Incidental Mutation 'IGL01474:Gm29326'
ID 88376
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 # IGL01474
Quality Score
Status
Chromosome 7
Chromosomal Location 29259790-29262240 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to T at 29262014 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: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acot12 A T 13: 91,920,902 (GRCm39) K336I possibly damaging Het
Acsbg2 A G 17: 57,168,621 (GRCm39) I166T possibly damaging Het
Adrm1b G T 3: 92,335,650 (GRCm39) Q351K probably damaging Het
Bpifc T A 10: 85,836,503 (GRCm39) M1L probably damaging Het
Ccnb2 T A 9: 70,326,305 (GRCm39) N44I probably benign Het
Cdc73 C T 1: 143,547,070 (GRCm39) V276M probably benign Het
Cnot7 A G 8: 40,960,490 (GRCm39) probably null Het
Col11a1 T A 3: 114,010,783 (GRCm39) probably benign Het
Coro1c T C 5: 114,020,216 (GRCm39) probably benign Het
Crocc A G 4: 140,762,703 (GRCm39) probably benign Het
Dync2h1 A T 9: 7,102,493 (GRCm39) Y396N probably benign Het
Gm2888 T A 14: 3,032,041 (GRCm38) D116E probably damaging Het
Greb1 A G 12: 16,734,502 (GRCm39) V1496A probably benign Het
H2bc18 A G 3: 96,177,125 (GRCm39) probably benign Het
Hdac7 A G 15: 97,695,820 (GRCm39) probably null Het
Hectd4 A G 5: 121,474,712 (GRCm39) T2778A possibly damaging Het
Hivep2 A T 10: 14,019,406 (GRCm39) H2059L probably damaging Het
Ift88 A T 14: 57,715,531 (GRCm39) I525F probably benign Het
Irag1 A T 7: 110,470,640 (GRCm39) S898T possibly damaging Het
Itga5 G A 15: 103,262,697 (GRCm39) Q324* probably null Het
Klhl14 T G 18: 21,690,911 (GRCm39) H513P probably damaging Het
Lama5 A T 2: 179,838,363 (GRCm39) D837E probably damaging Het
Muc6 C A 7: 141,237,572 (GRCm39) C215F probably damaging Het
Myh15 A G 16: 48,952,461 (GRCm39) K844E probably damaging Het
Neb A G 2: 52,218,917 (GRCm39) V31A unknown Het
Nipbl A G 15: 8,340,693 (GRCm39) I2009T possibly damaging Het
Or2ag18 A G 7: 106,405,147 (GRCm39) I174T probably benign Het
Piwil2 T C 14: 70,635,667 (GRCm39) R536G probably benign Het
Pld3 A G 7: 27,232,044 (GRCm39) V412A probably damaging Het
Prkaa2 A C 4: 104,906,529 (GRCm39) probably null Het
Rdh9 T C 10: 127,626,814 (GRCm39) L289P probably damaging Het
Rusc2 C T 4: 43,416,434 (GRCm39) S580L probably damaging Het
Sidt2 A G 9: 45,858,280 (GRCm39) probably null Het
Slc18b1 A T 10: 23,679,748 (GRCm39) K92N probably benign Het
Slc20a2 G A 8: 23,025,573 (GRCm39) V92M possibly damaging Het
Slc4a11 A T 2: 130,527,464 (GRCm39) F644I probably damaging Het
Spata31d1d A T 13: 59,878,029 (GRCm39) probably benign Het
Spef2 T C 15: 9,663,244 (GRCm39) M846V probably benign Het
Syncrip T C 9: 88,362,800 (GRCm39) T3A probably benign Het
Other mutations in Gm29326
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01482:Gm29326 APN 7 29,260,136 (GRCm39) exon noncoding transcript
IGL02336:Gm29326 APN 7 29,260,833 (GRCm39) exon noncoding transcript
Posted On 2013-11-18