Incidental Mutation 'IGL01593:Gm17541'
ID 91645
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm17541
Ensembl Gene ENSMUSG00000091732
Gene Name predicted gene, 17541
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL01593
Quality Score
Status
Chromosome 12
Chromosomal Location 4739405-4739917 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to A at 4739868 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000151896 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000062580] [ENSMUST00000219007] [ENSMUST00000220311]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000062580
SMART Domains Protein: ENSMUSP00000052758
Gene: ENSMUSG00000020640

DomainStartEndE-ValueType
EH 15 109 8.44e-41 SMART
EFh 58 86 7.18e-3 SMART
low complexity region 156 169 N/A INTRINSIC
low complexity region 215 231 N/A INTRINSIC
EH 238 333 4.06e-43 SMART
EFh 282 310 6.16e-2 SMART
coiled coil region 366 462 N/A INTRINSIC
coiled coil region 516 556 N/A INTRINSIC
coiled coil region 580 715 N/A INTRINSIC
SH3 721 778 2.65e-21 SMART
low complexity region 791 811 N/A INTRINSIC
SH3 855 909 8.83e-18 SMART
SH3 945 999 9.1e-20 SMART
SH3 1017 1077 1.55e-13 SMART
SH3 1091 1146 7.22e-23 SMART
RhoGEF 1174 1355 1.93e-56 SMART
PH 1396 1507 1.16e-9 SMART
C2 1531 1628 3.96e-19 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000080062
SMART Domains Protein: ENSMUSP00000129198
Gene: ENSMUSG00000091732

DomainStartEndE-ValueType
Pfam:Ribosomal_L18ae 4 127 2.1e-53 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000219007
Predicted Effect noncoding transcript
Transcript: ENSMUST00000219832
Predicted Effect probably benign
Transcript: ENSMUST00000220311
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc12 A T 8: 87,284,279 (GRCm39) I310N probably damaging Het
Abtb3 T A 10: 85,490,339 (GRCm39) probably benign Het
Ackr4 C T 9: 103,963,130 (GRCm39) probably benign Het
Ankib1 A T 5: 3,782,590 (GRCm39) D346E probably benign Het
Asap2 G T 12: 21,263,203 (GRCm39) A273S probably null Het
Atp6v0d2 C A 4: 19,881,436 (GRCm39) R219L probably damaging Het
Atp6v1e2 A T 17: 87,251,727 (GRCm39) F224I probably damaging Het
Bnc2 T C 4: 84,194,478 (GRCm39) probably null Het
Cd33 A G 7: 43,179,705 (GRCm39) L241P possibly damaging Het
Clec4g A T 8: 3,769,474 (GRCm39) probably null Het
Dym C T 18: 75,247,852 (GRCm39) probably benign Het
Enpp5 A G 17: 44,391,612 (GRCm39) T14A probably benign Het
Ggt1 T C 10: 75,421,121 (GRCm39) probably null Het
Gpr39 A T 1: 125,605,188 (GRCm39) I39F probably benign Het
Kcnb1 G T 2: 166,948,127 (GRCm39) F240L probably damaging Het
Kcnt1 T A 2: 25,788,766 (GRCm39) V400E probably damaging Het
Klhdc7a A G 4: 139,694,125 (GRCm39) I274T probably damaging Het
Lrwd1 A T 5: 136,163,483 (GRCm39) L71Q probably damaging Het
Mycbp2 A T 14: 103,528,723 (GRCm39) probably null Het
Nckap1 A T 2: 80,350,914 (GRCm39) M725K probably benign Het
Odad2 T C 18: 7,127,345 (GRCm39) K956R probably benign Het
Or2b7 T A 13: 21,739,389 (GRCm39) I268F probably damaging Het
Pole2 C T 12: 69,269,873 (GRCm39) probably null Het
Prss32 A G 17: 24,074,982 (GRCm39) T111A probably benign Het
Rgs9 A G 11: 109,139,875 (GRCm39) probably benign Het
Slc2a4 A G 11: 69,835,654 (GRCm39) C361R probably damaging Het
Ston1 G A 17: 88,944,438 (GRCm39) G615R probably null Het
Tas2r139 T G 6: 42,117,891 (GRCm39) W8G probably benign Het
Tmem101 A T 11: 102,046,704 (GRCm39) L55Q probably damaging Het
Tnni3k T C 3: 154,646,666 (GRCm39) probably null Het
Uba2 A G 7: 33,845,689 (GRCm39) V478A probably damaging Het
Vps13a T C 19: 16,739,545 (GRCm39) D52G probably damaging Het
Other mutations in Gm17541
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02006:Gm17541 APN 12 4,739,619 (GRCm39) intron probably benign
IGL02525:Gm17541 APN 12 4,739,907 (GRCm39) intron probably benign
R0266:Gm17541 UTSW 12 4,739,487 (GRCm39) intron probably benign
R0501:Gm17541 UTSW 12 4,739,730 (GRCm39) intron probably benign
R1375:Gm17541 UTSW 12 4,739,825 (GRCm39) intron probably benign
R4283:Gm17541 UTSW 12 4,739,656 (GRCm39) intron probably benign
R5256:Gm17541 UTSW 12 4,739,672 (GRCm39) intron probably benign
R5512:Gm17541 UTSW 12 4,739,452 (GRCm39) intron probably benign
Posted On 2013-12-09