Incidental Mutation 'IGL01526:9130204L05Rik'
ID89584
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: 0.117) question?
Stock #IGL01526
Quality Score
Status
Chromosome3
Chromosomal Location91088137-91090803 bp(-) (GRCm38)
Type of Mutationutr 3 prime
DNA Base Change (assembly) T to A at 91088305 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: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1500002C15Rik G T 4: 155,734,171 probably benign Het
4933430I17Rik G T 4: 62,532,621 R107L possibly damaging Het
Acvr1 A T 2: 58,458,985 D388E probably benign Het
Art3 T C 5: 92,414,340 S354P probably damaging Het
Bpnt1 C A 1: 185,345,394 S102* probably null Het
C530008M17Rik T A 5: 76,857,631 M613K unknown Het
Ces1a G T 8: 93,045,098 P24T probably damaging Het
Cfap65 A T 1: 74,911,078 S1171T probably damaging Het
Csn2 T C 5: 87,694,979 H47R possibly damaging Het
Gm14496 T A 2: 181,995,665 D177E probably benign Het
Hmbs A G 9: 44,339,548 V126A possibly damaging Het
Ica1l A G 1: 60,015,757 M105T probably damaging Het
Morc2a G A 11: 3,650,428 E17K probably benign Het
Mroh8 T C 2: 157,238,312 probably benign Het
Mroh9 G T 1: 163,055,603 L436I probably damaging Het
Nup54 T C 5: 92,417,475 D461G probably benign Het
Olfr1123 A T 2: 87,418,975 D309V probably damaging Het
Olfr315 A G 11: 58,778,297 T57A probably benign Het
Pcid2 G A 8: 13,085,319 probably benign Het
Ppp1r3b G T 8: 35,384,718 R237L probably benign Het
Prdm11 A G 2: 93,012,757 V119A probably damaging Het
Serpina5 T A 12: 104,101,890 V70E probably damaging Het
Skap2 C T 6: 51,907,914 D249N probably benign Het
Slc22a29 A T 19: 8,207,178 probably benign Het
Slc4a1ap C A 5: 31,528,227 T283K possibly damaging Het
Slc6a21 T G 7: 45,287,796 I575S probably damaging Het
Smpd1 T G 7: 105,554,775 W82G probably benign Het
Snx14 T A 9: 88,381,500 M897L probably damaging Het
Tjp1 A G 7: 65,322,658 V586A probably damaging Het
Tmc8 T C 11: 117,792,084 probably benign Het
Trim34a A G 7: 104,260,499 Y298C probably damaging Het
Ube3c T C 5: 29,667,962 V1000A probably damaging Het
Other mutations in 9130204L05Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00231:9130204L05Rik APN 3 91088358 missense probably benign 0.01
IGL01372:9130204L05Rik APN 3 91088309 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
R8351:9130204L05Rik UTSW 3 91088364 missense probably benign 0.01
Z1177:9130204L05Rik UTSW 3 91088356 missense probably benign 0.01
Posted On2013-12-03