Incidental Mutation 'R3079:Or51a7'
ID 265333
Institutional Source Beutler Lab
Gene Symbol Or51a7
Ensembl Gene ENSMUSG00000073962
Gene Name olfactory receptor family 51 subfamily A member 7
Synonyms GA_x6K02T2PBJ9-5676385-5677371, MOR8-5, Olfr576
MMRRC Submission 040569-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.198) question?
Stock # R3079 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 102614309-102615247 bp(+) (GRCm39)
Type of Mutation splice site (5 bp from exon)
DNA Base Change (assembly) C to T at 102622254 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000059586 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000051505] [ENSMUST00000098213] [ENSMUST00000185326] [ENSMUST00000214080] [ENSMUST00000215237]
AlphaFold A0A0G2JFH3
Predicted Effect probably null
Transcript: ENSMUST00000051505
SMART Domains Protein: ENSMUSP00000059586
Gene: ENSMUSG00000043354

DomainStartEndE-ValueType
Pfam:7tm_4 34 312 3.3e-140 PFAM
Pfam:7TM_GPCR_Srsx 38 310 1.2e-6 PFAM
Pfam:7tm_1 44 295 7.5e-22 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000098213
SMART Domains Protein: ENSMUSP00000143172
Gene: ENSMUSG00000073962

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 35 301 6.2e-12 PFAM
Pfam:7tm_1 41 291 2.5e-29 PFAM
Pfam:7tm_4 140 284 3.1e-28 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000185326
SMART Domains Protein: ENSMUSP00000142459
Gene: ENSMUSG00000073962

DomainStartEndE-ValueType
Pfam:7TM_GPCR_Srsx 35 300 9.7e-12 PFAM
Pfam:7tm_1 41 291 1.8e-29 PFAM
Pfam:7tm_4 140 284 2.6e-28 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000214080
Predicted Effect probably benign
Transcript: ENSMUST00000215237
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.0%
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: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aaas A T 15: 102,248,879 (GRCm39) L168H probably damaging Het
Abca15 T C 7: 119,984,392 (GRCm39) W1158R probably damaging Het
Anks4b A T 7: 119,781,146 (GRCm39) D59V probably damaging Het
Aqp11 A T 7: 97,386,795 (GRCm39) C134S probably benign Het
Arhgap35 A G 7: 16,296,501 (GRCm39) Y855H probably damaging Het
Ces1c A C 8: 93,846,975 (GRCm39) L93R probably damaging Het
Cit A G 5: 116,063,545 (GRCm39) D462G probably damaging Het
Col6a6 T C 9: 105,631,422 (GRCm39) R1494G probably benign Het
Edc4 T C 8: 106,611,750 (GRCm39) S109P possibly damaging Het
Elp4 T C 2: 105,639,790 (GRCm39) K130E possibly damaging Het
Gemin5 A T 11: 58,036,345 (GRCm39) V666E probably damaging Het
Hba-x A G 11: 32,227,616 (GRCm39) D62G probably damaging Het
Hnrnpul1 A T 7: 25,432,540 (GRCm39) Y474* probably null Het
Ighv5-6 T A 12: 113,589,237 (GRCm39) D81V probably damaging Het
Krt1 C T 15: 101,754,622 (GRCm39) G543S unknown Het
Mbtps1 A G 8: 120,257,944 (GRCm39) V431A probably benign Het
Mbtps1 T C 8: 120,265,602 (GRCm39) D315G probably damaging Het
Mrc2 T C 11: 105,227,539 (GRCm39) S591P probably damaging Het
Msh5 T C 17: 35,265,208 (GRCm39) E48G probably benign Het
Mybpc2 T C 7: 44,155,505 (GRCm39) D916G probably damaging Het
Nebl A G 2: 17,381,462 (GRCm39) V738A possibly damaging Het
Nlrp1b T C 11: 71,108,794 (GRCm39) R236G probably benign Het
Obsl1 G T 1: 75,467,467 (GRCm39) R1436S probably damaging Het
Or14j4 T C 17: 37,921,169 (GRCm39) T158A probably benign Het
Padi2 T C 4: 140,677,189 (GRCm39) V659A probably damaging Het
Pnpla6 T G 8: 3,591,512 (GRCm39) S1169A probably benign Het
Pramel30 T G 4: 144,058,098 (GRCm39) L235R probably damaging Het
Prl6a1 A G 13: 27,502,983 (GRCm39) D193G possibly damaging Het
Rce1 G T 19: 4,674,750 (GRCm39) C138* probably null Het
Shoc1 G T 4: 59,047,848 (GRCm39) T1257N possibly damaging Het
Shroom3 G T 5: 93,090,945 (GRCm39) V1151F probably damaging Het
Skint2 A G 4: 112,496,870 (GRCm39) T259A probably benign Het
Slc66a1 G T 4: 139,033,829 (GRCm39) A30D probably damaging Het
Slco5a1 C T 1: 12,949,486 (GRCm39) G635S probably damaging Het
Slfn1 T C 11: 83,011,986 (GRCm39) V34A probably benign Het
Syt4 A G 18: 31,574,738 (GRCm39) V293A probably benign Het
Trh T C 6: 92,219,551 (GRCm39) E255G possibly damaging Het
Ube4a G T 9: 44,871,371 (GRCm39) N9K probably damaging Het
Uck1 A T 2: 32,148,089 (GRCm39) probably benign Het
Vmn1r222 A G 13: 23,416,631 (GRCm39) M194T possibly damaging Het
Vmn2r91 T G 17: 18,355,973 (GRCm39) probably null Het
Wbp2 C T 11: 115,970,534 (GRCm39) probably null Het
Zdbf2 A G 1: 63,346,636 (GRCm39) I1672V probably benign Het
Other mutations in Or51a7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01112:Or51a7 APN 7 102,615,235 (GRCm39) splice site probably benign
IGL01695:Or51a7 APN 7 102,614,790 (GRCm39) missense probably damaging 0.97
IGL01707:Or51a7 APN 7 102,615,126 (GRCm39) missense probably damaging 0.97
IGL02637:Or51a7 APN 7 102,622,250 (GRCm39) utr 3 prime probably benign
R1636:Or51a7 UTSW 7 102,614,898 (GRCm39) missense possibly damaging 0.94
R3077:Or51a7 UTSW 7 102,615,223 (GRCm39) missense probably benign 0.06
R3803:Or51a7 UTSW 7 102,615,228 (GRCm39) critical splice donor site probably null
R4342:Or51a7 UTSW 7 102,615,231 (GRCm39) missense probably benign 0.03
R4866:Or51a7 UTSW 7 102,614,927 (GRCm39) missense probably benign 0.01
R5193:Or51a7 UTSW 7 102,615,143 (GRCm39) missense possibly damaging 0.52
R5194:Or51a7 UTSW 7 102,615,071 (GRCm39) missense probably benign 0.01
R9002:Or51a7 UTSW 7 102,614,618 (GRCm39) missense probably damaging 1.00
R9590:Or51a7 UTSW 7 102,614,553 (GRCm39) missense probably benign 0.07
Predicted Primers PCR Primer
(F):5'- GGATCATCTATATTTCTGCTGCCATG -3'
(R):5'- ATACATGCGTTTCACACATCTCTG -3'

Sequencing Primer
(F):5'- CTCCATATCCTCCTGTAAAAGG -3'
(R):5'- CTATACTCCCATGATAGGATTGTCTG -3'
Posted On 2015-02-05