Incidental Mutation 'R5823:Gm38119'
ID 450019
Institutional Source Beutler Lab
Gene Symbol Gm38119
Ensembl Gene ENSMUSG00000103084
Gene Name predicted gene, 38119
Synonyms
MMRRC Submission 043215-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.141) question?
Stock # R5823 (G1)
Quality Score 225
Status Not validated
Chromosome 3
Chromosomal Location 92644958-92646403 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 92645380 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Glutamine at position 71 (H71Q)
Ref Sequence ENSEMBL: ENSMUSP00000141812 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000192027]
AlphaFold A0A0A6YX29
Predicted Effect unknown
Transcript: ENSMUST00000192027
AA Change: H71Q
SMART Domains Protein: ENSMUSP00000141812
Gene: ENSMUSG00000103084
AA Change: H71Q

DomainStartEndE-ValueType
Pfam:LCE 43 113 1.6e-6 PFAM
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.5%
  • 10x: 97.7%
  • 20x: 92.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930505A04Rik C T 11: 30,376,349 (GRCm39) V173M probably damaging Het
Acsl3 G T 1: 78,666,003 (GRCm39) R143L probably benign Het
Ankrd11 A T 8: 123,622,529 (GRCm39) I420K probably benign Het
Aoc1l2 T A 6: 48,907,486 (GRCm39) I162N probably damaging Het
Cwh43 A G 5: 73,569,213 (GRCm39) E85G probably benign Het
Dnah1 G T 14: 30,988,375 (GRCm39) F3442L possibly damaging Het
Dock6 T A 9: 21,716,124 (GRCm39) N1737I probably damaging Het
Fcf1 A G 12: 85,020,921 (GRCm39) Y55C possibly damaging Het
Fer1l6 T A 15: 58,462,352 (GRCm39) Y802* probably null Het
Fgf9 T G 14: 58,320,759 (GRCm39) S10A probably damaging Het
Fhad1 A G 4: 141,682,617 (GRCm39) I508T possibly damaging Het
Flnc T C 6: 29,461,201 (GRCm39) V2692A probably damaging Het
Hcn1 A T 13: 117,739,388 (GRCm39) H50L unknown Het
Helz2 T C 2: 180,878,189 (GRCm39) T870A possibly damaging Het
Iqcf4 T C 9: 106,445,800 (GRCm39) I116V probably benign Het
Lama5 T A 2: 179,834,285 (GRCm39) I1383F probably benign Het
Lmo2 C T 2: 103,811,417 (GRCm39) T150I probably damaging Het
Mgat4f T A 1: 134,318,655 (GRCm39) W476R probably damaging Het
Myh13 A G 11: 67,251,294 (GRCm39) E1391G probably damaging Het
Mylk T A 16: 34,715,317 (GRCm39) probably null Het
Nat10 A T 2: 103,560,612 (GRCm39) V731D probably damaging Het
Ncapd2 A G 6: 125,145,663 (GRCm39) V1328A probably benign Het
Nfu1 C A 6: 87,002,541 (GRCm39) Q207K probably damaging Het
Nipsnap2 T A 5: 129,816,833 (GRCm39) probably null Het
Npc1 T C 18: 12,324,846 (GRCm39) K1216E possibly damaging Het
Or2r3 C A 6: 42,448,906 (GRCm39) V69L probably benign Het
Phf3 T C 1: 30,843,764 (GRCm39) I1732V probably damaging Het
Rasgrp4 G T 7: 28,837,142 (GRCm39) R67L probably benign Het
Rubcn T C 16: 32,670,091 (GRCm39) D88G probably damaging Het
Slc30a2 T C 4: 134,073,289 (GRCm39) I112T probably damaging Het
Slc35d2 A G 13: 64,268,419 (GRCm39) I78T probably damaging Het
Slc9a4 T A 1: 40,658,277 (GRCm39) M600K probably damaging Het
Slfn8 A G 11: 82,907,562 (GRCm39) I327T probably benign Het
Tas2r118 A G 6: 23,969,470 (GRCm39) I197T probably benign Het
Tex15 A G 8: 34,060,962 (GRCm39) I405V possibly damaging Het
Thsd7b T C 1: 129,605,821 (GRCm39) S521P probably benign Het
Trim36 A G 18: 46,302,407 (GRCm39) L535P probably damaging Het
Trim63 A T 4: 134,043,842 (GRCm39) I102F probably damaging Het
Wdr47 G A 3: 108,550,401 (GRCm39) V809M probably damaging Het
Other mutations in Gm38119
AlleleSourceChrCoordTypePredicted EffectPPH Score
R6892:Gm38119 UTSW 3 92,645,529 (GRCm39) missense unknown
R7721:Gm38119 UTSW 3 92,645,337 (GRCm39) missense unknown
R7747:Gm38119 UTSW 3 92,645,328 (GRCm39) missense unknown
R8710:Gm38119 UTSW 3 92,645,197 (GRCm39) small deletion probably benign
R8788:Gm38119 UTSW 3 92,645,537 (GRCm39) missense unknown
R9131:Gm38119 UTSW 3 92,645,403 (GRCm39) nonsense probably null
RF050:Gm38119 UTSW 3 92,645,196 (GRCm39) missense not run
Predicted Primers PCR Primer
(F):5'- GTCTGAAGTCTTCCTCACCCAG -3'
(R):5'- TCAAAGTGCCCTCCAAATGC -3'

Sequencing Primer
(F):5'- GTCTTCCTCACCCAGGTCAACAG -3'
(R):5'- TGCCCACCCAAATGTCCTATC -3'
Posted On 2016-12-20