Incidental Mutation 'R5311:Gm14403'
ID 404836
Institutional Source Beutler Lab
Gene Symbol Gm14403
Ensembl Gene ENSMUSG00000094786
Gene Name predicted gene 14403
Synonyms
MMRRC Submission 042894-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.145) question?
Stock # R5311 (G1)
Quality Score 150
Status Not validated
Chromosome 2
Chromosomal Location 177190008-177201556 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) AAACCCTA to AA at 177201448 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000104575 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000108940] [ENSMUST00000108947]
AlphaFold A2BFU4
Predicted Effect probably benign
Transcript: ENSMUST00000108940
SMART Domains Protein: ENSMUSP00000104568
Gene: ENSMUSG00000094786

DomainStartEndE-ValueType
internal_repeat_1 1 73 1.34e-11 PROSPERO
internal_repeat_1 169 241 1.34e-11 PROSPERO
Predicted Effect probably benign
Transcript: ENSMUST00000108947
SMART Domains Protein: ENSMUSP00000104575
Gene: ENSMUSG00000094786

DomainStartEndE-ValueType
KRAB 4 66 4.86e-13 SMART
ZnF_C2H2 76 97 2.31e2 SMART
ZnF_C2H2 103 125 1.2e-3 SMART
ZnF_C2H2 131 153 1.18e-2 SMART
ZnF_C2H2 159 179 4.57e0 SMART
ZnF_C2H2 187 209 5.59e-4 SMART
ZnF_C2H2 215 237 1.12e-3 SMART
ZnF_C2H2 243 265 1.18e-2 SMART
ZnF_C2H2 271 293 8.6e-5 SMART
ZnF_C2H2 299 321 3.16e-3 SMART
ZnF_C2H2 327 349 1.84e-4 SMART
ZnF_C2H2 355 377 3.44e-4 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000142549
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.3%
  • 20x: 95.2%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ap5z1 A G 5: 142,453,442 (GRCm39) K137E possibly damaging Het
Atm A C 9: 53,429,923 (GRCm39) V371G probably benign Het
Cacna2d3 A G 14: 29,068,987 (GRCm39) Y247H probably damaging Het
Ccdc180 T C 4: 45,917,556 (GRCm39) V927A probably damaging Het
Cdc45 C T 16: 18,614,647 (GRCm39) R205H probably damaging Het
Edar G A 10: 58,443,257 (GRCm39) P290S possibly damaging Het
Ext2 T C 2: 93,526,606 (GRCm39) I677V probably benign Het
Fam53a A G 5: 33,765,080 (GRCm39) S209P probably damaging Het
Fshr A T 17: 89,318,441 (GRCm39) probably null Het
Gfm2 G A 13: 97,299,659 (GRCm39) A406T probably damaging Het
Gm14295 A T 2: 176,502,465 (GRCm39) I652L probably benign Het
Gm5431 T A 11: 48,779,716 (GRCm39) E402V probably damaging Het
Gm6899 GGAGGCCGCCCAGTGGCAGAGGCCGCCCAGTGGCAGAGGC GGAGGCCGCCCAGTGGCAGAGGC 11: 26,543,725 (GRCm39) probably null Het
Itih2 T C 2: 10,115,346 (GRCm39) D342G probably benign Het
Lgi2 A T 5: 52,711,827 (GRCm39) D164E probably damaging Het
Lrriq1 A G 10: 103,050,448 (GRCm39) I768T probably damaging Het
Map1a C A 2: 121,132,868 (GRCm39) A990E probably damaging Het
Mdh1b A G 1: 63,759,163 (GRCm39) V143A probably benign Het
Mrgprb3 C T 7: 48,293,059 (GRCm39) C164Y probably damaging Het
Mtpap T A 18: 4,386,328 (GRCm39) V316E probably damaging Het
Mybpc3 T A 2: 90,959,023 (GRCm39) C655* probably null Het
Myh15 A G 16: 48,986,204 (GRCm39) E1558G possibly damaging Het
Mylk A G 16: 34,742,127 (GRCm39) T880A probably benign Het
Nckap1 T A 2: 80,370,466 (GRCm39) D408V probably damaging Het
Nos3 A T 5: 24,582,343 (GRCm39) H605L probably benign Het
Nrxn2 C A 19: 6,581,428 (GRCm39) D411E probably benign Het
Or1af1 T C 2: 37,109,633 (GRCm39) V44A probably benign Het
Or8j3b T A 2: 86,205,094 (GRCm39) I221L possibly damaging Het
Pde4d C A 13: 109,769,398 (GRCm39) P29T probably benign Het
Pde4d C T 13: 109,769,399 (GRCm39) P29L probably benign Het
Pkhd1 A G 1: 20,636,094 (GRCm39) V412A possibly damaging Het
Rev1 T A 1: 38,118,474 (GRCm39) I480L probably benign Het
Rimbp3 A G 16: 17,028,708 (GRCm39) T711A probably benign Het
RP23-191E1.1 T A 3: 106,204,784 (GRCm39) noncoding transcript Het
Serpina11 A T 12: 103,952,221 (GRCm39) I183N probably damaging Het
Siglec1 T C 2: 130,921,236 (GRCm39) H645R probably damaging Het
Skint7 G A 4: 111,837,501 (GRCm39) R93H probably damaging Het
Slfn8 T C 11: 82,894,910 (GRCm39) E632G probably damaging Het
Tmem8b G A 4: 43,673,992 (GRCm39) V208I probably benign Het
Trps1 G A 15: 50,528,156 (GRCm39) T658I probably damaging Het
Ubash3a A G 17: 31,438,691 (GRCm39) T287A probably damaging Het
Ugt2b35 G A 5: 87,159,139 (GRCm39) W444* probably null Het
Vmn1r219 T A 13: 23,347,063 (GRCm39) V84D probably damaging Het
Vmn2r10 T C 5: 109,154,121 (GRCm39) Y61C probably damaging Het
Vmn2r104 G A 17: 20,250,163 (GRCm39) P703S probably damaging Het
Wdsub1 T A 2: 59,708,873 (GRCm39) probably benign Het
Zfp667 A G 7: 6,308,715 (GRCm39) Q461R probably benign Het
Zfp941 C A 7: 140,391,872 (GRCm39) G496* probably null Het
Other mutations in Gm14403
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01835:Gm14403 APN 2 177,199,049 (GRCm39) missense probably damaging 0.99
IGL02660:Gm14403 APN 2 177,201,257 (GRCm39) missense probably damaging 1.00
R0492:Gm14403 UTSW 2 177,200,359 (GRCm39) missense probably benign 0.09
R0932:Gm14403 UTSW 2 177,198,810 (GRCm39) missense probably benign 0.01
R0975:Gm14403 UTSW 2 177,201,217 (GRCm39) missense probably damaging 1.00
R1468:Gm14403 UTSW 2 177,199,024 (GRCm39) splice site probably benign
R1853:Gm14403 UTSW 2 177,200,932 (GRCm39) missense probably damaging 1.00
R3011:Gm14403 UTSW 2 177,200,786 (GRCm39) missense probably benign
R3803:Gm14403 UTSW 2 177,200,569 (GRCm39) missense probably benign 0.04
R4589:Gm14403 UTSW 2 177,200,428 (GRCm39) missense probably benign 0.29
R4805:Gm14403 UTSW 2 177,200,492 (GRCm39) missense probably damaging 0.97
R5085:Gm14403 UTSW 2 177,200,282 (GRCm39) missense probably benign 0.04
R5425:Gm14403 UTSW 2 177,201,448 (GRCm39) unclassified probably benign
R5643:Gm14403 UTSW 2 177,199,054 (GRCm39) missense possibly damaging 0.87
R5644:Gm14403 UTSW 2 177,199,054 (GRCm39) missense possibly damaging 0.87
R5739:Gm14403 UTSW 2 177,201,040 (GRCm39) missense probably damaging 1.00
R5982:Gm14403 UTSW 2 177,200,345 (GRCm39) missense probably damaging 0.98
R6197:Gm14403 UTSW 2 177,201,448 (GRCm39) unclassified probably benign
R6198:Gm14403 UTSW 2 177,201,448 (GRCm39) unclassified probably benign
R6892:Gm14403 UTSW 2 177,201,040 (GRCm39) missense probably damaging 1.00
R7090:Gm14403 UTSW 2 177,201,114 (GRCm39) missense possibly damaging 0.87
R7168:Gm14403 UTSW 2 177,201,318 (GRCm39) missense probably damaging 0.96
R7510:Gm14403 UTSW 2 177,200,403 (GRCm39) missense probably benign 0.01
R7623:Gm14403 UTSW 2 177,200,405 (GRCm39) missense probably benign
R8049:Gm14403 UTSW 2 177,200,311 (GRCm39) missense probably benign 0.00
R8557:Gm14403 UTSW 2 177,201,354 (GRCm39) missense probably damaging 0.99
R9224:Gm14403 UTSW 2 177,200,336 (GRCm39) missense probably benign
R9333:Gm14403 UTSW 2 177,200,919 (GRCm39) missense probably benign 0.42
R9632:Gm14403 UTSW 2 177,201,421 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TGGTAAAGCCTTTGCACAAAG -3'
(R):5'- ATTTAGAGGCCAATGCTTTGTG -3'

Sequencing Primer
(F):5'- GCAGTCATCTCCGAAAACATAACTG -3'
(R):5'- CCAATGCTTTGTGAAAAAGGTG -3'
Posted On 2016-07-22