Incidental Mutation 'IGL02269:4933414I15Rik'
ID 287060
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4933414I15Rik
Ensembl Gene ENSMUSG00000072983
Gene Name RIKEN cDNA 4933414I15 gene
Synonyms ENSMUSG00000051192
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # IGL02269
Quality Score
Status
Chromosome 11
Chromosomal Location 50940711-50943765 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 50942598 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 59 (V59A)
Ref Sequence ENSEMBL: ENSMUSP00000104751 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000109123]
AlphaFold Q9D4D5
Predicted Effect unknown
Transcript: ENSMUST00000109123
AA Change: V59A
Predicted Effect noncoding transcript
Transcript: ENSMUST00000156329
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2ml1 C A 6: 128,553,338 probably benign Het
Akap13 G A 7: 75,602,911 R263H probably benign Het
B3galt5 A G 16: 96,315,530 D121G possibly damaging Het
Becn1 A G 11: 101,291,535 probably benign Het
Carmil1 A T 13: 24,155,410 L150* probably null Het
Cep170 A T 1: 176,769,366 M475K probably benign Het
Cyp24a1 C T 2: 170,496,572 G68D probably damaging Het
Cyp3a44 A T 5: 145,805,737 I18N probably benign Het
Dmrt2 T C 19: 25,678,459 V474A probably benign Het
Dtnb A G 12: 3,596,691 D64G probably damaging Het
Epb41l3 T C 17: 69,247,573 S223P probably damaging Het
Ephb2 A G 4: 136,771,049 Y240H possibly damaging Het
Extl3 T C 14: 65,077,583 Y50C probably damaging Het
Fat3 A C 9: 15,915,577 S4360A possibly damaging Het
Fbxo9 A T 9: 78,087,553 V230E probably damaging Het
Frmd4a T C 2: 4,604,234 M971T probably benign Het
Gm7275 A G 16: 48,073,822 noncoding transcript Het
Hyal6 C T 6: 24,740,859 T337I probably damaging Het
Obsl1 C T 1: 75,487,713 V1650M probably damaging Het
Olfr143 A T 9: 38,253,936 D173V possibly damaging Het
Olfr341 A T 2: 36,479,567 S188T possibly damaging Het
Olfr619 T A 7: 103,603,882 I76N probably damaging Het
Olfr860 A T 9: 19,845,728 I297N possibly damaging Het
Pcdh7 A C 5: 57,913,322 E1114A probably damaging Het
Pde8a C T 7: 81,308,802 probably benign Het
Pdzrn4 A T 15: 92,769,850 S628C probably damaging Het
Pear1 C T 3: 87,756,264 G376S probably damaging Het
Plekha6 C T 1: 133,287,849 T644M possibly damaging Het
Plpp1 T A 13: 112,856,992 C153S probably damaging Het
Ptpn3 G A 4: 57,197,510 T793M possibly damaging Het
Rdh13 A T 7: 4,445,498 L5Q possibly damaging Het
Rimbp2 G T 5: 128,774,295 D862E probably damaging Het
Rita1 C T 5: 120,609,793 A147T probably damaging Het
Scamp1 C T 13: 94,232,186 probably benign Het
Scamp3 A G 3: 89,180,734 T178A probably benign Het
Sh3tc1 A G 5: 35,706,284 V853A probably benign Het
Snrnp200 C T 2: 127,229,991 T1197M possibly damaging Het
Sult3a1 T C 10: 33,879,263 F275L probably benign Het
Tenm4 A T 7: 96,823,822 I905F probably damaging Het
Tgm3 T A 2: 130,024,518 S119T probably benign Het
Tmem131l A T 3: 83,938,050 D424E possibly damaging Het
Tmem45b G T 9: 31,427,983 C145* probably null Het
Unc5c G A 3: 141,788,982 R352H probably damaging Het
Vmn2r12 A G 5: 109,086,477 L623P probably damaging Het
Vmn2r68 T C 7: 85,221,739 M779V possibly damaging Het
Zfhx2 T C 14: 55,071,936 N902S probably benign Het
Other mutations in 4933414I15Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02598:4933414I15Rik APN 11 50943621 start codon destroyed probably null
BB010:4933414I15Rik UTSW 11 50942400 missense unknown
BB020:4933414I15Rik UTSW 11 50942400 missense unknown
R2384:4933414I15Rik UTSW 11 50942506 missense unknown
R5226:4933414I15Rik UTSW 11 50942589 missense unknown
R6514:4933414I15Rik UTSW 11 50942742 missense unknown
R7933:4933414I15Rik UTSW 11 50942400 missense unknown
R8219:4933414I15Rik UTSW 11 50942536 missense unknown
R8700:4933414I15Rik UTSW 11 50942517 missense unknown
Posted On 2015-04-16