Incidental Mutation 'IGL02388:9230019H11Rik'
ID291634
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 9230019H11Rik
Ensembl Gene ENSMUSG00000071434
Gene NameRIKEN cDNA 9230019H11 gene
Synonyms
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.308) question?
Stock #IGL02388
Quality Score
Status
Chromosome10
Chromosomal Location3119841-3129546 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to T at 3125050 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000095874
SMART Domains Protein: ENSMUSP00000093559
Gene: ENSMUSG00000071434

DomainStartEndE-ValueType
signal peptide 1 30 N/A INTRINSIC
PDB:1KCG|C 57 207 2e-6 PDB
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217333
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930597O21Rik A T 6: 66,896,113 probably benign Het
Abca8a A G 11: 110,078,815 probably benign Het
Asphd1 A T 7: 126,946,712 probably benign Het
Ccdc77 G A 6: 120,331,897 A301V probably benign Het
Cep350 G T 1: 155,953,753 T135K probably benign Het
Chrna7 A T 7: 63,107,691 D153E probably damaging Het
Clec4b2 G T 6: 123,202,228 probably null Het
Cyp2c67 T C 19: 39,643,355 N133D probably benign Het
Dglucy T C 12: 100,856,998 I484T probably damaging Het
Dtna G T 18: 23,597,514 M319I probably benign Het
E2f5 T A 3: 14,588,280 M152K probably benign Het
Emsy A T 7: 98,641,666 M58K probably damaging Het
Epha1 A G 6: 42,365,016 Y367H probably damaging Het
Etv1 A G 12: 38,781,799 S32G possibly damaging Het
Fam114a1 A T 5: 65,008,980 probably benign Het
Fbxo30 T A 10: 11,290,378 N281K probably benign Het
Galnt12 G T 4: 47,117,941 R412L probably damaging Het
Gm5786 T A 12: 59,081,596 noncoding transcript Het
Gm9845 T C 3: 39,358,467 noncoding transcript Het
Hecw2 A G 1: 53,925,699 V656A probably benign Het
Hpse2 A T 19: 43,294,253 V187D probably damaging Het
Itsn2 T A 12: 4,629,557 M122K possibly damaging Het
Kcnj11 A G 7: 46,099,789 S37P probably benign Het
Kif13b T C 14: 64,800,358 I1491T probably damaging Het
Krt36 T A 11: 100,105,164 K145* probably null Het
Loxhd1 A G 18: 77,369,137 I499V probably benign Het
Map3k4 G T 17: 12,271,610 N311K probably damaging Het
Mical2 C A 7: 112,335,413 H880N probably benign Het
Myo1d A T 11: 80,637,997 C666* probably null Het
Nlrx1 C T 9: 44,264,005 R158H probably benign Het
Olfr1115 T A 2: 87,251,951 Y5N probably benign Het
Olfr1251 T C 2: 89,666,972 S305G probably benign Het
Olfr1494 C A 19: 13,749,630 H175N possibly damaging Het
Olfr380 A T 11: 73,453,280 L311I probably benign Het
Olfr45 A G 7: 140,691,111 T69A probably benign Het
Pdgfrl A G 8: 40,977,057 R154G probably benign Het
Pitpnb T C 5: 111,330,833 F7S possibly damaging Het
Ppm1n G A 7: 19,279,172 R285C probably damaging Het
Prdm11 A T 2: 92,975,612 I331N possibly damaging Het
Ptprb C T 10: 116,367,521 P2066L probably damaging Het
Ric8b T C 10: 84,992,271 probably benign Het
Setx A G 2: 29,173,653 I2320M probably damaging Het
Skil C A 3: 31,111,638 S368* probably null Het
Slc1a5 G T 7: 16,785,719 probably null Het
Trpm7 A C 2: 126,819,891 V1079G possibly damaging Het
Tulp1 A G 17: 28,358,659 F2L probably damaging Het
Zbtb17 A G 4: 141,461,913 Y48C probably damaging Het
Zfp605 T A 5: 110,127,640 I208N possibly damaging 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
IGL02560:9230019H11Rik APN 10 3125866 exon noncoding transcript
IGL03293:9230019H11Rik APN 10 3125699 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 On2015-04-16