Incidental Mutation 'R6791:Gm4302'
ID 532597
Institutional Source Beutler Lab
Gene Symbol Gm4302
Ensembl Gene ENSMUSG00000091101
Gene Name predicted gene 4302
Synonyms
MMRRC Submission 044904-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.504) question?
Stock # R6791 (G1)
Quality Score 132.467
Status Not validated
Chromosome 10
Chromosomal Location 100176698-100177624 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) TGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA to TGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA at 100177361 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000151319 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168769] [ENSMUST00000186197] [ENSMUST00000218922]
AlphaFold E9PX25
Predicted Effect probably benign
Transcript: ENSMUST00000168769
SMART Domains Protein: ENSMUSP00000131605
Gene: ENSMUSG00000091101

DomainStartEndE-ValueType
RRM 87 159 8.99e-17 SMART
coiled coil region 209 286 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000186197
SMART Domains Protein: ENSMUSP00000140999
Gene: ENSMUSG00000094314

DomainStartEndE-ValueType
RRM 84 156 3.8e-19 SMART
coiled coil region 206 286 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000218922
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.7%
  • 20x: 96.7%
Validation Efficiency 100% (52/52)
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca13 T A 11: 9,328,504 (GRCm39) C3526S probably damaging Het
Adgrf2 T C 17: 43,021,774 (GRCm39) N350S probably benign Het
Atp12a G A 14: 56,624,439 (GRCm39) probably null Het
AW551984 T G 9: 39,511,955 (GRCm39) S19R probably damaging Het
Bet1l A G 7: 140,434,418 (GRCm39) I77T possibly damaging Het
Cfap206 T C 4: 34,711,414 (GRCm39) I494M possibly damaging Het
Cog3 A G 14: 75,968,118 (GRCm39) I415T probably damaging Het
Col15a1 C T 4: 47,300,518 (GRCm39) P1060S probably damaging Het
Ctrb1 A G 8: 112,415,981 (GRCm39) V71A possibly damaging Het
Ddhd2 T C 8: 26,242,242 (GRCm39) Y211C probably benign Het
Fbxl20 T C 11: 98,000,336 (GRCm39) T128A probably benign Het
Fdps A G 3: 89,002,659 (GRCm39) probably null Het
Gm8369 T A 19: 11,489,200 (GRCm39) probably benign Het
Grm6 T C 11: 50,750,601 (GRCm39) V588A possibly damaging Het
Heatr6 T C 11: 83,649,167 (GRCm39) L174S probably benign Het
Kif1a G A 1: 92,993,859 (GRCm39) P364S probably damaging Het
Klk7 A G 7: 43,462,684 (GRCm39) D163G probably benign Het
Kmt2e TGCCGCCGCCGCCGCCACCGCCGCCGCCGC TGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGC 5: 23,704,474 (GRCm39) probably benign Het
Lamb3 T C 1: 193,017,169 (GRCm39) S787P possibly damaging Het
Lrp5 C T 19: 3,650,753 (GRCm39) C1227Y probably damaging Het
Mgst1 G A 6: 138,118,805 (GRCm39) probably benign Het
Mllt6 T C 11: 97,571,428 (GRCm39) S1022P probably damaging Het
Mtmr2 T C 9: 13,716,678 (GRCm39) I521T probably benign Het
Naalad2 T C 9: 18,296,426 (GRCm39) T75A possibly damaging Het
Nadsyn1 A T 7: 143,372,845 (GRCm39) I83N probably damaging Het
Naip2 T C 13: 100,291,468 (GRCm39) S1157G probably benign Het
Neurl4 T A 11: 69,799,336 (GRCm39) L904Q probably damaging Het
Ngp A C 9: 110,249,017 (GRCm39) I30L probably benign Het
Or5af1 T C 11: 58,722,903 (GRCm39) Y308H probably benign Het
Or6c5c G A 10: 129,299,023 (GRCm39) M159I probably benign Het
Orm2 A T 4: 63,282,196 (GRCm39) M125L probably benign Het
Pax2 A T 19: 44,777,260 (GRCm39) D151V possibly damaging Het
Polg A G 7: 79,109,857 (GRCm39) V382A probably benign Het
Ppargc1b C A 18: 61,440,747 (GRCm39) G724W probably damaging Het
Pramel11 T A 4: 143,622,252 (GRCm39) I368F probably benign Het
Prss16 A T 13: 22,190,237 (GRCm39) V307E probably damaging Het
Prss54 T G 8: 96,291,283 (GRCm39) probably null Het
Rspo1 A G 4: 124,900,976 (GRCm39) H108R probably benign Het
Sh3bp5l C A 11: 58,237,098 (GRCm39) H352N probably damaging Het
Skor1 T C 9: 63,047,636 (GRCm39) probably null Het
Smad6 A G 9: 63,919,509 (GRCm39) Y289H probably benign Het
Spart G A 3: 55,034,982 (GRCm39) G456D probably damaging Het
Spg11 T C 2: 121,923,924 (GRCm39) E799G probably damaging Het
Tbc1d4 T G 14: 101,845,695 (GRCm39) K68Q probably damaging Het
Treml2 A G 17: 48,616,247 (GRCm39) M296V probably benign Het
Ugt2b1 C A 5: 87,067,116 (GRCm39) D436Y probably damaging Het
Usp9y A T Y: 1,325,042 (GRCm39) probably null Homo
Vmn2r6 T C 3: 64,445,580 (GRCm39) Y626C probably damaging Het
Xpc G A 6: 91,483,839 (GRCm39) A169V probably benign Het
Zfp131 A G 13: 120,228,129 (GRCm39) V506A probably damaging Het
Zfp74 A G 7: 29,633,860 (GRCm39) I616T probably benign Het
Other mutations in Gm4302
AlleleSourceChrCoordTypePredicted EffectPPH Score
LCD18:Gm4302 UTSW 10 100,177,306 (GRCm39) missense probably benign 0.20
R6375:Gm4302 UTSW 10 100,177,258 (GRCm39) missense probably benign 0.03
R6878:Gm4302 UTSW 10 100,177,377 (GRCm39) unclassified probably benign
R6878:Gm4302 UTSW 10 100,177,369 (GRCm39) unclassified probably benign
R6878:Gm4302 UTSW 10 100,177,361 (GRCm39) unclassified probably benign
R7072:Gm4302 UTSW 10 100,177,521 (GRCm39) missense unknown
R7135:Gm4302 UTSW 10 100,177,589 (GRCm39) missense unknown
R7490:Gm4302 UTSW 10 100,177,445 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- GCCCTATGAACATCCACCTTG -3'
(R):5'- TAATAATCCAGCTGGGCGTC -3'

Sequencing Primer
(F):5'- CACCTTGTCACTTCACAGATTGATAG -3'
(R):5'- ACAGATAGCTGCTGCAGTTC -3'
Posted On 2018-08-29