Incidental Mutation 'R1106:Or4c102'
ID 98464
Institutional Source Beutler Lab
Gene Symbol Or4c102
Ensembl Gene ENSMUSG00000068808
Gene Name olfactory receptor family 4 subfamily C member 102
Synonyms GA_x6K02T2Q125-50079044-50079964, Olfr1189, MOR237-2
MMRRC Submission 039179-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.107) question?
Stock # R1106 (G1)
Quality Score 225
Status Not validated
Chromosome 2
Chromosomal Location 88422150-88423070 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 88422355 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 69 (V69A)
Ref Sequence ENSEMBL: ENSMUSP00000149696 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000090700] [ENSMUST00000213679]
AlphaFold A2AV11
Predicted Effect probably benign
Transcript: ENSMUST00000090700
AA Change: V69A

PolyPhen 2 Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000088201
Gene: ENSMUSG00000068808
AA Change: V69A

DomainStartEndE-ValueType
Pfam:7tm_4 29 303 9.6e-42 PFAM
Pfam:7tm_1 39 285 4.4e-19 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000213679
AA Change: V69A

PolyPhen 2 Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.3%
  • 20x: 92.5%
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: 20 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Asic5 C A 3: 81,911,897 (GRCm39) F122L probably damaging Het
Caml A G 13: 55,772,538 (GRCm39) T61A probably benign Het
Cfap20 A T 8: 96,147,873 (GRCm39) I156N probably damaging Het
Col1a2 G A 6: 4,518,822 (GRCm39) probably benign Het
Dio2 A G 12: 90,704,985 (GRCm39) L25P probably damaging Het
Eps8 G A 6: 137,491,322 (GRCm39) P352L probably damaging Het
Gnai2 A G 9: 107,497,385 (GRCm39) I3T probably damaging Het
Hexim2 T C 11: 103,029,319 (GRCm39) S124P probably damaging Het
Klk1b16 C T 7: 43,788,937 (GRCm39) R57C probably damaging Het
Mier3 A T 13: 111,844,763 (GRCm39) D205V probably damaging Het
Or2y14 A G 11: 49,404,519 (GRCm39) D18G probably damaging Het
Ptprz1 A G 6: 22,965,748 (GRCm39) D192G probably damaging Het
Samd3 G A 10: 26,147,689 (GRCm39) V455M possibly damaging Het
Slc9c1 C A 16: 45,376,170 (GRCm39) Q419K possibly damaging Het
Syce1 C A 7: 140,359,809 (GRCm39) L83F probably damaging Het
Tas2r139 A G 6: 42,118,479 (GRCm39) T204A probably benign Het
Ush2a G A 1: 188,643,180 (GRCm39) E4181K possibly damaging Het
Vps37a T A 8: 40,965,247 (GRCm39) I33N probably damaging Het
Zfp335 TTGCTGCTGCTGCTGCTGCT TTGCTGCTGCTGCTGCT 2: 164,749,471 (GRCm39) probably benign Het
Zik1 G A 7: 10,224,312 (GRCm39) R262C probably damaging Het
Other mutations in Or4c102
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02306:Or4c102 APN 2 88,422,950 (GRCm39) missense probably benign 0.22
R0115:Or4c102 UTSW 2 88,422,999 (GRCm39) missense probably damaging 1.00
R0481:Or4c102 UTSW 2 88,422,999 (GRCm39) missense probably damaging 1.00
R0565:Or4c102 UTSW 2 88,422,353 (GRCm39) missense probably benign 0.39
R1501:Or4c102 UTSW 2 88,422,492 (GRCm39) missense possibly damaging 0.94
R1616:Or4c102 UTSW 2 88,422,352 (GRCm39) missense probably damaging 0.99
R1763:Or4c102 UTSW 2 88,422,780 (GRCm39) missense probably benign 0.02
R1847:Or4c102 UTSW 2 88,422,516 (GRCm39) missense probably damaging 1.00
R1989:Or4c102 UTSW 2 88,422,943 (GRCm39) missense probably damaging 0.99
R3436:Or4c102 UTSW 2 88,422,448 (GRCm39) missense probably damaging 1.00
R3500:Or4c102 UTSW 2 88,422,285 (GRCm39) missense probably damaging 1.00
R4410:Or4c102 UTSW 2 88,422,765 (GRCm39) missense probably benign 0.03
R4463:Or4c102 UTSW 2 88,422,976 (GRCm39) missense possibly damaging 0.77
R5005:Or4c102 UTSW 2 88,422,348 (GRCm39) missense probably benign 0.00
R5174:Or4c102 UTSW 2 88,422,992 (GRCm39) missense probably damaging 1.00
R5557:Or4c102 UTSW 2 88,422,897 (GRCm39) missense probably damaging 1.00
R6354:Or4c102 UTSW 2 88,422,478 (GRCm39) missense probably damaging 1.00
R6850:Or4c102 UTSW 2 88,422,650 (GRCm39) nonsense probably null
R7522:Or4c102 UTSW 2 88,423,005 (GRCm39) missense possibly damaging 0.94
R7837:Or4c102 UTSW 2 88,422,723 (GRCm39) missense possibly damaging 0.80
R8252:Or4c102 UTSW 2 88,423,011 (GRCm39) missense probably damaging 1.00
R8345:Or4c102 UTSW 2 88,422,435 (GRCm39) missense probably benign 0.10
R9346:Or4c102 UTSW 2 88,423,062 (GRCm39) missense probably benign
R9425:Or4c102 UTSW 2 88,422,877 (GRCm39) missense probably damaging 0.99
R9632:Or4c102 UTSW 2 88,423,057 (GRCm39) missense probably benign 0.05
Predicted Primers PCR Primer
(F):5'- CCCACAAGGCTGTGAAATCACTCATTC -3'
(R):5'- GCGACATAGCGATCATAGGCCATAAC -3'

Sequencing Primer
(F):5'- CAGAGTTTATTCTGTTGGGAGTTAC -3'
(R):5'- CGATCATAGGCCATAACAATGAG -3'
Posted On 2014-01-05