Incidental Mutation 'IGL01372:9130204L05Rik'
ID76204
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 9130204L05Rik
Ensembl Gene ENSMUSG00000091175
Gene NameRIKEN cDNA 9130204L05 gene
SynonymsLOC229550
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.113) question?
Stock #IGL01372
Quality Score
Status
Chromosome3
Chromosomal Location91088137-91090803 bp(-) (GRCm38)
Type of Mutationutr 3 prime
DNA Base Change (assembly) A to G at 91088309 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000130512 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166173]
Predicted Effect probably benign
Transcript: ENSMUST00000166173
SMART Domains Protein: ENSMUSP00000130512
Gene: ENSMUSG00000091175

DomainStartEndE-ValueType
Pfam:S_100 9 48 4.4e-10 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca7 G A 10: 80,006,255 D1049N probably benign Het
Ankdd1a A T 9: 65,504,139 L362Q probably damaging Het
Ankib1 A T 5: 3,772,594 N37K probably damaging Het
Ankrd55 T A 13: 112,323,143 D90E probably damaging Het
Atp1a2 T C 1: 172,278,943 R831G probably damaging Het
Bcar3 A G 3: 122,523,294 D638G probably damaging Het
Cabp4 T A 19: 4,139,323 E78D probably benign Het
Cmtm8 A G 9: 114,790,687 V130A possibly damaging Het
Cyth3 A G 5: 143,692,638 T66A possibly damaging Het
Dmbt1 A T 7: 131,103,679 I1171F possibly damaging Het
Dnah10 G A 5: 124,779,154 G2060D probably damaging Het
Dnah11 T C 12: 118,192,399 H172R probably damaging Het
Dnah5 C T 15: 28,230,490 A178V probably benign Het
Efcab6 T G 15: 84,044,304 M30L possibly damaging Het
Ehbp1l1 T C 19: 5,715,789 probably benign Het
Eps15 G A 4: 109,322,106 E230K probably damaging Het
Fam91a1 A G 15: 58,430,062 I258M probably damaging Het
Gm5581 G A 6: 131,168,403 noncoding transcript Het
Hrh1 G A 6: 114,479,997 V80I probably damaging Het
Ldhd G A 8: 111,628,400 H290Y probably benign Het
Lepr G A 4: 101,735,577 E130K possibly damaging Het
Mycbpap T C 11: 94,506,456 I40V possibly damaging Het
Nrap T A 19: 56,329,102 probably null Het
Olfr206 A G 16: 59,345,161 I180T probably damaging Het
Olfr342 T A 2: 36,527,451 I13N probably benign Het
Opn5 T A 17: 42,580,544 probably null Het
Otop3 A T 11: 115,345,104 T521S possibly damaging Het
Pcsk5 T G 19: 17,617,744 T409P probably damaging Het
Pde9a T A 17: 31,461,711 F322Y probably benign Het
Pgm5 T A 19: 24,733,621 I406F probably damaging Het
Prrc2b T C 2: 32,223,930 S1998P probably damaging Het
Prune2 T C 19: 17,125,069 Y2531H probably damaging Het
Ptprk T C 10: 28,569,927 V932A probably benign Het
Rapgef6 T A 11: 54,668,611 probably benign Het
Rgsl1 T A 1: 153,826,141 Y224F probably damaging Het
Rps6kl1 A T 12: 85,146,889 C143S probably damaging Het
Slc5a5 G A 8: 70,890,376 probably benign Het
Tfb2m A G 1: 179,542,313 S182P probably damaging Het
Tmc3 A G 7: 83,612,538 H608R probably damaging Het
Trim37 T A 11: 87,184,946 H459Q probably benign Het
Vmn2r71 A T 7: 85,620,814 probably benign Het
Xirp2 T C 2: 67,513,990 S2192P possibly damaging Het
Other mutations in 9130204L05Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00231:9130204L05Rik APN 3 91088358 missense probably benign 0.01
IGL01526:9130204L05Rik APN 3 91088305 utr 3 prime probably benign
IGL02894:9130204L05Rik APN 3 91088393 missense probably benign 0.18
IGL03110:9130204L05Rik APN 3 91088319 missense unknown
IGL03250:9130204L05Rik APN 3 91090408 utr 5 prime probably benign
R2357:9130204L05Rik UTSW 3 91088426 missense probably benign 0.35
R3795:9130204L05Rik UTSW 3 91088423 missense possibly damaging 0.73
R5315:9130204L05Rik UTSW 3 91090330 missense possibly damaging 0.56
R5495:9130204L05Rik UTSW 3 91090295 missense possibly damaging 0.93
R6314:9130204L05Rik UTSW 3 91088376 missense possibly damaging 0.56
Posted On2013-10-07