Incidental Mutation 'R6919:Or8g22'
ID 554322
Institutional Source Beutler Lab
Gene Symbol Or8g22
Ensembl Gene ENSMUSG00000095194
Gene Name olfactory receptor family 8 subfamily G member 22, pseudogene 1
Synonyms Olfr936, MOR171-37, EG628171, GA_x6K02T2PVTD-32743332-32742397
MMRRC Submission 045039-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # R6919 (G1)
Quality Score 225.009
Status Validated
Chromosome 9
Chromosomal Location 38957910-38958845 bp(-) (GRCm39)
Type of Mutation utr 5 prime
DNA Base Change (assembly) A to G at 38958827 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000137209 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000178303] [ENSMUST00000216912]
AlphaFold J3KMV2
Predicted Effect probably benign
Transcript: ENSMUST00000178303
SMART Domains Protein: ENSMUSP00000137209
Gene: ENSMUSG00000095194

DomainStartEndE-ValueType
Pfam:7tm_1 1 246 6e-21 PFAM
Pfam:7tm_4 1 264 6.9e-49 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000216912
AA Change: L7P
Meta Mutation Damage Score 0.1362 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.3%
  • 20x: 97.8%
Validation Efficiency 99% (84/85)
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, Feb 2010]
Allele List at MGI
Other mutations in this stock
Total: 83 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700086D15Rik A G 11: 65,043,356 (GRCm39) probably benign Het
6430548M08Rik T C 8: 120,872,221 (GRCm39) S50P probably damaging Het
Aacs A G 5: 125,583,227 (GRCm39) D261G probably benign Het
Abcc4 T A 14: 118,832,306 (GRCm39) T775S probably benign Het
Acsl6 A G 11: 54,232,582 (GRCm39) probably null Het
Agbl5 T A 5: 31,062,061 (GRCm39) F196I probably benign Het
Ahnak2 T C 12: 112,741,118 (GRCm39) T985A possibly damaging Het
Ak1 A T 2: 32,521,134 (GRCm39) D101V possibly damaging Het
Alx1 A G 10: 102,861,061 (GRCm39) Y156H probably damaging Het
Angptl7 T A 4: 148,584,488 (GRCm39) S87C probably benign Het
Ankrd36 A G 11: 5,579,299 (GRCm39) T188A probably benign Het
Arhgap11a A C 2: 113,670,054 (GRCm39) S356R possibly damaging Het
Ascc3 G T 10: 50,521,849 (GRCm39) E455* probably null Het
Atp6v0a2 G A 5: 124,789,225 (GRCm39) probably null Het
B3gnt7 T C 1: 86,233,416 (GRCm39) W104R probably damaging Het
Bbs9 G A 9: 22,723,840 (GRCm39) probably null Het
Cc2d2a T A 5: 43,860,557 (GRCm39) D544E probably benign Het
Cic C T 7: 24,971,202 (GRCm39) T311I probably benign Het
Cngb1 T A 8: 95,975,003 (GRCm39) R1157W probably null Het
Cntln A G 4: 85,033,605 (GRCm39) H1310R probably benign Het
Cntnap5c A T 17: 58,600,948 (GRCm39) I764F probably benign Het
Col26a1 T C 5: 136,773,088 (GRCm39) Q362R possibly damaging Het
Cyp2c29 G A 19: 39,279,585 (GRCm39) R100K probably benign Het
D17H6S53E C G 17: 35,346,222 (GRCm39) D44E probably damaging Het
Dap3 A G 3: 88,838,296 (GRCm39) V65A probably damaging Het
Dna2 A T 10: 62,792,782 (GRCm39) I266F probably damaging Het
Dnah14 G A 1: 181,412,631 (GRCm39) G57E probably benign Het
Dock9 A T 14: 121,880,564 (GRCm39) V333E probably benign Het
Dpm1 A G 2: 168,072,195 (GRCm39) Y27H probably damaging Het
Dsp A T 13: 38,351,631 (GRCm39) Y150F possibly damaging Het
Emilin3 A T 2: 160,750,018 (GRCm39) I577N probably damaging Het
Erap1 A G 13: 74,819,552 (GRCm39) T189A probably benign Het
Fat2 A G 11: 55,173,597 (GRCm39) I2372T possibly damaging Het
Fbn2 A T 18: 58,257,259 (GRCm39) probably null Het
Gnl1 A T 17: 36,298,425 (GRCm39) R390* probably null Het
Hivep1 A G 13: 42,336,928 (GRCm39) I2336V probably benign Het
Il17rb C G 14: 29,726,228 (GRCm39) probably null Het
Itga9 T C 9: 118,716,883 (GRCm39) W396R probably damaging Het
Katnal2 A G 18: 77,098,734 (GRCm39) V152A probably benign Het
Kcnk3 A G 5: 30,779,744 (GRCm39) T265A probably benign Het
Klhl1 T C 14: 96,374,030 (GRCm39) Y672C probably benign Het
Leng8 C A 7: 4,146,625 (GRCm39) N412K possibly damaging Het
Lrrc9 T A 12: 72,553,167 (GRCm39) F1356L probably benign Het
Map7 A G 10: 20,046,828 (GRCm39) probably benign Het
Mei1 T C 15: 81,966,131 (GRCm39) F251S probably damaging Het
Mia2 A G 12: 59,176,681 (GRCm39) E9G possibly damaging Het
Ms4a13 C A 19: 11,149,249 (GRCm39) W182C probably benign Het
Muc16 C T 9: 18,571,595 (GRCm39) R308K unknown Het
Or4c103 G A 2: 88,514,028 (GRCm39) T16I possibly damaging Het
Pcnt A G 10: 76,221,632 (GRCm39) V1998A probably benign Het
Pgm2 A T 5: 64,254,368 (GRCm39) N51I probably benign Het
Piezo1 T A 8: 123,217,020 (GRCm39) H1333L probably damaging Het
Prg2 G A 2: 84,813,600 (GRCm39) V199M probably damaging Het
Prss51 T C 14: 64,334,937 (GRCm39) V182A probably damaging Het
Psmb9 A T 17: 34,402,199 (GRCm39) Y132* probably null Het
Ralyl T C 3: 13,842,091 (GRCm39) Y76H probably damaging Het
Rnaset2a A T 17: 8,349,114 (GRCm39) D174E probably benign Het
Rnft1 G A 11: 86,386,156 (GRCm39) probably null Het
Robo2 T C 16: 73,758,755 (GRCm39) Y676C probably damaging Het
Samd9l T G 6: 3,376,313 (GRCm39) Y316S possibly damaging Het
Siah3 T A 14: 75,693,578 (GRCm39) F28Y possibly damaging Het
Slc28a3 C T 13: 58,721,257 (GRCm39) probably null Het
Slc8a1 A G 17: 81,696,301 (GRCm39) F911S probably damaging Het
Spata31e2 T C 1: 26,722,015 (GRCm39) Y1055C probably benign Het
Speg T A 1: 75,364,552 (GRCm39) L156* probably null Het
Spopl T G 2: 23,407,873 (GRCm39) M269L probably benign Het
Tacr1 C T 6: 82,534,054 (GRCm39) T360I probably benign Het
Tasor T A 14: 27,171,758 (GRCm39) L397* probably null Het
Tmem262 A G 19: 6,130,767 (GRCm39) E95G probably benign Het
Tmem68 G T 4: 3,569,669 (GRCm39) T7N possibly damaging Het
Top3a T A 11: 60,640,319 (GRCm39) I460F probably damaging Het
Trafd1 G A 5: 121,522,137 (GRCm39) R5* probably null Het
Trim16 T A 11: 62,731,695 (GRCm39) V435D possibly damaging Het
Tspan17 A G 13: 54,943,846 (GRCm39) D236G probably damaging Het
Tssk2 A T 16: 17,717,565 (GRCm39) M323L probably benign Het
Ubqln5 A G 7: 103,778,215 (GRCm39) V203A probably benign Het
Utrn A T 10: 12,569,214 (GRCm39) L1134* probably null Het
Vmn1r37 C T 6: 66,708,704 (GRCm39) S73F possibly damaging Het
Vps13c A G 9: 67,834,734 (GRCm39) K1688E probably damaging Het
Zbtb39 A G 10: 127,577,711 (GRCm39) D95G probably damaging Het
Zfhx3 T A 8: 109,527,160 (GRCm39) I1019N probably damaging Het
Zfp207 C T 11: 80,286,329 (GRCm39) probably benign Het
Zmiz1 C T 14: 25,644,062 (GRCm39) T169M probably damaging Het
Other mutations in Or8g22
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01928:Or8g22 APN 9 38,958,709 (GRCm39) missense unknown
R0086:Or8g22 UTSW 9 38,958,191 (GRCm39) missense probably benign 0.00
R0561:Or8g22 UTSW 9 38,958,669 (GRCm39) missense probably damaging 0.99
R0650:Or8g22 UTSW 9 38,957,996 (GRCm39) missense probably benign 0.01
R1221:Or8g22 UTSW 9 38,958,483 (GRCm39) missense probably damaging 1.00
R1384:Or8g22 UTSW 9 38,958,200 (GRCm39) missense possibly damaging 0.70
R1680:Or8g22 UTSW 9 38,958,296 (GRCm39) missense probably benign 0.43
R1733:Or8g22 UTSW 9 38,958,678 (GRCm39) missense unknown
R3767:Or8g22 UTSW 9 38,958,707 (GRCm39) missense unknown
R4786:Or8g22 UTSW 9 38,958,783 (GRCm39) nonsense probably null
R4944:Or8g22 UTSW 9 38,958,158 (GRCm39) missense probably damaging 1.00
R5186:Or8g22 UTSW 9 38,958,265 (GRCm39) nonsense probably null
R5403:Or8g22 UTSW 9 38,957,999 (GRCm39) missense probably damaging 1.00
R6037:Or8g22 UTSW 9 38,958,403 (GRCm39) missense probably damaging 1.00
R6037:Or8g22 UTSW 9 38,958,403 (GRCm39) missense probably damaging 1.00
R6156:Or8g22 UTSW 9 38,958,671 (GRCm39) missense possibly damaging 0.90
R6217:Or8g22 UTSW 9 38,958,039 (GRCm39) makesense probably null
R6711:Or8g22 UTSW 9 38,958,162 (GRCm39) makesense probably null
R7022:Or8g22 UTSW 9 38,958,379 (GRCm39) nonsense probably null
R7275:Or8g22 UTSW 9 38,958,815 (GRCm39) utr 5 prime probably benign
R7290:Or8g22 UTSW 9 38,958,694 (GRCm39) missense unknown
R7644:Or8g22 UTSW 9 38,958,638 (GRCm39) missense probably damaging 1.00
R8906:Or8g22 UTSW 9 38,958,077 (GRCm39) missense possibly damaging 0.87
R9099:Or8g22 UTSW 9 38,958,026 (GRCm39) missense probably benign 0.00
Z1176:Or8g22 UTSW 9 38,958,215 (GRCm39) missense probably damaging 0.98
Predicted Primers PCR Primer
(F):5'- TGACAGTAGATTGGCAGAGGTC -3'
(R):5'- GTAGCTGTGCTTTTGACACCC -3'

Sequencing Primer
(F):5'- TCAATGAAGGACAGACTGCTGAG -3'
(R):5'- GTCTCTGCCATTTATAATTTAGGCAC -3'
Posted On 2019-05-30