,979,033 (GRCm39) I172T possibly damaging Het
Syt16 T C 12: 74,269,437 (GRCm39) V92A possibly damaging Het
Tenm4 A G 7: 96,523,474 (GRCm39) Y1672C probably damaging Het
Tmem131 A G 1: 36,838,468 (GRCm39) Y1486H probably damaging Het
Tmem132a A G 19: 10,838,888 (GRCm39) probably benign Het
Usp40 A T 1: 87,921,920 (GRCm39) D314E probably damaging Het
Vmn2r79 G A 7: 86,686,481 (GRCm39) V621I probably benign Het
Wnk4 A G 11: 101,167,509 (GRCm39) probably benign Het
Wwc1 C A 11: 35,789,445 (GRCm39) probably null Het
Other mutations in Or13c7d
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02701:Or13c7d APN 4 43,770,366 (GRCm39) missense probably benign 0.31
IGL02839:Or13c7d APN 4 43,770,943 (GRCm39) nonsense probably null
IGL02956:Or13c7d APN 4 43,770,399 (GRCm39) missense probably benign 0.15
IGL03058:Or13c7d APN 4 43,770,255 (GRCm39) missense probably damaging 1.00
R1164:Or13c7d UTSW 4 43,770,991 (GRCm39) missense probably benign 0.03
R1796:Or13c7d UTSW 4 43,770,495 (GRCm39) missense possibly damaging 0.90
R1812:Or13c7d UTSW 4 43,770,230 (GRCm39) nonsense probably null
R4906:Or13c7d UTSW 4 43,770,476 (GRCm39) missense possibly damaging 0.76
R5426:Or13c7d UTSW 4 43,770,168 (GRCm39) missense probably benign 0.04
R5684:Or13c7d UTSW 4 43,770,624 (GRCm39) missense probably benign 0.03
R6002:Or13c7d UTSW 4 43,770,063 (GRCm39) missense probably benign
R7174:Or13c7d UTSW 4 43,770,691 (GRCm39) missense not run
R7431:Or13c7d UTSW 4 43,770,882 (GRCm39) missense probably damaging 1.00
R8423:Or13c7d UTSW 4 43,770,598 (GRCm39) missense possibly damaging 0.65
R8770:Or13c7d UTSW 4 43,770,813 (GRCm39) missense probably damaging 1.00
R8789:Or13c7d UTSW 4 43,770,793 (GRCm39) missense probably damaging 0.96
R8989:Or13c7d UTSW 4 43,770,346 (GRCm39) missense possibly damaging 0.76
R9616:Or13c7d UTSW 4 43,770,193 (GRCm39) nonsense probably null
Z1176:Or13c7d UTSW 4 43,770,267 (GRCm39) missense probably damaging 1.00
Posted On 2013-11-05