Incidental Mutation 'IGL02193:Gm5900'
ID 283952
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm5900
Ensembl Gene ENSMUSG00000094685
Gene Name predicted pseudogene 5900
Synonyms
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.453) question?
Stock # IGL02193
Quality Score
Status
Chromosome 7
Chromosomal Location 104599122-104599496 bp(-) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) A to C at 104599231 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000179862
SMART Domains Protein: ENSMUSP00000136999
Gene: ENSMUSG00000094685

DomainStartEndE-ValueType
MAPKK1_Int 3 121 6.65e-63 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Agl A G 3: 116,572,815 (GRCm39) L812P probably damaging Het
Ankmy1 A T 1: 92,808,767 (GRCm39) F714I probably benign Het
Armh3 G T 19: 45,961,323 (GRCm39) T118K probably benign Het
Celf5 A G 10: 81,306,507 (GRCm39) I52T probably damaging Het
Clstn1 T C 4: 149,729,809 (GRCm39) V771A probably benign Het
Enpep G T 3: 129,075,336 (GRCm39) L661I possibly damaging Het
Faxc A G 4: 21,993,486 (GRCm39) N377D possibly damaging Het
Gabrb3 A G 7: 57,442,264 (GRCm39) E190G probably damaging Het
Gm4787 C T 12: 81,425,302 (GRCm39) M285I probably benign Het
Gm6133 A G 18: 78,393,308 (GRCm39) N101D probably benign Het
Gtse1 A G 15: 85,746,531 (GRCm39) K116E probably benign Het
H2-D1 T G 17: 35,484,785 (GRCm39) H215Q possibly damaging Het
Hdc A T 2: 126,443,700 (GRCm39) probably benign Het
Hnrnph3 T C 10: 62,853,056 (GRCm39) H195R probably damaging Het
Ipo8 T C 6: 148,678,782 (GRCm39) T939A probably damaging Het
Irag1 A T 7: 110,498,162 (GRCm39) L411Q probably damaging Het
Krt79 G T 15: 101,848,340 (GRCm39) P104T possibly damaging Het
Lama4 A T 10: 38,918,670 (GRCm39) M384L probably benign Het
Lamb2 T G 9: 108,366,559 (GRCm39) D1590E probably benign Het
Ly6i A T 15: 74,854,879 (GRCm39) C10* probably null Het
Mamdc4 G A 2: 25,454,458 (GRCm39) A1082V probably benign Het
Nlrp4a T A 7: 26,159,117 (GRCm39) L799H probably damaging Het
Nlrp4a G T 7: 26,148,703 (GRCm39) K103N possibly damaging Het
Or2y13 C T 11: 49,414,571 (GRCm39) T7I possibly damaging Het
Or5al6 A T 2: 85,977,059 (GRCm39) N6K probably benign Het
Or6b1 T C 6: 42,815,753 (GRCm39) probably benign Het
Otud6b T C 4: 14,812,543 (GRCm39) H268R probably damaging Het
Peg3 T C 7: 6,714,927 (GRCm39) E138G probably damaging Het
Phactr1 T C 13: 42,863,176 (GRCm39) probably benign Het
Psmf1 A G 2: 151,562,733 (GRCm39) probably benign Het
Rab32 T C 10: 10,422,199 (GRCm39) probably benign Het
Rfwd3 C T 8: 111,999,647 (GRCm39) probably benign Het
Scart2 A G 7: 139,828,913 (GRCm39) T191A probably benign Het
Slc25a3 A G 10: 90,953,977 (GRCm39) V245A probably benign Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Thoc1 A G 18: 9,992,863 (GRCm39) D545G probably benign Het
Tpst1 T A 5: 130,130,737 (GRCm39) M69K possibly damaging Het
Trank1 T C 9: 111,196,344 (GRCm39) V1456A probably benign Het
Trappc6a T A 7: 19,249,144 (GRCm39) C124S possibly damaging Het
Tsc22d2 T A 3: 58,367,628 (GRCm39) probably benign Het
Other mutations in Gm5900
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01584:Gm5900 APN 7 104,599,361 (GRCm39) exon noncoding transcript
IGL02653:Gm5900 APN 7 104,599,340 (GRCm39) exon noncoding transcript
R2509:Gm5900 UTSW 7 104,599,571 (GRCm39) unclassified noncoding transcript
R2510:Gm5900 UTSW 7 104,599,571 (GRCm39) unclassified noncoding transcript
R5129:Gm5900 UTSW 7 104,599,223 (GRCm39) exon noncoding transcript
R5898:Gm5900 UTSW 7 104,599,468 (GRCm39) exon noncoding transcript
Posted On 2015-04-16