Incidental Mutation 'R0392:Gm11146'
ID 31772
Institutional Source Beutler Lab
Gene Symbol Gm11146
Ensembl Gene ENSMUSG00000079546
Gene Name predicted gene 11146
Synonyms
MMRRC Submission 038598-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.101) question?
Stock # R0392 (G1)
Quality Score 225
Status Validated
Chromosome 16
Chromosomal Location (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to A at 77394054 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000109869 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000114231]
AlphaFold F6WTR5
Predicted Effect noncoding transcript
Transcript: ENSMUST00000068704
SMART Domains Protein: ENSMUSP00000070456
Gene: ENSMUSG00000052450

DomainStartEndE-ValueType
low complexity region 23 42 N/A INTRINSIC
low complexity region 105 116 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000083596
Predicted Effect noncoding transcript
Transcript: ENSMUST00000083623
Predicted Effect probably benign
Transcript: ENSMUST00000114231
Predicted Effect noncoding transcript
Transcript: ENSMUST00000170849
SMART Domains Protein: ENSMUSP00000127794
Gene: ENSMUSG00000090386

DomainStartEndE-ValueType
transmembrane domain 20 42 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182398
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182601
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182656
Predicted Effect noncoding transcript
Transcript: ENSMUST00000194553
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182986
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182820
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183099
Predicted Effect noncoding transcript
Transcript: ENSMUST00000183327
Predicted Effect noncoding transcript
Transcript: ENSMUST00000231957
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.0%
  • 10x: 95.5%
  • 20x: 90.6%
Validation Efficiency 100% (31/31)
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930527J03Rik ACCC ACC 1: 178,276,503 (GRCm38) noncoding transcript Het
Bcan T A 3: 87,900,869 (GRCm39) K455* probably null Het
Casp12 T A 9: 5,348,973 (GRCm39) probably benign Het
Ccdc61 T C 7: 18,625,027 (GRCm39) M504V probably benign Het
Cd53 A T 3: 106,670,592 (GRCm39) V147E probably damaging Het
Cyp2b13 T C 7: 25,785,308 (GRCm39) Y226H probably benign Het
Cyp2j7 T C 4: 96,087,671 (GRCm39) D413G probably damaging Het
Dcbld1 T C 10: 52,193,230 (GRCm39) I254T possibly damaging Het
Ddx39a T G 8: 84,448,366 (GRCm39) M206R probably damaging Het
Dgki T A 6: 36,977,113 (GRCm39) T666S probably damaging Het
Dnaaf8 T C 16: 4,795,363 (GRCm39) noncoding transcript Het
Dnah7a C A 1: 53,543,357 (GRCm39) C2271F probably damaging Het
Emilin3 A G 2: 160,752,799 (GRCm39) probably benign Het
Epha4 T C 1: 77,483,610 (GRCm39) K133R probably benign Het
Ift88 A T 14: 57,733,617 (GRCm39) probably benign Het
Ighv10-3 A G 12: 114,487,460 (GRCm39) probably benign Het
Lamp5 T C 2: 135,902,817 (GRCm39) S179P probably damaging Het
Map4 T C 9: 109,907,113 (GRCm39) S788P probably damaging Het
Or5m13 T A 2: 85,749,106 (GRCm39) I279N possibly damaging Het
Otog T C 7: 45,899,499 (GRCm39) W267R probably benign Het
Pafah1b2 T C 9: 45,880,151 (GRCm39) I175M probably benign Het
Pcdhb12 A G 18: 37,570,011 (GRCm39) K386E possibly damaging Het
Pcnt T C 10: 76,220,660 (GRCm39) N2056S probably benign Het
Pold2 T C 11: 5,826,776 (GRCm39) I53V possibly damaging Het
Rsf1 T A 7: 97,328,212 (GRCm39) D1071E probably benign Het
Rtp3 A T 9: 110,818,621 (GRCm39) M20K probably damaging Het
S1pr5 T A 9: 21,156,277 (GRCm39) I50F probably damaging Het
Slc47a1 A G 11: 61,262,608 (GRCm39) S94P probably damaging Het
Slitrk5 G A 14: 111,916,465 (GRCm39) V30I probably benign Het
St8sia5 G A 18: 77,342,102 (GRCm39) V271M probably damaging Het
Sult2b1 G T 7: 45,383,062 (GRCm39) T240N probably damaging Het
Other mutations in Gm11146
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02119:Gm11146 APN 16 77,385,498 (GRCm39) splice site probably null
R1302:Gm11146 UTSW 16 77,398,970 (GRCm39) missense unknown
R2055:Gm11146 UTSW 16 77,391,969 (GRCm39) intron probably benign
R4843:Gm11146 UTSW 16 77,392,144 (GRCm39) intron probably benign
Predicted Primers PCR Primer
(F):5'- TCATCTCAGGTAAAACGAAAAGGCACAA -3'
(R):5'- GCCAGTAAGCACACATGAAGCCA -3'

Sequencing Primer
(F):5'- GTAAAACGAAAAGGCACAAATGTAG -3'
(R):5'- TGGCCTACACAAATTTTCACC -3'
Posted On 2013-04-24