Incidental Mutation 'IGL02839:Or13c7d'
ID 361775
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Or13c7d
Ensembl Gene ENSMUSG00000044801
Gene Name olfactory receptor family 13 subfamily C member 7D
Synonyms mOR37e, MOR262-5, Olfr37e, GA_x6K02T2N78B-16165641-16166600, Olfr159
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # IGL02839
Quality Score
Status
Chromosome 4
Chromosomal Location 43770050-43771009 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 43770943 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Lysine to Stop codon at position 23 (K23*)
Ref Sequence ENSEMBL: ENSMUSP00000060784 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053931]
AlphaFold Q9QZ19
Predicted Effect probably null
Transcript: ENSMUST00000053931
AA Change: K23*
SMART Domains Protein: ENSMUSP00000060784
Gene: ENSMUSG00000044801
AA Change: K23*

DomainStartEndE-ValueType
Pfam:7tm_4 32 315 6.9e-60 PFAM
Pfam:7tm_1 42 297 2.4e-25 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000120783
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: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A3galt2 T C 4: 128,653,816 (GRCm39) probably null Het
Aldh1l1 T C 6: 90,546,857 (GRCm39) F387L possibly damaging Het
Aldh5a1 A G 13: 25,095,603 (GRCm39) S505P probably damaging Het
Aox1 A G 1: 58,107,943 (GRCm39) T642A probably benign Het
Atg16l2 T C 7: 100,942,604 (GRCm39) I364V probably damaging Het
Atp2c2 T C 8: 120,475,859 (GRCm39) V584A possibly damaging Het
Axl A T 7: 25,466,216 (GRCm39) probably null Het
Camta1 T C 4: 151,228,969 (GRCm39) Q621R probably damaging Het
Cdca4 A T 12: 112,785,511 (GRCm39) D72E probably damaging Het
Col1a2 T A 6: 4,538,748 (GRCm39) Y1223N unknown Het
Drc1 T C 5: 30,507,767 (GRCm39) M263T probably benign Het
Eef1akmt1 A T 14: 57,787,238 (GRCm39) Y213N probably damaging Het
Fat3 C A 9: 15,830,466 (GRCm39) D4343Y probably damaging Het
Ftdc1 A G 16: 58,436,210 (GRCm39) Y38H probably damaging Het
Gucy2d T C 7: 98,093,196 (GRCm39) V191A possibly damaging Het
Hdac5 A G 11: 102,095,734 (GRCm39) L355P probably damaging Het
Hdgfl3 C T 7: 81,550,160 (GRCm39) G58D probably damaging Het
Hnrnpul1 A G 7: 25,432,667 (GRCm39) probably null Het
Klf12 A T 14: 100,137,675 (GRCm39) C290* probably null Het
Mtmr3 A T 11: 4,437,994 (GRCm39) I820N probably benign Het
Myo7a A T 7: 97,740,329 (GRCm39) L555Q probably damaging Het
Nrsn1 A G 13: 25,437,527 (GRCm39) C134R probably damaging Het
Or1p1 T A 11: 74,180,196 (GRCm39) C241* probably null Het
Or4c11c G A 2: 88,661,992 (GRCm39) C177Y probably damaging Het
Or56a3b A C 7: 104,771,563 (GRCm39) T300P probably damaging Het
Or5ac24 A T 16: 59,165,753 (GRCm39) C104S probably benign Het
Or5t9 T A 2: 86,659,712 (GRCm39) N205K probably benign Het
Pik3r6 A G 11: 68,417,238 (GRCm39) E60G probably damaging Het
Pkhd1l1 T A 15: 44,392,939 (GRCm39) I1758N probably damaging Het
Poc1b A G 10: 98,980,460 (GRCm39) probably benign Het
Rnf103 G T 6: 71,486,689 (GRCm39) R440L probably benign Het
Siglec1 A G 2: 130,926,852 (GRCm39) V237A possibly damaging Het
Skic2 T C 17: 35,066,774 (GRCm39) T165A probably benign Het
Slit3 A G 11: 35,539,874 (GRCm39) N762S possibly damaging Het
Trank1 A G 9: 111,193,824 (GRCm39) N616S probably damaging Het
Trav14d-3-dv8 C A 14: 53,316,247 (GRCm39) Q36K possibly damaging Het
Ttll6 T C 11: 96,049,646 (GRCm39) V788A probably damaging Het
Ube4b A T 4: 149,452,856 (GRCm39) S357T probably damaging Het
Unc80 A G 1: 66,710,834 (GRCm39) H2701R possibly damaging Het
Wdfy3 A G 5: 102,116,786 (GRCm39) S85P probably damaging Het
Other mutations in Or13c7d
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01401:Or13c7d APN 4 43,770,112 (GRCm39) missense probably damaging 1.00
IGL02701:Or13c7d APN 4 43,770,366 (GRCm39) missense probably benign 0.31
IGL02956:Or13c7d APN 4 43,770,399 (GRCm39) missense probably benign 0.15
IGL03058:Or13c7d APN 4 43,770,255 (GRCm39) missense probably damaging 1.00
R1164:Or13c7d UTSW 4 43,770,991 (GRCm39) missense probably benign 0.03
R1796:Or13c7d UTSW 4 43,770,495 (GRCm39) missense possibly damaging 0.90
R1812:Or13c7d UTSW 4 43,770,230 (GRCm39) nonsense probably null
R4906:Or13c7d UTSW 4 43,770,476 (GRCm39) missense possibly damaging 0.76
R5426:Or13c7d UTSW 4 43,770,168 (GRCm39) missense probably benign 0.04
R5684:Or13c7d UTSW 4 43,770,624 (GRCm39) missense probably benign 0.03
R6002:Or13c7d UTSW 4 43,770,063 (GRCm39) missense probably benign
R7174:Or13c7d UTSW 4 43,770,691 (GRCm39) missense not run
R7431:Or13c7d UTSW 4 43,770,882 (GRCm39) missense probably damaging 1.00
R8423:Or13c7d UTSW 4 43,770,598 (GRCm39) missense possibly damaging 0.65
R8770:Or13c7d UTSW 4 43,770,813 (GRCm39) missense probably damaging 1.00
R8789:Or13c7d UTSW 4 43,770,793 (GRCm39) missense probably damaging 0.96
R8989:Or13c7d UTSW 4 43,770,346 (GRCm39) missense possibly damaging 0.76
R9616:Or13c7d UTSW 4 43,770,193 (GRCm39) nonsense probably null
Z1176:Or13c7d UTSW 4 43,770,267 (GRCm39) missense probably damaging 1.00
Posted On 2015-12-18