Incidental Mutation 'IGL02962:1700017N19Rik'
ID 365408
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700017N19Rik
Ensembl Gene ENSMUSG00000056912
Gene Name RIKEN cDNA 1700017N19 gene
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.063) question?
Stock # IGL02962
Quality Score
Status
Chromosome 10
Chromosomal Location 100426346-100454257 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to A at 100446455 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000151731 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000041162] [ENSMUST00000186825] [ENSMUST00000187119] [ENSMUST00000188736] [ENSMUST00000190386] [ENSMUST00000190708] [ENSMUST00000191033] [ENSMUST00000191336] [ENSMUST00000218464]
AlphaFold A0A087WPJ1
Predicted Effect probably null
Transcript: ENSMUST00000041162
Predicted Effect probably benign
Transcript: ENSMUST00000186825
Predicted Effect probably benign
Transcript: ENSMUST00000187119
Predicted Effect probably benign
Transcript: ENSMUST00000188736
Predicted Effect probably benign
Transcript: ENSMUST00000190386
Predicted Effect probably null
Transcript: ENSMUST00000190708
Predicted Effect probably null
Transcript: ENSMUST00000191033
Predicted Effect probably benign
Transcript: ENSMUST00000191336
Predicted Effect probably null
Transcript: ENSMUST00000218464
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9530068E07Rik T C 11: 52,294,362 (GRCm39) V209A possibly damaging Het
Abca3 T A 17: 24,619,383 (GRCm39) V907E probably damaging Het
Acvrl1 T C 15: 101,033,382 (GRCm39) Y90H probably benign Het
Aff3 T C 1: 38,574,737 (GRCm39) D81G probably damaging Het
Amn G T 12: 111,240,951 (GRCm39) V152L probably damaging Het
Arhgap44 A G 11: 64,957,987 (GRCm39) probably benign Het
Atad5 T A 11: 79,999,405 (GRCm39) V895D possibly damaging Het
Card9 T G 2: 26,248,029 (GRCm39) probably null Het
Ccer1 T C 10: 97,529,702 (GRCm39) S122P unknown Het
Ccr2 A G 9: 123,905,712 (GRCm39) probably benign Het
Dsg1a T A 18: 20,473,381 (GRCm39) I818N possibly damaging Het
Ear10 G T 14: 44,160,774 (GRCm39) L18I probably damaging Het
Mertk A G 2: 128,619,374 (GRCm39) Y544C probably damaging Het
Miga1 A T 3: 151,990,978 (GRCm39) probably benign Het
Myo18a T C 11: 77,669,061 (GRCm39) V307A probably damaging Het
Or5p64 A T 7: 107,854,910 (GRCm39) I145N possibly damaging Het
Or7a38 T A 10: 78,752,773 (GRCm39) L33H probably damaging Het
Pou2f3 T C 9: 43,036,384 (GRCm39) probably benign Het
Pramel23 T A 4: 143,423,910 (GRCm39) E293V probably benign Het
Prickle2 A C 6: 92,353,403 (GRCm39) S744A probably benign Het
Prkcb T A 7: 122,024,270 (GRCm39) probably null Het
Prkd2 A G 7: 16,603,757 (GRCm39) T813A probably benign Het
Prkra G A 2: 76,463,891 (GRCm39) T257M probably damaging Het
Rbm18 C T 2: 36,012,886 (GRCm39) R102Q probably damaging Het
Rbsn A G 6: 92,167,307 (GRCm39) S446P probably benign Het
Rpgrip1l A T 8: 91,996,990 (GRCm39) V28D possibly damaging Het
Sdccag8 A T 1: 176,775,928 (GRCm39) K613I probably damaging Het
Serbp1 G A 6: 67,244,103 (GRCm39) G8D probably damaging Het
Slc6a2 T A 8: 93,699,390 (GRCm39) Y139* probably null Het
Slc7a2 T A 8: 41,358,621 (GRCm39) F321L probably damaging Het
Slco1b2 G A 6: 141,594,279 (GRCm39) S48N probably damaging Het
Ssbp2 G T 13: 91,790,490 (GRCm39) V118L possibly damaging Het
Sugp1 T A 8: 70,512,512 (GRCm39) probably benign Het
Taar5 C A 10: 23,846,883 (GRCm39) R94S possibly damaging Het
Tgs1 G T 4: 3,586,181 (GRCm39) A353S probably benign Het
Trav1 A G 14: 52,666,099 (GRCm39) E32G probably damaging Het
Trp53bp2 T C 1: 182,259,160 (GRCm39) V71A probably benign Het
Vmn2r50 T C 7: 9,784,252 (GRCm39) Y74C probably damaging Het
Wars1 A T 12: 108,841,706 (GRCm39) M147K probably damaging Het
Other mutations in 1700017N19Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01565:1700017N19Rik APN 10 100,439,222 (GRCm39) missense probably damaging 1.00
IGL02159:1700017N19Rik APN 10 100,446,527 (GRCm39) missense probably damaging 1.00
IGL02556:1700017N19Rik APN 10 100,446,579 (GRCm39) critical splice donor site probably null
IGL02629:1700017N19Rik APN 10 100,445,006 (GRCm39) splice site probably benign
IGL02692:1700017N19Rik APN 10 100,439,410 (GRCm39) missense probably benign 0.05
R0145:1700017N19Rik UTSW 10 100,437,783 (GRCm39) missense probably damaging 0.96
R0402:1700017N19Rik UTSW 10 100,445,115 (GRCm39) missense probably damaging 0.99
R1514:1700017N19Rik UTSW 10 100,448,729 (GRCm39) missense probably damaging 1.00
R1519:1700017N19Rik UTSW 10 100,439,390 (GRCm39) missense probably damaging 0.98
R1680:1700017N19Rik UTSW 10 100,439,390 (GRCm39) missense probably damaging 0.98
R1686:1700017N19Rik UTSW 10 100,448,722 (GRCm39) missense probably damaging 0.97
R3951:1700017N19Rik UTSW 10 100,451,158 (GRCm39) splice site probably benign
R3952:1700017N19Rik UTSW 10 100,451,158 (GRCm39) splice site probably benign
R4423:1700017N19Rik UTSW 10 100,441,495 (GRCm39) missense probably damaging 0.99
R4905:1700017N19Rik UTSW 10 100,448,680 (GRCm39) splice site probably null
R5507:1700017N19Rik UTSW 10 100,445,095 (GRCm39) missense probably benign 0.02
R5898:1700017N19Rik UTSW 10 100,451,070 (GRCm39) missense probably benign 0.20
R5898:1700017N19Rik UTSW 10 100,448,762 (GRCm39) missense possibly damaging 0.56
R5977:1700017N19Rik UTSW 10 100,451,106 (GRCm39) missense probably damaging 0.99
R7034:1700017N19Rik UTSW 10 100,445,118 (GRCm39) critical splice donor site probably null
R7036:1700017N19Rik UTSW 10 100,445,118 (GRCm39) critical splice donor site probably null
R7394:1700017N19Rik UTSW 10 100,445,038 (GRCm39) missense probably benign 0.01
R7412:1700017N19Rik UTSW 10 100,448,691 (GRCm39) nonsense probably null
R7870:1700017N19Rik UTSW 10 100,441,505 (GRCm39) missense probably benign
R7914:1700017N19Rik UTSW 10 100,428,538 (GRCm39) missense probably benign
R8466:1700017N19Rik UTSW 10 100,437,873 (GRCm39) missense probably benign 0.00
R8558:1700017N19Rik UTSW 10 100,430,497 (GRCm39) missense probably benign 0.23
R9004:1700017N19Rik UTSW 10 100,454,197 (GRCm39) unclassified probably benign
R9105:1700017N19Rik UTSW 10 100,439,407 (GRCm39) nonsense probably null
R9641:1700017N19Rik UTSW 10 100,430,498 (GRCm39) missense possibly damaging 0.91
Z1088:1700017N19Rik UTSW 10 100,441,501 (GRCm39) missense probably damaging 1.00
Z1176:1700017N19Rik UTSW 10 100,448,291 (GRCm39) missense probably damaging 0.98
Posted On 2015-12-18