Incidental Mutation 'IGL02536:Olfr624'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Olfr624
Ensembl Gene ENSMUSG00000045780
Gene Nameolfactory receptor 624
SynonymsMOR4-2P, GA_x6K02T2PBJ9-6394126-6393197
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.157) question?
Stock #IGL02536
Quality Score
Chromosomal Location103665461-103671191 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to A at 103670957 bp
Amino Acid Change Isoleucine to Phenylalanine at position 25 (I25F)
Ref Sequence ENSEMBL: ENSMUSP00000049938 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000062144]
Predicted Effect possibly damaging
Transcript: ENSMUST00000062144
AA Change: I25F

PolyPhen 2 Score 0.778 (Sensitivity: 0.85; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000049938
Gene: ENSMUSG00000045780
AA Change: I25F

Pfam:7tm_4 27 306 3.3e-138 PFAM
Pfam:7tm_1 37 288 1.8e-19 PFAM
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: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930449A18Rik T A 3: 59,778,244 noncoding transcript Het
Abca8b C T 11: 109,981,748 R9H probably benign Het
Adamts8 T A 9: 30,962,072 S858T probably benign Het
Alg1 C T 16: 5,239,159 Q245* probably null Het
Ankmy1 T C 1: 92,886,188 Y423C probably damaging Het
Anp32a A T 9: 62,371,828 T55S probably damaging Het
Arhgef9 A C X: 95,058,837 V406G probably damaging Het
Bdkrb1 T C 12: 105,605,000 F275S possibly damaging Het
Card9 C T 2: 26,358,832 V102I possibly damaging Het
Ccdc130 A T 8: 84,260,616 Y109* probably null Het
Ccdc81 A T 7: 89,877,580 probably benign Het
Cd101 T A 3: 101,003,597 D915V probably damaging Het
Cdk10 A G 8: 123,227,015 D77G possibly damaging Het
Ctnnd1 T C 2: 84,605,196 T827A probably benign Het
Dspp A C 5: 104,175,665 T225P probably damaging Het
Evpl T C 11: 116,221,209 E1885G probably damaging Het
Fstl4 C T 11: 53,134,024 probably benign Het
Gm5930 T A 14: 44,337,558 N57I probably damaging Het
Gnl2 C T 4: 125,052,608 Q541* probably null Het
Igkv3-1 T C 6: 70,704,051 V78A probably benign Het
Inpp5a T C 7: 139,567,422 I321T probably benign Het
Kif20b T A 19: 34,974,559 S1746T probably benign Het
Lrrc8c T C 5: 105,607,172 I271T probably benign Het
Mrps10 T C 17: 47,375,003 Y152H probably damaging Het
Myl9 C T 2: 156,778,549 S2L probably damaging Het
Myof A T 19: 37,949,655 H870Q probably damaging Het
Nfatc4 A T 14: 55,829,910 I456F probably damaging Het
Notch2 A G 3: 98,102,407 H550R probably benign Het
Olfr113 T A 17: 37,574,926 I166F probably damaging Het
Olfr275 T A 4: 52,825,817 V140D possibly damaging Het
Olfr911-ps1 T C 9: 38,524,164 L144P probably damaging Het
P2rx1 A T 11: 73,012,474 I230F probably damaging Het
Pcnt A G 10: 76,380,229 V2275A possibly damaging Het
Pip5k1a G A 3: 95,064,396 T465I probably benign Het
Pnkd G A 1: 74,351,900 R415H probably damaging Het
Prdx4 T A X: 155,332,447 I132F probably damaging Het
Pvr A G 7: 19,918,792 M66T probably benign Het
Rnf216 A G 5: 143,080,240 I531T probably benign Het
Rps6ka4 A T 19: 6,832,071 F405Y probably damaging Het
Serpinb2 A G 1: 107,524,949 probably benign Het
Sfxn1 A G 13: 54,085,494 K12R probably benign Het
Slc17a7 A G 7: 45,170,946 E275G probably damaging Het
Tnpo2 A T 8: 85,045,067 I245F probably benign Het
Ush2a A T 1: 188,957,266 probably null Het
Zcchc4 C T 5: 52,808,316 R321W probably damaging Het
Other mutations in Olfr624
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02419:Olfr624 APN 7 103670475 nonsense probably null
IGL02684:Olfr624 APN 7 103670384 missense probably benign 0.06
FR4548:Olfr624 UTSW 7 103670960 small insertion probably benign
FR4548:Olfr624 UTSW 7 103670967 nonsense probably null
FR4976:Olfr624 UTSW 7 103670966 small insertion probably benign
R0295:Olfr624 UTSW 7 103670311 missense probably damaging 1.00
R0518:Olfr624 UTSW 7 103670489 missense possibly damaging 0.56
R0521:Olfr624 UTSW 7 103670489 missense possibly damaging 0.56
R1352:Olfr624 UTSW 7 103670311 missense probably damaging 1.00
R1779:Olfr624 UTSW 7 103670638 missense probably benign 0.15
R1878:Olfr624 UTSW 7 103670182 missense probably damaging 1.00
R1965:Olfr624 UTSW 7 103670896 missense probably damaging 1.00
R2162:Olfr624 UTSW 7 103670872 missense possibly damaging 0.95
R2316:Olfr624 UTSW 7 103670467 missense probably damaging 0.97
R3792:Olfr624 UTSW 7 103670146 missense probably damaging 1.00
R3848:Olfr624 UTSW 7 103670701 missense probably damaging 0.99
R4120:Olfr624 UTSW 7 103671014 missense probably benign
R4183:Olfr624 UTSW 7 103670971 missense possibly damaging 0.87
R4853:Olfr624 UTSW 7 103670803 missense probably damaging 1.00
R6351:Olfr624 UTSW 7 103670956 missense possibly damaging 0.50
R7717:Olfr624 UTSW 7 103670945 missense probably benign
RF005:Olfr624 UTSW 7 103670785 frame shift probably null
X0026:Olfr624 UTSW 7 103670395 missense probably benign
Posted On2015-04-16