Incidental Mutation 'R0028:AC159748.1'
ID 15560
Institutional Source Beutler Lab
Gene Symbol AC159748.1
Ensembl Gene
Gene Name
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # R0028 (G1)
Quality Score
Status Validated
Chromosome 10
Chromosomal Location
Type of Mutation synonymous
DNA Base Change (assembly) T to C at 5542006 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000150262 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000041639] [ENSMUST00000214945] [ENSMUST00000215295]
AlphaFold no structure available at present
Predicted Effect silent
Transcript: ENSMUST00000041639
SMART Domains Protein: ENSMUSP00000039440
Gene: ENSMUSG00000096054

DomainStartEndE-ValueType
CH 29 139 4.55e-14 SMART
low complexity region 145 167 N/A INTRINSIC
CH 187 285 9.67e-18 SMART
coiled coil region 425 452 N/A INTRINSIC
Blast:SPEC 493 599 2e-28 BLAST
Blast:SPEC 606 695 7e-40 BLAST
Blast:SPEC 701 815 1e-32 BLAST
Blast:SPEC 815 913 4e-41 BLAST
Blast:SPEC 920 1013 9e-53 BLAST
Blast:SPEC 1117 1219 2e-60 BLAST
coiled coil region 1267 1329 N/A INTRINSIC
low complexity region 1349 1368 N/A INTRINSIC
coiled coil region 1399 1427 N/A INTRINSIC
Predicted Effect silent
Transcript: ENSMUST00000214945
Predicted Effect silent
Transcript: ENSMUST00000215295
Coding Region Coverage
  • 1x: 80.7%
  • 3x: 72.7%
  • 10x: 50.3%
  • 20x: 30.1%
Validation Efficiency 96% (74/77)
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca3 T C 17: 24,596,698 (GRCm39) F384L probably benign Het
Adamts12 C T 15: 11,215,710 (GRCm39) R244C probably damaging Het
Bms1 T C 6: 118,393,480 (GRCm39) I131V probably benign Het
Ccdc107 A G 4: 43,495,549 (GRCm39) T151A probably benign Het
Col1a2 G A 6: 4,518,822 (GRCm39) probably benign Het
Col4a4 A G 1: 82,465,231 (GRCm39) probably null Het
Creb1 A G 1: 64,609,307 (GRCm39) D126G probably damaging Het
Ddb1 T A 19: 10,596,610 (GRCm39) V443E probably damaging Het
Dnmt3a T A 12: 3,950,337 (GRCm39) S634T probably damaging Het
Fras1 A C 5: 96,825,175 (GRCm39) N1455T probably benign Het
Fyb1 A G 15: 6,674,395 (GRCm39) probably benign Het
Gpr141 C T 13: 19,936,599 (GRCm39) V59M probably damaging Het
Ikbke T C 1: 131,199,921 (GRCm39) I222V possibly damaging Het
Macf1 A T 4: 123,275,895 (GRCm39) H6222Q probably damaging Het
Mapk8ip3 C T 17: 25,123,871 (GRCm39) probably benign Het
Phactr1 A T 13: 43,210,655 (GRCm39) D74V probably damaging Het
Prickle2 T C 6: 92,399,323 (GRCm39) I185V probably benign Het
Rnasel A T 1: 153,630,465 (GRCm39) D327V probably benign Het
Slc25a13 T C 6: 6,181,047 (GRCm39) N46D probably benign Het
Slc28a2 T A 2: 122,282,083 (GRCm39) F261L probably damaging Het
Slc6a15 A T 10: 103,252,541 (GRCm39) Y568F probably benign Het
Slc7a1 A G 5: 148,272,321 (GRCm39) V452A probably benign Het
Tectb T C 19: 55,183,109 (GRCm39) I330T probably benign Het
Tmem92 C T 11: 94,669,778 (GRCm39) V118I possibly damaging Het
Tmf1 T C 6: 97,135,059 (GRCm39) E985G probably damaging Het
Traf5 T A 1: 191,758,421 (GRCm39) probably benign Het
Trip11 T C 12: 101,851,016 (GRCm39) E731G probably damaging Het
Unc5a A G 13: 55,151,726 (GRCm39) S50G possibly damaging Het
Wrnip1 T C 13: 33,004,280 (GRCm39) L517P probably damaging Het
Zfp202 T A 9: 40,123,048 (GRCm39) H603Q probably damaging Het
Posted On 2012-12-21