Incidental Mutation 'IGL03060:Gm9637'
ID 409393
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm9637
Ensembl Gene ENSMUSG00000093814
Gene Name predicted gene 9637
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.254) question?
Stock # IGL03060
Quality Score
Status
Chromosome 14
Chromosomal Location 3067106-3067978 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) G to A at 19402173 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000179141
SMART Domains Protein: ENSMUSP00000137522
Gene: ENSMUSG00000093814

DomainStartEndE-ValueType
S_TKc 36 283 1.12e-85 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Afap1l2 G A 19: 56,902,682 (GRCm39) Q720* probably null Het
Amph A G 13: 19,278,984 (GRCm39) E153G probably damaging Het
Atad2 T C 15: 57,985,842 (GRCm39) probably benign Het
Atosa A G 9: 74,917,450 (GRCm39) D683G probably damaging Het
Cep152 C T 2: 125,461,907 (GRCm39) probably benign Het
Cntn2 C T 1: 132,456,678 (GRCm39) V123I probably benign Het
Dhrs2 C A 14: 55,474,775 (GRCm39) Q137K probably benign Het
Fam124a A G 14: 62,843,353 (GRCm39) Y287C probably benign Het
Flg2 C T 3: 93,110,920 (GRCm39) R983W unknown Het
Helz2 A G 2: 180,871,015 (GRCm39) probably null Het
Iars1 G A 13: 49,843,923 (GRCm39) probably null Het
Igll1 A T 16: 16,680,291 (GRCm39) probably null Het
Iqch A G 9: 63,432,196 (GRCm39) Y361H probably damaging Het
Lrp1b A T 2: 40,527,765 (GRCm39) H105Q probably benign Het
Mapk6 A G 9: 75,305,084 (GRCm39) M111T probably damaging Het
Mrtfa G A 15: 80,929,523 (GRCm39) R27W probably damaging Het
Mt1 T A 8: 94,906,522 (GRCm39) probably benign Het
Myh7b A T 2: 155,474,671 (GRCm39) D1768V probably damaging Het
Myo6 A T 9: 80,168,159 (GRCm39) Q441L probably benign Het
Nt5c3b A T 11: 100,327,045 (GRCm39) Y84N probably damaging Het
Ntmt2 T C 1: 163,544,692 (GRCm39) D97G probably damaging Het
Or1e29 A G 11: 73,667,289 (GRCm39) F288S probably damaging Het
Paxx A G 2: 25,350,196 (GRCm39) L137P probably damaging Het
Ptprz1 T C 6: 22,972,834 (GRCm39) V248A probably damaging Het
Rif1 T A 2: 52,002,149 (GRCm39) C1868S probably damaging Het
Sec23a A T 12: 59,032,891 (GRCm39) C403S probably benign Het
Skint4 G A 4: 111,975,432 (GRCm39) V131I probably benign Het
Sugp2 T C 8: 70,695,837 (GRCm39) V270A possibly damaging Het
Tmed9 A G 13: 55,743,321 (GRCm39) D151G possibly damaging Het
Tubgcp4 A G 2: 121,007,071 (GRCm39) probably benign Het
Uaca A G 9: 60,777,148 (GRCm39) R512G probably damaging Het
Unc80 A G 1: 66,676,169 (GRCm39) Y1999C possibly damaging Het
Vwf T A 6: 125,640,523 (GRCm39) C2320S probably damaging Het
Other mutations in Gm9637
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02304:Gm9637 APN 14 19,402,545 (GRCm38) exon noncoding transcript
IGL02449:Gm9637 APN 14 19,402,436 (GRCm38) exon noncoding transcript
IGL02492:Gm9637 APN 14 19,402,182 (GRCm38) exon noncoding transcript
R0062:Gm9637 UTSW 14 19,402,570 (GRCm38) exon noncoding transcript
R0621:Gm9637 UTSW 14 19,402,011 (GRCm38) exon noncoding transcript
R1122:Gm9637 UTSW 14 19,401,879 (GRCm38) exon noncoding transcript
R1762:Gm9637 UTSW 14 19,402,408 (GRCm38) exon noncoding transcript
R1812:Gm9637 UTSW 14 19,402,395 (GRCm38) exon noncoding transcript
R2880:Gm9637 UTSW 14 19,401,978 (GRCm38) exon noncoding transcript
R3685:Gm9637 UTSW 14 19,401,950 (GRCm38) exon noncoding transcript
R3810:Gm9637 UTSW 14 19,402,398 (GRCm38) exon noncoding transcript
R3812:Gm9637 UTSW 14 19,402,398 (GRCm38) exon noncoding transcript
R5415:Gm9637 UTSW 14 19,402,143 (GRCm38) exon noncoding transcript
R8245:Gm9637 UTSW 14 19,402,598 (GRCm38) missense noncoding transcript
Z1088:Gm9637 UTSW 14 19,401,731 (GRCm38) exon noncoding transcript
Posted On 2016-08-02