Incidental Mutation 'R1489:2700097O09Rik'
ID 163614
Institutional Source Beutler Lab
Gene Symbol 2700097O09Rik
Ensembl Gene ENSMUSG00000062198
Gene Name RIKEN cDNA 2700097O09 gene
Synonyms
MMRRC Submission 039541-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.142) question?
Stock # R1489 (G1)
Quality Score 225
Status Validated
Chromosome 12
Chromosomal Location 55045661-55080110 bp(-) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 55059510 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 143 (S143P)
Ref Sequence ENSEMBL: ENSMUSP00000021406 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000021406]
AlphaFold Q6PGK3
Predicted Effect possibly damaging
Transcript: ENSMUST00000021406
AA Change: S143P

PolyPhen 2 Score 0.937 (Sensitivity: 0.80; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000021406
Gene: ENSMUSG00000062198
AA Change: S143P

DomainStartEndE-ValueType
Pfam:Methyltransf_18 143 253 3.1e-8 PFAM
Pfam:CheR 172 269 7.5e-8 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000156852
Predicted Effect noncoding transcript
Transcript: ENSMUST00000222572
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.4%
  • 10x: 96.7%
  • 20x: 93.9%
Validation Efficiency 96% (52/54)
Allele List at MGI
Other mutations in this stock
Total: 49 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930522H14Rik T C 4: 109,505,457 K218E possibly damaging Het
Abcb1a T A 5: 8,686,300 probably null Het
Adam39 A G 8: 40,824,994 T141A possibly damaging Het
Adam6b T A 12: 113,491,451 S629R probably benign Het
Ap3b2 C A 7: 81,463,690 E924* probably null Het
Armc3 A T 2: 19,310,047 Y856F probably benign Het
Asap1 A G 15: 64,172,730 L142P probably damaging Het
Atg9a T A 1: 75,186,090 D427V probably damaging Het
Atl2 G A 17: 79,852,706 A17V probably benign Het
Atxn2l A T 7: 126,496,467 S379T probably damaging Het
C1ql3 G T 2: 13,010,642 P69Q possibly damaging Het
Cap2 A T 13: 46,609,635 I114F probably damaging Het
Cox16 T C 12: 81,474,615 N135S probably null Het
Dnajc13 A T 9: 104,231,035 H180Q possibly damaging Het
Dpy19l3 A T 7: 35,725,410 Y73* probably null Het
Duox2 T A 2: 122,293,396 M436L probably benign Het
Exoc6 T A 19: 37,597,120 M481K possibly damaging Het
Fbxw2 GCCCCC GCCCCCCCC 2: 34,812,817 probably benign Het
Fmn1 T A 2: 113,365,212 V419E unknown Het
Fndc4 T C 5: 31,293,451 *232W probably null Het
Foxc1 C T 13: 31,808,612 R469* probably null Het
Fsip2 A G 2: 82,979,811 H2158R probably benign Het
Ghdc C T 11: 100,768,257 G373D probably benign Het
Gm10330 A T 12: 23,780,031 S50T probably benign Het
Gm8251 A G 1: 44,057,790 F1383L probably benign Het
Gm8251 T C 1: 44,061,507 I144V probably benign Het
Hlx G T 1: 184,731,987 A52D probably damaging Het
Lonrf1 A G 8: 36,222,954 V650A probably damaging Het
Map1a T C 2: 121,300,437 V578A possibly damaging Het
Mbd3 C G 10: 80,393,906 D190H probably damaging Het
Mcpt9 T C 14: 56,027,519 K175R probably benign Het
Mia3 A G 1: 183,338,674 S85P probably benign Het
Myrip T C 9: 120,432,529 F403L probably damaging Het
Nox4 A G 7: 87,304,889 Y134C probably damaging Het
Numb A G 12: 83,795,443 L642P probably damaging Het
Pappa A T 4: 65,180,948 Y568F possibly damaging Het
Pdzrn4 T C 15: 92,677,712 L333P probably benign Het
Prl A T 13: 27,057,636 S3C probably damaging Het
Ptprc T C 1: 138,120,086 T60A possibly damaging Het
Rbm10 C T X: 20,637,664 probably benign Het
Slc7a7 C T 14: 54,408,646 R120H probably damaging Het
Smpd1 T C 7: 105,556,554 probably null Het
Spta1 A G 1: 174,231,325 E1942G probably damaging Het
Tmem38a A G 8: 72,579,635 Y66C probably damaging Het
Tnnt1 A T 7: 4,507,525 Y232* probably null Het
Tpte T C 8: 22,349,389 probably null Het
Virma T C 4: 11,521,164 V907A probably damaging Het
Vmn1r174 C T 7: 23,754,556 Q216* probably null Het
Zswim3 T C 2: 164,819,981 V127A probably benign Het
Other mutations in 2700097O09Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00418:2700097O09Rik APN 12 55048963 missense probably damaging 1.00
IGL02618:2700097O09Rik APN 12 55057301 nonsense probably null
IGL03340:2700097O09Rik APN 12 55080001 missense probably benign 0.10
R0844:2700097O09Rik UTSW 12 55080073 missense possibly damaging 0.62
R4722:2700097O09Rik UTSW 12 55061137 missense probably benign 0.24
R4786:2700097O09Rik UTSW 12 55059536 missense possibly damaging 0.88
R4981:2700097O09Rik UTSW 12 55048987 splice site probably null
R5216:2700097O09Rik UTSW 12 55061162 missense probably damaging 1.00
R6787:2700097O09Rik UTSW 12 55079983 missense probably benign 0.06
R7014:2700097O09Rik UTSW 12 55045942 missense probably benign
R7895:2700097O09Rik UTSW 12 55059510 missense probably benign 0.03
R8688:2700097O09Rik UTSW 12 55057351 missense probably damaging 1.00
R8690:2700097O09Rik UTSW 12 55061172 missense possibly damaging 0.89
Predicted Primers PCR Primer
(F):5'- GCAGAGTTTAGGAGCCTGCCAATG -3'
(R):5'- AGTTCCCTCCAGGTCAGAGGAAAG -3'

Sequencing Primer
(F):5'- AGCTGTCACTAGCAGGAGAA -3'
(R):5'- caggtgaggtggtgcag -3'
Posted On 2014-03-28