Incidental Mutation 'R0060:1810065E05Rik'
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ID201410
Institutional Source Beutler Lab
Gene Symbol 1810065E05Rik
Ensembl Gene ENSMUSG00000013653
Gene NameRIKEN cDNA 1810065E05 gene
Synonyms
MMRRC Submission 038353-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.225) question?
Stock #R0060 (G1)
Quality Score31
Status Validated
Chromosome11
Chromosomal Location58421111-58426024 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) A to C at 58422182 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000013797 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000013797]
Predicted Effect probably benign
Transcript: ENSMUST00000013797
SMART Domains Protein: ENSMUSP00000013797
Gene: ENSMUSG00000013653

DomainStartEndE-ValueType
signal peptide 1 26 N/A INTRINSIC
low complexity region 222 235 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.0%
Validation Efficiency 98% (60/61)
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A630091E08Rik A G 7: 98,543,668 noncoding transcript Het
Abca8a T C 11: 110,070,480 T539A probably damaging Het
Ankrd60 A T 2: 173,572,613 M1K probably null Het
Arnt2 G A 7: 84,347,530 R63C probably damaging Het
Cabcoco1 A T 10: 68,533,862 probably null Het
Capn7 T C 14: 31,365,604 probably benign Het
Cd109 G A 9: 78,703,107 E1145K probably damaging Het
Celsr1 A T 15: 85,922,198 V2353D probably damaging Het
Cep350 C T 1: 155,928,626 D904N probably damaging Het
Chl1 T A 6: 103,711,058 probably benign Het
Colec10 G A 15: 54,439,146 probably benign Het
Cst11 T A 2: 148,770,402 Q105L probably damaging Het
Eps8l3 T C 3: 107,879,541 L11S probably damaging Het
Gsdme A G 6: 50,221,029 I317T possibly damaging Het
Itgad T C 7: 128,202,986 S979P probably damaging Het
Mga T C 2: 119,960,961 probably null Het
Nubpl T C 12: 52,310,687 probably benign Het
Olfr1105 T C 2: 87,033,774 Y149C probably damaging Het
Olfr124 T C 17: 37,806,000 L285P probably damaging Het
Pard3b G A 1: 61,639,315 E25K probably damaging Het
Phactr1 T A 13: 42,682,721 Y8* probably null Het
Phf14 T C 6: 11,953,317 S352P probably damaging Het
Ppp1r16a C T 15: 76,690,799 probably benign Het
Prap1 G T 7: 140,093,477 probably benign Het
Prdm8 T A 5: 98,185,260 F229I probably benign Het
Rfx6 T C 10: 51,677,840 F11L probably benign Het
Rfx8 T A 1: 39,718,405 probably benign Het
Rif1 C T 2: 52,111,117 R1528C probably damaging Het
Ripk4 G A 16: 97,763,518 probably benign Het
Satb1 T A 17: 51,740,203 I695F probably damaging Het
Sema4d A G 13: 51,705,257 probably benign Het
Slc30a4 T A 2: 122,685,184 T381S probably benign Het
Suv39h2 T C 2: 3,464,916 Y134C probably damaging Het
Tcerg1 C T 18: 42,524,008 A185V unknown Het
Tep1 T A 14: 50,866,029 D268V probably damaging Het
Tmem89 T A 9: 108,915,417 V126D probably damaging Het
Trf T C 9: 103,220,922 T46A probably benign Het
Trmt6 C T 2: 132,806,769 R415Q possibly damaging Het
Trp53bp1 T C 2: 121,204,525 K1625E probably damaging Het
Zcchc4 T A 5: 52,807,078 I292N possibly damaging Het
Other mutations in 1810065E05Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01772:1810065E05Rik APN 11 58422884 missense probably benign 0.30
R0060:1810065E05Rik UTSW 11 58422182 splice site probably benign
R2141:1810065E05Rik UTSW 11 58423926 missense probably damaging 1.00
R2156:1810065E05Rik UTSW 11 58422308 critical splice donor site probably null
R4925:1810065E05Rik UTSW 11 58425714 nonsense probably null
R5010:1810065E05Rik UTSW 11 58422804 missense possibly damaging 0.77
R5716:1810065E05Rik UTSW 11 58421768 missense possibly damaging 0.77
R6026:1810065E05Rik UTSW 11 58425755 missense probably benign 0.06
Predicted Primers PCR Primer
(F):5'- ATCGAAGAGCCTCCTTGCTGTCTG -3'
(R):5'- TTCATTCCCACCACCCTGAGGAAG -3'

Sequencing Primer
(F):5'- gcatccacgggactcac -3'
(R):5'- CTGAGGAAGCTACACTCCTAAC -3'
Posted On2014-06-06