Incidental Mutation 'R2382:Gm21286'
ID 247557
Institutional Source Beutler Lab
Gene Symbol Gm21286
Ensembl Gene ENSMUSG00000094948
Gene Name predicted gene, 21286
Synonyms
MMRRC Submission 040357-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.115) question?
Stock # R2382 (G1)
Quality Score 225
Status Not validated
Chromosome 4
Chromosomal Location 60792907-60795648 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to G at 60794283 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: ENSMUST00000098035
SMART Domains Protein: ENSMUSP00000137167
Gene: ENSMUSG00000094948

DomainStartEndE-ValueType
Pfam:Lipocalin 1 92 1.3e-15 PFAM
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 96.9%
  • 20x: 93.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik G T 12: 71,211,320 (GRCm39) E685* probably null Het
2700049A03Rik A T 12: 71,211,321 (GRCm39) E685V possibly damaging Het
Aarsd1 T A 11: 101,304,904 (GRCm39) I64F probably damaging Het
Agrn T A 4: 156,260,973 (GRCm39) D574V probably damaging Het
Atg4b T C 1: 93,712,564 (GRCm39) C16R probably damaging Het
Ccdc141 A T 2: 76,841,886 (GRCm39) L1515Q probably damaging Het
Ccdc141 A T 2: 76,905,342 (GRCm39) V368E probably benign Het
Clk1 A T 1: 58,460,448 (GRCm39) S61T probably benign Het
Dhx38 A T 8: 110,282,772 (GRCm39) D631E probably damaging Het
Dner C G 1: 84,348,544 (GRCm39) E719Q probably damaging Het
E030025P04Rik G A 11: 109,034,880 (GRCm39) Q3* probably null Het
Eif4g2 T A 7: 110,674,253 (GRCm39) T613S probably benign Het
Fn1 C G 1: 71,687,278 (GRCm39) G193A probably damaging Het
Ftdc1 T C 16: 58,436,239 (GRCm39) probably null Het
Gls2 A G 10: 128,039,711 (GRCm39) E286G probably damaging Het
Hoxa13 A T 6: 52,236,125 (GRCm39) V304D probably damaging Het
Hpse2 A T 19: 42,920,061 (GRCm39) M346K probably benign Het
Igkv1-99 A T 6: 68,519,481 (GRCm39) probably benign Het
Kcnq2 A G 2: 180,753,900 (GRCm39) Y237H probably damaging Het
Kmt2a T A 9: 44,732,207 (GRCm39) probably benign Het
Kntc1 A G 5: 123,898,411 (GRCm39) D180G probably damaging Het
Macf1 G A 4: 123,268,625 (GRCm39) T4682M probably damaging Het
Mfsd6 T A 1: 52,747,569 (GRCm39) H432L probably benign Het
Mgat5b T A 11: 116,810,322 (GRCm39) D7E probably damaging Het
Msh6 G A 17: 88,292,159 (GRCm39) V305I probably benign Het
Notch1 A T 2: 26,363,793 (GRCm39) H880Q probably benign Het
Or2g25 A C 17: 37,970,822 (GRCm39) V134G probably benign Het
Or7a37 G A 10: 78,805,990 (GRCm39) C169Y probably damaging Het
Or7a41 A T 10: 78,870,968 (GRCm39) I113F possibly damaging Het
Pmepa1 G A 2: 173,069,926 (GRCm39) R210W probably damaging Het
Pnliprp2 A G 19: 58,757,062 (GRCm39) N308S probably benign Het
Ppwd1 T C 13: 104,343,621 (GRCm39) T595A probably damaging Het
Prdm13 T C 4: 21,678,277 (GRCm39) T738A possibly damaging Het
Rab11fip3 T A 17: 26,209,841 (GRCm39) K1062* probably null Het
Reep3 A T 10: 66,932,569 (GRCm39) V11E possibly damaging Het
Slco1a8 G A 6: 141,936,206 (GRCm39) S293F probably benign Het
Slco3a1 T C 7: 73,996,524 (GRCm39) D294G probably benign Het
Sycp2 A G 2: 178,019,811 (GRCm39) probably null Het
Zfp292 A G 4: 34,806,426 (GRCm39) V2206A possibly damaging Het
Other mutations in Gm21286
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01396:Gm21286 APN 4 60,794,323 (GRCm39) splice site noncoding transcript
R1510:Gm21286 UTSW 4 60,794,931 (GRCm39) exon noncoding transcript
Predicted Primers PCR Primer
(F):5'- GGAAGTCCAGCATTGGTGAAAC -3'
(R):5'- AGATGGTGCTCATTTGACTAGTAGG -3'

Sequencing Primer
(F):5'- TCCAGCATTGGTGAAACTTAGAAG -3'
(R):5'- AGGTTCAAGTTCCTGAGTTCAGAC -3'
Posted On 2014-11-11