Incidental Mutation 'IGL01873:Gm6665'
ID 178773
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm6665
Ensembl Gene ENSMUSG00000091561
Gene Name predicted gene 6665
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL01873
Quality Score
Status
Chromosome 18
Chromosomal Location 31952915-31953572 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 31953355 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Glycine at position 38 (S38G)
Ref Sequence ENSEMBL: ENSMUSP00000129853 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025264] [ENSMUST00000082319] [ENSMUST00000165131]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000025264
SMART Domains Protein: ENSMUSP00000025264
Gene: ENSMUSG00000024400

DomainStartEndE-ValueType
WD40 107 147 2.15e-1 SMART
WD40 150 189 5.77e-5 SMART
WD40 191 230 1.89e-9 SMART
WD40 233 274 2.59e-7 SMART
WD40 277 316 2.73e-6 SMART
WD40 320 360 1.71e-7 SMART
WD40 364 403 1.52e-4 SMART
low complexity region 481 499 N/A INTRINSIC
coiled coil region 531 559 N/A INTRINSIC
low complexity region 573 587 N/A INTRINSIC
low complexity region 608 624 N/A INTRINSIC
low complexity region 628 668 N/A INTRINSIC
low complexity region 679 722 N/A INTRINSIC
low complexity region 725 761 N/A INTRINSIC
internal_repeat_1 778 803 3.47e-9 PROSPERO
low complexity region 806 818 N/A INTRINSIC
internal_repeat_1 821 845 3.47e-9 PROSPERO
low complexity region 848 881 N/A INTRINSIC
low complexity region 920 935 N/A INTRINSIC
low complexity region 938 951 N/A INTRINSIC
low complexity region 1000 1018 N/A INTRINSIC
low complexity region 1041 1049 N/A INTRINSIC
low complexity region 1057 1100 N/A INTRINSIC
low complexity region 1137 1154 N/A INTRINSIC
low complexity region 1190 1207 N/A INTRINSIC
low complexity region 1251 1262 N/A INTRINSIC
low complexity region 1287 1330 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000082319
SMART Domains Protein: ENSMUSP00000080936
Gene: ENSMUSG00000024400

DomainStartEndE-ValueType
WD40 107 147 2.15e-1 SMART
WD40 150 189 5.77e-5 SMART
WD40 191 230 1.89e-9 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000165131
AA Change: S38G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000129853
Gene: ENSMUSG00000091561
AA Change: S38G

DomainStartEndE-ValueType
Pfam:GST_N 1 47 6.3e-12 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Chd9 A G 8: 91,660,395 (GRCm39) T452A probably benign Het
Coq8a T A 1: 180,006,542 (GRCm39) Q115L probably damaging Het
Cul9 T C 17: 46,813,378 (GRCm39) E2326G probably damaging Het
Cyp2c69 A G 19: 39,869,693 (GRCm39) probably benign Het
Dennd5b A T 6: 148,946,027 (GRCm39) M528K probably benign Het
Gm10717 C T 9: 3,025,616 (GRCm39) S67L probably benign Het
Gm21738 G A 14: 19,416,979 (GRCm38) S144L probably benign Het
Gm5862 A C 5: 26,227,769 (GRCm39) W41G probably benign Het
Gsg1l A G 7: 125,557,615 (GRCm39) V171A probably damaging Het
Ighv5-2 A T 12: 113,542,350 (GRCm39) S42T probably benign Het
Itch C T 2: 155,010,670 (GRCm39) T46I possibly damaging Het
Itsn2 T G 12: 4,682,366 (GRCm39) probably benign Het
Lime1 T C 2: 181,024,667 (GRCm39) V107A probably benign Het
Mertk T C 2: 128,571,195 (GRCm39) S50P possibly damaging Het
Myo5b T A 18: 74,713,467 (GRCm39) V104E probably damaging Het
Nckap1 A T 2: 80,383,729 (GRCm39) I145K possibly damaging Het
Ppp4r3a A T 12: 101,008,094 (GRCm39) I794N possibly damaging Het
Psapl1 C A 5: 36,362,569 (GRCm39) P387Q possibly damaging Het
Ripk1 T A 13: 34,193,707 (GRCm39) L23Q probably damaging Het
Srrm4 G T 5: 116,729,527 (GRCm39) probably benign Het
St6galnac1 T A 11: 116,657,437 (GRCm39) T376S probably damaging Het
Tmem74 T C 15: 43,730,782 (GRCm39) D87G probably benign Het
Trav19 A G 14: 54,083,173 (GRCm39) R83G probably benign Het
Tubgcp4 T C 2: 121,018,665 (GRCm39) probably null Het
Vmn2r129 C T 4: 156,690,549 (GRCm39) noncoding transcript Het
Zfat T C 15: 68,096,744 (GRCm39) N23S probably benign Het
Other mutations in Gm6665
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00962:Gm6665 APN 18 31,953,204 (GRCm39) missense probably benign 0.00
R1551:Gm6665 UTSW 18 31,953,340 (GRCm39) missense probably damaging 0.99
R1797:Gm6665 UTSW 18 31,953,186 (GRCm39) missense possibly damaging 0.49
R1922:Gm6665 UTSW 18 31,953,318 (GRCm39) missense probably benign 0.11
R6123:Gm6665 UTSW 18 31,952,937 (GRCm39) missense probably benign 0.00
R8468:Gm6665 UTSW 18 31,953,453 (GRCm39) missense possibly damaging 0.90
RF020:Gm6665 UTSW 18 31,953,430 (GRCm39) frame shift probably null
RF050:Gm6665 UTSW 18 31,953,430 (GRCm39) frame shift probably null
Posted On 2014-05-07