Incidental Mutation 'R7147:Or52h7'
ID 553875
Institutional Source Beutler Lab
Gene Symbol Or52h7
Ensembl Gene ENSMUSG00000073927
Gene Name olfactory receptor family 52 subfamily H member 7
Synonyms MOR31-8, Olfr652, GA_x6K02T2PBJ9-7191524-7192471
MMRRC Submission 045224-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # R7147 (G1)
Quality Score 215.009
Status Not validated
Chromosome 7
Chromosomal Location 104213359-104214419 bp(+) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) A to G at 104213273 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000152027 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098175] [ENSMUST00000215410] [ENSMUST00000216131] [ENSMUST00000219111]
AlphaFold B9EHE6
Predicted Effect probably benign
Transcript: ENSMUST00000098175
SMART Domains Protein: ENSMUSP00000095777
Gene: ENSMUSG00000073927

DomainStartEndE-ValueType
transmembrane domain 7 25 N/A INTRINSIC
Pfam:7tm_4 36 315 2.6e-105 PFAM
Pfam:7TM_GPCR_Srsx 40 312 6.9e-9 PFAM
Pfam:7tm_1 46 297 4.7e-17 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000215410
Predicted Effect probably benign
Transcript: ENSMUST00000216131
Predicted Effect probably benign
Transcript: ENSMUST00000219111
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
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: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adcy4 C T 14: 56,017,182 (GRCm39) G303D probably damaging Het
Adgra3 C T 5: 50,118,587 (GRCm39) G987D probably damaging Het
Akap11 A G 14: 78,748,905 (GRCm39) S1161P Het
Ampd3 G A 7: 110,404,059 (GRCm39) E528K probably damaging Het
Arl8b G A 6: 108,791,976 (GRCm39) R79Q probably damaging Het
Atf4 AAGCGGGCTGAGC AAGC 15: 80,141,500 (GRCm39) probably benign Het
Cald1 A T 6: 34,723,231 (GRCm39) Q105L Het
Casd1 T C 6: 4,624,187 (GRCm39) Y327H probably benign Het
Chodl T A 16: 78,743,629 (GRCm39) C239S probably damaging Het
D130043K22Rik A T 13: 25,066,546 (GRCm39) H781L probably benign Het
Dlg1 A T 16: 31,610,672 (GRCm39) M318L probably benign Het
Dlgap1 T C 17: 70,969,753 (GRCm39) S520P probably benign Het
Dmxl2 T C 9: 54,324,013 (GRCm39) I950V probably benign Het
Dnah17 T A 11: 117,985,755 (GRCm39) T1441S probably benign Het
Dock7 A T 4: 98,849,654 (GRCm39) N1638K unknown Het
Ect2 A T 3: 27,204,239 (GRCm39) D23E probably benign Het
Ephx1 T A 1: 180,829,384 (GRCm39) T55S probably damaging Het
F11 T C 8: 45,703,183 (GRCm39) Y169C probably damaging Het
Fbxw27 A G 9: 109,618,391 (GRCm39) probably null Het
Fhl5 T A 4: 25,213,777 (GRCm39) probably null Het
Gm5145 G A 17: 20,791,323 (GRCm39) E234K probably damaging Het
Gpr39 G A 1: 125,800,238 (GRCm39) D330N possibly damaging Het
Greb1 C T 12: 16,783,428 (GRCm39) R102H probably damaging Het
H4c17 A G 13: 21,996,159 (GRCm39) D69G probably damaging Het
Ighmbp2 T C 19: 3,321,676 (GRCm39) K361R probably benign Het
Inpp4b A G 8: 82,629,400 (GRCm39) D245G probably damaging Het
Ints14 T C 9: 64,891,267 (GRCm39) V416A possibly damaging Het
Kif21a A G 15: 90,865,086 (GRCm39) S529P probably benign Het
Limk1 A G 5: 134,686,195 (GRCm39) M609T probably benign Het
Lrrc75a G A 11: 62,496,795 (GRCm39) P256S probably damaging Het
Mcc T C 18: 44,626,580 (GRCm39) R339G probably damaging Het
Mdga1 C T 17: 30,065,495 (GRCm39) W371* probably null Het
Mei4 T A 9: 81,809,649 (GRCm39) L244Q probably damaging Het
Mical2 C T 7: 111,922,810 (GRCm39) P605L possibly damaging Het
Mrgprf G T 7: 144,862,128 (GRCm39) R230L possibly damaging Het
Nlgn1 T A 3: 26,187,509 (GRCm39) R125S probably benign Het
Papola A T 12: 105,774,897 (GRCm39) probably benign Het
Pold2 T C 11: 5,823,095 (GRCm39) D360G probably benign Het
Prr12 T C 7: 44,683,274 (GRCm39) R1797G unknown Het
Psmg2 C T 18: 67,786,338 (GRCm39) P233S probably benign Het
Ptprh A G 7: 4,553,781 (GRCm39) W857R probably damaging Het
Raet1e A T 10: 22,057,179 (GRCm39) M168L probably benign Het
Rhbdl2 A T 4: 123,703,908 (GRCm39) Y61F probably damaging Het
Sacm1l A G 9: 123,398,016 (GRCm39) N236S probably damaging Het
Sbf2 A T 7: 110,046,268 (GRCm39) S310T probably benign Het
Sdr42e2 A T 7: 120,412,238 (GRCm39) R33S probably damaging Het
Sh3d19 T A 3: 86,011,584 (GRCm39) I390N possibly damaging Het
Slco3a1 A G 7: 74,154,042 (GRCm39) Y177H probably damaging Het
Smo G A 6: 29,758,448 (GRCm39) G531D possibly damaging Het
Snx25 A C 8: 46,558,233 (GRCm39) V258G probably damaging Het
Spata31d1b T A 13: 59,866,028 (GRCm39) S1059T probably benign Het
Srgap2 C T 1: 131,238,332 (GRCm39) C274Y Het
Srrm1 A G 4: 135,074,137 (GRCm39) I48T probably damaging Het
Syne1 A T 10: 5,199,340 (GRCm39) V3719E probably damaging Het
Tcerg1 T A 18: 42,683,128 (GRCm39) M616K probably benign Het
Tgtp2 G C 11: 48,950,135 (GRCm39) R146G probably damaging Het
Tie1 A T 4: 118,341,610 (GRCm39) V234D probably damaging Het
Tom1 A G 8: 75,783,895 (GRCm39) N293S probably damaging Het
Trim13 A T 14: 61,842,080 (GRCm39) K32N probably damaging Het
Trim6 G A 7: 103,874,777 (GRCm39) V5I probably benign Het
Vps11 A T 9: 44,266,379 (GRCm39) L436* probably null Het
Vps50 C T 6: 3,567,750 (GRCm39) Q549* probably null Het
Vtcn1 T A 3: 100,791,210 (GRCm39) F83I probably damaging Het
Zfp131 T C 13: 120,228,079 (GRCm39) T523A probably benign Het
Zfp758 A T 17: 22,594,981 (GRCm39) Y489F possibly damaging Het
Zfp804a T C 2: 82,088,531 (GRCm39) Y787H probably benign Het
Zfp9 C T 6: 118,441,963 (GRCm39) C233Y probably damaging Het
Other mutations in Or52h7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01311:Or52h7 APN 7 104,214,036 (GRCm39) missense probably damaging 1.00
IGL01620:Or52h7 APN 7 104,214,220 (GRCm39) missense probably damaging 0.97
IGL01712:Or52h7 APN 7 104,214,226 (GRCm39) missense probably benign
IGL02211:Or52h7 APN 7 104,214,333 (GRCm39) nonsense probably null
IGL03328:Or52h7 APN 7 104,213,677 (GRCm39) missense probably damaging 1.00
K7894:Or52h7 UTSW 7 104,213,739 (GRCm39) missense probably benign 0.12
R0138:Or52h7 UTSW 7 104,214,210 (GRCm39) missense probably benign
R0632:Or52h7 UTSW 7 104,213,544 (GRCm39) missense probably benign 0.00
R1457:Or52h7 UTSW 7 104,214,278 (GRCm39) missense probably damaging 1.00
R1494:Or52h7 UTSW 7 104,214,038 (GRCm39) nonsense probably null
R1879:Or52h7 UTSW 7 104,214,118 (GRCm39) missense possibly damaging 0.93
R2188:Or52h7 UTSW 7 104,213,883 (GRCm39) missense probably benign 0.00
R2323:Or52h7 UTSW 7 104,213,826 (GRCm39) missense probably benign 0.01
R3862:Or52h7 UTSW 7 104,214,145 (GRCm39) missense probably benign 0.01
R3908:Or52h7 UTSW 7 104,213,848 (GRCm39) missense probably benign 0.01
R4942:Or52h7 UTSW 7 104,214,212 (GRCm39) missense probably benign 0.00
R5443:Or52h7 UTSW 7 104,213,583 (GRCm39) missense probably benign 0.14
R5572:Or52h7 UTSW 7 104,214,201 (GRCm39) missense probably benign 0.08
R6045:Or52h7 UTSW 7 104,213,974 (GRCm39) missense probably benign 0.42
R6973:Or52h7 UTSW 7 104,214,183 (GRCm39) missense probably benign 0.42
R7349:Or52h7 UTSW 7 104,213,857 (GRCm39) missense probably benign
R7968:Or52h7 UTSW 7 104,213,857 (GRCm39) missense probably benign 0.01
R8031:Or52h7 UTSW 7 104,214,316 (GRCm39) missense probably damaging 0.99
R8129:Or52h7 UTSW 7 104,213,584 (GRCm39) missense probably benign 0.07
R8198:Or52h7 UTSW 7 104,214,140 (GRCm39) missense probably benign 0.01
R8296:Or52h7 UTSW 7 104,213,593 (GRCm39) missense probably benign
R8345:Or52h7 UTSW 7 104,213,431 (GRCm39) start codon destroyed probably null 0.08
R8475:Or52h7 UTSW 7 104,214,066 (GRCm39) missense probably benign
R8875:Or52h7 UTSW 7 104,213,670 (GRCm39) missense probably benign 0.00
R8881:Or52h7 UTSW 7 104,213,619 (GRCm39) missense possibly damaging 0.58
R8927:Or52h7 UTSW 7 104,214,229 (GRCm39) missense probably damaging 1.00
R8928:Or52h7 UTSW 7 104,214,229 (GRCm39) missense probably damaging 1.00
X0024:Or52h7 UTSW 7 104,213,457 (GRCm39) missense possibly damaging 0.94
Predicted Primers PCR Primer
(F):5'- GAGTCTGTCTTTGTGAAGCCC -3'
(R):5'- GCCATTATGGTCATGGGTTAAATG -3'

Sequencing Primer
(F):5'- CATAGGACCTTGTACATGCTAGGC -3'
(R):5'- ATGGTCATGGGTTAAATGATTCTCC -3'
Posted On 2019-05-15