Incidental Mutation 'IGL02536:4930449A18Rik'
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Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930449A18Rik
Ensembl Gene ENSMUSG00000074589
Gene NameRIKEN cDNA 4930449A18 gene
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.329) question?
Stock #IGL02536
Quality Score
Chromosomal Location59777809-59846817 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to A at 59778244 bp
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000094228
SMART Domains Protein: ENSMUSP00000091781
Gene: ENSMUSG00000074589

SCOP:d1qfma2 104 157 3e-8 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8b C T 11: 109,981,748 R9H probably benign Het
Adamts8 T A 9: 30,962,072 S858T probably benign Het
Alg1 C T 16: 5,239,159 Q245* probably null Het
Ankmy1 T C 1: 92,886,188 Y423C probably damaging Het
Anp32a A T 9: 62,371,828 T55S probably damaging Het
Arhgef9 A C X: 95,058,837 V406G probably damaging Het
Bdkrb1 T C 12: 105,605,000 F275S possibly damaging Het
Card9 C T 2: 26,358,832 V102I possibly damaging Het
Ccdc130 A T 8: 84,260,616 Y109* probably null Het
Ccdc81 A T 7: 89,877,580 probably benign Het
Cd101 T A 3: 101,003,597 D915V probably damaging Het
Cdk10 A G 8: 123,227,015 D77G possibly damaging Het
Ctnnd1 T C 2: 84,605,196 T827A probably benign Het
Dspp A C 5: 104,175,665 T225P probably damaging Het
Evpl T C 11: 116,221,209 E1885G probably damaging Het
Fstl4 C T 11: 53,134,024 probably benign Het
Gm5930 T A 14: 44,337,558 N57I probably damaging Het
Gnl2 C T 4: 125,052,608 Q541* probably null Het
Igkv3-1 T C 6: 70,704,051 V78A probably benign Het
Inpp5a T C 7: 139,567,422 I321T probably benign Het
Kif20b T A 19: 34,974,559 S1746T probably benign Het
Lrrc8c T C 5: 105,607,172 I271T probably benign Het
Mrps10 T C 17: 47,375,003 Y152H probably damaging Het
Myl9 C T 2: 156,778,549 S2L probably damaging Het
Myof A T 19: 37,949,655 H870Q probably damaging Het
Nfatc4 A T 14: 55,829,910 I456F probably damaging Het
Notch2 A G 3: 98,102,407 H550R probably benign Het
Olfr113 T A 17: 37,574,926 I166F probably damaging Het
Olfr275 T A 4: 52,825,817 V140D possibly damaging Het
Olfr624 T A 7: 103,670,957 I25F possibly damaging Het
Olfr911-ps1 T C 9: 38,524,164 L144P probably damaging Het
P2rx1 A T 11: 73,012,474 I230F probably damaging Het
Pcnt A G 10: 76,380,229 V2275A possibly damaging Het
Pip5k1a G A 3: 95,064,396 T465I probably benign Het
Pnkd G A 1: 74,351,900 R415H probably damaging Het
Prdx4 T A X: 155,332,447 I132F probably damaging Het
Pvr A G 7: 19,918,792 M66T probably benign Het
Rnf216 A G 5: 143,080,240 I531T probably benign Het
Rps6ka4 A T 19: 6,832,071 F405Y probably damaging Het
Serpinb2 A G 1: 107,524,949 probably benign Het
Sfxn1 A G 13: 54,085,494 K12R probably benign Het
Slc17a7 A G 7: 45,170,946 E275G probably damaging Het
Tnpo2 A T 8: 85,045,067 I245F probably benign Het
Ush2a A T 1: 188,957,266 probably null Het
Zcchc4 C T 5: 52,808,316 R321W probably damaging Het
Other mutations in 4930449A18Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4243:4930449A18Rik UTSW 3 59825782 exon noncoding transcript
R4245:4930449A18Rik UTSW 3 59825782 exon noncoding transcript
R4368:4930449A18Rik UTSW 3 59846778 exon noncoding transcript
R4466:4930449A18Rik UTSW 3 59838466 exon noncoding transcript
R4755:4930449A18Rik UTSW 3 59825859 exon noncoding transcript
R4842:4930449A18Rik UTSW 3 59841732 exon noncoding transcript
R5214:4930449A18Rik UTSW 3 59825884 splice site noncoding transcript
R5436:4930449A18Rik UTSW 3 59846693 exon noncoding transcript
Posted On2015-04-16