Incidental Mutation 'IGL03344:1700011L22Rik'
List |< first << previous [record 85 of 55675] next >> last >|
ID417386
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700011L22Rik
Ensembl Gene ENSMUSG00000031682
Gene NameRIKEN cDNA 1700011L22 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.030) question?
Stock #IGL03344
Quality Score
Status
Chromosome8
Chromosomal Location79210431-79248570 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to T at 79248376 bp
ZygosityHeterozygous
Amino Acid Change Isoleucine to Asparagine at position 26 (I26N)
Ref Sequence ENSEMBL: ENSMUSP00000034109 (fasta)
Gene Model
Predicted Effect probably damaging
Transcript: ENSMUST00000034109
AA Change: I26N

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000210889
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2410089E03Rik C A 15: 8,187,458 P720Q possibly damaging Het
AI314180 A C 4: 58,828,538 V965G probably damaging Het
Armc4 C A 18: 7,129,434 G915* probably null Het
Atxn7l1 A G 12: 33,326,066 N47D probably damaging Het
BC003331 T C 1: 150,363,544 E386G probably damaging Het
Cer1 A T 4: 82,884,825 W87R probably damaging Het
Chrna2 A G 14: 66,150,966 K477E probably damaging Het
Chtf8 G A 8: 106,886,272 P12S probably damaging Het
Deaf1 A T 7: 141,297,548 H555Q probably benign Het
Dopey1 T G 9: 86,536,144 I1975M probably damaging Het
Fsd2 C A 7: 81,559,909 V62L probably benign Het
Fxyd6 T G 9: 45,392,250 L81R probably benign Het
Htt T A 5: 34,879,828 S2086T probably benign Het
Htt T A 5: 34,907,466 S3008T probably benign Het
Mybbp1a G T 11: 72,445,202 R447L probably damaging Het
Nup210 A G 6: 91,021,429 V792A possibly damaging Het
Olfr342 T C 2: 36,528,128 S239P probably damaging Het
Olfr392 T A 11: 73,814,177 I302L probably benign Het
Prokr1 T C 6: 87,588,500 D121G possibly damaging Het
Puf60 A G 15: 76,070,380 V548A possibly damaging Het
Serpina3c T C 12: 104,147,264 I408V probably benign Het
Ska2 A G 11: 87,109,313 Het
Slc4a9 T A 18: 36,535,601 Y745N probably damaging Het
Speer4f1 A G 5: 17,480,334 E209G possibly damaging Het
Spg20 T C 3: 55,121,685 M299T probably benign Het
Tmem202 T C 9: 59,519,068 T272A possibly damaging Het
Vegfc T A 8: 54,157,151 I114N possibly damaging Het
Vmn1r61 T A 7: 5,610,494 T274S possibly damaging Het
Zfpm2 A G 15: 41,102,774 N753S probably benign Het
Zmym6 A G 4: 127,120,521 T624A probably damaging Het
Other mutations in 1700011L22Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02969:1700011L22Rik APN 8 79220237 splice site probably benign
IGL02835:1700011L22Rik UTSW 8 79210655 nonsense probably null
R0331:1700011L22Rik UTSW 8 79229392 missense probably benign 0.08
R0904:1700011L22Rik UTSW 8 79248489 start gained probably benign
R3801:1700011L22Rik UTSW 8 79248293 missense probably benign 0.06
R3804:1700011L22Rik UTSW 8 79248293 missense probably benign 0.06
R4606:1700011L22Rik UTSW 8 79210745 missense probably benign 0.00
R6045:1700011L22Rik UTSW 8 79229367 missense probably benign 0.00
Posted On2016-08-02