Incidental Mutation 'R7707:Gm10375'
ID 594370
Institutional Source Beutler Lab
Gene Symbol Gm10375
Ensembl Gene ENSMUSG00000095528
Gene Name predicted gene 10375
Synonyms
MMRRC Submission 067893-MU
Accession Numbers
Essential gene? Not available question?
Stock # R7707 (G1)
Quality Score 168.009
Status Not validated
Chromosome 14
Chromosomal Location 43840084-43845470 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) G to A at 43842332 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Stop codon at position 133 (Q133*)
Ref Sequence ENSEMBL: ENSMUSP00000098257 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000100692]
AlphaFold Q5EBJ2
Predicted Effect probably null
Transcript: ENSMUST00000100692
AA Change: Q133*
SMART Domains Protein: ENSMUSP00000098257
Gene: ENSMUSG00000095528
AA Change: Q133*

DomainStartEndE-ValueType
Pfam:Takusan 8 89 5.1e-25 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 99% (72/73)
Allele List at MGI
Other mutations in this stock
Total: 75 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2900026A02Rik T A 5: 113,285,852 (GRCm39) M1L probably benign Het
Ap1s3 T C 1: 79,591,964 (GRCm39) K129E probably benign Het
Ap3b2 C T 7: 81,126,530 (GRCm39) V357I possibly damaging Het
Aplp1 A T 7: 30,142,523 (GRCm39) C140S probably damaging Het
Arhgef1 G A 7: 24,616,306 (GRCm39) D317N probably damaging Het
Asb4 A G 6: 5,430,968 (GRCm39) H401R probably benign Het
Bpi A T 2: 158,103,093 (GRCm39) E79D probably benign Het
Cant1 C T 11: 118,301,724 (GRCm39) V198M possibly damaging Het
Casp9 C T 4: 141,532,778 (GRCm39) R225C probably benign Het
Ccdc88b C A 19: 6,834,837 (GRCm39) R82L probably benign Het
Cfap251 A T 5: 123,391,950 (GRCm39) E28V probably benign Het
Chrm4 A G 2: 91,757,699 (GRCm39) T36A probably benign Het
Cntln A T 4: 84,802,853 (GRCm39) D51V probably damaging Het
Commd8 A T 5: 72,320,081 (GRCm39) F120Y probably damaging Het
Cpne6 A C 14: 55,753,771 (GRCm39) T410P probably damaging Het
Ctnnb1 A T 9: 120,781,931 (GRCm39) I315F possibly damaging Het
Dnah9 A G 11: 66,009,784 (GRCm39) V701A probably damaging Het
Efcab9 A G 11: 32,472,851 (GRCm39) Y199H possibly damaging Het
Endou T A 15: 97,610,983 (GRCm39) probably null Het
Fhip1a A G 3: 85,583,560 (GRCm39) V412A probably benign Het
Foxc2 C T 8: 121,844,641 (GRCm39) P430S probably benign Het
Gas2l3 T A 10: 89,250,220 (GRCm39) K299N probably damaging Het
Gorab T C 1: 163,220,009 (GRCm39) D211G probably damaging Het
Grin3b T A 10: 79,811,735 (GRCm39) S747T possibly damaging Het
Gucd1 C A 10: 75,347,120 (GRCm39) probably benign Het
Gucy2d T C 7: 98,100,876 (GRCm39) F400L possibly damaging Het
Hivep3 G A 4: 119,591,156 (GRCm39) V55M Het
Igsf3 A G 3: 101,367,238 (GRCm39) N1157S probably benign Het
Irak3 A T 10: 119,982,489 (GRCm39) D324E probably damaging Het
Jup G T 11: 100,273,878 (GRCm39) A221D possibly damaging Het
Kctd17 CAGCTGGAGGAGC CAGC 15: 78,321,113 (GRCm39) probably benign Het
Lgr4 A G 2: 109,827,936 (GRCm39) probably null Het
Lrrc34 T C 3: 30,679,041 (GRCm39) D352G probably benign Het
Metrn C A 17: 26,014,384 (GRCm39) A175S probably benign Het
Nr2c1 T A 10: 94,024,027 (GRCm39) S411T probably benign Het
Or4c11 A G 2: 88,695,153 (GRCm39) D68G possibly damaging Het
Or5h22 T A 16: 58,894,634 (GRCm39) I270F possibly damaging Het
Orc3 T A 4: 34,598,691 (GRCm39) K172* probably null Het
Oxnad1 A G 14: 31,823,965 (GRCm39) probably null Het
Pcdh7 A G 5: 57,877,672 (GRCm39) N409S probably damaging Het
Pcdha11 A T 18: 37,144,845 (GRCm39) N312I probably benign Het
Pds5a G T 5: 65,767,476 (GRCm39) P121Q unknown Het
Phc1 A G 6: 122,300,739 (GRCm39) I380T unknown Het
Phldb3 C A 7: 24,326,022 (GRCm39) H535N possibly damaging Het
Proser3 T C 7: 30,239,216 (GRCm39) Q600R probably benign Het
Ptprz1 A G 6: 23,002,295 (GRCm39) M1462V probably benign Het
Pyroxd2 T C 19: 42,726,586 (GRCm39) T243A probably damaging Het
Ralgapa1 C A 12: 55,824,077 (GRCm39) D268Y probably null Het
Rapgef5 A C 12: 117,679,079 (GRCm39) Y419S probably damaging Het
Rbm24 C A 13: 46,582,605 (GRCm39) Q175K possibly damaging Het
Robo4 A T 9: 37,324,418 (GRCm39) D982V probably damaging Het
Sbf2 T C 7: 109,929,920 (GRCm39) probably null Het
Serping1 A T 2: 84,604,043 (GRCm39) probably null Het
Shank1 C T 7: 43,993,725 (GRCm39) S798F unknown Het
Slc15a5 A T 6: 138,056,745 (GRCm39) M57K probably damaging Het
Slc35g1 T A 19: 38,391,571 (GRCm39) C284* probably null Het
Src G A 2: 157,306,578 (GRCm39) D194N probably damaging Het
Srfbp1 A G 18: 52,616,726 (GRCm39) T84A probably damaging Het
Sspo A T 6: 48,438,461 (GRCm39) T1510S probably benign Het
Taar1 A T 10: 23,797,135 (GRCm39) I278F possibly damaging Het
Taf1a T C 1: 183,185,583 (GRCm39) Y281H possibly damaging Het
Thbs3 A T 3: 89,132,207 (GRCm39) Y798F possibly damaging Het
Tnpo1 T C 13: 99,027,295 (GRCm39) T7A probably benign Het
Traf7 A T 17: 24,729,683 (GRCm39) probably null Het
Trbv19 G A 6: 41,155,547 (GRCm39) V9I possibly damaging Het
Trim17 C T 11: 58,856,110 (GRCm39) Q56* probably null Het
Ttn G T 2: 76,732,406 (GRCm39) A4643E unknown Het
Ugt2b36 A G 5: 87,229,367 (GRCm39) probably null Het
Uso1 A G 5: 92,349,795 (GRCm39) *960W probably null Het
Usp2 G T 9: 43,984,757 (GRCm39) probably null Het
Wdr20rt A G 12: 65,272,981 (GRCm39) D148G probably damaging Het
Wif1 T C 10: 120,919,864 (GRCm39) F204L probably damaging Het
Wwp1 T C 4: 19,627,645 (GRCm39) D750G probably benign Het
Zfp1006 A T 8: 129,945,660 (GRCm39) C388* probably null Het
Zmynd12 A T 4: 119,302,063 (GRCm39) D234V probably damaging Het
Other mutations in Gm10375
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03252:Gm10375 APN 14 43,842,289 (GRCm39) missense probably damaging 1.00
R4651:Gm10375 UTSW 14 43,844,326 (GRCm39) critical splice donor site probably null
R4652:Gm10375 UTSW 14 43,844,326 (GRCm39) critical splice donor site probably null
R7077:Gm10375 UTSW 14 43,840,427 (GRCm39) missense probably benign
R7313:Gm10375 UTSW 14 43,842,314 (GRCm39) missense possibly damaging 0.80
Predicted Primers PCR Primer
(F):5'- AGAGAGCCTGCATAAGTTTCAGG -3'
(R):5'- ATGCTCCATGGCCAATCTGG -3'

Sequencing Primer
(F):5'- GCCTGCATAAGTTTCAGGATGTTAC -3'
(R):5'- CCATGGCCAATCTGGATACTTG -3'
Posted On 2019-11-12