Incidental Mutation 'IGL03101:AA474408'
ID 418743
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol AA474408
Ensembl Gene ENSMUSG00000073867
Gene Name expressed sequence AA474408
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL03101
Quality Score
Status
Chromosome 7
Chromosomal Location 109657194-109660532 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) A to T at 109660177 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000148235 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000084727] [ENSMUST00000084731] [ENSMUST00000169638] [ENSMUST00000208951] [ENSMUST00000209505] [ENSMUST00000211798]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000084727
SMART Domains Protein: ENSMUSP00000081778
Gene: ENSMUSG00000061079

DomainStartEndE-ValueType
ZnF_C2H2 236 260 5.5e-3 SMART
ZnF_C2H2 266 290 6.42e-4 SMART
ZnF_C2H2 296 320 4.01e-5 SMART
ZnF_C2H2 326 350 1.38e-3 SMART
ZnF_C2H2 356 380 3.95e-4 SMART
ZnF_C2H2 386 410 2.4e-3 SMART
ZnF_C2H2 416 439 1.79e-2 SMART
low complexity region 443 457 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000084731
SMART Domains Protein: ENSMUSP00000081782
Gene: ENSMUSG00000066232

DomainStartEndE-ValueType
IBN_N 22 101 3.06e-15 SMART
Pfam:Cse1 168 452 2.8e-12 PFAM
low complexity region 701 712 N/A INTRINSIC
low complexity region 881 900 N/A INTRINSIC
low complexity region 923 939 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000098110
SMART Domains Protein: ENSMUSP00000095714
Gene: ENSMUSG00000073867

DomainStartEndE-ValueType
SCOP:d1gosa1 29 85 4e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000169638
SMART Domains Protein: ENSMUSP00000126015
Gene: ENSMUSG00000061079

DomainStartEndE-ValueType
ZnF_C2H2 209 233 5.5e-3 SMART
ZnF_C2H2 239 263 6.42e-4 SMART
ZnF_C2H2 269 293 4.01e-5 SMART
ZnF_C2H2 299 323 1.38e-3 SMART
ZnF_C2H2 329 353 3.95e-4 SMART
ZnF_C2H2 359 383 2.4e-3 SMART
ZnF_C2H2 389 412 1.79e-2 SMART
low complexity region 416 430 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185931
Predicted Effect probably benign
Transcript: ENSMUST00000208951
Predicted Effect probably benign
Transcript: ENSMUST00000209505
Predicted Effect probably benign
Transcript: ENSMUST00000211798
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc1 T A 16: 14,207,732 (GRCm39) V23D probably damaging Het
Adam8 G T 7: 139,568,456 (GRCm39) N260K possibly damaging Het
Ap3b1 A T 13: 94,591,906 (GRCm39) I457L probably benign Het
Apaf1 T C 10: 90,867,421 (GRCm39) N808S possibly damaging Het
Arhgef26 A G 3: 62,327,082 (GRCm39) T532A possibly damaging Het
Cfap65 G T 1: 74,967,592 (GRCm39) T162N possibly damaging Het
Clec12b A G 6: 129,356,480 (GRCm39) probably null Het
Creb3 T C 4: 43,563,081 (GRCm39) V60A probably benign Het
Cyp11b1 A G 15: 74,707,703 (GRCm39) F469L probably benign Het
Defb28 A T 2: 152,362,047 (GRCm39) E69V possibly damaging Het
Etnppl T C 3: 130,415,967 (GRCm39) L118S probably damaging Het
Fsip1 T C 2: 118,072,144 (GRCm39) Y213C probably damaging Het
Glb1l2 A G 9: 26,676,421 (GRCm39) W480R probably damaging Het
Herc1 A T 9: 66,395,279 (GRCm39) M4205L probably benign Het
Kif5a A T 10: 127,071,478 (GRCm39) probably benign Het
Lmbrd2 C T 15: 9,186,695 (GRCm39) R557C probably damaging Het
Map4k3 A G 17: 80,963,284 (GRCm39) probably null Het
Npc1 A G 18: 12,331,596 (GRCm39) I858T probably benign Het
Or7e173 T C 9: 19,938,725 (GRCm39) T170A probably benign Het
Pecam1 A G 11: 106,588,177 (GRCm39) V92A probably damaging Het
Rbm43 A T 2: 51,816,757 (GRCm39) I70N probably benign Het
Rps6kb1 T C 11: 86,393,708 (GRCm39) Y474C probably benign Het
Slco2a1 G A 9: 102,954,205 (GRCm39) G459R possibly damaging Het
Snca T A 6: 60,804,595 (GRCm39) probably benign Het
Spata31f1e T C 4: 42,793,424 (GRCm39) D236G possibly damaging Het
Stap2 T A 17: 56,309,029 (GRCm39) I113F probably damaging Het
Tas2r140 T C 6: 40,468,764 (GRCm39) M198T probably benign Het
Trim9 T C 12: 70,393,428 (GRCm39) E172G probably damaging Het
Ttll7 T C 3: 146,602,445 (GRCm39) V81A possibly damaging Het
Vmn2r103 A G 17: 19,993,782 (GRCm39) Y53C probably damaging Het
Vmn2r22 C A 6: 123,614,295 (GRCm39) A432S probably benign Het
Zfp943 T C 17: 22,211,156 (GRCm39) S81P probably damaging Het
Other mutations in AA474408
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01356:AA474408 APN 7 109,660,189 (GRCm39) unclassified probably benign
Posted On 2016-08-02