Incidental Mutation 'IGL01665:Gm7964'
ID103273
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Gm7964
Ensembl Gene ENSMUSG00000063902
Gene Namepredicted gene 7964
Synonyms
Accession Numbers
Is this an essential gene? Possibly essential (E-score: 0.746) question?
Stock #IGL01665
Quality Score
Status
Chromosome7
Chromosomal Location83755904-83757356 bp(+) (GRCm38)
Type of Mutationexon
DNA Base Change (assembly) T to A at 83757133 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
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: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5430419D17Rik G T 7: 131,246,657 G847* probably null Het
Acsbg1 T A 9: 54,622,720 I231L probably benign Het
Adcyap1 T A 17: 93,200,078 V22D probably damaging Het
Adgra3 T C 5: 50,006,930 T236A possibly damaging Het
Adipor2 A T 6: 119,361,926 L122H probably benign Het
Atp1a4 T C 1: 172,246,724 I321V probably benign Het
Bhmt2 A T 13: 93,663,153 Y258* probably null Het
C230029F24Rik T A 1: 49,338,094 noncoding transcript Het
Ccpg1 T A 9: 73,005,877 F232I probably damaging Het
Cd83 A T 13: 43,801,677 T195S probably benign Het
Cfap70 G A 14: 20,403,118 T897M probably damaging Het
Cyp3a11 T A 5: 145,868,665 M181L probably benign Het
Frem2 C T 3: 53,549,662 V2090I probably benign Het
Gm45234 A G 6: 124,746,608 probably benign Het
Igsf9 T A 1: 172,492,171 C39* probably null Het
Il1rap A T 16: 26,722,713 D568V probably damaging Het
Ints7 C T 1: 191,613,219 probably benign Het
Lsamp C T 16: 42,144,012 R250* probably null Het
Oit3 T A 10: 59,438,909 D23V probably damaging Het
Pcdh17 T A 14: 84,447,002 L303Q probably damaging Het
Pcdhb1 T A 18: 37,267,397 N800K probably benign Het
Plce1 A G 19: 38,524,887 D210G probably benign Het
Plekhb2 T A 1: 34,869,330 Y152N probably damaging Het
Rbp3 T C 14: 33,956,131 S679P probably benign Het
Rps6kc1 T C 1: 190,911,657 T2A possibly damaging Het
Tmem167 T A 13: 90,098,385 S9R probably damaging Het
Xpnpep1 A T 19: 52,997,032 S522T probably benign Het
Other mutations in Gm7964
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01691:Gm7964 APN 7 83756136 exon noncoding transcript
IGL02232:Gm7964 APN 7 83756307 exon noncoding transcript
IGL02525:Gm7964 APN 7 83756042 exon noncoding transcript
R0512:Gm7964 UTSW 7 83755950 exon noncoding transcript
R0543:Gm7964 UTSW 7 83756394 exon noncoding transcript
R0723:Gm7964 UTSW 7 83756166 exon noncoding transcript
R1977:Gm7964 UTSW 7 83757352 missense possibly damaging 0.56
R2397:Gm7964 UTSW 7 83757113 exon noncoding transcript
R3623:Gm7964 UTSW 7 83756421 missense probably benign 0.02
R3769:Gm7964 UTSW 7 83756130 missense probably damaging 0.98
R4222:Gm7964 UTSW 7 83756822 missense probably damaging 1.00
R4224:Gm7964 UTSW 7 83756822 missense probably damaging 1.00
R4796:Gm7964 UTSW 7 83755901 unclassified probably null
R4869:Gm7964 UTSW 7 83756142 missense possibly damaging 0.51
R5086:Gm7964 UTSW 7 83757352 missense possibly damaging 0.56
R5944:Gm7964 UTSW 7 83756535 missense probably benign 0.00
Posted On2014-01-21