Incidental Mutation 'IGL03244:Or9k2'
ID 414330
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or9k2
Ensembl Gene ENSMUSG00000058084
Gene Name olfactory receptor family 9 subfamily K member 2
Synonyms GA_x6K02T2PULF-11834065-11833103, Olfr825, MOR210-1
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.370) question?
Stock # IGL03244
Quality Score
Status
Chromosome 10
Chromosomal Location 129998231-129999193 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 129998269 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 309 (K309*)
Ref Sequence ENSEMBL: ENSMUSP00000149981 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000076814] [ENSMUST00000216530]
AlphaFold Q8VFU7
Predicted Effect probably null
Transcript: ENSMUST00000076814
AA Change: K309*
SMART Domains Protein: ENSMUSP00000076091
Gene: ENSMUSG00000058084
AA Change: K309*

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 null
Transcript: ENSMUST00000216530
AA Change: K309*
Predicted Effect noncoding transcript
Transcript: ENSMUST00000218167
Coding Region Coverage
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: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ank2 C A 3: 126,749,519 (GRCm39) E503D probably damaging Het
Aoc1 T C 6: 48,882,756 (GRCm39) Y233H possibly damaging Het
Apaf1 A T 10: 90,885,211 (GRCm39) probably benign Het
Asah2 T C 19: 31,964,342 (GRCm39) Y696C probably damaging Het
Atp8b3 A T 10: 80,370,292 (GRCm39) D112E probably damaging Het
B3gat3 T C 19: 8,903,215 (GRCm39) Y191H probably damaging Het
Capns2 T C 8: 93,628,738 (GRCm39) I209T probably damaging Het
Ccnl2 T C 4: 155,905,479 (GRCm39) I303T probably benign Het
Cdk5rap2 A T 4: 70,199,672 (GRCm39) S817R probably benign Het
Cep57 A T 9: 13,729,683 (GRCm39) L36* probably null Het
Cers4 T A 8: 4,566,878 (GRCm39) V60E probably damaging Het
Ces2e T C 8: 105,655,451 (GRCm39) Y125H probably benign Het
Cyp4f18 T C 8: 72,742,489 (GRCm39) E497G probably benign Het
Ddx24 A T 12: 103,383,864 (GRCm39) M575K possibly damaging Het
Dmxl2 A T 9: 54,323,655 (GRCm39) V1243E probably damaging Het
Elf2 A T 3: 51,165,193 (GRCm39) Y270* probably null Het
Ep400 A G 5: 110,875,429 (GRCm39) L844S unknown Het
F13a1 A T 13: 37,172,870 (GRCm39) I170N possibly damaging Het
Gm16506 T A 14: 43,961,603 (GRCm39) probably benign Het
Grm4 A G 17: 27,653,797 (GRCm39) F463L probably damaging Het
H2-M10.2 A T 17: 36,596,463 (GRCm39) N127K probably benign Het
Lrrc49 T C 9: 60,495,140 (GRCm39) Y691C probably damaging Het
Mbip A C 12: 56,384,547 (GRCm39) probably null Het
Plod1 C T 4: 148,007,580 (GRCm39) probably null Het
Primpol A G 8: 47,039,475 (GRCm39) W382R probably damaging Het
Rufy2 A G 10: 62,840,483 (GRCm39) E418G probably benign Het
Samm50 T C 15: 84,098,341 (GRCm39) V460A probably benign Het
Senp2 T C 16: 21,859,329 (GRCm39) V460A probably damaging Het
Simc1 A G 13: 54,698,442 (GRCm39) H453R probably benign Het
Slc22a22 A G 15: 57,112,948 (GRCm39) probably benign Het
Spag1 A T 15: 36,234,529 (GRCm39) D763V probably benign Het
Thsd7a T A 6: 12,504,167 (GRCm39) probably benign Het
Tppp G T 13: 74,169,535 (GRCm39) V92F possibly damaging Het
Vmn1r32 G A 6: 66,530,489 (GRCm39) L96F probably damaging Het
Vmn2r53 C A 7: 12,340,435 (GRCm39) A13S probably damaging Het
Vmn2r75 G A 7: 85,820,933 (GRCm39) probably benign Het
Zfp750 C A 11: 121,404,513 (GRCm39) G121* probably null Het
Other mutations in Or9k2
AlleleSourceChrCoordTypePredicted EffectPPH Score
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
R5899:Or9k2 UTSW 10 129,998,542 (GRCm39) missense probably benign 0.00
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
Posted On 2016-08-02