Incidental Mutation 'IGL01691:Gm7964'
ID 104111
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7964
Ensembl Gene ENSMUSG00000063902
Gene Name predicted gene 7964
Synonyms
Accession Numbers
Essential gene? Probably essential (E-score: 0.930) question?
Stock # IGL01691
Quality Score
Status
Chromosome 7
Chromosomal Location 83405112-83406489 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to C at 83405344 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: ENSMUST00000051522
SMART Domains Protein: ENSMUSP00000095927
Gene: ENSMUSG00000063902

DomainStartEndE-ValueType
KH 41 109 4.56e-11 SMART
KH 143 214 2.62e-11 SMART
low complexity region 262 277 N/A INTRINSIC
low complexity region 284 300 N/A INTRINSIC
low complexity region 306 314 N/A INTRINSIC
low complexity region 322 334 N/A INTRINSIC
low complexity region 364 380 N/A INTRINSIC
KH 385 455 7.45e-16 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actl6a T A 3: 32,774,349 (GRCm39) M282K possibly damaging Het
Adam22 T C 5: 8,142,742 (GRCm39) N831S probably damaging Het
Adamdec1 C T 14: 68,810,556 (GRCm39) R200Q probably damaging Het
Asb15 A G 6: 24,567,271 (GRCm39) I531V probably benign Het
Btrc T A 19: 45,501,117 (GRCm39) D223E probably benign Het
Ccdc30 T A 4: 119,250,761 (GRCm39) E161V probably damaging Het
Cd38 G A 5: 44,060,928 (GRCm39) probably benign Het
Clec2d T C 6: 129,161,185 (GRCm39) F94S probably damaging Het
Cwf19l1 C T 19: 44,109,311 (GRCm39) probably null Het
Dnah2 A T 11: 69,430,269 (GRCm39) N96K probably benign Het
Ephb6 G A 6: 41,591,449 (GRCm39) R202H probably benign Het
Gm43191 T A 3: 116,471,616 (GRCm39) I218L probably benign Het
Gm7168 G A 17: 14,169,140 (GRCm39) S169N probably damaging Het
Kif20b T C 19: 34,913,143 (GRCm39) probably benign Het
Kmt2e A G 5: 23,702,089 (GRCm39) T906A probably benign Het
Mboat2 A G 12: 25,004,221 (GRCm39) N341D probably damaging Het
Msh6 T C 17: 88,292,907 (GRCm39) V554A probably benign Het
Ndc80 T C 17: 71,815,634 (GRCm39) T384A possibly damaging Het
Or1af1 G T 2: 37,110,038 (GRCm39) C179F probably damaging Het
Or8g18 G A 9: 39,149,315 (GRCm39) T135I probably benign Het
Ptpn5 G T 7: 46,732,906 (GRCm39) H312Q probably benign Het
Rftn2 C T 1: 55,253,445 (GRCm39) V53I probably damaging Het
Rgs20 T C 1: 4,987,145 (GRCm39) T124A probably benign Het
Sox18 T C 2: 181,313,143 (GRCm39) S58G possibly damaging Het
Togaram2 A G 17: 72,036,485 (GRCm39) M1012V probably null Het
Usp48 A T 4: 137,350,583 (GRCm39) probably null Het
Other mutations in Gm7964
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01665:Gm7964 APN 7 83,406,341 (GRCm39) exon noncoding transcript
IGL02232:Gm7964 APN 7 83,405,515 (GRCm39) exon noncoding transcript
IGL02525:Gm7964 APN 7 83,405,250 (GRCm39) exon noncoding transcript
R0512:Gm7964 UTSW 7 83,405,158 (GRCm39) exon noncoding transcript
R0543:Gm7964 UTSW 7 83,405,602 (GRCm39) exon noncoding transcript
R0723:Gm7964 UTSW 7 83,405,374 (GRCm39) exon noncoding transcript
R1977:Gm7964 UTSW 7 83,406,560 (GRCm39) missense possibly damaging 0.56
R2397:Gm7964 UTSW 7 83,406,321 (GRCm39) exon noncoding transcript
R3623:Gm7964 UTSW 7 83,405,629 (GRCm39) missense probably benign 0.02
R3769:Gm7964 UTSW 7 83,405,338 (GRCm39) missense probably damaging 0.98
R4222:Gm7964 UTSW 7 83,406,030 (GRCm39) missense probably damaging 1.00
R4224:Gm7964 UTSW 7 83,406,030 (GRCm39) missense probably damaging 1.00
R4796:Gm7964 UTSW 7 83,405,109 (GRCm39) splice site probably null
R4869:Gm7964 UTSW 7 83,405,350 (GRCm39) missense possibly damaging 0.51
R5086:Gm7964 UTSW 7 83,406,560 (GRCm39) missense possibly damaging 0.56
R5944:Gm7964 UTSW 7 83,405,743 (GRCm39) missense probably benign 0.00
Posted On 2014-01-21