Incidental Mutation 'R0650:Or51q1c'
ID 261993
Institutional Source Beutler Lab
Gene Symbol Or51q1c
Ensembl Gene ENSMUSG00000094063
Gene Name olfactory receptor family 51 subfamily Q member 1C
Synonyms Olfr638, MOR5-1, GA_x6K02T2PBJ9-6737723-6738670
MMRRC Submission 038835-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.175) question?
Stock # R0650 (G1)
Quality Score 165
Status Not validated
Chromosome 7
Chromosomal Location 103652466-103653431 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 103652446 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000151996 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000138055] [ENSMUST00000209757] [ENSMUST00000215653] [ENSMUST00000218325]
AlphaFold Q8VH20
Predicted Effect probably null
Transcript: ENSMUST00000098184
SMART Domains Protein: ENSMUSP00000095786
Gene: ENSMUSG00000094063

DomainStartEndE-ValueType
Pfam:7tm_4 39 318 2.6e-119 PFAM
Pfam:7TM_GPCR_Srsx 43 198 9.8e-10 PFAM
Pfam:7tm_1 49 300 7.8e-19 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 null
Transcript: ENSMUST00000209757
Predicted Effect probably benign
Transcript: ENSMUST00000215653
Predicted Effect probably null
Transcript: ENSMUST00000218325
Coding Region Coverage
  • 1x: 99.5%
  • 3x: 99.0%
  • 10x: 97.8%
  • 20x: 96.0%
Validation Efficiency 99% (77/78)
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: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700020N15Rik A G X: 68,989,391 (GRCm39) S96G unknown Het
4930447C04Rik T C 12: 72,956,830 (GRCm39) D120G probably damaging Het
Actmap A T 7: 26,902,072 (GRCm39) H233L probably damaging Het
Adgrg5 T A 8: 95,660,785 (GRCm39) probably null Het
Afg3l2 G T 18: 67,548,627 (GRCm39) H534Q possibly damaging Het
Ankar G A 1: 72,695,380 (GRCm39) probably benign Het
Arid2 T A 15: 96,299,930 (GRCm39) F1814L possibly damaging Het
Asb15 C T 6: 24,566,163 (GRCm39) A372V probably damaging Het
Atg16l1 A T 1: 87,709,421 (GRCm39) D403V possibly damaging Het
Bnc2 T C 4: 84,211,433 (GRCm39) D407G probably benign Het
Ccdc121 T C 5: 31,643,312 (GRCm39) probably benign Het
Cdan1 A G 2: 120,556,526 (GRCm39) V633A probably benign Het
Cfap46 T C 7: 139,185,571 (GRCm39) Y2482C unknown Het
Chd8 T C 14: 52,439,761 (GRCm39) E964G probably benign Het
Cyp2s1 A G 7: 25,508,683 (GRCm39) V253A probably damaging Het
Depdc1b A G 13: 108,460,443 (GRCm39) N18D probably damaging Het
Fis1 T A 5: 136,991,048 (GRCm39) V4E probably damaging Het
Gba2 T A 4: 43,570,424 (GRCm39) probably null Het
Gm2381 C T 7: 42,469,504 (GRCm39) G207R probably damaging Het
Gpr89 T A 3: 96,804,640 (GRCm39) probably benign Het
Gtf2i A G 5: 134,290,691 (GRCm39) probably benign Het
Herc2 T G 7: 55,762,958 (GRCm39) S896A probably damaging Het
Huwe1 T C X: 150,659,309 (GRCm39) S921P probably damaging Het
Iqgap1 T A 7: 80,386,143 (GRCm39) K936I probably damaging Het
Kcna4 T A 2: 107,125,927 (GRCm39) Y220* probably null Het
Krt18 A G 15: 101,937,920 (GRCm39) D139G possibly damaging Het
Krt87 T C 15: 101,384,921 (GRCm39) N392D probably damaging Het
L3mbtl4 G A 17: 69,081,286 (GRCm39) C558Y probably damaging Het
Lamc2 T A 1: 153,019,622 (GRCm39) I440F possibly damaging Het
Lrrc28 T C 7: 67,267,833 (GRCm39) N98S probably damaging Het
Lrrk1 G A 7: 65,942,084 (GRCm39) A718V probably damaging Het
Mrgprx2 T C 7: 48,132,666 (GRCm39) I51V probably damaging Het
Myt1 A T 2: 181,424,408 (GRCm39) R25* probably null Het
Npdc1 C T 2: 25,298,021 (GRCm39) T199I probably benign Het
Nup98 T A 7: 101,801,660 (GRCm39) Y755F probably damaging Het
Or5p69 T A 7: 107,966,996 (GRCm39) C100S probably damaging Het
Or5p76 G T 7: 108,122,289 (GRCm39) N289K probably damaging Het
Or8g22 T A 9: 38,957,996 (GRCm39) M240L probably benign Het
Osgin1 A T 8: 120,172,211 (GRCm39) Y335F probably damaging Het
Pde10a A T 17: 9,161,797 (GRCm39) I493F probably damaging Het
Pdgfrb A G 18: 61,212,780 (GRCm39) I895V probably benign Het
Peg10 T TCCCCANNANNNN 6: 4,756,475 (GRCm39) probably benign Het
Pidd1 A T 7: 141,020,726 (GRCm39) L457* probably null Het
Pik3c2a A G 7: 115,945,482 (GRCm39) probably benign Het
Pkd1l3 C G 8: 110,350,281 (GRCm39) D375E possibly damaging Het
Plcg1 C T 2: 160,595,283 (GRCm39) probably benign Het
Prr13 A C 15: 102,370,650 (GRCm39) *138C probably null Het
Prrc2b T C 2: 32,119,267 (GRCm39) probably benign Het
Psph T C 5: 129,868,633 (GRCm39) probably benign Het
Ripor1 A G 8: 106,344,746 (GRCm39) probably benign Het
Scg3 A G 9: 75,576,617 (GRCm39) S253P probably damaging Het
Sema6a G A 18: 47,423,112 (GRCm39) probably null Het
Sgk1 A G 10: 21,758,556 (GRCm39) N7D probably damaging Het
Skor2 T C 18: 76,964,255 (GRCm39) F940L probably benign Het
Slbp T C 5: 33,802,833 (GRCm39) probably benign Het
Snrnp40 C G 4: 130,271,836 (GRCm39) probably null Het
Susd5 A T 9: 113,911,603 (GRCm39) H171L possibly damaging Het
Sybu T C 15: 44,536,664 (GRCm39) E354G probably benign Het
Synpo T C 18: 60,735,412 (GRCm39) N845D possibly damaging Het
Tdrd6 A T 17: 43,939,050 (GRCm39) I666N probably damaging Het
Tm9sf4 T C 2: 153,029,285 (GRCm39) I111T probably benign Het
Tnc T C 4: 63,926,971 (GRCm39) T852A probably benign Het
Tnfrsf10b T A 14: 70,013,625 (GRCm39) I185K probably damaging Het
Tnks1bp1 A G 2: 84,892,974 (GRCm39) E305G possibly damaging Het
Tnrc6b T C 15: 80,668,959 (GRCm39) V22A probably benign Het
Ttn A T 2: 76,598,956 (GRCm39) F19319Y probably damaging Het
Ubr5 T C 15: 38,031,051 (GRCm39) probably benign Het
Ugt2b5 T A 5: 87,287,627 (GRCm39) Q191L probably benign Het
Urod T C 4: 116,848,473 (GRCm39) T300A probably benign Het
Vmn1r213 A G 13: 23,195,564 (GRCm39) probably benign Het
Znfx1 G A 2: 166,889,574 (GRCm39) Q723* probably null Het
Other mutations in Or51q1c
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01412:Or51q1c APN 7 103,652,842 (GRCm39) missense probably damaging 1.00
IGL01901:Or51q1c APN 7 103,653,274 (GRCm39) missense probably damaging 1.00
IGL02040:Or51q1c APN 7 103,652,614 (GRCm39) missense probably damaging 1.00
IGL02756:Or51q1c APN 7 103,652,866 (GRCm39) missense probably damaging 1.00
R0122:Or51q1c UTSW 7 103,652,565 (GRCm39) missense probably damaging 1.00
R0137:Or51q1c UTSW 7 103,652,709 (GRCm39) missense probably benign 0.13
R0312:Or51q1c UTSW 7 103,653,232 (GRCm39) missense probably damaging 1.00
R0652:Or51q1c UTSW 7 103,652,446 (GRCm39) splice site probably null
R1382:Or51q1c UTSW 7 103,652,927 (GRCm39) missense probably benign 0.01
R1700:Or51q1c UTSW 7 103,653,329 (GRCm39) nonsense probably null
R1723:Or51q1c UTSW 7 103,652,518 (GRCm39) missense probably damaging 0.97
R1745:Or51q1c UTSW 7 103,653,270 (GRCm39) missense probably benign 0.02
R1840:Or51q1c UTSW 7 103,653,324 (GRCm39) missense probably benign 0.00
R3408:Or51q1c UTSW 7 103,652,550 (GRCm39) nonsense probably null
R3413:Or51q1c UTSW 7 103,653,039 (GRCm39) missense probably damaging 0.99
R4441:Or51q1c UTSW 7 103,653,279 (GRCm39) missense probably damaging 1.00
R4727:Or51q1c UTSW 7 103,653,097 (GRCm39) missense probably benign 0.00
R5096:Or51q1c UTSW 7 103,652,667 (GRCm39) missense probably benign 0.08
R5851:Or51q1c UTSW 7 103,652,659 (GRCm39) missense probably benign 0.13
R6133:Or51q1c UTSW 7 103,652,532 (GRCm39) missense possibly damaging 0.58
R6529:Or51q1c UTSW 7 103,653,133 (GRCm39) missense probably benign 0.06
R6572:Or51q1c UTSW 7 103,648,391 (GRCm39) splice site probably null
R6799:Or51q1c UTSW 7 103,648,006 (GRCm39) critical splice donor site probably null
R7267:Or51q1c UTSW 7 103,653,046 (GRCm39) missense probably benign
R9140:Or51q1c UTSW 7 103,653,322 (GRCm39) missense probably damaging 1.00
X0018:Or51q1c UTSW 7 103,652,638 (GRCm39) missense probably benign
X0063:Or51q1c UTSW 7 103,652,734 (GRCm39) missense probably damaging 0.99
Predicted Primers
Posted On 2015-02-04