Incidental Mutation 'IGL03293:9230019H11Rik'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 9230019H11Rik
Ensembl Gene ENSMUSG00000071434
Gene NameRIKEN cDNA 9230019H11 gene
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.335) question?
Stock #IGL03293
Quality Score
Chromosomal Location3119841-3129546 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) A to G at 3125699 bp
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000095874
SMART Domains Protein: ENSMUSP00000093559
Gene: ENSMUSG00000071434

signal peptide 1 30 N/A INTRINSIC
PDB:1KCG|C 57 207 2e-6 PDB
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217333
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A830018L16Rik T A 1: 11,545,151 probably null Het
Akr1c14 C T 13: 4,079,130 R45* probably null Het
Ccdc62 T A 5: 123,951,225 L309I possibly damaging Het
Ccdc66 T A 14: 27,490,671 N565I probably damaging Het
Cerkl G T 2: 79,342,375 A318E probably damaging Het
Clec4n A T 6: 123,232,146 T57S probably benign Het
Cluh A G 11: 74,665,752 E921G probably benign Het
Cnbd1 C T 4: 18,860,565 E394K possibly damaging Het
Dmgdh G T 13: 93,706,701 M348I probably benign Het
Dnajc13 G A 9: 104,174,426 S1744L possibly damaging Het
Dspp A T 5: 104,177,561 S597C unknown Het
Dync1h1 A T 12: 110,628,734 N1360I probably benign Het
Eepd1 A G 9: 25,603,412 H505R possibly damaging Het
Gcnt7 T C 2: 172,454,383 T174A possibly damaging Het
Gnb1 T C 4: 155,540,547 probably benign Het
Gpam A G 19: 55,071,016 S800P probably benign Het
Gsr T C 8: 33,694,996 probably benign Het
Herc2 A G 7: 56,155,130 K2302R probably benign Het
Hipk1 C A 3: 103,777,259 A347S possibly damaging Het
Iqgap2 T C 13: 95,731,434 N222S probably damaging Het
Marco T A 1: 120,494,795 M46L probably benign Het
Morc2b A T 17: 33,138,363 V145D probably damaging Het
Mprip C A 11: 59,696,163 P54Q probably damaging Het
Ndufv2 A T 17: 66,083,449 C175* probably null Het
Olfr1181 T C 2: 88,423,227 D266G probably damaging Het
Olfr272 A G 4: 52,910,835 *320Q probably null Het
Orc3 A C 4: 34,595,210 I195S probably damaging Het
Otos C A 1: 92,644,413 E64* probably null Het
Plxna2 T C 1: 194,804,945 S1603P probably damaging Het
Rlf A T 4: 121,148,330 I1151N probably benign Het
Scaper A G 9: 55,874,823 V283A probably benign Het
Sdccag3 A T 2: 26,387,676 probably benign Het
Slc25a43 A G X: 36,775,599 T270A probably benign Het
Slc35a5 A G 16: 45,143,781 V78A probably damaging Het
Smurf1 A T 5: 144,881,799 D636E probably benign Het
Tchhl1 A T 3: 93,470,275 E95D probably damaging Het
Tcp10a A G 17: 7,326,492 E72G possibly damaging Het
Tmem232 A G 17: 65,450,374 S275P probably damaging Het
Ugt1a5 T C 1: 88,166,818 F256S probably damaging Het
Vmn2r5 A G 3: 64,491,326 V744A probably benign Het
Vmn2r53 A T 7: 12,598,422 S433R probably benign Het
Vmn2r9 A T 5: 108,848,131 I217N probably damaging Het
Wdr83 G T 8: 85,080,587 A10E probably benign Het
Other mutations in 9230019H11Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01018:9230019H11Rik APN 10 3120231 unclassified noncoding transcript
IGL01018:9230019H11Rik APN 10 3120209 unclassified noncoding transcript
IGL01018:9230019H11Rik APN 10 3125031 unclassified noncoding transcript
IGL01018:9230019H11Rik APN 10 3125193 exon noncoding transcript
IGL02388:9230019H11Rik APN 10 3125050 unclassified noncoding transcript
IGL02560:9230019H11Rik APN 10 3125866 exon noncoding transcript
R0357:9230019H11Rik UTSW 10 3120307 unclassified noncoding transcript
R0357:9230019H11Rik UTSW 10 3125788 exon noncoding transcript
R0582:9230019H11Rik UTSW 10 3125082 unclassified noncoding transcript
R0680:9230019H11Rik UTSW 10 3125133 exon noncoding transcript
R1116:9230019H11Rik UTSW 10 3120180 unclassified noncoding transcript
R1519:9230019H11Rik UTSW 10 3125230 exon noncoding transcript
R1717:9230019H11Rik UTSW 10 3125050 unclassified noncoding transcript
R2112:9230019H11Rik UTSW 10 3126459 exon noncoding transcript
R5410:9230019H11Rik UTSW 10 3126473 exon noncoding transcript
Posted On2016-08-02