Incidental Mutation 'R5939:Gm10428'
ID 462441
Institutional Source Beutler Lab
Gene Symbol Gm10428
Ensembl Gene ENSMUSG00000096083
Gene Name predicted gene 10428
Synonyms
MMRRC Submission 043243-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.142) question?
Stock # R5939 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 62643926-62644324 bp(+) (GRCm39)
Type of Mutation utr 3 prime
DNA Base Change (assembly) A to C at 62644288 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: R121S
Predicted Effect noncoding transcript
Transcript: ENSMUST00000207474
Predicted Effect probably benign
Transcript: ENSMUST00000207597
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 97.9%
  • 20x: 93.9%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam32 A T 8: 25,404,138 (GRCm39) F225I probably damaging Het
Ager G T 17: 34,817,175 (GRCm39) C38F probably damaging Het
Arel1 C A 12: 84,973,066 (GRCm39) R577L probably damaging Het
Armh1 T C 4: 117,087,119 (GRCm39) Y182C probably damaging Het
Cabp2 G T 19: 4,136,470 (GRCm39) C172F possibly damaging Het
Cenps C A 4: 149,214,658 (GRCm39) probably benign Het
D630045J12Rik A C 6: 38,171,904 (GRCm39) S755A possibly damaging Het
Duox1 A T 2: 122,176,832 (GRCm39) H1451L probably damaging Het
Dync2h1 A G 9: 7,037,801 (GRCm39) V3359A probably damaging Het
Erlin2 T C 8: 27,526,554 (GRCm39) F305L probably benign Het
Gnal G A 18: 67,324,456 (GRCm39) V204M probably damaging Het
Intu T C 3: 40,647,014 (GRCm39) V629A probably damaging Het
Lrguk G T 6: 34,055,688 (GRCm39) C435F probably damaging Het
Man1c1 C T 4: 134,293,147 (GRCm39) V543M probably damaging Het
Mcm3ap A G 10: 76,344,195 (GRCm39) H1779R probably benign Het
Neb T C 2: 52,147,606 (GRCm39) T2776A probably benign Het
Nek10 A T 14: 14,931,290 (GRCm38) Y754F possibly damaging Het
Nr3c1 A G 18: 39,553,706 (GRCm39) I664T probably benign Het
Nrip1 T C 16: 76,089,010 (GRCm39) E849G probably damaging Het
Nrros A G 16: 31,962,272 (GRCm39) F546L probably benign Het
Or12e8 A C 2: 87,188,048 (GRCm39) I87L possibly damaging Het
Or5d39 T C 2: 87,979,853 (GRCm39) Y170C probably damaging Het
Pcdhb16 A G 18: 37,611,117 (GRCm39) T26A probably benign Het
Penk A G 4: 4,138,010 (GRCm39) F45S probably benign Het
Pgap4 T A 4: 49,586,412 (GRCm39) Q252L probably damaging Het
Ppp2r3d A T 9: 101,089,824 (GRCm39) N166K probably benign Het
Psmb1 A G 17: 15,718,440 (GRCm39) F29L probably damaging Het
Rab23 T C 1: 33,762,990 (GRCm39) V20A probably damaging Het
Ryr1 C T 7: 28,815,552 (GRCm39) A113T probably damaging Het
Ryr2 C T 13: 11,805,218 (GRCm39) R882K probably damaging Het
Slc6a6 A G 6: 91,731,929 (GRCm39) N586S probably benign Het
Slc9c1 A G 16: 45,368,031 (GRCm39) I207V probably benign Het
Spef2 G A 15: 9,614,301 (GRCm39) T1215I probably benign Het
Thoc2l T C 5: 104,667,073 (GRCm39) Y532H possibly damaging Het
Tmc7 C T 7: 118,144,950 (GRCm39) A537T probably benign Het
Tmem70 T C 1: 16,747,615 (GRCm39) V243A probably benign Het
Top2b T C 14: 16,422,786 (GRCm38) Y1408H probably damaging Het
Tpcn1 A T 5: 120,677,892 (GRCm39) F642I probably damaging Het
Xirp1 T G 9: 119,847,575 (GRCm39) D436A probably benign 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
R6611:Gm10428 UTSW 11 62,644,115 (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'- TCACATGTGCCTACATCTATAGGG -3'
(R):5'- GCTATCAGAGAACGGCTTTGG -3'

Sequencing Primer
(F):5'- CCTCAAAATAAATGATGAAGTCTGCC -3'
(R):5'- CGGCTTTGGAAAAGATTTATCACAG -3'
Posted On 2017-02-28