Incidental Mutation 'R6002:Or13c7d'
ID 478412
Institutional Source Beutler Lab
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
MMRRC Submission 044181-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # R6002 (G1)
Quality Score 225.009
Status Not validated
Chromosome 4
Chromosomal Location 43770050-43771009 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 43770063 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 316 (H316R)
Ref Sequence ENSEMBL: ENSMUSP00000060784 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053931]
AlphaFold Q9QZ19
Predicted Effect probably benign
Transcript: ENSMUST00000053931
AA Change: H316R

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000060784
Gene: ENSMUSG00000044801
AA Change: H316R

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
  • 1x: 99.8%
  • 3x: 99.4%
  • 10x: 96.6%
  • 20x: 88.5%
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: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4932414N04Rik T A 2: 68,492,768 (GRCm39) probably null Het
Adam28 A G 14: 68,879,511 (GRCm39) L179P probably benign Het
Amer2 G T 14: 60,616,231 (GRCm39) G142V possibly damaging Het
Ap2a1 A G 7: 44,553,819 (GRCm39) probably null Het
Arhgap32 A G 9: 32,168,275 (GRCm39) T753A probably benign Het
Capsl A G 15: 9,461,874 (GRCm39) D90G probably damaging Het
Cd96 A T 16: 45,938,349 (GRCm39) S39T possibly damaging Het
Cdx2 T A 5: 147,240,044 (GRCm39) T211S probably damaging Het
Chd9 A G 8: 91,705,515 (GRCm39) Y251C probably damaging Het
Chrna6 C T 8: 27,896,774 (GRCm39) V368I probably benign Het
Coro1a G T 7: 126,302,252 (GRCm39) Q32K probably benign Het
Cps1 T A 1: 67,211,914 (GRCm39) V694E possibly damaging Het
Eif3h A G 15: 51,662,672 (GRCm39) Y125H probably benign Het
Fbxw22 A C 9: 109,210,750 (GRCm39) Y420* probably null Het
Fgf21 T C 7: 45,264,651 (GRCm39) Y27C probably benign Het
Gm7356 A G 17: 14,221,001 (GRCm39) S343P probably benign Het
Hmcn2 A G 2: 31,310,321 (GRCm39) D3305G probably damaging Het
Ift70a1 T C 2: 75,811,121 (GRCm39) T321A possibly damaging Het
Kdm4c T A 4: 74,323,206 (GRCm39) F1046Y possibly damaging Het
Klk1b27 T A 7: 43,705,114 (GRCm39) W94R probably benign Het
Nwd2 A T 5: 63,962,143 (GRCm39) M576L probably benign Het
Or4d2 A T 11: 87,784,633 (GRCm39) V39E probably damaging Het
Or5b122 T C 19: 13,562,781 (GRCm39) probably benign Het
Or5p54 A G 7: 107,554,376 (GRCm39) H176R probably damaging Het
Pappa T A 4: 65,215,645 (GRCm39) V1184D probably damaging Het
Pcyox1 T A 6: 86,369,164 (GRCm39) M152L probably benign Het
Pdha2 A G 3: 140,917,457 (GRCm39) V17A probably benign Het
Pi4k2b A T 5: 52,914,247 (GRCm39) I328L probably benign Het
Ppp1r13l T C 7: 19,111,895 (GRCm39) F814L probably benign Het
Prag1 A T 8: 36,571,337 (GRCm39) H640L probably benign Het
Prl5a1 T C 13: 28,329,465 (GRCm39) I48T probably benign Het
Rabgap1 A G 2: 37,363,614 (GRCm39) T132A probably benign Het
Sec31b T C 19: 44,524,203 (GRCm39) I146V probably benign Het
Slc30a9 A G 5: 67,499,460 (GRCm39) Y306C probably damaging Het
Stat3 A G 11: 100,794,569 (GRCm39) S247P probably benign Het
Tbc1d1 C A 5: 64,490,776 (GRCm39) L747I probably damaging Het
Tbc1d24 A T 17: 24,402,761 (GRCm39) M1K probably null Het
Vezt A C 10: 93,836,336 (GRCm39) V104G probably damaging Het
Zbtb41 A G 1: 139,351,397 (GRCm39) D170G probably damaging Het
Zswim2 C A 2: 83,746,032 (GRCm39) D469Y probably damaging Het
Other mutations in Or13c7d
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01401:Or13c7d APN 4 43,770,112 (GRCm39) missense probably damaging 1.00
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
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
Predicted Primers PCR Primer
(F):5'- GGAGAATTACCTATTCATACAGAGCTC -3'
(R):5'- CCATCCTGTTCATGTACGGG -3'

Sequencing Primer
(F):5'- AAACTTGTGTCTGATCCCTGGAAC -3'
(R):5'- GTTCATGTACGGGAAGCCCAAATC -3'
Posted On 2017-06-26