Incidental Mutation 'R9161:Or51a10'
ID 731269
Institutional Source Beutler Lab
Gene Symbol Or51a10
Ensembl Gene ENSMUSG00000049797
Gene Name olfactory receptor family 51 subfamily A member 10
Synonyms MOR13-6, GA_x6K02T2PBJ9-6784380-6783436, Olfr642
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.077) question?
Stock # R9161 (G1)
Quality Score 63.0073
Status Validated
Chromosome 7
Chromosomal Location 103698615-103699559 bp(-) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) C to A at 103699725 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000148961 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000052660] [ENSMUST00000074064] [ENSMUST00000138055] [ENSMUST00000214299]
AlphaFold Q924X8
Predicted Effect probably benign
Transcript: ENSMUST00000052660
SMART Domains Protein: ENSMUSP00000061462
Gene: ENSMUSG00000049797

DomainStartEndE-ValueType
Pfam:7tm_4 33 312 8.5e-119 PFAM
Pfam:7TM_GPCR_Srsx 37 309 1.7e-7 PFAM
Pfam:7tm_1 43 294 4.1e-23 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000074064
SMART Domains Protein: ENSMUSP00000073707
Gene: ENSMUSG00000090219

DomainStartEndE-ValueType
Pfam:7tm_4 33 312 2.6e-124 PFAM
Pfam:7TM_GPCR_Srsx 37 255 3.1e-7 PFAM
Pfam:7tm_1 43 294 3.2e-21 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000138055
SMART Domains Protein: ENSMUSP00000139240
Gene: ENSMUSG00000109824

DomainStartEndE-ValueType
transmembrane domain 29 51 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000214299
Meta Mutation Damage Score 0.0846 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.2%
Validation Efficiency 98% (58/59)
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: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adprhl1 T A 8: 13,272,270 (GRCm39) N1496I probably damaging Het
Arglu1 T C 8: 8,733,941 (GRCm39) E125G possibly damaging Het
Atad2 A T 15: 57,989,185 (GRCm39) I225N possibly damaging Het
Atrn T C 2: 130,777,470 (GRCm39) F173S probably damaging Het
BC024063 T A 10: 81,945,044 (GRCm39) H221Q probably benign Het
Bnip5 T A 17: 29,128,387 (GRCm39) K175N probably damaging Het
Btbd16 C T 7: 130,417,516 (GRCm39) R344C probably damaging Het
Cdh24 A T 14: 54,876,097 (GRCm39) Y182N probably damaging Het
Cdkl4 A G 17: 80,851,120 (GRCm39) L194P probably damaging Het
Cep152 T A 2: 125,408,574 (GRCm39) R1327* probably null Het
Ckap5 A T 2: 91,445,653 (GRCm39) M1797L probably benign Het
Clasp1 A T 1: 118,474,651 (GRCm39) N895I probably damaging Het
Col15a1 G C 4: 47,288,200 (GRCm39) probably benign Het
Cotl1 G T 8: 120,549,456 (GRCm39) D85E probably benign Het
Cryba4 A C 5: 112,396,039 (GRCm39) probably null Het
Dync1h1 A G 12: 110,625,023 (GRCm39) K3817E probably benign Het
Ehd3 A T 17: 74,134,480 (GRCm39) R280* probably null Het
Erp29 T C 5: 121,583,146 (GRCm39) E260G possibly damaging Het
Fam135b T A 15: 71,334,417 (GRCm39) R926W possibly damaging Het
Fbn1 T C 2: 125,192,270 (GRCm39) N1413S probably damaging Het
Fbxw8 A G 5: 118,251,727 (GRCm39) V262A probably damaging Het
Gabrb1 A G 5: 72,187,199 (GRCm39) D164G probably damaging Het
Galnt15 T A 14: 31,780,116 (GRCm39) I471N probably damaging Het
Get1 A T 16: 95,953,139 (GRCm39) R77W probably damaging Het
Gon4l A G 3: 88,808,955 (GRCm39) N1733S probably damaging Het
Hmcn2 A G 2: 31,242,758 (GRCm39) T562A probably benign Het
Inha A G 1: 75,484,144 (GRCm39) I85V probably damaging Het
Kif28 A C 1: 179,526,244 (GRCm39) V897G probably benign Het
Map1s G A 8: 71,366,250 (GRCm39) R385H probably damaging Het
Map2 T C 1: 66,477,503 (GRCm39) V1750A possibly damaging Het
Mbd1 C T 18: 74,407,792 (GRCm39) P273L probably benign Het
Megf6 A G 4: 154,352,172 (GRCm39) T1226A probably benign Het
Muc5ac T A 7: 141,353,026 (GRCm39) C791S possibly damaging Het
Nlrc5 A C 8: 95,213,274 (GRCm39) H883P probably damaging Het
Nrip3 C T 7: 109,365,777 (GRCm39) R91H probably damaging Het
Or10w1 G A 19: 13,632,038 (GRCm39) V82M probably damaging Het
Or12j3 C T 7: 139,952,989 (GRCm39) C178Y probably damaging Het
Or8g21 A T 9: 38,905,816 (GRCm39) I305K possibly damaging Het
Or8k16 A G 2: 85,520,231 (GRCm39) T153A probably benign Het
Pdgfrb T G 18: 61,197,053 (GRCm39) L163R probably damaging Het
Pik3ip1 G T 11: 3,281,945 (GRCm39) R34L possibly damaging Het
Pip4k2b A G 11: 97,615,245 (GRCm39) F205S possibly damaging Het
Pttg1ip A C 10: 77,425,487 (GRCm39) N60T probably benign Het
Rab3ip C T 10: 116,750,066 (GRCm39) E356K probably damaging Het
Rai1 A G 11: 60,076,682 (GRCm39) N249D probably benign Het
Rd3l T C 12: 111,946,753 (GRCm39) K8E probably damaging Het
Rnf32 A G 5: 29,408,058 (GRCm39) K96E probably damaging Het
Rsf1 GGCG GGCGACCGCCGCG 7: 97,229,113 (GRCm39) probably benign Het
Slc4a1ap A G 5: 31,685,474 (GRCm39) K251E Het
Spink5 T A 18: 44,147,986 (GRCm39) N875K probably damaging Het
Taf6 G T 5: 138,178,160 (GRCm39) A447D probably benign Het
Tbxas1 A T 6: 38,999,989 (GRCm39) I259F probably damaging Het
Tcap G T 11: 98,275,256 (GRCm39) R130L probably damaging Het
Tyms T C 5: 30,266,040 (GRCm39) E293G Het
Vmn1r20 C A 6: 57,408,759 (GRCm39) F28L probably benign Het
Vmn2r120 A T 17: 57,831,864 (GRCm39) D308E Het
Vmn2r69 T A 7: 85,056,177 (GRCm39) I654F possibly damaging Het
Zfp990 G T 4: 145,261,509 (GRCm39) V52L possibly damaging Het
Other mutations in Or51a10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01457:Or51a10 APN 7 103,699,376 (GRCm39) missense probably damaging 1.00
IGL01933:Or51a10 APN 7 103,699,021 (GRCm39) missense probably damaging 1.00
IGL01980:Or51a10 APN 7 103,699,300 (GRCm39) missense probably benign 0.21
IGL02161:Or51a10 APN 7 103,698,797 (GRCm39) missense possibly damaging 0.66
IGL02639:Or51a10 APN 7 103,698,988 (GRCm39) missense probably damaging 0.99
I2289:Or51a10 UTSW 7 103,698,961 (GRCm39) missense probably damaging 1.00
R0418:Or51a10 UTSW 7 103,698,979 (GRCm39) missense probably benign 0.00
R1647:Or51a10 UTSW 7 103,699,376 (GRCm39) missense probably damaging 1.00
R1648:Or51a10 UTSW 7 103,699,376 (GRCm39) missense probably damaging 1.00
R1701:Or51a10 UTSW 7 103,699,402 (GRCm39) missense possibly damaging 0.95
R2142:Or51a10 UTSW 7 103,699,507 (GRCm39) missense probably damaging 1.00
R2165:Or51a10 UTSW 7 103,698,845 (GRCm39) missense probably benign 0.22
R2655:Or51a10 UTSW 7 103,698,638 (GRCm39) missense probably benign 0.03
R6216:Or51a10 UTSW 7 103,698,902 (GRCm39) missense probably damaging 1.00
R6759:Or51a10 UTSW 7 103,699,334 (GRCm39) missense probably damaging 1.00
R6925:Or51a10 UTSW 7 103,698,947 (GRCm39) missense probably benign 0.16
R7243:Or51a10 UTSW 7 103,698,962 (GRCm39) missense probably damaging 1.00
R7684:Or51a10 UTSW 7 103,698,667 (GRCm39) missense probably damaging 0.99
R7699:Or51a10 UTSW 7 103,699,800 (GRCm39) start gained probably benign
R8316:Or51a10 UTSW 7 103,698,829 (GRCm39) missense probably damaging 1.00
R8458:Or51a10 UTSW 7 103,698,875 (GRCm39) missense possibly damaging 0.93
R8836:Or51a10 UTSW 7 103,699,055 (GRCm39) missense probably benign 0.07
R9519:Or51a10 UTSW 7 103,698,636 (GRCm39) missense probably benign 0.00
Z1176:Or51a10 UTSW 7 103,699,480 (GRCm39) missense probably benign
Predicted Primers PCR Primer
(F):5'- CAAGGTTCTCATGAGGGTTGC -3'
(R):5'- CATAGGAGAGAGTAAATCAGCTTCAAC -3'

Sequencing Primer
(F):5'- CTCATGAGGGTTGCTGAGGAGC -3'
(R):5'- GAAAGGCCAGATTATACAGAT -3'
Posted On 2022-10-10