Incidental Mutation 'R4465:Gm11541'
ID 330309
Institutional Source Beutler Lab
Gene Symbol Gm11541
Ensembl Gene ENSMUSG00000056008
Gene Name predicted gene 11541
Synonyms
MMRRC Submission 041580-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.133) question?
Stock # R4465 (G1)
Quality Score 225
Status Not validated
Chromosome 11
Chromosomal Location 94585324-94595325 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 94595048 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Serine at position 7 (C7S)
Ref Sequence ENSEMBL: ENSMUSP00000066721 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000069852]
AlphaFold Q8C4D8
Predicted Effect unknown
Transcript: ENSMUST00000069852
AA Change: C7S
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
0610040J01Rik G T 5: 64,056,182 (GRCm39) probably benign Het
Acsbg2 A G 17: 57,168,580 (GRCm39) Y180H probably damaging Het
Adgrb3 G T 1: 25,133,447 (GRCm39) T1213K probably damaging Het
Atrn A G 2: 130,802,388 (GRCm39) T510A probably benign Het
Clasp1 C A 1: 118,488,808 (GRCm39) T857N probably damaging Het
Cldn8 A C 16: 88,359,619 (GRCm39) M102R probably damaging Het
Col12a1 C A 9: 79,580,192 (GRCm39) V1562F possibly damaging Het
Cyp4f40 T A 17: 32,890,186 (GRCm39) D285E probably benign Het
Dis3 G A 14: 99,321,550 (GRCm39) S599L possibly damaging Het
Dnah11 T C 12: 117,951,186 (GRCm39) T3041A probably benign Het
Erbin T C 13: 103,981,393 (GRCm39) N511D probably benign Het
F11 T A 8: 45,694,511 (GRCm39) I617F probably damaging Het
Klk12 A T 7: 43,422,807 (GRCm39) R245W probably damaging Het
Lao1 C A 4: 118,822,504 (GRCm39) S141R probably benign Het
Lrrk2 A G 15: 91,632,023 (GRCm39) K1316E probably damaging Het
Map3k6 A G 4: 132,973,644 (GRCm39) Y445C possibly damaging Het
Mup6 T C 4: 60,004,000 (GRCm39) I31T probably damaging Het
Ndnf T A 6: 65,681,180 (GRCm39) D486E probably benign Het
Or2a54 T C 6: 43,092,852 (GRCm39) Y59H probably damaging Het
Or8h7 A T 2: 86,721,494 (GRCm39) N8K probably benign Het
Or8k37 A T 2: 86,469,478 (GRCm39) N191K probably benign Het
Rab19 T C 6: 39,365,060 (GRCm39) S107P probably damaging Het
Slc22a29 A T 19: 8,140,088 (GRCm39) L439* probably null Het
Slc5a1 A G 5: 33,303,860 (GRCm39) E225G possibly damaging Het
Slx4 A G 16: 3,806,919 (GRCm39) V508A possibly damaging Het
Snx25 A G 8: 46,521,266 (GRCm39) S373P possibly damaging Het
Stag2 A G X: 41,322,749 (GRCm39) S400G probably benign Homo
Tas2r107 A G 6: 131,636,972 (GRCm39) Y26H probably benign Het
Tmem181a T A 17: 6,346,061 (GRCm39) L185H probably damaging Het
Zdhhc22 G A 12: 87,034,997 (GRCm39) L152F probably benign Het
Zfpm2 T G 15: 40,959,557 (GRCm39) M80R probably benign Het
Other mutations in Gm11541
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01451:Gm11541 APN 11 94,586,495 (GRCm39) missense unknown
IGL01689:Gm11541 APN 11 94,595,020 (GRCm39) missense unknown
R2698:Gm11541 UTSW 11 94,586,441 (GRCm39) nonsense probably null
R5526:Gm11541 UTSW 11 94,594,944 (GRCm39) missense unknown
X0018:Gm11541 UTSW 11 94,586,451 (GRCm39) missense unknown
Predicted Primers PCR Primer
(F):5'- AGGTAGAGCTCCCTTCTCTC -3'
(R):5'- AGATGCCCCACGACTTTCAG -3'

Sequencing Primer
(F):5'- TAGGCCTGGAAACTTCTAGCC -3'
(R):5'- ACGACTTTCAGGACTTTGGTAC -3'
Posted On 2015-07-21