Incidental Mutation 'R9793:Or4f14c'
ID 734734
Institutional Source Beutler Lab
Gene Symbol Or4f14c
Ensembl Gene ENSMUSG00000109033
Gene Name olfactory receptor family 4 subfamily F member 14C
Synonyms Olfr1315, GA_x6K02T2Q125-73157028-73156524, MOR245-1
MMRRC Submission
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.261) question?
Stock # R9793 (G1)
Quality Score 225.009
Status Not validated
Chromosome 2
Chromosomal Location 111940657-111941160 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 111941330 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 89 (H89R)
Ref Sequence ENSEMBL: ENSMUSP00000146586 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000207542] [ENSMUST00000208654] [ENSMUST00000217078]
AlphaFold A0A140LI66
Predicted Effect probably benign
Transcript: ENSMUST00000207542
AA Change: H89R

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
Predicted Effect probably benign
Transcript: ENSMUST00000208654
AA Change: H91R

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
Predicted Effect probably benign
Transcript: ENSMUST00000217078
AA Change: H89R

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.8%
  • 10x: 99.5%
  • 20x: 98.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Add2 A T 6: 86,078,135 (GRCm39) probably null Het
Afap1l1 T C 18: 61,874,822 (GRCm39) D453G possibly damaging Het
Agrn A G 4: 156,261,129 (GRCm39) V656A probably benign Het
Aldh3a1 T C 11: 61,108,927 (GRCm39) Y443H probably damaging Het
Alpk3 T C 7: 80,750,881 (GRCm39) probably null Het
Ano1 A T 7: 144,175,434 (GRCm39) W495R probably damaging Het
Apc T A 18: 34,447,628 (GRCm39) L1508Q probably damaging Het
Cald1 A T 6: 34,723,071 (GRCm39) M52L Het
Ccdc9b T C 2: 118,587,784 (GRCm39) S517G unknown Het
Cdk11b T A 4: 155,732,378 (GRCm39) H510Q unknown Het
Cdk12 T A 11: 98,102,051 (GRCm39) D636E unknown Het
Cfap53 A G 18: 74,438,741 (GRCm39) D306G probably benign Het
Cntln C T 4: 84,985,798 (GRCm39) L951F probably benign Het
Cntnap4 T C 8: 113,608,357 (GRCm39) V1259A probably benign Het
Cntnap5c A T 17: 58,409,192 (GRCm39) T477S probably benign Het
Cyp4a30b A G 4: 115,316,167 (GRCm39) T298A probably benign Het
Dop1b T A 16: 93,598,503 (GRCm39) D2006E probably benign Het
Ermard T C 17: 15,281,441 (GRCm39) L617P probably damaging Het
Glipr1l2 A G 10: 111,942,905 (GRCm39) I253M probably benign Het
Gm40460 CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG 7: 141,794,554 (GRCm39) probably benign Het
Grik3 A G 4: 125,526,315 (GRCm39) T183A probably damaging Het
Hao1 T A 2: 134,372,552 (GRCm39) Y152F possibly damaging Het
Hdac7 T C 15: 97,698,671 (GRCm39) T629A possibly damaging Het
Hmcn1 G A 1: 150,608,689 (GRCm39) P1498S possibly damaging Het
Iqcf3 T A 9: 106,434,714 (GRCm39) K41N probably benign Het
Kif26a C T 12: 112,142,887 (GRCm39) A1047V probably damaging Het
Lrriq3 T C 3: 154,893,313 (GRCm39) M338T probably benign Het
Map1a T C 2: 121,121,304 (GRCm39) probably null Het
Ncoa2 G T 1: 13,260,355 (GRCm39) Q107K possibly damaging Het
Nsd2 A G 5: 34,003,489 (GRCm39) D213G possibly damaging Het
Nuggc T C 14: 65,847,345 (GRCm39) S131P probably damaging Het
Nwd2 A G 5: 63,964,232 (GRCm39) E1272G probably damaging Het
Or2y1 A T 11: 49,385,882 (GRCm39) N174I probably damaging Het
Or4a78 T C 2: 89,497,811 (GRCm39) I140V probably benign Het
Or52m1 G A 7: 102,289,788 (GRCm39) V112I probably benign Het
Or5b113 A T 19: 13,342,514 (GRCm39) H174L probably damaging Het
Or8h9 T A 2: 86,789,119 (GRCm39) I228F probably damaging Het
Otud7a C T 7: 63,378,845 (GRCm39) R232W probably damaging Het
Pacsin3 C A 2: 91,094,160 (GRCm39) A363D probably benign Het
Pcdh17 C T 14: 84,770,350 (GRCm39) R943* probably null Het
Pkd1 A G 17: 24,800,172 (GRCm39) T2978A probably benign Het
Pkhd1l1 T C 15: 44,406,983 (GRCm39) S2407P probably benign Het
Ppip5k2 A T 1: 97,671,822 (GRCm39) Y489* probably null Het
Rasgrp1 T C 2: 117,118,429 (GRCm39) D520G probably benign Het
Rbm20 C A 19: 53,852,551 (GRCm39) T1177K probably benign Het
Rex2 A C 4: 147,142,039 (GRCm39) N176H probably damaging Het
Rsl1d1 T C 16: 11,017,300 (GRCm39) N194S possibly damaging Het
Sel1l3 C A 5: 53,329,924 (GRCm39) R477L probably benign Het
Sidt2 A G 9: 45,850,563 (GRCm39) Y851H probably damaging Het
Sirpb1b G A 3: 15,640,074 (GRCm39) probably benign Het
Slc6a7 C A 18: 61,138,866 (GRCm39) R214L probably benign Het
Srrt G C 5: 137,294,835 (GRCm39) I739M probably benign Het
Tbc1d22a T C 15: 86,119,839 (GRCm39) L81P probably damaging Het
Trim42 A G 9: 97,245,429 (GRCm39) I457T probably damaging Het
Ttc23l T A 15: 10,537,731 (GRCm39) I180F probably benign Het
Usp9y T C Y: 1,364,679 (GRCm39) M1045V probably benign Het
Vim A G 2: 13,579,598 (GRCm39) D119G probably benign Het
Vmn2r118 T C 17: 55,899,496 (GRCm39) T803A probably damaging Het
Vwa3a C A 7: 120,383,307 (GRCm39) A636D probably damaging Het
Wdr26 A G 1: 181,036,812 (GRCm39) F143S probably damaging Het
Other mutations in Or4f14c
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6854:Or4f14c UTSW 2 111,940,992 (GRCm39) missense probably benign 0.29
R6905:Or4f14c UTSW 2 111,940,703 (GRCm39) missense probably damaging 0.99
R8671:Or4f14c UTSW 2 111,941,333 (GRCm39) missense probably damaging 1.00
R8753:Or4f14c UTSW 2 111,940,802 (GRCm39) missense probably benign 0.00
R9051:Or4f14c UTSW 2 111,941,441 (GRCm39) missense probably damaging 0.99
R9653:Or4f14c UTSW 2 111,941,261 (GRCm39) missense probably damaging 0.98
R9792:Or4f14c UTSW 2 111,941,330 (GRCm39) missense probably benign 0.00
R9795:Or4f14c UTSW 2 111,941,330 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TGTATAAGGCCAACTATCCAAGC -3'
(R):5'- GGGACATCCAGCTTCTTCTC -3'

Sequencing Primer
(F):5'- GGCCAACTATCCAAGCAATAACTAC -3'
(R):5'- GGACATCCAGCTTCTTCTCTTTGTG -3'
Posted On 2022-11-14