Incidental Mutation 'IGL01556:Gm1840'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm1840
Ensembl Gene ENSMUSG00000043192
Gene Namepredicted gene 1840
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.889) question?
Stock #IGL01556
Quality Score
Chromosomal Location5639584-5640996 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) A to G at 5639833 bp
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000051687
SMART Domains Protein: ENSMUSP00000127885
Gene: ENSMUSG00000043192

Pfam:PGI 48 130 1.2e-34 PFAM
Pfam:PGI 127 463 1.2e-181 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts18 T C 8: 113,845,109 I81V probably benign Het
Armc3 T A 2: 19,269,146 D330E probably damaging Het
Atp6v0b A G 4: 117,885,865 F49S probably damaging Het
Atp8b3 A C 10: 80,530,968 Y265* probably null Het
Cdh11 A G 8: 102,679,644 Y66H probably damaging Het
Cntn5 T A 9: 9,673,908 M730L probably benign Het
Cntrl A G 2: 35,173,059 T1556A probably benign Het
Dixdc1 A G 9: 50,706,134 S128P probably damaging Het
Doxl2 A C 6: 48,975,684 D181A possibly damaging Het
Egfr T C 11: 16,905,382 L889S probably damaging Het
F830045P16Rik A G 2: 129,463,720 Y245H probably benign Het
Fam124a G A 14: 62,587,732 C225Y probably damaging Het
Frem2 T C 3: 53,535,281 T2612A probably benign Het
Gkap1 A T 13: 58,263,292 I89N probably benign Het
Gm8247 A T 14: 44,586,354 K75* probably null Het
Hdac11 T A 6: 91,173,180 H320Q probably benign Het
Iyd A G 10: 3,547,091 I149V probably benign Het
Krtap4-6 T A 11: 99,665,850 Q17L unknown Het
Lrrc24 T A 15: 76,722,575 D207V probably damaging Het
Mfsd12 G A 10: 81,363,024 C425Y probably damaging Het
Muc5b A G 7: 141,863,240 T3308A probably benign Het
Myo18b A G 5: 112,757,449 probably benign Het
Ndufa6 C T 15: 82,354,081 V50M possibly damaging Het
Nin A G 12: 70,043,188 V1151A probably benign Het
Nrf1 A G 6: 30,126,367 probably benign Het
Pcdhb20 T C 18: 37,504,799 I126T possibly damaging Het
Pdgfra G T 5: 75,177,691 L535F probably damaging Het
Pkn2 A T 3: 142,829,317 I212K possibly damaging Het
Slc5a9 T A 4: 111,898,636 T22S probably benign Het
Slitrk1 A G 14: 108,913,018 L87S probably damaging Het
Spert A G 14: 75,584,111 F16S probably damaging Het
Syne2 C A 12: 76,087,815 R29S probably damaging Het
Zc3h12b C A X: 95,927,115 F551L probably damaging Het
Zfp664 C A 5: 124,886,188 C215* probably null Het
Other mutations in Gm1840
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00497:Gm1840 APN 8 5640563 exon noncoding transcript
IGL01721:Gm1840 APN 8 5639896 exon noncoding transcript
IGL02008:Gm1840 APN 8 5639896 exon noncoding transcript
IGL02200:Gm1840 APN 8 5639968 exon noncoding transcript
IGL02285:Gm1840 APN 8 5640373 exon noncoding transcript
IGL02354:Gm1840 APN 8 5640896 exon noncoding transcript
IGL02361:Gm1840 APN 8 5640896 exon noncoding transcript
IGL03052:Gm1840 APN 8 5639816 exon noncoding transcript
R0114:Gm1840 UTSW 8 5640359 exon noncoding transcript
R0480:Gm1840 UTSW 8 5639888 exon noncoding transcript
R4760:Gm1840 UTSW 8 5640473 exon noncoding transcript
R5076:Gm1840 UTSW 8 5640130 exon noncoding transcript
Posted On2013-12-09