Incidental Mutation 'R4885:Or5an1c'
ID 375675
Institutional Source Beutler Lab
Gene Symbol Or5an1c
Ensembl Gene ENSMUSG00000067519
Gene Name olfactory receptor family 5 subfamily AN member 1C
Synonyms MOR214-1, Olfr262, GA_x6K02T2N4A9-18144-19082, MOR214-9
MMRRC Submission 042851-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.076) question?
Stock # R4885 (G1)
Quality Score 225
Status Validated
Chromosome 19
Chromosomal Location 12218085-12219023 bp(-) (GRCm39)
Type of Mutation splice site (3 bp from exon)
DNA Base Change (assembly) T to G at 12218082 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000085120 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000087818]
AlphaFold Q8VFV8
Predicted Effect probably null
Transcript: ENSMUST00000087818
SMART Domains Protein: ENSMUSP00000085120
Gene: ENSMUSG00000067519

DomainStartEndE-ValueType
Pfam:7tm_4 32 309 2.3e-55 PFAM
Pfam:7tm_1 42 291 1.2e-20 PFAM
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.7%
  • 20x: 93.6%
Validation Efficiency 99% (77/78)
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: 72 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcf3 A G 16: 20,370,425 (GRCm39) T317A probably benign Het
Adck1 G A 12: 88,407,865 (GRCm39) A199T probably benign Het
Adgrb1 A T 15: 74,444,011 (GRCm39) M1038L probably benign Het
Anapc10 C T 8: 80,455,779 (GRCm39) T76I probably benign Het
Atosa T C 9: 74,913,649 (GRCm39) L94P probably damaging Het
Bptf C T 11: 106,965,474 (GRCm39) S1177N probably benign Het
Bsn A T 9: 107,984,726 (GRCm39) Y337* probably null Het
Ccl20 T A 1: 83,095,580 (GRCm39) V48E possibly damaging Het
Ccnl1 C T 3: 65,864,320 (GRCm39) D122N probably damaging Het
Chat C G 14: 32,176,567 (GRCm39) G69A probably damaging Het
Cr2 T A 1: 194,841,039 (GRCm39) I418F possibly damaging Het
Dmxl1 G C 18: 50,011,862 (GRCm39) A1340P probably damaging Het
Eef2k G A 7: 120,491,155 (GRCm39) R547Q probably benign Het
Eml2 G A 7: 18,937,935 (GRCm39) S793N probably benign Het
Enox1 T A 14: 77,958,290 (GRCm39) L632Q probably damaging Het
Fabp9 T C 3: 10,259,738 (GRCm39) K92E probably damaging Het
Fam234a T C 17: 26,432,559 (GRCm39) H530R probably benign Het
Fancm C T 12: 65,149,417 (GRCm39) Q728* probably null Het
Fgd3 G A 13: 49,417,465 (GRCm39) T666M possibly damaging Het
Foxs1 T C 2: 152,774,301 (GRCm39) M251V probably benign Het
Fsip2 A T 2: 82,818,438 (GRCm39) M4724L probably benign Het
Gemin6 G A 17: 80,535,327 (GRCm39) E96K probably damaging Het
Gfi1 C A 5: 107,871,152 (GRCm39) V80F probably damaging Het
H3c13 G T 3: 96,176,277 (GRCm39) V90F possibly damaging Het
Hectd1 A G 12: 51,847,505 (GRCm39) V442A probably damaging Het
Ift80 A G 3: 68,857,829 (GRCm39) I272T probably damaging Het
Impact C G 18: 13,119,430 (GRCm39) A214G probably damaging Het
Insl6 C T 19: 29,302,556 (GRCm39) E54K probably benign Het
Irak3 T A 10: 120,018,586 (GRCm39) D54V probably damaging Het
Itk C T 11: 46,227,171 (GRCm39) probably null Het
Ivl A T 3: 92,479,718 (GRCm39) C116S probably benign Het
Kcnq4 G A 4: 120,570,260 (GRCm39) A361V probably benign Het
L1td1 C T 4: 98,625,548 (GRCm39) P581L probably benign Het
Lrp1b T C 2: 41,358,905 (GRCm39) E656G probably benign Het
Macrod2 A G 2: 140,261,985 (GRCm39) T89A possibly damaging Het
Mettl13 T C 1: 162,364,837 (GRCm39) D514G probably damaging Het
Mfsd13b A T 7: 120,590,711 (GRCm39) I151F possibly damaging Het
Mical3 G A 6: 120,912,214 (GRCm39) P1882S probably damaging Het
Mycbp2 T C 14: 103,383,382 (GRCm39) E394G possibly damaging Het
Myo16 T A 8: 10,488,892 (GRCm39) S688T probably damaging Het
Neb T C 2: 52,176,058 (GRCm39) Y1467C probably damaging Het
Nhsl3 C T 4: 129,118,238 (GRCm39) R214Q probably damaging Het
Nkx6-3 C A 8: 23,643,914 (GRCm39) P105Q possibly damaging Het
Nlrp1b T C 11: 71,108,710 (GRCm39) T264A possibly damaging Het
Nnat G A 2: 157,403,678 (GRCm39) C122Y probably damaging Het
Notch3 G A 17: 32,360,351 (GRCm39) R1527C probably damaging Het
Or2y16 C T 11: 49,335,449 (GRCm39) T257I probably damaging Het
Or5h18 A G 16: 58,847,518 (GRCm39) Y251H probably damaging Het
Pds5b C T 5: 150,639,927 (GRCm39) T14I probably benign Het
Phf19 A T 2: 34,789,718 (GRCm39) I334N probably damaging Het
Pik3ap1 T C 19: 41,364,365 (GRCm39) D118G probably benign Het
Pkhd1 T A 1: 20,140,712 (GRCm39) E3886V possibly damaging Het
Pkp1 A G 1: 135,846,690 (GRCm39) S21P possibly damaging Het
Pramel32 T A 4: 88,546,219 (GRCm39) L374F possibly damaging Het
Rack1 C A 11: 48,696,463 (GRCm39) A290E probably damaging Het
Rbm15 A G 3: 107,239,570 (GRCm39) V276A probably benign Het
Rnf216 A T 5: 143,076,335 (GRCm39) L183* probably null Het
Sc5d T C 9: 42,166,922 (GRCm39) I206V probably benign Het
Scpep1 A G 11: 88,826,737 (GRCm39) I233T probably benign Het
Sh3pxd2a A G 19: 47,257,132 (GRCm39) Y529H probably damaging Het
Slc1a4 A C 11: 20,254,384 (GRCm39) V494G probably damaging Het
Slc38a7 T C 8: 96,575,230 (GRCm39) T17A probably benign Het
Smg6 T C 11: 74,932,744 (GRCm39) S73P probably damaging Het
Stk32b T C 5: 37,624,141 (GRCm39) Y202C probably damaging Het
Tas2r140 A G 6: 40,468,334 (GRCm39) S55G probably damaging Het
Tcf12 C T 9: 71,766,122 (GRCm39) G504S probably null Het
Ttc3 G C 16: 94,227,690 (GRCm39) probably null Het
Ttc3 T C 16: 94,220,324 (GRCm39) I568T probably damaging Het
Ttc41 T G 10: 86,594,966 (GRCm39) N913K possibly damaging Het
Vrk1 G A 12: 106,024,231 (GRCm39) V236M probably damaging Het
Wscd1 C T 11: 71,650,972 (GRCm39) R100C probably damaging Het
Zc3h18 C T 8: 123,128,445 (GRCm39) probably benign Het
Other mutations in Or5an1c
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01432:Or5an1c APN 19 12,218,891 (GRCm39) missense probably damaging 0.99
IGL02170:Or5an1c APN 19 12,218,120 (GRCm39) missense probably benign
IGL02748:Or5an1c APN 19 12,218,204 (GRCm39) missense probably benign 0.01
IGL02896:Or5an1c APN 19 12,218,353 (GRCm39) nonsense probably null
R0365:Or5an1c UTSW 19 12,218,440 (GRCm39) missense probably benign 0.13
R0374:Or5an1c UTSW 19 12,218,505 (GRCm39) missense probably damaging 1.00
R1226:Or5an1c UTSW 19 12,218,950 (GRCm39) missense probably benign
R1319:Or5an1c UTSW 19 12,218,866 (GRCm39) missense probably damaging 1.00
R1426:Or5an1c UTSW 19 12,218,546 (GRCm39) missense possibly damaging 0.81
R1453:Or5an1c UTSW 19 12,218,956 (GRCm39) missense probably benign
R1675:Or5an1c UTSW 19 12,218,195 (GRCm39) missense probably benign 0.37
R1773:Or5an1c UTSW 19 12,219,023 (GRCm39) start codon destroyed probably null 0.03
R1778:Or5an1c UTSW 19 12,218,819 (GRCm39) missense probably benign
R1820:Or5an1c UTSW 19 12,218,612 (GRCm39) missense probably damaging 1.00
R3161:Or5an1c UTSW 19 12,218,860 (GRCm39) missense probably benign 0.06
R3412:Or5an1c UTSW 19 12,218,954 (GRCm39) missense probably benign 0.00
R4387:Or5an1c UTSW 19 12,218,503 (GRCm39) missense probably damaging 0.98
R4389:Or5an1c UTSW 19 12,218,503 (GRCm39) missense probably damaging 0.98
R4782:Or5an1c UTSW 19 12,218,936 (GRCm39) missense probably benign 0.01
R4915:Or5an1c UTSW 19 12,218,737 (GRCm39) missense probably benign 0.31
R5254:Or5an1c UTSW 19 12,218,612 (GRCm39) missense probably damaging 1.00
R5726:Or5an1c UTSW 19 12,218,644 (GRCm39) missense probably damaging 0.99
R6579:Or5an1c UTSW 19 12,218,726 (GRCm39) missense probably benign
R7062:Or5an1c UTSW 19 12,218,089 (GRCm39) missense probably benign
R7424:Or5an1c UTSW 19 12,218,318 (GRCm39) missense possibly damaging 0.65
R9491:Or5an1c UTSW 19 12,218,606 (GRCm39) missense probably benign 0.01
R9736:Or5an1c UTSW 19 12,218,920 (GRCm39) missense probably damaging 0.97
Predicted Primers PCR Primer
(F):5'- CATCAAATCAGTTGGTTCATGCAG -3'
(R):5'- GTGCTTCTCACTTGACAGCTG -3'

Sequencing Primer
(F):5'- GAGACAGGGTTTCTCTATATAGCCC -3'
(R):5'- ACCTCCAGTATCTTTGTCTATTTGAG -3'
Posted On 2016-03-17