Incidental Mutation 'R2906:Gm6430'
ID 261638
Institutional Source Beutler Lab
Gene Symbol Gm6430
Ensembl Gene ENSMUSG00000044757
Gene Name predicted gene 6430
Synonyms
MMRRC Submission 040493-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.236) question?
Stock # R2906 (G1)
Quality Score 225
Status Validated
Chromosome 1
Chromosomal Location 96952406-96953653 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) A to T at 96952554 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000054664
SMART Domains Protein: ENSMUSP00000136398
Gene: ENSMUSG00000044757

DomainStartEndE-ValueType
RRM 12 86 3.26e-5 SMART
RRM 112 184 2.38e-7 SMART
low complexity region 233 254 N/A INTRINSIC
RRM 290 360 2.43e-13 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188810
Meta Mutation Damage Score 0.2698 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.4%
  • 20x: 95.2%
Validation Efficiency 97% (37/38)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam32 A T 8: 25,353,520 (GRCm39) W690R probably damaging Het
Adgrg6 A G 10: 14,308,694 (GRCm39) I800T probably benign Het
Afg3l2 G A 18: 67,573,292 (GRCm39) T170M probably damaging Het
Ap1b1 T A 11: 4,981,641 (GRCm39) N516K probably damaging Het
Armcx6 A T X: 133,650,199 (GRCm39) C211S probably damaging Het
Atp7b G A 8: 22,501,570 (GRCm39) T781I probably damaging Het
Cd96 T C 16: 45,871,850 (GRCm39) T432A possibly damaging Het
Col13a1 T C 10: 61,696,267 (GRCm39) probably benign Het
Ddx4 G T 13: 112,757,311 (GRCm39) probably benign Het
Dnm1l A T 16: 16,132,175 (GRCm39) S666T probably damaging Het
Duoxa1 C T 2: 122,135,155 (GRCm39) V197M probably benign Het
Gtf2a1l G A 17: 89,002,083 (GRCm39) R313H possibly damaging Het
Gucy2c A T 6: 136,685,385 (GRCm39) V852E probably damaging Het
Kcnk1 G T 8: 126,722,538 (GRCm39) V114L probably benign Het
Klra3 G T 6: 130,310,302 (GRCm39) Q73K probably damaging Het
Lax1 A T 1: 133,616,643 (GRCm39) M1K probably null Het
Lce1k T C 3: 92,713,882 (GRCm39) S101G unknown Het
Med12l T C 3: 59,164,503 (GRCm39) L1365P probably damaging Het
Mtx2 T C 2: 74,697,253 (GRCm39) S83P probably damaging Het
Naip2 A C 13: 100,298,504 (GRCm39) C511G probably damaging Het
Nefh A G 11: 4,890,216 (GRCm39) I801T probably benign Het
Or8g24 A G 9: 38,989,669 (GRCm39) V124A probably benign Het
Oxct2b A G 4: 123,010,823 (GRCm39) I248V probably benign Het
Pcdhgb2 A T 18: 37,823,908 (GRCm39) I300F probably damaging Het
Ptprc G A 1: 137,992,272 (GRCm39) A1285V possibly damaging Het
Rassf3 A G 10: 121,250,297 (GRCm39) L172P probably damaging Het
Rbm26 T A 14: 105,380,270 (GRCm39) T516S probably benign Het
Rpusd1 T C 17: 25,949,705 (GRCm39) S292P probably benign Het
Scamp5 A G 9: 57,351,146 (GRCm39) V172A probably damaging Het
Snx25 T C 8: 46,502,560 (GRCm39) probably null Het
Tmprss11g A G 5: 86,640,661 (GRCm39) probably benign Het
Ttll3 G C 6: 113,369,471 (GRCm39) probably benign Het
Uggt2 C T 14: 119,256,919 (GRCm39) S1105N probably benign Het
Usp45 T A 4: 21,834,338 (GRCm39) Y805* probably null Het
Zfp639 T C 3: 32,573,900 (GRCm39) L175P probably damaging Het
Zfp995 T C 17: 22,099,247 (GRCm39) D329G probably benign Het
Other mutations in Gm6430
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02610:Gm6430 APN 1 96,952,560 (GRCm39) intron noncoding transcript
R2225:Gm6430 UTSW 1 96,953,441 (GRCm39) unclassified noncoding transcript
R4258:Gm6430 UTSW 1 96,952,561 (GRCm39) intron noncoding transcript
R4407:Gm6430 UTSW 1 96,953,297 (GRCm39) unclassified noncoding transcript
Predicted Primers PCR Primer
(F):5'- TTGTGTGACATCAGCCCTGTC -3'
(R):5'- TTCCTTTGTGCATCCAAATGGG -3'

Sequencing Primer
(F):5'- AGCCCTGTCAAGTGTCCATGATG -3'
(R):5'- ATCATTGGCACTGTCGGC -3'
Posted On 2015-01-23