Incidental Mutation 'R5199:Or5ac21'
ID 400634
Institutional Source Beutler Lab
Gene Symbol Or5ac21
Ensembl Gene ENSMUSG00000068182
Gene Name olfactory receptor family 5 subfamily AC member 21
Synonyms GA_x54KRFPKG5P-55517445-55518365, Olfr203, MOR182-5
MMRRC Submission 042775-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.140) question?
Stock # R5199 (G1)
Quality Score 225
Status Validated
Chromosome 16
Chromosomal Location 59123518-59124438 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 59124103 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Isoleucine at position 196 (F196I)
Ref Sequence ENSEMBL: ENSMUSP00000149906 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000089305] [ENSMUST00000201687] [ENSMUST00000215893]
AlphaFold L7N205
Predicted Effect probably benign
Transcript: ENSMUST00000089305
AA Change: F197I

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000086719
Gene: ENSMUSG00000068182
AA Change: F197I

DomainStartEndE-ValueType
Pfam:7tm_4 31 307 1e-46 PFAM
Pfam:7tm_1 41 290 7.6e-20 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000201687
AA Change: F196I

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000144622
Gene: ENSMUSG00000048810
AA Change: F196I

DomainStartEndE-ValueType
Pfam:7tm_4 30 306 3.4e-46 PFAM
Pfam:7tm_1 40 289 1.4e-19 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000215893
AA Change: F196I

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.7%
Validation Efficiency 100% (57/57)
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: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl2fm1 T C 3: 59,843,906 (GRCm39) L200P probably damaging Het
Adam1a T C 5: 121,659,215 (GRCm39) E26G probably benign Het
Adar T A 3: 89,653,251 (GRCm39) M797K probably damaging Het
Amdhd1 A T 10: 93,361,847 (GRCm39) C352S probably damaging Het
AW554918 C A 18: 25,473,356 (GRCm39) R387S probably damaging Het
Cabp1 A G 5: 115,324,102 (GRCm39) V5A possibly damaging Het
Carmil1 A G 13: 24,295,853 (GRCm39) L387P probably damaging Het
Cds2 T A 2: 132,140,403 (GRCm39) H200Q probably damaging Het
Cep170b T A 12: 112,710,581 (GRCm39) L1470Q probably damaging Het
Cnnm1 A G 19: 43,483,425 (GRCm39) D956G possibly damaging Het
Cnot8 C T 11: 58,006,100 (GRCm39) Q210* probably null Het
Cpne8 G A 15: 90,532,812 (GRCm39) T65I probably benign Het
Crygn A G 5: 24,961,156 (GRCm39) V50A probably damaging Het
Cxcr4 A G 1: 128,517,283 (GRCm39) V126A probably damaging Het
Cyp4f15 A G 17: 32,921,346 (GRCm39) D464G probably benign Het
Dapp1 C T 3: 137,687,146 (GRCm39) S12N probably benign Het
Dhps G A 8: 85,800,035 (GRCm39) G162R probably damaging Het
Dsp T G 13: 38,376,878 (GRCm39) Y1554* probably null Het
Etl4 G T 2: 20,748,853 (GRCm39) R397L probably damaging Het
Ezh2 C T 6: 47,528,659 (GRCm39) C291Y probably benign Het
Gbp9 T C 5: 105,231,678 (GRCm39) S303G probably benign Het
Gm11444 A C 11: 85,738,845 (GRCm39) S83A unknown Het
Gpat4 A G 8: 23,672,712 (GRCm39) V46A possibly damaging Het
Haus6 T C 4: 86,501,222 (GRCm39) D883G possibly damaging Het
Hinfp T C 9: 44,207,689 (GRCm39) E439G probably benign Het
Ifna14 T A 4: 88,489,599 (GRCm39) Y146F probably damaging Het
Igkv3-3 A T 6: 70,664,488 (GRCm39) Y110F probably damaging Het
Kansl2-ps A G 7: 72,322,942 (GRCm39) noncoding transcript Het
Klrh1 T A 6: 129,752,781 (GRCm39) Y8F possibly damaging Het
Mcmdc2 T C 1: 9,990,660 (GRCm39) V279A probably benign Het
Mug2 T A 6: 122,017,619 (GRCm39) V452D probably benign Het
Ndufb3 C G 1: 58,630,281 (GRCm39) probably benign Het
Oas1d G T 5: 121,057,208 (GRCm39) K271N probably benign Het
Or4c110 T A 2: 88,832,107 (GRCm39) H175L possibly damaging Het
Or9g3 A G 2: 85,590,558 (GRCm39) L54P probably damaging Het
Otx1 C A 11: 21,947,037 (GRCm39) A91S probably damaging Het
Pcnt T A 10: 76,254,378 (GRCm39) H817L probably benign Het
Per3 G T 4: 151,097,352 (GRCm39) S724R probably benign Het
Phlpp1 T A 1: 106,101,124 (GRCm39) V464E probably damaging Het
Psme4 A G 11: 30,803,272 (GRCm39) E38G probably benign Het
Qtrt2 T C 16: 43,687,788 (GRCm39) N264S probably benign Het
Ranbp2 G A 10: 58,300,265 (GRCm39) R557H probably benign Het
Rptor T A 11: 119,494,642 (GRCm39) S3T probably benign Het
Saxo1 T A 4: 86,406,019 (GRCm39) Y60F probably damaging Het
St3gal1 A G 15: 66,985,564 (GRCm39) V30A probably benign Het
Tmem245 G A 4: 56,925,149 (GRCm39) S324L probably benign Het
Topbp1 A G 9: 103,223,871 (GRCm39) probably benign Het
Urb1 T C 16: 90,589,636 (GRCm39) T382A possibly damaging Het
Vmn1r178 A T 7: 23,593,814 (GRCm39) L214F probably benign Het
Vmn2r82 G A 10: 79,231,921 (GRCm39) C640Y probably damaging Het
Vsx2 A G 12: 84,639,984 (GRCm39) D281G probably benign Het
Zfp804b A T 5: 6,820,013 (GRCm39) C1017S probably benign Het
Other mutations in Or5ac21
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02003:Or5ac21 APN 16 59,123,996 (GRCm39) missense probably damaging 0.99
IGL02294:Or5ac21 APN 16 59,123,975 (GRCm39) missense probably damaging 1.00
IGL02412:Or5ac21 APN 16 59,123,555 (GRCm39) missense probably damaging 1.00
IGL02899:Or5ac21 APN 16 59,123,649 (GRCm39) missense probably damaging 1.00
R0792:Or5ac21 UTSW 16 59,124,352 (GRCm39) missense probably damaging 0.99
R1551:Or5ac21 UTSW 16 59,123,766 (GRCm39) missense probably benign 0.03
R1701:Or5ac21 UTSW 16 59,123,651 (GRCm39) missense probably benign 0.23
R1975:Or5ac21 UTSW 16 59,124,091 (GRCm39) missense probably damaging 0.98
R2272:Or5ac21 UTSW 16 59,123,807 (GRCm39) missense possibly damaging 0.55
R5843:Or5ac21 UTSW 16 59,123,724 (GRCm39) missense probably damaging 1.00
R5928:Or5ac21 UTSW 16 59,123,521 (GRCm39) missense probably damaging 1.00
R6708:Or5ac21 UTSW 16 59,124,416 (GRCm39) missense probably damaging 1.00
R6747:Or5ac21 UTSW 16 59,124,004 (GRCm39) missense probably benign 0.03
R6894:Or5ac21 UTSW 16 59,124,142 (GRCm39) missense probably damaging 0.98
R7324:Or5ac21 UTSW 16 59,123,611 (GRCm39) missense probably benign
R7380:Or5ac21 UTSW 16 59,124,391 (GRCm39) missense probably damaging 1.00
R7612:Or5ac21 UTSW 16 59,123,990 (GRCm39) missense probably damaging 1.00
R7775:Or5ac21 UTSW 16 59,123,614 (GRCm39) missense probably damaging 1.00
R8010:Or5ac21 UTSW 16 59,123,867 (GRCm39) missense probably damaging 1.00
R8408:Or5ac21 UTSW 16 59,124,418 (GRCm39) nonsense probably null
R8424:Or5ac21 UTSW 16 59,123,772 (GRCm39) missense possibly damaging 0.60
R8746:Or5ac21 UTSW 16 59,123,973 (GRCm39) missense probably benign 0.03
Z1176:Or5ac21 UTSW 16 59,123,532 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- GCTATGTAGCCATATGCAATCC -3'
(R):5'- CCAGGGCTCACGTACATAAAG -3'

Sequencing Primer
(F):5'- ATGTCCAACAGAGTGTGCACTTG -3'
(R):5'- TCACGTACATAAAGAAGAGAGTTCC -3'
Posted On 2016-07-06