Incidental Mutation 'IGL01744:2900092C05Rik'
ID152975
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 2900092C05Rik
Ensembl Gene ENSMUSG00000030385
Gene NameRIKEN cDNA 2900092C05 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.064) question?
Stock #IGL01744
Quality Score
Status
Chromosome7
Chromosomal Location12512517-12556323 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) T to C at 12550532 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Threonine at position 102 (I102T)
Ref Sequence ENSEMBL: ENSMUSP00000032541 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032541]
Predicted Effect possibly damaging
Transcript: ENSMUST00000032541
AA Change: I102T

PolyPhen 2 Score 0.915 (Sensitivity: 0.81; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000032541
Gene: ENSMUSG00000030385
AA Change: I102T

DomainStartEndE-ValueType
signal peptide 1 25 N/A INTRINSIC
transmembrane domain 96 118 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933412E24Rik C A 15: 60,015,575 A339S possibly damaging Het
Ackr2 A G 9: 121,909,119 T187A probably benign Het
Adam28 A G 14: 68,607,507 V777A probably benign Het
Add3 T A 19: 53,239,430 D515E probably damaging Het
Aire C A 10: 78,036,723 E354* probably null Het
AW551984 T C 9: 39,591,272 K670R probably benign Het
Bahcc1 T C 11: 120,271,737 V287A probably benign Het
Brca1 T C 11: 101,524,176 N1044S possibly damaging Het
Bub1b T A 2: 118,636,749 I851N probably damaging Het
Ceacam11 A T 7: 17,973,398 I36F possibly damaging Het
Copa A G 1: 172,113,189 E714G probably benign Het
Cth A T 3: 157,924,935 N32K probably benign Het
Cyp2a5 T A 7: 26,841,009 M349K probably damaging Het
D130052B06Rik A G 11: 33,623,966 S188G unknown Het
Fhdc1 G A 3: 84,444,735 A1061V possibly damaging Het
Flt1 T C 5: 147,571,461 N1161S probably benign Het
Gm10696 T A 3: 94,176,237 K89M probably damaging Het
Hip1 T C 5: 135,545,063 probably benign Het
Mapk11 A G 15: 89,146,843 probably benign Het
Mtif2 A G 11: 29,544,417 probably benign Het
Myo1f C A 17: 33,583,680 probably benign Het
Nipsnap1 G A 11: 4,889,912 R211H probably damaging Het
Olfr599 A G 7: 103,338,228 H58R probably damaging Het
Olfr781 T C 10: 129,333,457 I192T probably benign Het
Pcdh1 A T 18: 38,203,249 I111N probably damaging Het
Piezo2 T A 18: 63,042,788 I1841F probably damaging Het
Pirb G T 7: 3,717,176 Y399* probably null Het
Ppp1r36 A T 12: 76,439,232 N388I possibly damaging Het
Prr16 A G 18: 51,302,989 D180G possibly damaging Het
Prss39 A G 1: 34,502,199 probably null Het
Trank1 T A 9: 111,349,363 V373D probably damaging Het
Ubn1 A G 16: 5,072,059 E186G probably damaging Het
Zmym2 T C 14: 56,946,572 V997A probably benign Het
Other mutations in 2900092C05Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00714:2900092C05Rik APN 7 12556004 splice site probably benign
IGL03047:2900092C05Rik UTSW 7 12512641 missense possibly damaging 0.92
R0001:2900092C05Rik UTSW 7 12554607 splice site probably benign
R0607:2900092C05Rik UTSW 7 12554698 missense probably benign 0.19
R0831:2900092C05Rik UTSW 7 12550596 splice site probably benign
R1468:2900092C05Rik UTSW 7 12512580 start codon destroyed probably null 0.83
R1468:2900092C05Rik UTSW 7 12512580 start codon destroyed probably null 0.83
R1846:2900092C05Rik UTSW 7 12512882 missense probably benign 0.38
R1852:2900092C05Rik UTSW 7 12512702 splice site probably null
R1912:2900092C05Rik UTSW 7 12554655 missense probably benign 0.01
R3442:2900092C05Rik UTSW 7 12512656 nonsense probably null
R3694:2900092C05Rik UTSW 7 12550516 missense possibly damaging 0.46
R3751:2900092C05Rik UTSW 7 12556046 missense probably benign 0.02
R5977:2900092C05Rik UTSW 7 12554737 missense probably benign 0.17
R6158:2900092C05Rik UTSW 7 12512672 missense probably benign 0.37
R6777:2900092C05Rik UTSW 7 12512829 missense probably benign 0.00
R6931:2900092C05Rik UTSW 7 12512596 missense unknown
R7284:2900092C05Rik UTSW 7 12512678 nonsense probably null
R7406:2900092C05Rik UTSW 7 12515464 missense possibly damaging 0.66
Posted On2014-02-04