Incidental Mutation 'IGL00429:1700009J07Rik'
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ID332403
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 1700009J07Rik
Ensembl Gene ENSMUSG00000096573
Gene NameRIKEN cDNA 1700009J07 gene
Synonyms
Accession Numbers
Is this an essential gene? Not available question?
Stock #IGL00429
Quality Score
Status
Chromosome10
Chromosomal Location77893417-77896114 bp(+) (GRCm38)
Type of Mutation
DNA Base Change (assembly) G to A at 77893839 bp
ZygosityHeterozygous
Amino Acid Change
Predicted Effect probably benign
Transcript: ENSMUST00000057608
SMART Domains Protein: ENSMUSP00000059570
Gene: ENSMUSG00000051652

DomainStartEndE-ValueType
LRRNT 32 68 6.53e-9 SMART
LRR 67 86 7.17e1 SMART
LRR_TYP 87 110 1.87e-5 SMART
LRR 113 135 2.14e0 SMART
Blast:LRRCT 145 197 7e-10 BLAST
transmembrane domain 204 226 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000178996
SMART Domains Protein: ENSMUSP00000136431
Gene: ENSMUSG00000096573

DomainStartEndE-ValueType
internal_repeat_1 4 32 6.69e-6 PROSPERO
internal_repeat_1 52 80 6.69e-6 PROSPERO
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185309
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185513
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933411K16Rik T C 19: 42,052,544 L38P probably damaging Het
Abca1 A G 4: 53,059,255 probably null Het
Abca15 T A 7: 120,397,054 I1401N probably damaging Het
Adam3 A C 8: 24,694,278 Y569D probably damaging Het
Ap2a1 T C 7: 44,905,768 S458G probably damaging Het
Asxl3 C T 18: 22,525,223 P2097S probably benign Het
AW551984 T C 9: 39,592,849 D607G probably benign Het
Ccdc158 C A 5: 92,657,881 M338I probably benign Het
Cdh23 A G 10: 60,421,141 S735P probably damaging Het
Cdh9 T C 15: 16,828,362 V180A probably damaging Het
Cyp4a31 A T 4: 115,574,974 probably benign Het
Dus4l A G 12: 31,641,669 V180A probably benign Het
Dysf A T 6: 84,189,844 T1672S probably damaging Het
F830016B08Rik T A 18: 60,300,268 L141Q probably damaging Het
Fhod3 A G 18: 24,994,540 E313G probably damaging Het
Gm4884 A G 7: 41,044,385 T593A probably benign Het
Hist1h2bm T C 13: 21,722,140 S15P possibly damaging Het
Il18r1 G A 1: 40,498,652 E526K possibly damaging Het
Lama4 A T 10: 39,011,026 H109L possibly damaging Het
Mab21l1 A C 3: 55,783,136 Q48P probably damaging Het
Magi3 T A 3: 104,014,978 K1474N probably damaging Het
Mre11a T C 9: 14,802,813 F237L probably damaging Het
Mst1r A T 9: 107,913,250 probably benign Het
Myh2 C T 11: 67,180,790 Q478* probably null Het
Mylip C A 13: 45,408,567 P282T probably benign Het
Mymk T C 2: 27,062,787 Y103C probably damaging Het
Necab1 A T 4: 15,052,656 N107K probably damaging Het
Pclo T C 5: 14,680,739 probably benign Het
Phgdh T C 3: 98,328,315 K129E probably damaging Het
Plxna4 T C 6: 32,162,091 Y1714C probably damaging Het
Pm20d2 A G 4: 33,187,205 probably benign Het
Ppfibp2 A G 7: 107,697,594 T172A probably benign Het
Prkca T C 11: 108,343,508 T54A probably benign Het
Prlr A G 15: 10,328,324 D295G probably benign Het
Rdh12 A G 12: 79,211,402 I68V probably benign Het
Slc14a2 A G 18: 78,150,438 F850L possibly damaging Het
Smad2 A T 18: 76,298,495 S185C possibly damaging Het
Soga1 A C 2: 157,030,864 F909C probably damaging Het
Trav13n-4 T A 14: 53,363,831 L19Q probably benign Het
Ush2a T A 1: 188,400,114 C844* probably null Het
Vwce T A 19: 10,664,511 probably null Het
Wdr95 T C 5: 149,595,244 probably benign Het
Zfp143 T C 7: 110,091,772 I510T probably damaging Het
Zfp930 G T 8: 69,227,982 K90N probably damaging Het
Posted On2015-08-05