Incidental Mutation 'R2925:Or5m11b'
ID 255688
Institutional Source Beutler Lab
Gene Symbol Or5m11b
Ensembl Gene ENSMUSG00000059873
Gene Name olfactory receptor family 5 subfamily M member 11B
Synonyms GA_x6K02T2Q125-47454152-47455126, Olfr1029, MOR198-1P
MMRRC Submission 040510-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.054) question?
Stock # R2925 (G1)
Quality Score 191
Status Not validated
Chromosome 2
Chromosomal Location 85805557-85806617 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 85806125 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Stop codon at position 179 (C179*)
Ref Sequence ENSEMBL: ENSMUSP00000150637 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000056849] [ENSMUST00000082191] [ENSMUST00000217244]
AlphaFold A2ATE0
Predicted Effect probably benign
Transcript: ENSMUST00000056849
SMART Domains Protein: ENSMUSP00000053309
Gene: ENSMUSG00000044923

DomainStartEndE-ValueType
Pfam:7tm_4 37 314 2.4e-58 PFAM
Pfam:7tm_1 47 296 3.2e-27 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000082191
AA Change: C179*
SMART Domains Protein: ENSMUSP00000080828
Gene: ENSMUSG00000059873
AA Change: C179*

DomainStartEndE-ValueType
Pfam:7tm_4 31 308 4.2e-56 PFAM
Pfam:7tm_1 41 290 2.1e-25 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000217244
AA Change: C179*
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.2%
Validation Efficiency 95% (40/42)
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: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930503E14Rik T C 14: 44,407,755 (GRCm39) T93A probably damaging Het
Acte1 A T 7: 143,437,736 (GRCm39) R147* probably null Het
Akr1c21 A G 13: 4,626,349 (GRCm39) probably null Het
Alk A G 17: 72,910,202 (GRCm39) V168A probably benign Het
Ap4b1 A G 3: 103,727,997 (GRCm39) E337G probably damaging Het
Bltp1 G T 3: 37,061,271 (GRCm39) A3327S probably damaging Het
Btn2a2 A G 13: 23,665,984 (GRCm39) S283P probably damaging Het
Ctcfl C T 2: 172,936,489 (GRCm39) E628K probably damaging Het
Cul9 G A 17: 46,821,907 (GRCm39) T1856M probably benign Het
Defb41 T C 1: 18,330,857 (GRCm39) D30G probably damaging Het
Dnai1 A T 4: 41,597,919 (GRCm39) I74F probably damaging Het
Ecpas T A 4: 58,833,928 (GRCm39) K851* probably null Het
Fbln2 T A 6: 91,242,837 (GRCm39) C846S probably damaging Het
Fuom T C 7: 139,679,862 (GRCm39) T110A probably benign Het
Hsp90aa1 C A 12: 110,662,115 (GRCm39) probably null Het
Hsp90aa1 T A 12: 110,662,114 (GRCm39) M1L possibly damaging Het
Il12a TCAC TC 3: 68,605,320 (GRCm39) probably null Het
Kcnd3 C T 3: 105,566,082 (GRCm39) A421V probably damaging Het
Lyz3 C T 10: 117,070,336 (GRCm39) R147Q probably benign Het
Man2b2 A G 5: 36,981,446 (GRCm39) F224L probably benign Het
Mtbp G A 15: 55,483,210 (GRCm39) R429Q probably benign Het
Ncapg2 C A 12: 116,402,349 (GRCm39) T727K probably benign Het
Nek4 G A 14: 30,673,667 (GRCm39) G29S probably benign Het
Nsf C T 11: 103,821,578 (GRCm39) E26K possibly damaging Het
Nup214 A G 2: 31,888,015 (GRCm39) K15E probably damaging Het
Or5ac24 A T 16: 59,165,706 (GRCm39) Y119* probably null Het
Or8k32 C T 2: 86,368,891 (GRCm39) D121N probably damaging Het
Or9a4 T A 6: 40,548,342 (GRCm39) S7R probably benign Het
P2ry13 G A 3: 59,116,801 (GRCm39) H326Y probably benign Het
Plec A G 15: 76,062,452 (GRCm39) F2563S probably damaging Het
Rc3h1 A G 1: 160,782,546 (GRCm39) Y675C probably damaging Het
Samd3 T A 10: 26,127,785 (GRCm39) S288T probably benign Het
Scaf4 G T 16: 90,047,177 (GRCm39) P400Q unknown Het
Selplg T C 5: 113,958,240 (GRCm39) D22G possibly damaging Het
Slc30a6 T C 17: 74,708,999 (GRCm39) probably benign Het
Syt3 T A 7: 44,045,222 (GRCm39) V518E probably damaging Het
Tnks G A 8: 35,432,815 (GRCm39) A2V unknown Het
Upk3a A G 15: 84,902,350 (GRCm39) Y59C probably benign Het
Usp4 T C 9: 108,245,055 (GRCm39) L331P probably damaging Het
Zbed5 A G 5: 129,932,039 (GRCm39) T663A possibly damaging Het
Zbtb11 G A 16: 55,794,447 (GRCm39) R8Q probably benign Het
Other mutations in Or5m11b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02020:Or5m11b APN 2 85,805,579 (GRCm39) utr 5 prime probably benign
IGL02126:Or5m11b APN 2 85,806,517 (GRCm39) missense probably benign 0.00
IGL02584:Or5m11b APN 2 85,806,219 (GRCm39) missense probably damaging 0.96
IGL03410:Or5m11b APN 2 85,805,764 (GRCm39) missense probably damaging 0.99
R1466:Or5m11b UTSW 2 85,806,339 (GRCm39) missense probably damaging 1.00
R1466:Or5m11b UTSW 2 85,806,339 (GRCm39) missense probably damaging 1.00
R1499:Or5m11b UTSW 2 85,806,372 (GRCm39) missense possibly damaging 0.62
R1584:Or5m11b UTSW 2 85,806,339 (GRCm39) missense probably damaging 1.00
R2970:Or5m11b UTSW 2 85,806,454 (GRCm39) missense possibly damaging 0.75
R4571:Or5m11b UTSW 2 85,806,175 (GRCm39) missense probably damaging 0.97
R5533:Or5m11b UTSW 2 85,805,797 (GRCm39) missense possibly damaging 0.78
R5654:Or5m11b UTSW 2 85,806,500 (GRCm39) missense probably benign 0.00
R5827:Or5m11b UTSW 2 85,805,650 (GRCm39) missense probably benign 0.00
R5967:Or5m11b UTSW 2 85,806,535 (GRCm39) missense probably benign 0.01
R6291:Or5m11b UTSW 2 85,805,926 (GRCm39) missense probably damaging 1.00
R6735:Or5m11b UTSW 2 85,805,778 (GRCm39) missense possibly damaging 0.81
R6897:Or5m11b UTSW 2 85,805,700 (GRCm39) missense possibly damaging 0.45
R7053:Or5m11b UTSW 2 85,806,358 (GRCm39) missense possibly damaging 0.64
R7163:Or5m11b UTSW 2 85,805,932 (GRCm39) missense probably damaging 1.00
R7358:Or5m11b UTSW 2 85,805,780 (GRCm39) missense possibly damaging 0.81
R8047:Or5m11b UTSW 2 85,806,271 (GRCm39) missense possibly damaging 0.52
R8271:Or5m11b UTSW 2 85,806,085 (GRCm39) missense probably benign 0.40
R8271:Or5m11b UTSW 2 85,805,766 (GRCm39) missense probably damaging 1.00
R8364:Or5m11b UTSW 2 85,806,358 (GRCm39) missense possibly damaging 0.64
R9100:Or5m11b UTSW 2 85,806,096 (GRCm39) missense probably benign 0.00
R9190:Or5m11b UTSW 2 85,805,884 (GRCm39) missense possibly damaging 0.66
R9646:Or5m11b UTSW 2 85,806,446 (GRCm39) missense probably benign 0.18
Predicted Primers PCR Primer
(F):5'- CATGGCCTATGACCGCTATG -3'
(R):5'- AAACAATGTGACAGCCATCATGTG -3'

Sequencing Primer
(F):5'- ACCGCTATGTGGCCATATG -3'
(R):5'- CAAGTAGAGAATGCCTTGCGTCTTC -3'
Posted On 2014-12-29