Incidental Mutation 'IGL01482:Gm29326'
ID 88655
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm29326
Ensembl Gene ENSMUSG00000100400
Gene Name predicted gene 29326
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL01482
Quality Score
Status
Chromosome 7
Chromosomal Location 29259790-29262240 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to C at 29260136 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: ENSMUST00000053635
SMART Domains Protein: ENSMUSP00000049518
Gene: ENSMUSG00000046958

DomainStartEndE-ValueType
Blast:WD40 43 79 3e-11 BLAST
WD40 131 172 1.97e2 SMART
WD40 175 214 2.24e-2 SMART
Blast:WD40 257 296 4e-15 BLAST
WD40 393 437 1.32e2 SMART
WD40 494 533 2.15e-4 SMART
low complexity region 598 617 N/A INTRINSIC
low complexity region 1082 1094 N/A INTRINSIC
low complexity region 1107 1148 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000063585
SMART Domains Protein: ENSMUSP00000063695
Gene: ENSMUSG00000051976

DomainStartEndE-ValueType
low complexity region 15 28 N/A INTRINSIC
internal_repeat_1 35 67 3.29e-5 PROSPERO
internal_repeat_1 73 102 3.29e-5 PROSPERO
low complexity region 122 135 N/A INTRINSIC
coiled coil region 161 182 N/A INTRINSIC
low complexity region 216 233 N/A INTRINSIC
low complexity region 239 249 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185541
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
3110009E18Rik A T 1: 120,099,201 (GRCm39) D98V probably benign Het
Aatf G A 11: 84,361,536 (GRCm39) R356C possibly damaging Het
Abca15 A T 7: 119,981,969 (GRCm39) T1095S probably benign Het
Abca9 A G 11: 110,011,599 (GRCm39) F1148S probably benign Het
Adam12 G T 7: 133,569,577 (GRCm39) D299E probably damaging Het
Alyref A T 11: 120,486,762 (GRCm39) N166K possibly damaging Het
Atxn1 A T 13: 45,710,790 (GRCm39) I714N probably benign Het
Bves A G 10: 45,230,902 (GRCm39) E291G possibly damaging Het
Chrm2 A G 6: 36,500,692 (GRCm39) N183S possibly damaging Het
Dennd2a T C 6: 39,457,243 (GRCm39) H733R probably damaging Het
Erbb3 C T 10: 128,408,798 (GRCm39) G762S possibly damaging Het
Itgb2l A T 16: 96,239,948 (GRCm39) L17Q probably damaging Het
Jade1 T A 3: 41,567,937 (GRCm39) D668E probably benign Het
Ksr1 G A 11: 78,927,409 (GRCm39) T308I probably damaging Het
Mfap4 A G 11: 61,378,583 (GRCm39) D177G probably damaging Het
Mmut C T 17: 41,267,162 (GRCm39) R579C probably damaging Het
Muc2 A T 7: 141,307,797 (GRCm39) I369F probably damaging Het
Myh13 A T 11: 67,242,894 (GRCm39) M936L probably benign Het
Nckap5 G T 1: 125,950,897 (GRCm39) S1598Y probably damaging Het
Nlrp10 T A 7: 108,526,159 (GRCm39) M60L probably benign Het
Nlrp12 T C 7: 3,283,790 (GRCm39) N739S possibly damaging Het
Or5p58 A C 7: 107,694,693 (GRCm39) V28G probably benign Het
Pappa A T 4: 65,074,271 (GRCm39) H275L probably benign Het
Plekhm2 A G 4: 141,357,340 (GRCm39) S711P probably damaging Het
Ptpn1 G A 2: 167,809,712 (GRCm39) V107M probably damaging Het
Ptprf G A 4: 118,069,651 (GRCm39) R1498C probably damaging Het
Rhobtb2 A G 14: 70,034,037 (GRCm39) I396T possibly damaging Het
Ryr1 A G 7: 28,751,762 (GRCm39) F3668S probably damaging Het
Serpinb6d T C 13: 33,855,346 (GRCm39) V340A probably benign Het
Silc1 T A 12: 27,191,893 (GRCm39) noncoding transcript Het
Spaca3 G T 11: 80,758,510 (GRCm39) V158L probably benign Het
Tdp1 A G 12: 99,857,639 (GRCm39) N66S probably benign Het
Tmem132d A T 5: 128,346,270 (GRCm39) I84N probably damaging Het
Uggt2 T A 14: 119,295,057 (GRCm39) D523V probably damaging Het
Usp17la A T 7: 104,508,600 (GRCm39) M1L probably benign Het
Yeats2 C T 16: 20,041,671 (GRCm39) T1202I probably damaging Het
Other mutations in Gm29326
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01474:Gm29326 APN 7 29,262,014 (GRCm39) exon noncoding transcript
IGL02336:Gm29326 APN 7 29,260,833 (GRCm39) exon noncoding transcript
Posted On 2013-11-18