Incidental Mutation 'IGL01721:Gm1840'
ID105112
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm1840
Ensembl Gene ENSMUSG00000043192
Gene Namepredicted gene 1840
SynonymsLOC233995
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.897) question?
Stock #IGL01721
Quality Score
Status
Chromosome8
Chromosomal Location5639584-5640996 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) A to T at 5639896 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000051687
SMART Domains Protein: ENSMUSP00000127885
Gene: ENSMUSG00000043192

DomainStartEndE-ValueType
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: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700088E04Rik T C 15: 79,139,253 M51V possibly damaging Het
Acad8 A G 9: 26,992,267 probably benign Het
Atp2a2 A G 5: 122,500,792 V53A possibly damaging Het
Bicra T C 7: 15,988,699 T298A probably benign Het
Ccdc185 C T 1: 182,748,978 E49K possibly damaging Het
Cfhr2 A G 1: 139,813,614 S208P probably benign Het
Chd1 T C 17: 15,770,168 Y1661H probably damaging Het
Cntnap5a A G 1: 116,157,637 H435R probably benign Het
Cog8 A G 8: 107,054,065 V187A probably benign Het
Col24a1 A G 3: 145,538,567 H1532R probably benign Het
Dpp6 A G 5: 27,631,520 Y336C probably damaging Het
Drosha T A 15: 12,846,112 Y444* probably null Het
Egf A T 3: 129,697,722 C374* probably null Het
Eif2b3 C T 4: 117,058,804 H203Y probably damaging Het
Erbb4 A G 1: 68,254,563 V723A possibly damaging Het
Fbxo21 T C 5: 117,988,790 I202T probably benign Het
Gbp6 T C 5: 105,274,207 M544V probably benign Het
Gm10750 T C 2: 149,016,044 T96A unknown Het
Gm8232 A T 14: 44,437,183 probably null Het
Gsdma3 T C 11: 98,637,956 V412A possibly damaging Het
Hs6st1 A T 1: 36,068,935 H93L probably damaging Het
Hsf2 G A 10: 57,496,181 E77K probably benign Het
Ing3 T A 6: 21,968,880 probably benign Het
Ints6 T C 14: 62,713,739 I280M probably damaging Het
Kazn C A 4: 142,159,043 probably null Het
Klhl20 T C 1: 161,095,587 Y13C probably damaging Het
Krtap26-1 G A 16: 88,647,172 P187L probably damaging Het
Mga T A 2: 119,935,239 I1329K probably damaging Het
Mindy4 A G 6: 55,223,999 D223G probably damaging Het
Ncor2 T C 5: 125,050,937 E124G probably damaging Het
Nfat5 G A 8: 107,344,979 probably null Het
Nkain1 A G 4: 130,532,134 F184L probably benign Het
Olfr1061 T C 2: 86,413,333 T240A probably damaging Het
Rars A T 11: 35,828,664 F110L probably damaging Het
Rfx6 A C 10: 51,723,077 K509N probably damaging Het
Serpinb2 T C 1: 107,515,603 L44P probably damaging Het
Sin3a G A 9: 57,095,325 R167Q probably damaging Het
Sos2 T A 12: 69,603,867 T809S probably damaging Het
Stard9 A G 2: 120,703,330 E3356G probably damaging Het
Vmn1r52 A G 6: 90,178,923 T70A probably benign Het
Other mutations in Gm1840
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00497:Gm1840 APN 8 5640563 exon noncoding transcript
IGL01556:Gm1840 APN 8 5639833 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 On2014-01-21