Incidental Mutation 'IGL03070:1190007I07Rik'
List |< first << previous [record 34 of 55675] next >> last >|
ID417497
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1190007I07Rik
Ensembl Gene ENSMUSG00000063320
Gene NameRIKEN cDNA 1190007I07 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.187) question?
Stock #IGL03070
Quality Score
Status
Chromosome10
Chromosomal Location82619851-82623228 bp(-) (GRCm38)
Type of Mutationutr 3 prime
DNA Base Change (assembly) A to T at 82620116 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000139244 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000079648] [ENSMUST00000176200] [ENSMUST00000183363] [ENSMUST00000183416] [ENSMUST00000185168]
Predicted Effect probably benign
Transcript: ENSMUST00000079648
SMART Domains Protein: ENSMUSP00000078593
Gene: ENSMUSG00000063320

DomainStartEndE-ValueType
Pfam:DUF4516 1 46 1.5e-29 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000176200
SMART Domains Protein: ENSMUSP00000134868
Gene: ENSMUSG00000063320

DomainStartEndE-ValueType
Pfam:DUF4516 1 47 2.2e-28 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000183363
SMART Domains Protein: ENSMUSP00000139234
Gene: ENSMUSG00000063320

DomainStartEndE-ValueType
Pfam:DUF4516 1 47 2.2e-28 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000183416
SMART Domains Protein: ENSMUSP00000139041
Gene: ENSMUSG00000063320

DomainStartEndE-ValueType
Pfam:DUF4516 1 40 1.1e-21 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000185168
SMART Domains Protein: ENSMUSP00000139244
Gene: ENSMUSG00000063320

DomainStartEndE-ValueType
Pfam:DUF4516 1 47 2.2e-28 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam3 T C 8: 24,703,784 E404G probably damaging Het
Arid1a A G 4: 133,694,753 S778P unknown Het
Asah2 A T 19: 32,006,344 Y567N probably damaging Het
Crb1 G T 1: 139,241,258 H841N possibly damaging Het
Ehbp1l1 A G 19: 5,715,953 V1454A probably benign Het
Eif3d A G 15: 77,959,643 L501P probably damaging Het
Fam122a A C 19: 24,476,952 D135E probably damaging Het
Fbxo4 A T 15: 3,977,862 S107T possibly damaging Het
Galnt10 T C 11: 57,725,582 Y108H probably damaging Het
Hspbap1 T A 16: 35,818,726 D263E probably damaging Het
Kpna3 T C 14: 61,370,782 probably benign Het
Miox A G 15: 89,336,084 T160A possibly damaging Het
Mlxipl G A 5: 135,132,453 V409M possibly damaging Het
Mrps21 A T 3: 95,870,585 probably benign Het
Muc6 A G 7: 141,644,567 probably benign Het
Mup6 A T 4: 60,003,999 I31F probably damaging Het
Olfr593 A G 7: 103,212,697 H279R probably benign Het
Pgr T A 9: 8,903,664 I562N possibly damaging Het
Prag1 T A 8: 36,103,549 W429R probably benign Het
Prrc2c G T 1: 162,677,409 P2621Q probably damaging Het
Psip1 T G 4: 83,465,081 K232N probably damaging Het
Ryr1 T C 7: 29,070,659 Y2663C probably damaging Het
Trhr2 T A 8: 122,358,603 Q214L probably benign Het
Txndc11 A T 16: 11,075,287 Y860N probably damaging Het
Vmn2r72 C T 7: 85,752,041 probably benign Het
Yif1a T A 19: 5,088,729 H4Q possibly damaging Het
Other mutations in 1190007I07Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1985:1190007I07Rik UTSW 10 82620217 missense possibly damaging 0.71
Posted On2016-08-02