Incidental Mutation 'R6611:Gm10428'
ID 523601
Institutional Source Beutler Lab
Gene Symbol Gm10428
Ensembl Gene ENSMUSG00000096083
Gene Name predicted gene 10428
Synonyms
MMRRC Submission 044734-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.142) question?
Stock # R6611 (G1)
Quality Score 225.009
Status Not validated
Chromosome 11
Chromosomal Location 62643926-62644324 bp(+) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) A to T at 62644115 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147022 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000178750] [ENSMUST00000207597]
AlphaFold J3QNV7
Predicted Effect noncoding transcript
Transcript: ENSMUST00000117937
Predicted Effect noncoding transcript
Transcript: ENSMUST00000138105
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139798
Predicted Effect noncoding transcript
Transcript: ENSMUST00000175753
Predicted Effect unknown
Transcript: ENSMUST00000178750
AA Change: I64L
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207474
Predicted Effect probably benign
Transcript: ENSMUST00000207597
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.1%
  • 20x: 94.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 37 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1810009J06Rik A T 6: 40,943,713 (GRCm39) T126S probably benign Het
Bex6 A G 16: 32,005,483 (GRCm39) K97R probably benign Het
Brca2 T C 5: 150,459,658 (GRCm39) L311P probably damaging Het
Ccng2 C G 5: 93,421,202 (GRCm39) S237R probably benign Het
Cdc16 C A 8: 13,831,512 (GRCm39) P582T probably benign Het
Cep112 T C 11: 108,397,377 (GRCm39) I280T possibly damaging Het
Cfhr4 A G 1: 139,660,128 (GRCm39) Y666H probably damaging Het
Chd2 A G 7: 73,143,313 (GRCm39) F527L probably damaging Het
Drc3 G T 11: 60,255,773 (GRCm39) R120L probably damaging Het
Efcab6 T A 15: 83,777,036 (GRCm39) R1133S possibly damaging Het
Fer1l5 T C 1: 36,445,735 (GRCm39) V834A probably benign Het
Flnb A G 14: 7,915,318 (GRCm38) Y1483C probably damaging Het
Fstl4 A T 11: 53,077,552 (GRCm39) M770L probably benign Het
Hmbs C A 9: 44,252,988 (GRCm39) R15L probably damaging Het
Irx3 T C 8: 92,526,631 (GRCm39) T358A probably damaging Het
Kmt2a T A 9: 44,760,569 (GRCm39) I460L probably damaging Het
Mob2 G T 7: 141,563,293 (GRCm39) F55L probably damaging Het
Muc6 G C 7: 141,226,700 (GRCm39) probably benign Het
Ntrk2 T C 13: 59,202,228 (GRCm39) L612P probably damaging Het
Obscn A G 11: 58,955,056 (GRCm39) probably null Het
Or4d5 T C 9: 40,012,316 (GRCm39) I157V probably benign Het
Or5j1 A T 2: 86,879,577 (GRCm39) M1K probably null Het
Or8b44 A T 9: 38,410,534 (GRCm39) T190S probably damaging Het
Oxct2a T C 4: 123,216,640 (GRCm39) E247G probably damaging Het
Phykpl G T 11: 51,489,181 (GRCm39) A336S probably damaging Het
Pik3r4 T G 9: 105,521,476 (GRCm39) L14R probably damaging Het
Pnpla1 A G 17: 29,100,021 (GRCm39) N296S probably benign Het
Pramel7 A G 2: 87,320,393 (GRCm39) I300T probably damaging Het
Rictor T G 15: 6,780,140 (GRCm39) C132G probably damaging Het
Rsf1 G GACGGCGGCT 7: 97,229,116 (GRCm39) probably benign Homo
Slc9a9 G T 9: 94,821,531 (GRCm39) R306L probably benign Het
Smc5 A G 19: 23,206,283 (GRCm39) V681A probably benign Het
Snap91 C T 9: 86,672,180 (GRCm39) S646N probably benign Het
Ssh3 T C 19: 4,314,450 (GRCm39) N368S probably damaging Het
Syne1 A T 10: 4,995,273 (GRCm39) N8326K probably benign Het
Traf3 T G 12: 111,204,074 (GRCm39) L21R possibly damaging Het
Ubxn11 C A 4: 133,850,910 (GRCm39) T254K probably damaging Het
Other mutations in Gm10428
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0630:Gm10428 UTSW 11 62,644,256 (GRCm39) utr 3 prime probably benign
R1925:Gm10428 UTSW 11 62,644,179 (GRCm39) utr 3 prime probably benign
R5466:Gm10428 UTSW 11 62,643,932 (GRCm39) utr 3 prime probably benign
R5761:Gm10428 UTSW 11 62,644,169 (GRCm39) utr 3 prime probably benign
R5788:Gm10428 UTSW 11 62,644,107 (GRCm39) utr 3 prime probably benign
R5939:Gm10428 UTSW 11 62,644,288 (GRCm39) utr 3 prime probably benign
R7115:Gm10428 UTSW 11 62,644,206 (GRCm39) missense unknown
R8398:Gm10428 UTSW 11 62,644,173 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- ACGCAAAGAAGGCCTTTCC -3'
(R):5'- ACCCGAGTCAGAGACTAGTAAG -3'

Sequencing Primer
(F):5'- GCAAAGAAGGCCTTTCCGAATTC -3'
(R):5'- CAAGCTGCTCTAAGGGGCTC -3'
Posted On 2018-06-22