Incidental Mutation 'R3757:Gm10985'
ID 271471
Institutional Source Beutler Lab
Gene Symbol Gm10985
Ensembl Gene ENSMUSG00000078742
Gene Name predicted gene 10985
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # R3757 (G1)
Quality Score 107
Status Not validated
Chromosome 3
Chromosomal Location 53752507-53752699 bp(+) (GRCm39)
Type of Mutation frame shift
DNA Base Change (assembly) GCTCTCTCTCTCTCTCTCTCTCTCTCTCT to GCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT at 53752645 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000103649 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000108014]
AlphaFold F6T1P1
Predicted Effect probably null
Transcript: ENSMUST00000108014
Predicted Effect noncoding transcript
Transcript: ENSMUST00000158028
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.3%
Validation Efficiency 92% (35/38)
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamtsl3 T A 7: 81,986,415 (GRCm39) I9K probably benign Het
Arhgap31 T C 16: 38,457,362 (GRCm39) E82G probably damaging Het
Asap2 T A 12: 21,317,767 (GRCm39) S993T probably damaging Het
Bmpr1a A T 14: 34,156,624 (GRCm39) L134* probably null Het
Cacna1e A G 1: 154,509,442 (GRCm39) V271A probably damaging Het
Cacna2d4 A G 6: 119,218,124 (GRCm39) E153G probably damaging Het
Cage1 A C 13: 38,209,705 (GRCm39) F91V possibly damaging Het
Cdh24 T C 14: 54,869,637 (GRCm39) D760G possibly damaging Het
Col9a1 T C 1: 24,271,312 (GRCm39) probably null Het
Cts6 A T 13: 61,349,972 (GRCm39) Y36* probably null Het
Dennd3 C G 15: 73,394,083 (GRCm39) A36G probably benign Het
Dmxl1 G A 18: 50,068,384 (GRCm39) G2719D probably damaging Het
Dnajc28 G A 16: 91,413,755 (GRCm39) T187M probably damaging Het
Ep300 T A 15: 81,532,790 (GRCm39) V1676E unknown Het
Ercc4 C T 16: 12,962,360 (GRCm39) T668M probably benign Het
G530012D18Rik CAGAGAGA CAGAGAGAGA 1: 85,504,945 (GRCm39) probably null Het
H1f4 T A 13: 23,806,240 (GRCm39) K81* probably null Het
Havcr1 G T 11: 46,643,407 (GRCm39) R109L probably damaging Het
Krtap4-9 A G 11: 99,676,444 (GRCm39) probably benign Het
Layn T C 9: 50,970,856 (GRCm39) E229G probably benign Het
Lpcat3 T A 6: 124,676,955 (GRCm39) probably null Het
Lrrn1 T A 6: 107,546,169 (GRCm39) F656I possibly damaging Het
Lypd1 A G 1: 125,838,121 (GRCm39) probably benign Het
Or4k41 T A 2: 111,279,602 (GRCm39) V39E possibly damaging Het
Or5v1b T A 17: 37,841,246 (GRCm39) I126N probably damaging Het
Or6c207 T C 10: 129,104,934 (GRCm39) D86G probably damaging Het
Ptprt A T 2: 161,653,950 (GRCm39) L560Q probably damaging Het
Rbm11 T C 16: 75,393,469 (GRCm39) V55A probably damaging Het
Scn11a C T 9: 119,632,569 (GRCm39) V434I probably benign Het
Serpinc1 A G 1: 160,829,935 (GRCm39) T434A probably benign Het
Setd2 T C 9: 110,402,753 (GRCm39) I1798T probably damaging Het
Sfswap A G 5: 129,590,298 (GRCm39) Y265C probably damaging Het
Slc9a8 C A 2: 167,266,050 (GRCm39) T9K probably benign Het
Synpo T C 18: 60,736,062 (GRCm39) D389G probably damaging Het
Vmn1r181 C T 7: 23,683,909 (GRCm39) L125F possibly damaging Het
Wdfy4 A C 14: 32,745,331 (GRCm39) H2296Q probably benign Het
Other mutations in Gm10985
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02805:Gm10985 APN 3 53,752,514 (GRCm39) critical splice donor site probably null
R0027:Gm10985 UTSW 3 53,752,677 (GRCm39) frame shift probably null
R0184:Gm10985 UTSW 3 53,752,679 (GRCm39) missense probably damaging 0.99
R1027:Gm10985 UTSW 3 53,752,674 (GRCm39) missense probably damaging 0.99
R1216:Gm10985 UTSW 3 53,752,674 (GRCm39) missense probably damaging 0.99
R2126:Gm10985 UTSW 3 53,752,670 (GRCm39) frame shift probably null
R3870:Gm10985 UTSW 3 53,752,626 (GRCm39) frame shift probably null
R5567:Gm10985 UTSW 3 53,752,683 (GRCm39) missense probably damaging 0.99
R5585:Gm10985 UTSW 3 53,752,674 (GRCm39) missense probably damaging 0.99
R6782:Gm10985 UTSW 3 53,752,626 (GRCm39) frame shift probably null
R6818:Gm10985 UTSW 3 53,752,674 (GRCm39) missense probably damaging 0.99
R8398:Gm10985 UTSW 3 53,752,674 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- GCTGGCTGAAAGAACATCTG -3'
(R):5'- ATGGGTAGTTACAGTGTTAGCAAC -3'

Sequencing Primer
(F):5'- GAGGTAGTATGTCACGTTAGCCATC -3'
(R):5'- CACTCTTGCAATTTAATGAGAAAAGG -3'
Posted On 2015-03-18