Incidental Mutation 'R3726:Gm8730'
ID270792
Institutional Source Beutler Lab
Gene Symbol Gm8730
Ensembl Gene ENSMUSG00000063696
Gene Namepredicted pseudogene 8730
Synonyms
MMRRC Submission 040717-MU
Accession Numbers
Is this an essential gene? Probably essential (E-score: 0.875) question?
Stock #R3726 (G1)
Quality Score84
Status Validated
Chromosome8
Chromosomal Location102864779-102865853 bp(-) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to C at 102865032 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
Predicted Effect noncoding transcript
Transcript: ENSMUST00000076373
SMART Domains Protein: ENSMUSP00000132472
Gene: ENSMUSG00000063696

DomainStartEndE-ValueType
Pfam:Ribosomal_L10 5 106 3.1e-25 PFAM
low complexity region 109 117 N/A INTRINSIC
Pfam:Ribosomal_60s 231 316 3.7e-24 PFAM
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.2%
  • 20x: 94.9%
Validation Efficiency 100% (49/49)
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930402K13Rik AGAGGAG AGAG X: 9,105,103 probably benign Het
Caap1 A T 4: 94,501,143 V318D probably damaging Het
Camsap3 T C 8: 3,603,785 L485P probably damaging Het
Ccsap T C 8: 123,859,361 E17G possibly damaging Het
Cdk5rap2 C A 4: 70,235,437 K1716N possibly damaging Het
Coq3 T C 4: 21,892,941 probably benign Het
Daam2 T A 17: 49,469,738 D773V probably damaging Het
F11 A G 8: 45,248,638 S353P probably damaging Het
Fam209 T C 2: 172,473,995 S97P probably benign Het
Fam50b G A 13: 34,746,886 R115H probably damaging Het
Fbxo31 A G 8: 121,578,509 F83L probably damaging Het
Fsip2 G T 2: 82,988,967 A5015S possibly damaging Het
Galnt13 A G 2: 55,098,657 H497R probably damaging Het
Ggnbp2 A G 11: 84,854,094 C201R possibly damaging Het
Gsr A G 8: 33,671,537 K124R probably benign Het
Hdgf T C 3: 87,914,497 S140P probably benign Het
Iqcg C T 16: 33,029,041 E292K probably damaging Het
Lamb1 C T 12: 31,321,075 A1375V probably null Het
Lct T C 1: 128,304,226 M629V probably damaging Het
Lonp1 A G 17: 56,618,310 probably benign Het
Mrc2 G A 11: 105,348,431 probably null Het
Olfr805 A T 10: 129,723,115 V143D probably damaging Het
Pcdhb9 T C 18: 37,401,601 L216P possibly damaging Het
Ppp3cb A G 14: 20,530,942 probably null Het
Ptprm G A 17: 66,956,860 P464L possibly damaging Het
Rars2 A G 4: 34,645,787 T235A probably benign Het
Rimkla A T 4: 119,477,789 probably null Het
Rnf216 A T 5: 143,027,946 I708N probably damaging Het
Six5 T A 7: 19,096,930 V494E possibly damaging Het
Slc43a2 A G 11: 75,543,154 probably benign Het
Slmap C A 14: 26,427,242 R671S probably damaging Het
Smarcal1 T C 1: 72,626,596 F751S possibly damaging Het
Sptan1 G A 2: 30,018,419 D1711N possibly damaging Het
Sptssa T C 12: 54,656,395 E30G probably damaging Het
Taf1c A G 8: 119,603,070 F111L probably damaging Het
Thbs1 A G 2: 118,114,710 I255V probably benign Het
Tmem19 A G 10: 115,359,770 probably benign Het
Tmem59l A G 8: 70,487,301 L6S unknown Het
Tmod1 T C 4: 46,097,026 V273A probably benign Het
Trpm8 A T 1: 88,328,196 Y191F probably benign Het
Ube4a T C 9: 44,933,323 I934V probably damaging Het
Vpreb3 G A 10: 75,943,291 probably null Het
Vwf G T 6: 125,677,948 probably benign Het
Wdr53 T C 16: 32,256,720 C248R probably benign Het
Zfp217 A G 2: 170,119,210 V399A probably damaging Het
Zfp980 G A 4: 145,702,083 G461S probably benign Het
Other mutations in Gm8730
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02341:Gm8730 APN 8 102865143 exon noncoding transcript
R3105:Gm8730 UTSW 8 102865263 exon noncoding transcript
R3725:Gm8730 UTSW 8 102865032 exon noncoding transcript
R4689:Gm8730 UTSW 8 102865747 exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- TTAAGCAGGCTGACTTGGTTGC -3'
(R):5'- CGGCAGCATTTATAACCCGG -3'

Sequencing Primer
(F):5'- GTCGAAGAGACCGAATCCCATATC -3'
(R):5'- TTATAACCCGGAAGTGCTCG -3'
Posted On2015-03-18