Incidental Mutation 'IGL01586:9830107B12Rik'
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 9830107B12Rik
Ensembl Gene ENSMUSG00000073386
Gene NameRIKEN cDNA 9830107B12 gene
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL01586
Quality Score
Chromosomal Location48125605-48146307 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 48128515 bp
Amino Acid Change Tyrosine to Asparagine at position 144 (Y144N)
Ref Sequence ENSEMBL: ENSMUSP00000070138 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000063481]
Predicted Effect unknown
Transcript: ENSMUST00000063481
AA Change: Y144N
SMART Domains Protein: ENSMUSP00000070138
Gene: ENSMUSG00000073386
AA Change: Y144N

low complexity region 8 17 N/A INTRINSIC
IG 26 122 3.65e-6 SMART
low complexity region 144 158 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca9 A C 11: 110,154,417 C363W probably damaging Het
Acmsd G A 1: 127,759,710 R243H probably damaging Het
Adam33 T C 2: 131,054,050 T490A probably damaging Het
Ank1 A G 8: 23,120,912 D1411G probably benign Het
Arhgap39 T C 15: 76,730,438 E842G probably benign Het
Asgr2 T C 11: 70,105,367 probably benign Het
Bbs9 T C 9: 22,645,997 V14A possibly damaging Het
Cer1 A G 4: 82,884,843 S81P probably damaging Het
Cln6 T A 9: 62,844,618 H41Q probably damaging Het
Dock1 A G 7: 134,753,377 D334G probably damaging Het
Dpy19l2 A G 9: 24,666,975 I261T probably benign Het
Fhod3 T G 18: 25,090,747 I1050S probably damaging Het
Gbgt1 T C 2: 28,497,830 V22A probably benign Het
Izumo3 A G 4: 92,146,295 probably null Het
Kif11 T C 19: 37,384,233 probably benign Het
Krt2 C A 15: 101,811,390 G615V unknown Het
Midn A G 10: 80,156,643 probably benign Het
Mier1 C T 4: 103,155,572 T342I probably damaging Het
Mycbp2 A T 14: 103,140,869 probably null Het
Nrp1 A T 8: 128,432,032 S267C possibly damaging Het
Olfr145 A G 9: 37,897,976 T191A possibly damaging Het
Pcdh20 A T 14: 88,470,908 M28K probably benign Het
Prmt5 G A 14: 54,509,951 probably benign Het
Psmg2 G A 18: 67,653,223 V218I probably benign Het
Rps6ka5 T C 12: 100,570,914 E519G probably damaging Het
Samm50 T A 15: 84,195,838 I39N probably benign Het
Shc2 A T 10: 79,622,304 M515K probably damaging Het
Sorbs2 T A 8: 45,795,594 F608L probably damaging Het
Sos2 T C 12: 69,607,398 K727E probably damaging Het
Sox13 A T 1: 133,389,444 H150Q possibly damaging Het
Tmem132e T C 11: 82,434,669 V165A probably damaging Het
Trmt11 T C 10: 30,597,751 T43A probably benign Het
Tyrp1 G T 4: 80,844,898 V341L probably benign Het
Ugt2b35 C A 5: 87,011,391 H481Q probably benign Het
Zzz3 T A 3: 152,455,839 I290N possibly damaging Het
Other mutations in 9830107B12Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00771:9830107B12Rik APN 17 48145684 missense possibly damaging 0.74
IGL01457:9830107B12Rik APN 17 48128583 splice site probably benign
IGL01792:9830107B12Rik APN 17 48145509 missense probably damaging 1.00
IGL01978:9830107B12Rik APN 17 48145993 missense probably damaging 0.99
IGL02347:9830107B12Rik APN 17 48145664 nonsense probably null
R0044:9830107B12Rik UTSW 17 48146186 utr 5 prime probably benign
R4613:9830107B12Rik UTSW 17 48128557 missense probably benign 0.15
R5984:9830107B12Rik UTSW 17 48128555 missense probably benign 0.00
R7565:9830107B12Rik UTSW 17 48145579 missense possibly damaging 0.76
Posted On2013-12-09