Incidental Mutation 'R5899:Or9k2'
ID 457741
Institutional Source Beutler Lab
Gene Symbol Or9k2
Ensembl Gene ENSMUSG00000058084
Gene Name olfactory receptor family 9 subfamily K member 2
Synonyms GA_x6K02T2PULF-11834065-11833103, Olfr825, MOR210-1
MMRRC Submission 044098-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.370) question?
Stock # R5899 (G1)
Quality Score 225
Status Validated
Chromosome 10
Chromosomal Location 129998231-129999193 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 129998542 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Phenylalanine at position 218 (I218F)
Ref Sequence ENSEMBL: ENSMUSP00000149981 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076814] [ENSMUST00000216530]
AlphaFold Q8VFU7
Predicted Effect probably benign
Transcript: ENSMUST00000076814
AA Change: I218F

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
SMART Domains Protein: ENSMUSP00000076091
Gene: ENSMUSG00000058084
AA Change: I218F

DomainStartEndE-ValueType
Pfam:7tm_4 34 309 8.8e-54 PFAM
Pfam:7TM_GPCR_Srsx 38 251 9.6e-6 PFAM
Pfam:7tm_1 44 291 2e-22 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000216434
Predicted Effect probably benign
Transcript: ENSMUST00000216530
AA Change: I218F

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000218167
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.5%
  • 10x: 97.6%
  • 20x: 92.5%
Validation Efficiency 93% (56/60)
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: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ahi1 T C 10: 20,876,465 (GRCm39) I792T probably benign Het
Anks1b T A 10: 90,759,379 (GRCm39) probably null Het
Ano3 T G 2: 110,693,232 (GRCm39) D122A probably benign Het
Atp12a T C 14: 56,610,801 (GRCm39) V315A probably benign Het
B230104I21Rik G T 4: 154,433,986 (GRCm39) G57* probably null Het
Bpifb2 A G 2: 153,733,050 (GRCm39) K378E probably damaging Het
Cdk5rap2 T C 4: 70,161,830 (GRCm39) probably benign Het
Ceacam23 A G 7: 17,651,369 (GRCm39) D840G possibly damaging Het
Cflar A G 1: 58,791,927 (GRCm39) D410G probably benign Het
Clcn6 A G 4: 148,102,049 (GRCm39) V345A probably benign Het
Cnga1 C T 5: 72,776,404 (GRCm39) V20I possibly damaging Het
Ddx50 T A 10: 62,476,596 (GRCm39) K226* probably null Het
Dnah5 T C 15: 28,448,513 (GRCm39) V4192A possibly damaging Het
Dnah8 G A 17: 30,875,659 (GRCm39) D494N probably benign Het
Dock7 A T 4: 98,879,660 (GRCm39) C965S probably benign Het
Dst C T 1: 34,334,370 (GRCm39) A5083V probably damaging Het
E130208F15Rik T C 7: 30,021,726 (GRCm39) Q10R probably damaging Het
Fbxw15 T C 9: 109,384,741 (GRCm39) probably null Het
Fxr2 A G 11: 69,543,511 (GRCm39) N671D probably damaging Het
Gbp7 A G 3: 142,252,303 (GRCm39) T629A probably benign Het
Grm1 T C 10: 10,565,092 (GRCm39) Y1072C probably benign Het
Hmcn2 A T 2: 31,244,685 (GRCm39) E714V possibly damaging Het
Hsd17b13 T A 5: 104,113,730 (GRCm39) E205D probably benign Het
Igf2bp3 A G 6: 49,094,084 (GRCm39) probably benign Het
Il2ra A G 2: 11,689,248 (GRCm39) H259R probably benign Het
Klk15 G T 7: 43,588,247 (GRCm39) R185L probably benign Het
Map3k11 T G 19: 5,745,937 (GRCm39) probably null Het
Morn3 A G 5: 123,179,166 (GRCm39) W95R probably damaging Het
Nipbl A G 15: 8,364,328 (GRCm39) probably null Het
Nrap A T 19: 56,329,006 (GRCm39) V1145D possibly damaging Het
Or1e35 A G 11: 73,797,755 (GRCm39) S188P probably damaging Het
Or2l13b C T 16: 19,349,551 (GRCm39) G40R probably damaging Het
Pdcd11 A G 19: 47,093,198 (GRCm39) N492S possibly damaging Het
Ptgfr C T 3: 151,540,738 (GRCm39) V257I probably damaging Het
Racgap1 T C 15: 99,521,509 (GRCm39) E549G possibly damaging Het
Rfx3 T C 19: 27,808,165 (GRCm39) T193A probably damaging Het
Rplp0 T A 5: 115,699,489 (GRCm39) I149N probably benign Het
Samd7 T G 3: 30,810,883 (GRCm39) I300S probably benign Het
Scpep1 A G 11: 88,825,402 (GRCm39) probably null Het
Senp6 T C 9: 80,049,352 (GRCm39) probably benign Het
Serpinb2 G T 1: 107,447,446 (GRCm39) G78V probably damaging Het
Sesn1 T C 10: 41,687,189 (GRCm39) S58P probably benign Het
Skic3 A G 13: 76,259,938 (GRCm39) probably null Het
Spg11 T C 2: 121,928,680 (GRCm39) D591G possibly damaging Het
Spire2 A C 8: 124,080,833 (GRCm39) S26R probably damaging Het
Strip2 T A 6: 29,956,957 (GRCm39) probably benign Het
Ttn G A 2: 76,697,519 (GRCm39) probably benign Het
Vmn2r77 A G 7: 86,460,924 (GRCm39) Y750C probably damaging Het
Wnt11 T A 7: 98,488,383 (GRCm39) Y23* probably null Het
Zbp1 T A 2: 173,052,340 (GRCm39) D272V probably benign Het
Other mutations in Or9k2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03244:Or9k2 APN 10 129,998,269 (GRCm39) nonsense probably null
R1120:Or9k2 UTSW 10 129,998,406 (GRCm39) missense probably damaging 1.00
R1341:Or9k2 UTSW 10 129,999,185 (GRCm39) missense probably benign 0.00
R1754:Or9k2 UTSW 10 129,999,033 (GRCm39) missense probably benign 0.02
R2022:Or9k2 UTSW 10 129,999,049 (GRCm39) missense probably benign 0.00
R2027:Or9k2 UTSW 10 129,998,604 (GRCm39) missense probably benign 0.00
R3838:Or9k2 UTSW 10 129,998,275 (GRCm39) nonsense probably null
R3842:Or9k2 UTSW 10 129,998,770 (GRCm39) missense probably benign 0.00
R4737:Or9k2 UTSW 10 129,998,707 (GRCm39) missense probably benign 0.01
R5166:Or9k2 UTSW 10 129,998,430 (GRCm39) missense possibly damaging 0.60
R5744:Or9k2 UTSW 10 129,998,661 (GRCm39) missense possibly damaging 0.92
R7754:Or9k2 UTSW 10 129,998,698 (GRCm39) missense probably damaging 1.00
R8098:Or9k2 UTSW 10 129,998,916 (GRCm39) missense probably benign 0.32
R9393:Or9k2 UTSW 10 129,999,016 (GRCm39) missense probably benign 0.39
X0026:Or9k2 UTSW 10 129,998,600 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- ATCAGAGGGTTCAGCATAGGTG -3'
(R):5'- TCAGCTCTGTTCTCCAGACTAG -3'

Sequencing Primer
(F):5'- TCAGCATAGGTGTGACTAGGG -3'
(R):5'- TGTTCTCCAGACTAGCATGAC -3'
Posted On 2017-02-15