Incidental Mutation 'R0542:Or2l13b'
ID 50011
Institutional Source Beutler Lab
Gene Symbol Or2l13b
Ensembl Gene ENSMUSG00000061361
Gene Name olfactory receptor family 2 subfamily L member 13B
Synonyms GA_x54KRFPKG5P-15979009-15978071, Olfr168, MOR271-1
MMRRC Submission 038734-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.075) question?
Stock # R0542 (G1)
Quality Score 225
Status Validated
Chromosome 16
Chromosomal Location 19348730-19349668 bp(-) (GRCm39)
Type of Mutation makesense
DNA Base Change (assembly) A to T at 19348732 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Stop codon to Arginine at position 313 (*313R)
Ref Sequence ENSEMBL: ENSMUSP00000149405 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000078554] [ENSMUST00000213480]
AlphaFold Q8VF05
Predicted Effect probably null
Transcript: ENSMUST00000078554
AA Change: *313R
SMART Domains Protein: ENSMUSP00000077632
Gene: ENSMUSG00000061361
AA Change: *313R

DomainStartEndE-ValueType
Pfam:7tm_4 30 306 5e-50 PFAM
Pfam:7TM_GPCR_Srsx 34 295 3.7e-8 PFAM
Pfam:7tm_1 40 289 3.6e-27 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000213480
AA Change: *313R
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 95.0%
Validation Efficiency 99% (70/71)
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: 69 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abhd12b C A 12: 70,210,269 (GRCm39) N71K possibly damaging Het
Adgrl2 A G 3: 148,564,854 (GRCm39) I242T probably damaging Het
Adgrv1 A G 13: 81,721,437 (GRCm39) S714P probably damaging Het
Agap3 G A 5: 24,705,184 (GRCm39) R704Q possibly damaging Het
Ankrd11 T C 8: 123,622,509 (GRCm39) R448G probably damaging Het
Anks1b T C 10: 89,909,829 (GRCm39) probably benign Het
Caml A T 13: 55,770,974 (GRCm39) Q24L possibly damaging Het
Cdc14b G A 13: 64,391,497 (GRCm39) T124I probably benign Het
Clca3a2 A G 3: 144,781,571 (GRCm39) probably benign Het
Col12a1 A G 9: 79,512,610 (GRCm39) probably null Het
Crispld1 T C 1: 17,816,992 (GRCm39) V183A possibly damaging Het
Cstdc1 A G 2: 148,624,092 (GRCm39) N22S probably benign Het
Dhx40 C T 11: 86,695,082 (GRCm39) probably null Het
Dmxl1 T A 18: 50,026,761 (GRCm39) D1956E probably benign Het
Dsc2 A G 18: 20,184,283 (GRCm39) V35A probably damaging Het
Dync2i2 A G 2: 29,921,837 (GRCm39) V508A probably damaging Het
Elovl2 A G 13: 41,345,452 (GRCm39) probably benign Het
Gapvd1 T C 2: 34,615,048 (GRCm39) probably benign Het
Gnaq T A 19: 16,196,982 (GRCm39) I56N probably damaging Het
Gpr139 T C 7: 118,744,306 (GRCm39) D93G probably benign Het
Hars1 C T 18: 36,904,234 (GRCm39) R215H probably benign Het
Helz2 C A 2: 180,873,882 (GRCm39) W2204L probably damaging Het
Ift70b A G 2: 75,767,055 (GRCm39) V566A probably damaging Het
Itgb6 A T 2: 60,435,480 (GRCm39) C757S possibly damaging Het
Kpnb1 G A 11: 97,078,398 (GRCm39) T5I probably benign Het
Krt82 T C 15: 101,454,035 (GRCm39) probably benign Het
Lgals9 T A 11: 78,860,546 (GRCm39) K175N possibly damaging Het
Lrp2 A G 2: 69,258,998 (GRCm39) I4564T probably benign Het
Mblac1 A G 5: 138,192,798 (GRCm39) T47A possibly damaging Het
Med12l G A 3: 58,949,822 (GRCm39) D182N probably damaging Het
Megf9 A G 4: 70,353,585 (GRCm39) I407T probably benign Het
Mtmr6 A T 14: 60,529,578 (GRCm39) probably null Het
Mtor A G 4: 148,624,907 (GRCm39) T2173A probably benign Het
Mzt1 A T 14: 99,277,938 (GRCm39) probably benign Het
Narf T C 11: 121,143,690 (GRCm39) L444P probably damaging Het
Nsd1 A T 13: 55,408,271 (GRCm39) Q1305L possibly damaging Het
Ntsr1 A G 2: 180,184,374 (GRCm39) Y359C probably damaging Het
Olfm1 A G 2: 28,104,640 (GRCm39) D159G possibly damaging Het
Pcdh1 C T 18: 38,322,975 (GRCm39) V953I probably damaging Het
Pcdhb11 A T 18: 37,556,887 (GRCm39) D739V probably damaging Het
Pdgfd A G 9: 6,359,769 (GRCm39) N280S probably damaging Het
Per2 A T 1: 91,366,054 (GRCm39) probably null Het
Pfkp G T 13: 6,672,028 (GRCm39) C122* probably null Het
Plxna4 G A 6: 32,169,232 (GRCm39) R1322W probably damaging Het
Ppox A G 1: 171,106,818 (GRCm39) L202P probably damaging Het
Ppp1r3e G A 14: 55,114,588 (GRCm39) P58L probably benign Het
Prr23a2 A C 9: 98,739,086 (GRCm39) N148T probably benign Het
Psd T C 19: 46,302,649 (GRCm39) T842A probably damaging Het
Ranbp2 C T 10: 58,314,236 (GRCm39) A1652V probably benign Het
Rragd G A 4: 33,007,103 (GRCm39) V144M probably damaging Het
Sema6a T G 18: 47,381,643 (GRCm39) D968A probably damaging Het
Slc30a5 A T 13: 100,945,793 (GRCm39) probably null Het
Snx17 G T 5: 31,353,895 (GRCm39) probably null Het
Styxl2 A T 1: 165,928,853 (GRCm39) M253K possibly damaging Het
Syt14 G T 1: 192,613,111 (GRCm39) T563K probably damaging Het
Tada3 T C 6: 113,352,175 (GRCm39) K85E probably damaging Het
Tspear T C 10: 77,716,921 (GRCm39) V532A probably benign Het
Ttn A T 2: 76,723,453 (GRCm39) C6426S possibly damaging Het
Unc79 T C 12: 103,060,437 (GRCm39) probably benign Het
Usp19 A G 9: 108,371,584 (GRCm39) probably null Het
Vav3 G A 3: 109,434,746 (GRCm39) D426N probably damaging Het
Vezt T C 10: 93,842,958 (GRCm39) probably null Het
Vldlr G T 19: 27,213,655 (GRCm39) R114L probably benign Het
Wwc2 C T 8: 48,321,414 (GRCm39) V567I unknown Het
Zfp423 T C 8: 88,507,237 (GRCm39) T911A probably damaging Het
Zfp719 A G 7: 43,238,677 (GRCm39) probably null Het
Zkscan16 A T 4: 58,956,597 (GRCm39) H293L possibly damaging Het
Zkscan6 A C 11: 65,719,525 (GRCm39) N515T possibly damaging Het
Znfx1 A G 2: 166,897,575 (GRCm39) S450P probably damaging Het
Other mutations in Or2l13b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01635:Or2l13b APN 16 19,348,845 (GRCm39) missense probably benign 0.13
IGL02139:Or2l13b APN 16 19,349,640 (GRCm39) missense probably benign 0.05
IGL02347:Or2l13b APN 16 19,349,529 (GRCm39) missense probably damaging 1.00
IGL03402:Or2l13b APN 16 19,349,667 (GRCm39) start codon destroyed probably null 0.99
R1496:Or2l13b UTSW 16 19,349,133 (GRCm39) missense possibly damaging 0.94
R1707:Or2l13b UTSW 16 19,348,927 (GRCm39) missense probably benign 0.18
R2006:Or2l13b UTSW 16 19,349,455 (GRCm39) missense probably benign 0.02
R2220:Or2l13b UTSW 16 19,348,895 (GRCm39) nonsense probably null
R3734:Or2l13b UTSW 16 19,349,398 (GRCm39) missense probably damaging 0.99
R4134:Or2l13b UTSW 16 19,349,452 (GRCm39) missense possibly damaging 0.90
R4135:Or2l13b UTSW 16 19,349,452 (GRCm39) missense possibly damaging 0.90
R4538:Or2l13b UTSW 16 19,349,381 (GRCm39) nonsense probably null
R4631:Or2l13b UTSW 16 19,348,891 (GRCm39) nonsense probably null
R4633:Or2l13b UTSW 16 19,349,034 (GRCm39) missense possibly damaging 0.94
R4872:Or2l13b UTSW 16 19,349,383 (GRCm39) missense probably damaging 0.99
R4910:Or2l13b UTSW 16 19,348,768 (GRCm39) missense probably benign 0.03
R4945:Or2l13b UTSW 16 19,349,307 (GRCm39) missense probably benign 0.03
R5345:Or2l13b UTSW 16 19,349,527 (GRCm39) missense probably damaging 1.00
R5847:Or2l13b UTSW 16 19,349,076 (GRCm39) missense probably damaging 0.99
R5899:Or2l13b UTSW 16 19,349,551 (GRCm39) missense probably damaging 1.00
R7074:Or2l13b UTSW 16 19,348,855 (GRCm39) missense possibly damaging 0.90
R7439:Or2l13b UTSW 16 19,349,650 (GRCm39) missense probably benign 0.03
R7723:Or2l13b UTSW 16 19,349,358 (GRCm39) nonsense probably null
R7860:Or2l13b UTSW 16 19,349,167 (GRCm39) missense probably damaging 1.00
R8871:Or2l13b UTSW 16 19,349,536 (GRCm39) missense
R9515:Or2l13b UTSW 16 19,349,026 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- CATGTGTGGGCACAGTCCAAATTG -3'
(R):5'- TGTGAGCACAAGCCTGTTTCTCC -3'

Sequencing Primer
(F):5'- TGGGCACAGTCCAAATTGAATATG -3'
(R):5'- CAACTCACTTAACTGTGGTGAC -3'
Posted On 2013-06-12