Incidental Mutation 'R6591:Gm11099'
ID 524547
Institutional Source Beutler Lab
Gene Symbol Gm11099
Ensembl Gene ENSMUSG00000079353
Gene Name predicted gene 11099
Synonyms
MMRRC Submission 044715-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.171) question?
Stock # R6591 (G1)
Quality Score 225.009
Status Validated
Chromosome 2
Chromosomal Location 58749446-58797630 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) A to T at 58749485 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000153944 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000077687] [ENSMUST00000112589] [ENSMUST00000226455]
AlphaFold F7CV60
Predicted Effect probably benign
Transcript: ENSMUST00000077687
SMART Domains Protein: ENSMUSP00000076871
Gene: ENSMUSG00000036641

DomainStartEndE-ValueType
coiled coil region 173 195 N/A INTRINSIC
coiled coil region 289 353 N/A INTRINSIC
low complexity region 369 382 N/A INTRINSIC
coiled coil region 401 438 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000112589
Predicted Effect noncoding transcript
Transcript: ENSMUST00000134708
Predicted Effect probably benign
Transcript: ENSMUST00000226455
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.1%
  • 20x: 94.2%
Validation Efficiency 100% (34/34)
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2300009A05Rik A G 9: 63,306,236 (GRCm39) Y90H probably damaging Het
Agk A G 6: 40,369,624 (GRCm39) D337G probably benign Het
Amn A G 12: 111,241,831 (GRCm39) H299R possibly damaging Het
Angptl4 A G 17: 33,999,755 (GRCm39) probably null Het
AU040320 G A 4: 126,730,463 (GRCm39) M563I possibly damaging Het
Cachd1 T C 4: 100,846,683 (GRCm39) M1042T probably benign Het
Cd209c T A 8: 3,995,680 (GRCm39) I41L probably benign Het
Ceacam12 T A 7: 17,803,149 (GRCm39) V185D possibly damaging Het
Chpt1 A T 10: 88,321,762 (GRCm39) probably benign Het
Clca3a1 G C 3: 144,719,644 (GRCm39) A442G probably damaging Het
Cldn8 T C 16: 88,359,423 (GRCm39) I167M possibly damaging Het
Cln3 A G 7: 126,178,606 (GRCm39) V143A possibly damaging Het
Dusp11 T C 6: 85,938,507 (GRCm39) H4R possibly damaging Het
Ephb3 T A 16: 21,033,223 (GRCm39) F69Y probably damaging Het
Grik2 A T 10: 49,149,021 (GRCm39) Y521* probably null Het
Igf2r A G 17: 12,907,895 (GRCm39) L2143P probably damaging Het
Kcnk1 T C 8: 126,751,970 (GRCm39) V192A probably benign Het
Or4a81 A T 2: 89,619,332 (GRCm39) Y121* probably null Het
Or8k53 A C 2: 86,177,763 (GRCm39) S116A probably damaging Het
Parp3 A G 9: 106,350,891 (GRCm39) S329P probably benign Het
Pld3 A T 7: 27,231,741 (GRCm39) N483K probably benign Het
Rbm33 A T 5: 28,557,544 (GRCm39) E252D probably damaging Het
Ryr2 T C 13: 11,609,609 (GRCm39) T4406A probably benign Het
Sgsm3 A G 15: 80,893,063 (GRCm39) D380G possibly damaging Het
Sorl1 G T 9: 41,913,863 (GRCm39) D1355E probably damaging Het
Sptbn1 A G 11: 30,063,984 (GRCm39) S1945P probably damaging Het
Ube2m A T 7: 12,770,396 (GRCm39) F70I probably damaging Het
Ube3b A G 5: 114,546,185 (GRCm39) I664V probably benign Het
Ugt1a7c A G 1: 88,023,378 (GRCm39) E179G possibly damaging Het
Vps50 T C 6: 3,504,939 (GRCm39) probably null Het
Xpo1 T C 11: 23,236,875 (GRCm39) L718P probably damaging Het
Zfp354c A G 11: 50,705,602 (GRCm39) I491T probably benign Het
Other mutations in Gm11099
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1476:Gm11099 UTSW 2 58,749,482 (GRCm39) intron probably benign
R6691:Gm11099 UTSW 2 58,749,485 (GRCm39) intron probably benign
Predicted Primers PCR Primer
(F):5'- CAGCCCTACAGAAGGTGCT -3'
(R):5'- GTGTTTGGTGACTACATGTAAGTAT -3'

Sequencing Primer
(F):5'- CAGCCCTACAGAAGGTGCTAAAAG -3'
(R):5'- CATGTAAGTATTGCAATATGGTCGTG -3'
Posted On 2018-06-22