Incidental Mutation 'IGL02412:Gm2058'
ID 294372
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm2058
Ensembl Gene ENSMUSG00000074903
Gene Name predicted gene 2058
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL02412
Quality Score
Status
Chromosome 7
Chromosomal Location 39238355-39239141 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) G to A at 39238457 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000178791
SMART Domains Protein: ENSMUSP00000136025
Gene: ENSMUSG00000074903

DomainStartEndE-ValueType
UBCc 5 150 7.04e-55 SMART
low complexity region 163 177 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181075
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alms1 T A 6: 85,605,854 (GRCm39) F2032L possibly damaging Het
Caps2 T C 10: 112,039,941 (GRCm39) probably null Het
Ccdc88b A T 19: 6,824,012 (GRCm39) F1414I probably damaging Het
Cr1l T G 1: 194,797,080 (GRCm39) Y319S probably damaging Het
Cr1l C T 1: 194,797,074 (GRCm39) G283E probably damaging Het
Csmd2 G A 4: 128,407,165 (GRCm39) probably benign Het
Dhx37 T A 5: 125,508,692 (GRCm39) K81M probably damaging Het
Dzip3 T A 16: 48,778,820 (GRCm39) M326L probably benign Het
Exosc10 A G 4: 148,652,849 (GRCm39) D488G probably benign Het
Gm43638 T A 5: 87,633,995 (GRCm39) Q204L possibly damaging Het
Gm4847 T C 1: 166,469,307 (GRCm39) D119G probably damaging Het
Gnb3 A C 6: 124,814,425 (GRCm39) M120R probably benign Het
Il16 A C 7: 83,301,899 (GRCm39) D74E probably benign Het
Kpna1 T C 16: 35,851,561 (GRCm39) F382L probably benign Het
Krt33a G T 11: 99,902,805 (GRCm39) Q340K probably benign Het
Lrrc17 T A 5: 21,765,877 (GRCm39) S120T possibly damaging Het
Mapk3 C A 7: 126,362,210 (GRCm39) Y56* probably null Het
Mfhas1 C T 8: 36,055,969 (GRCm39) A148V probably benign Het
Npr2 A G 4: 43,647,005 (GRCm39) I713V probably damaging Het
Obp1a T A X: 77,131,980 (GRCm39) Y108F probably damaging Het
Or51f1d A T 7: 102,701,359 (GRCm39) M285L probably benign Het
Or5ac21 T A 16: 59,123,555 (GRCm39) L13H probably damaging Het
Or6n1 T C 1: 173,916,809 (GRCm39) F68L probably benign Het
Or7e178 T A 9: 20,225,935 (GRCm39) S86C probably benign Het
Pias1 A T 9: 62,800,421 (GRCm39) N430K probably benign Het
Ralgapa2 G T 2: 146,254,052 (GRCm39) A836D probably damaging Het
Rftn2 T C 1: 55,245,497 (GRCm39) E238G probably benign Het
Samt4 T G X: 153,267,118 (GRCm39) S86A probably damaging Het
Setd2 T C 9: 110,379,842 (GRCm39) M1219T probably benign Het
Sh3pxd2b T A 11: 32,337,992 (GRCm39) D99E probably damaging Het
Sh3rf1 A T 8: 61,825,723 (GRCm39) T573S probably benign Het
Sugct A G 13: 17,837,386 (GRCm39) W82R probably damaging Het
Syt4 T G 18: 31,576,896 (GRCm39) K153Q probably benign Het
Tbrg1 T C 9: 37,563,908 (GRCm39) probably null Het
Tex36 C T 7: 133,189,137 (GRCm39) R145K probably benign Het
Tfap2b A T 1: 19,289,427 (GRCm39) D166V probably damaging Het
Trhde T C 10: 114,322,830 (GRCm39) Y694C probably damaging Het
Trpc1 G A 9: 95,618,914 (GRCm39) L146F probably damaging Het
Ttc29 G A 8: 79,003,569 (GRCm39) E262K possibly damaging Het
Ttn A T 2: 76,547,293 (GRCm39) I32251N probably damaging Het
Ttn G T 2: 76,612,691 (GRCm39) D17129E probably benign Het
Ucma T A 2: 4,981,636 (GRCm39) I47N probably damaging Het
Vmn1r13 A T 6: 57,187,474 (GRCm39) K211M possibly damaging Het
Vmn2r95 A C 17: 18,660,218 (GRCm39) H210P probably damaging Het
Xpc T C 6: 91,476,767 (GRCm39) E444G probably benign Het
Yy1 T C 12: 108,760,023 (GRCm39) probably benign Het
Zfp217 A G 2: 169,954,422 (GRCm39) probably benign Het
Zfp318 T A 17: 46,720,043 (GRCm39) Y1080* probably null Het
Other mutations in Gm2058
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01338:Gm2058 APN 7 39,238,580 (GRCm39) exon noncoding transcript
IGL01366:Gm2058 APN 7 39,238,658 (GRCm39) exon noncoding transcript
Posted On 2015-04-16