Incidental Mutation 'IGL01665:Gm7964'
ID 103273
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 # IGL01665
Quality Score
Status
Chromosome 7
Chromosomal Location 83405112-83406489 bp(+) (GRCm39)
Type of Mutation exon
DNA Base Change (assembly) T to A at 83406341 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: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsbg1 T A 9: 54,530,004 (GRCm39) I231L probably benign Het
Adcyap1 T A 17: 93,507,506 (GRCm39) V22D probably damaging Het
Adgra3 T C 5: 50,164,272 (GRCm39) T236A possibly damaging Het
Adipor2 A T 6: 119,338,887 (GRCm39) L122H probably benign Het
Atp1a4 T C 1: 172,074,291 (GRCm39) I321V probably benign Het
Bhmt2 A T 13: 93,799,661 (GRCm39) Y258* probably null Het
C230029F24Rik T A 1: 49,377,253 (GRCm39) noncoding transcript Het
Ccpg1 T A 9: 72,913,159 (GRCm39) F232I probably damaging Het
Cd83 A T 13: 43,955,153 (GRCm39) T195S probably benign Het
Cdcp3 G T 7: 130,848,386 (GRCm39) G847* probably null Het
Cfap70 G A 14: 20,453,186 (GRCm39) T897M probably damaging Het
Cyp3a11 T A 5: 145,805,475 (GRCm39) M181L probably benign Het
Frem2 C T 3: 53,457,083 (GRCm39) V2090I probably benign Het
Gm45234 A G 6: 124,723,571 (GRCm39) probably benign Het
Igsf9 T A 1: 172,319,738 (GRCm39) C39* probably null Het
Il1rap A T 16: 26,541,463 (GRCm39) D568V probably damaging Het
Ints7 C T 1: 191,345,331 (GRCm39) probably benign Het
Lsamp C T 16: 41,964,375 (GRCm39) R250* probably null Het
Oit3 T A 10: 59,274,731 (GRCm39) D23V probably damaging Het
Pcdh17 T A 14: 84,684,442 (GRCm39) L303Q probably damaging Het
Pcdhb1 T A 18: 37,400,450 (GRCm39) N800K probably benign Het
Plce1 A G 19: 38,513,331 (GRCm39) D210G probably benign Het
Plekhb2 T A 1: 34,908,411 (GRCm39) Y152N probably damaging Het
Rbp3 T C 14: 33,678,088 (GRCm39) S679P probably benign Het
Rps6kc1 T C 1: 190,643,854 (GRCm39) T2A possibly damaging Het
Tmem167 T A 13: 90,246,504 (GRCm39) S9R probably damaging Het
Xpnpep1 A T 19: 52,985,463 (GRCm39) S522T probably benign Het
Other mutations in Gm7964
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01691:Gm7964 APN 7 83,405,344 (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