Incidental Mutation 'R5332:Gm8444'
ID 423319
Institutional Source Beutler Lab
Gene Symbol Gm8444
Ensembl Gene ENSMUSG00000069439
Gene Name predicted gene 8444
Synonyms
MMRRC Submission 042914-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.395) question?
Stock # R5332 (G1)
Quality Score 225
Status Not validated
Chromosome 15
Chromosomal Location 81727547-81727914 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 81727902 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000061390 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000050467] [ENSMUST00000092020]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000050467
SMART Domains Protein: ENSMUSP00000061390
Gene: ENSMUSG00000048546

DomainStartEndE-ValueType
btg1 1 106 3.69e-64 SMART
Pfam:PAM2 128 145 1e-7 PFAM
low complexity region 175 189 N/A INTRINSIC
low complexity region 194 218 N/A INTRINSIC
low complexity region 226 243 N/A INTRINSIC
Pfam:PAM2 249 266 5.9e-9 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000092020
SMART Domains Protein: ENSMUSP00000089648
Gene: ENSMUSG00000069439

DomainStartEndE-ValueType
Pfam:Ribosomal_L29 2 58 2.3e-22 PFAM
low complexity region 90 103 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.7%
  • 10x: 97.5%
  • 20x: 95.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc12 G T 8: 87,251,459 (GRCm39) probably null Het
Ace T A 11: 105,864,705 (GRCm39) probably null Het
Bax T C 7: 45,116,195 (GRCm39) D2G probably damaging Het
Clec16a G A 16: 10,549,543 (GRCm39) C872Y probably damaging Het
Cmya5 T A 13: 93,232,703 (GRCm39) Y795F probably damaging Het
Coro2b T C 9: 62,336,512 (GRCm39) D254G probably damaging Het
Crhbp G T 13: 95,572,963 (GRCm39) P261H probably damaging Het
Cyp4f14 T C 17: 33,125,065 (GRCm39) D452G probably benign Het
Gria1 T A 11: 57,218,447 (GRCm39) M900K possibly damaging Het
Kcnj3 A G 2: 55,327,559 (GRCm39) H116R probably damaging Het
Lin9 T A 1: 180,496,763 (GRCm39) L351I probably benign Het
Map3k2 A G 18: 32,340,509 (GRCm39) D172G probably damaging Het
Mmp1b T C 9: 7,384,897 (GRCm39) I251V possibly damaging Het
Mpdz A C 4: 81,210,817 (GRCm39) H1689Q probably damaging Het
Mybpc3 C T 2: 90,953,283 (GRCm39) A176V probably damaging Het
Or5b124 A T 19: 13,610,729 (GRCm39) T85S possibly damaging Het
Otud7a T A 7: 63,385,574 (GRCm39) I352N probably damaging Het
Ptrh1 T C 2: 32,666,758 (GRCm39) V109A probably damaging Het
Pxn A G 5: 115,682,428 (GRCm39) T14A probably damaging Het
Rtn4 T A 11: 29,683,645 (GRCm39) L173Q probably damaging Het
Ryr3 A G 2: 112,733,038 (GRCm39) S603P probably damaging Het
Scara5 CG C 14: 65,997,111 (GRCm39) probably null Het
Scgb2b19 T C 7: 32,978,006 (GRCm39) N97S probably benign Het
Shank2 T A 7: 143,965,029 (GRCm39) I872N possibly damaging Het
Spink5 A G 18: 44,125,984 (GRCm39) E421G possibly damaging Het
Ush2a A G 1: 188,083,276 (GRCm39) Y273C probably damaging Het
Vmn2r121 T C X: 123,043,272 (GRCm39) T120A probably benign Het
Vmn2r52 T A 7: 9,903,052 (GRCm39) I459L probably benign Het
Zfp974 A C 7: 27,625,715 (GRCm39) S52A probably benign Het
Other mutations in Gm8444
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1167:Gm8444 UTSW 15 81,727,581 (GRCm39) unclassified probably benign
R2006:Gm8444 UTSW 15 81,727,775 (GRCm39) unclassified probably benign
R3054:Gm8444 UTSW 15 81,727,845 (GRCm39) unclassified probably benign
R4274:Gm8444 UTSW 15 81,727,734 (GRCm39) unclassified probably benign
R5807:Gm8444 UTSW 15 81,727,654 (GRCm39) unclassified probably benign
R6036:Gm8444 UTSW 15 81,727,794 (GRCm39) unclassified probably benign
R6036:Gm8444 UTSW 15 81,727,794 (GRCm39) unclassified probably benign
R6187:Gm8444 UTSW 15 81,727,807 (GRCm39) unclassified probably benign
Predicted Primers PCR Primer
(F):5'- TGGCTAATAACAGTGAGGACTTGG -3'
(R):5'- TGGCCGCTAGAGATAATTACAG -3'

Sequencing Primer
(F):5'- GGCGATAGATTTGCGAACCACTC -3'
(R):5'- AGCGGAATCTAATGCCTCTG -3'
Posted On 2016-08-04