Incidental Mutation 'IGL03147:Mir205hg'
ID 453099
Institutional Source Beutler Lab
Gene Symbol Mir205hg
Ensembl Gene ENSMUSG00000097850
Gene Name Mir205 host gene
Synonyms 4631405K08Rik
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.420) question?
Stock # IGL03147 (G1)
Quality Score 54
Status Validated
Chromosome 1
Chromosomal Location 193189546-193192482 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to A at 193189768 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: ENSMUST00000083599
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180420
Coding Region Coverage
  • 1x: 0.0%
  • 3x: 0.0%
  • 10x: 0.0%
  • 20x: 0.0%
Validation Efficiency 91% (39/43)
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933416I08Rik TCC TCCC X: 52,692,862 (GRCm39) noncoding transcript Het
Acan A G 7: 78,740,804 (GRCm39) E390G probably damaging Het
Ano3 A G 2: 110,527,763 (GRCm39) S552P probably damaging Het
Ccser1 A G 6: 61,289,144 (GRCm39) S436G probably benign Het
Chek2 A G 5: 110,996,536 (GRCm39) D166G probably damaging Het
Cilp TGGG TGG 9: 65,187,412 (GRCm39) probably null Het
Crb1 CG C 1: 139,164,824 (GRCm39) probably null Het
Deup1 A T 9: 15,521,910 (GRCm39) M85K probably damaging Het
Dnaaf10 G A 11: 17,179,845 (GRCm39) G282E probably damaging Het
Exo1 A G 1: 175,716,354 (GRCm39) Y157C probably damaging Het
Ext1 T A 15: 52,951,468 (GRCm39) I539F probably damaging Het
Gcn1 T C 5: 115,748,917 (GRCm39) V1849A possibly damaging Het
Gpr161 A G 1: 165,144,877 (GRCm39) T389A probably benign Het
Hjurp TGGG TTGCGGG 1: 88,194,002 (GRCm39) probably benign Het
Mmp1a TG TGG 9: 7,465,083 (GRCm38) probably null Het
Muc6 G A 7: 141,218,313 (GRCm39) S2120F possibly damaging Het
Ncoa1 T A 12: 4,309,342 (GRCm39) Y1318F probably damaging Het
Or4c120 A G 2: 89,001,316 (GRCm39) M80T probably benign Het
Pml T C 9: 58,137,326 (GRCm39) H491R possibly damaging Het
Rbmxl2 T G 7: 106,808,858 (GRCm39) S48A probably benign Het
Rgs6 A G 12: 83,138,620 (GRCm39) D318G probably damaging Het
Rmc1 T C 18: 12,302,286 (GRCm39) probably benign Het
Sfi1 G A 11: 3,136,080 (GRCm39) T84I possibly damaging Het
Slc2a2 A G 3: 28,773,519 (GRCm39) M275V possibly damaging Het
Sp110 GC GCC 1: 85,519,288 (GRCm39) probably null Het
Specc1 T C 11: 62,009,108 (GRCm39) V288A probably benign Het
Speer4c1 A C 5: 15,919,214 (GRCm39) probably benign Het
Srsf11 C T 3: 157,732,377 (GRCm39) V118I probably damaging Het
St8sia2 C A 7: 73,616,567 (GRCm39) C136F probably damaging Het
Stmn3 A T 2: 180,950,993 (GRCm39) I21N possibly damaging Het
Trak2 G A 1: 58,949,222 (GRCm39) T526M probably benign Het
Ttn T A 2: 76,542,311 (GRCm39) K25231N probably damaging Het
Ugt1a1 AT A 1: 88,140,093 (GRCm39) probably null Het
Vmn1r11 A T 6: 57,114,650 (GRCm39) I68F probably damaging Het
Zfr T A 15: 12,140,638 (GRCm39) Y228* probably null Het
Predicted Primers PCR Primer
(F):5'- CATTTCCGAAGCATTGGTTTTAGG -3'
(R):5'- GTATTCAGGTCCTCACCAGGTC -3'

Sequencing Primer
(F):5'- CATTGGTTTTAGGAAGAAAGGCCAC -3'
(R):5'- TCACCAGGTCCTGAATGAATG -3'
Posted On 2017-01-27