Incidental Mutation 'R8144:1700017B05Rik'
ID 632697
Institutional Source Beutler Lab
Gene Symbol 1700017B05Rik
Ensembl Gene ENSMUSG00000032300
Gene Name RIKEN cDNA 1700017B05 gene
Synonyms D9Ertd278e
MMRRC Submission 067572-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.159) question?
Stock # R8144 (G1)
Quality Score 149.008
Status Validated
Chromosome 9
Chromosomal Location 57160400-57169895 bp(-) (GRCm39)
Type of Mutation start gained
DNA Base Change (assembly) A to C at 57166388 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000149643 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034846] [ENSMUST00000213199] [ENSMUST00000215298] [ENSMUST00000217657]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000034846
SMART Domains Protein: ENSMUSP00000034846
Gene: ENSMUSG00000032300

DomainStartEndE-ValueType
low complexity region 265 284 N/A INTRINSIC
low complexity region 293 299 N/A INTRINSIC
low complexity region 334 347 N/A INTRINSIC
low complexity region 649 675 N/A INTRINSIC
low complexity region 692 728 N/A INTRINSIC
low complexity region 785 799 N/A INTRINSIC
low complexity region 933 951 N/A INTRINSIC
low complexity region 963 977 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000213199
Predicted Effect probably benign
Transcript: ENSMUST00000215298
Predicted Effect probably benign
Transcript: ENSMUST00000217657
Coding Region Coverage
  • 1x: 99.7%
  • 3x: 99.4%
  • 10x: 98.0%
  • 20x: 90.8%
Validation Efficiency 96% (50/52)
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2ml1 T C 6: 128,546,962 (GRCm39) D389G possibly damaging Het
Acy1 A T 9: 106,313,319 (GRCm39) probably null Het
Adcy2 G A 13: 68,882,754 (GRCm39) Q328* probably null Het
Arhgef40 T A 14: 52,235,632 (GRCm39) V1171E probably damaging Het
Arrb1 G A 7: 99,247,659 (GRCm39) probably null Het
Atxn1l G A 8: 110,459,233 (GRCm39) A343V probably benign Het
C3 A T 17: 57,533,276 (GRCm39) V109E probably damaging Het
Clptm1 A T 7: 19,367,827 (GRCm39) V595E possibly damaging Het
Cpne6 T C 14: 55,750,066 (GRCm39) C66R possibly damaging Het
Dhrs3 T C 4: 144,646,474 (GRCm39) S175P probably damaging Het
Eif2b1 A T 5: 124,711,208 (GRCm39) M187K probably damaging Het
Eln CTCCAGCTCCGAT C 5: 134,758,003 (GRCm39) probably benign Het
Evc2 T C 5: 37,537,911 (GRCm39) L533P probably damaging Het
Fam221b T G 4: 43,665,465 (GRCm39) Q331P probably damaging Het
Fam221b G T 4: 43,665,466 (GRCm39) Q331K probably benign Het
Golga3 T C 5: 110,333,745 (GRCm39) V127A probably damaging Het
Itsn1 C T 16: 91,708,893 (GRCm39) P1719L unknown Het
Lars1 T G 18: 42,351,591 (GRCm39) H871P probably damaging Het
Mamdc4 A T 2: 25,457,019 (GRCm39) V590E probably damaging Het
Mdga2 A G 12: 66,702,037 (GRCm39) I457T probably damaging Het
Morc2a T C 11: 3,634,039 (GRCm39) V717A probably benign Het
Or1p1c C A 11: 74,160,384 (GRCm39) H56Q probably damaging Het
Or8d2b A T 9: 38,788,662 (GRCm39) L63F probably damaging Het
Pank4 A T 4: 155,054,537 (GRCm39) Q170L probably benign Het
Pde4dip G T 3: 97,622,742 (GRCm39) A1489D probably damaging Het
Pde8b A T 13: 95,359,278 (GRCm39) I15N probably damaging Het
Pex16 A C 2: 92,205,985 (GRCm39) E26A probably damaging Het
Poglut2 A G 1: 44,149,966 (GRCm39) Y408H probably damaging Het
Polq C T 16: 36,849,846 (GRCm39) P367S probably benign Het
Polr1a T A 6: 71,927,600 (GRCm39) V817E probably benign Het
Pthlh T C 6: 147,158,663 (GRCm39) D99G probably damaging Het
Rasgrp4 A T 7: 28,848,542 (GRCm39) S556C probably damaging Het
Rhobtb1 G T 10: 69,125,388 (GRCm39) V653L possibly damaging Het
Rin2 G A 2: 145,664,225 (GRCm39) R33Q probably benign Het
Rmc1 A T 18: 12,318,704 (GRCm39) probably null Het
Sh3rf2 C T 18: 42,274,124 (GRCm39) T430I probably benign Het
Slc14a2 A G 18: 78,227,759 (GRCm39) probably null Het
Slc39a8 C T 3: 135,590,404 (GRCm39) Q366* probably null Het
Spata31h1 A T 10: 82,130,433 (GRCm39) L859* probably null Het
Tagln3 G T 16: 45,544,554 (GRCm39) A39D probably benign Het
Tfdp1 T A 8: 13,423,015 (GRCm39) C307S probably benign Het
Tlr11 T C 14: 50,599,945 (GRCm39) S644P probably damaging Het
Tnpo3 T C 6: 29,558,761 (GRCm39) D723G probably benign Het
Xpo5 A G 17: 46,519,145 (GRCm39) N195D probably benign Het
Zfp11 T C 5: 129,733,694 (GRCm39) Y589C possibly damaging Het
Zfp712 T C 13: 67,189,172 (GRCm39) T452A probably benign Het
Other mutations in 1700017B05Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01011:1700017B05Rik APN 9 57,165,529 (GRCm39) missense probably damaging 1.00
IGL01287:1700017B05Rik APN 9 57,165,040 (GRCm39) missense probably damaging 1.00
IGL01798:1700017B05Rik APN 9 57,163,921 (GRCm39) missense probably benign 0.10
IGL01933:1700017B05Rik APN 9 57,164,650 (GRCm39) missense possibly damaging 0.95
IGL02146:1700017B05Rik APN 9 57,164,023 (GRCm39) missense possibly damaging 0.82
IGL02158:1700017B05Rik APN 9 57,163,902 (GRCm39) splice site probably null
IGL02277:1700017B05Rik APN 9 57,165,708 (GRCm39) missense probably benign 0.05
IGL02707:1700017B05Rik APN 9 57,165,928 (GRCm39) missense probably benign
IGL02887:1700017B05Rik APN 9 57,166,168 (GRCm39) missense probably damaging 1.00
IGL02936:1700017B05Rik APN 9 57,165,687 (GRCm39) missense possibly damaging 0.69
R0583:1700017B05Rik UTSW 9 57,164,926 (GRCm39) missense probably benign 0.04
R0926:1700017B05Rik UTSW 9 57,164,832 (GRCm39) missense probably damaging 0.99
R1812:1700017B05Rik UTSW 9 57,164,740 (GRCm39) nonsense probably null
R1903:1700017B05Rik UTSW 9 57,165,635 (GRCm39) missense possibly damaging 0.69
R4542:1700017B05Rik UTSW 9 57,163,875 (GRCm39) missense probably damaging 1.00
R4596:1700017B05Rik UTSW 9 57,165,088 (GRCm39) missense probably benign 0.03
R4631:1700017B05Rik UTSW 9 57,165,270 (GRCm39) missense probably damaging 1.00
R4869:1700017B05Rik UTSW 9 57,161,488 (GRCm39) missense probably damaging 1.00
R5265:1700017B05Rik UTSW 9 57,166,177 (GRCm39) missense probably damaging 1.00
R5361:1700017B05Rik UTSW 9 57,164,468 (GRCm39) missense probably damaging 1.00
R6216:1700017B05Rik UTSW 9 57,164,910 (GRCm39) missense probably benign 0.33
R6356:1700017B05Rik UTSW 9 57,161,292 (GRCm39) missense probably benign 0.11
R6579:1700017B05Rik UTSW 9 57,161,507 (GRCm39) missense possibly damaging 0.89
R6774:1700017B05Rik UTSW 9 57,163,908 (GRCm39) missense probably damaging 1.00
R6921:1700017B05Rik UTSW 9 57,166,019 (GRCm39) missense probably damaging 1.00
R7089:1700017B05Rik UTSW 9 57,166,041 (GRCm39) missense probably damaging 1.00
R7196:1700017B05Rik UTSW 9 57,165,505 (GRCm39) frame shift probably null
R7197:1700017B05Rik UTSW 9 57,165,505 (GRCm39) frame shift probably null
R7728:1700017B05Rik UTSW 9 57,163,822 (GRCm39) missense probably damaging 1.00
R7770:1700017B05Rik UTSW 9 57,165,894 (GRCm39) missense probably damaging 0.99
R7812:1700017B05Rik UTSW 9 57,165,141 (GRCm39) missense probably damaging 0.99
R8141:1700017B05Rik UTSW 9 57,165,688 (GRCm39) missense probably benign
R8925:1700017B05Rik UTSW 9 57,165,805 (GRCm39) nonsense probably null
R8927:1700017B05Rik UTSW 9 57,165,805 (GRCm39) nonsense probably null
R9186:1700017B05Rik UTSW 9 57,164,472 (GRCm39) missense probably damaging 0.99
R9194:1700017B05Rik UTSW 9 57,166,371 (GRCm39) start codon destroyed probably null 1.00
R9299:1700017B05Rik UTSW 9 57,163,792 (GRCm39) missense possibly damaging 0.91
Predicted Primers PCR Primer
(F):5'- GATCCTGCCTTCGAAGTACC -3'
(R):5'- GGCCACAGCACACATACTTG -3'

Sequencing Primer
(F):5'- GCCTTCGAAGTACCCCCTATGG -3'
(R):5'- CAAGTTTTTGAGGCCAGCC -3'
Posted On 2020-06-30