Incidental Mutation 'R1069:Mir100hg'
ID 86130
Institutional Source Beutler Lab
Gene Symbol Mir100hg
Ensembl Gene
Gene Name Mir100 Mirlet7a-2 Mir125b-1 cluster host gene
Synonyms 3110039I08Rik, 2610203C20Rik, D230004N17Rik
MMRRC Submission 039155-MU
Accession Numbers
Essential gene? Not available question?
Stock # R1069 (G1)
Quality Score 225
Status Validated
Chromosome 9
Chromosomal Location 41287822-41526481 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 41501594 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Histidine at position 151 (R151H)
Ref Sequence ENSEMBL: ENSMUSP00000155652 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098868]
AlphaFold no structure available at present
Predicted Effect possibly damaging
Transcript: ENSMUST00000098868
AA Change: R151H

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180622
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180818
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181214
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181296
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181814
Predicted Effect noncoding transcript
Transcript: ENSMUST00000181955
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188277
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188774
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212079
Predicted Effect noncoding transcript
Transcript: ENSMUST00000188945
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212373
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.5%
  • 20x: 95.4%
Validation Efficiency 100% (33/33)
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921524L21Rik A G 18: 6,624,037 (GRCm39) N106S probably benign Het
Akr1c21 C A 13: 4,625,333 (GRCm39) probably benign Het
Alpk2 G A 18: 65,438,085 (GRCm39) R1570C probably benign Het
Atp8b3 G A 10: 80,366,852 (GRCm39) R249C probably damaging Het
Cacnb4 C A 2: 52,345,623 (GRCm39) R252I probably damaging Het
Cars1 T C 7: 143,123,844 (GRCm39) T480A probably benign Het
Ccnf A T 17: 24,442,971 (GRCm39) C745* probably null Het
Ccr8 A G 9: 119,923,283 (GRCm39) I133V probably benign Het
Cndp1 G A 18: 84,652,777 (GRCm39) probably benign Het
Dgkq T C 5: 108,803,903 (GRCm39) probably benign Het
Ecd A G 14: 20,383,504 (GRCm39) C312R probably damaging Het
Eddm13 A T 7: 6,258,921 (GRCm39) probably null Het
Gstm1 T C 3: 107,920,064 (GRCm39) S226G probably damaging Het
Gtf3c3 C T 1: 54,456,937 (GRCm39) A488T probably damaging Het
Hacd4 T A 4: 88,355,739 (GRCm39) I49L probably damaging Het
Hid1 T C 11: 115,247,591 (GRCm39) N269S probably damaging Het
Ifitm3 A T 7: 140,589,813 (GRCm39) probably benign Het
Kctd9 C T 14: 67,966,869 (GRCm39) probably benign Het
Kif20b T C 19: 34,928,251 (GRCm39) L1131P probably damaging Het
Kif2c T C 4: 117,035,350 (GRCm39) T33A probably damaging Het
Lipc T C 9: 70,730,819 (GRCm39) T38A probably benign Het
Lrguk A C 6: 34,025,818 (GRCm39) I205L possibly damaging Het
Ncapg T A 5: 45,833,272 (GRCm39) probably benign Het
Ptprd A G 4: 75,916,724 (GRCm39) probably benign Het
Ptprd T A 4: 76,018,870 (GRCm39) K635* probably null Het
Sap130 G A 18: 31,844,682 (GRCm39) V898I probably damaging Het
Sned1 G A 1: 93,209,376 (GRCm39) V830M possibly damaging Het
Svep1 C T 4: 58,070,239 (GRCm39) G2516R probably damaging Het
Tas2r131 C T 6: 132,934,788 (GRCm39) R7K probably benign Het
Tfpi A G 2: 84,284,136 (GRCm39) probably benign Het
Trim80 T C 11: 115,338,909 (GRCm39) C580R probably damaging Het
Ttn T A 2: 76,800,273 (GRCm39) I312F unknown Het
Other mutations in Mir100hg
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1548:Mir100hg UTSW 9 41,492,672 (GRCm39) missense probably damaging 0.97
R3941:Mir100hg UTSW 9 41,501,570 (GRCm39) missense probably damaging 0.97
Predicted Primers PCR Primer
(F):5'- CACAAGACTGCTGCTGCATTGATTC -3'
(R):5'- ATCGCCTGTGACTGCTTTGCTG -3'

Sequencing Primer
(F):5'- AAAGAGCATTGTCTCTCCAGTGTC -3'
(R):5'- CATTAACACATTTGGGCAAAGC -3'
Posted On 2013-11-18