Incidental Mutation 'IGL02173:4930533K18Rik'
ID282989
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 4930533K18Rik
Ensembl Gene ENSMUSG00000047692
Gene NameRIKEN cDNA 4930533K18 gene
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.166) question?
Stock #IGL02173
Quality Score
Status
Chromosome10
Chromosomal Location70868280-70875986 bp(+) (GRCm38)
Type of Mutationunclassified
DNA Base Change (assembly) A to G at 70872230 bp
ZygosityHeterozygous
Amino Acid Change
Predicted Effect noncoding transcript
Transcript: ENSMUST00000058942
Predicted Effect noncoding transcript
Transcript: ENSMUST00000217867
Predicted Effect noncoding transcript
Transcript: ENSMUST00000218757
Predicted Effect noncoding transcript
Transcript: ENSMUST00000219192
Predicted Effect noncoding transcript
Transcript: ENSMUST00000219293
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700113H08Rik A T 10: 87,225,892 H68L possibly damaging Het
4933409G03Rik A G 2: 68,613,057 T182A unknown Het
Abca2 T A 2: 25,441,897 D1340E probably benign Het
Abcc12 G A 8: 86,566,442 A39V probably damaging Het
Acap2 T C 16: 31,108,147 R510G possibly damaging Het
Ace G T 11: 105,988,991 R719L probably benign Het
Adarb1 A C 10: 77,321,825 F263V probably damaging Het
Ambra1 T C 2: 91,917,668 S1130P probably benign Het
Aqp7 A T 4: 41,034,379 L260* probably null Het
Cntn5 G T 9: 9,748,396 S493R probably damaging Het
Crhr2 A G 6: 55,103,180 F138S probably damaging Het
D2hgdh T A 1: 93,829,889 D175E probably benign Het
Dtx4 G T 19: 12,473,257 Y530* probably null Het
Elp4 T A 2: 105,702,743 H419L probably damaging Het
Etv6 A G 6: 134,248,727 D218G possibly damaging Het
Exoc5 A G 14: 49,034,801 probably benign Het
Fyb C T 15: 6,580,695 P250S probably benign Het
Gaa A G 11: 119,274,913 Y84C probably damaging Het
Galns A T 8: 122,598,626 S262R probably damaging Het
Gm4737 T C 16: 46,154,078 N312S probably benign Het
Kctd16 T C 18: 40,530,853 I345T probably benign Het
Lats2 A G 14: 57,697,260 V671A probably damaging Het
Maml3 C A 3: 51,690,787 L179F probably damaging Het
Myo1f T C 17: 33,607,344 L1089P probably damaging Het
Nadsyn1 A T 7: 143,804,006 probably benign Het
Olfr1502 A G 19: 13,862,014 T74A probably benign Het
Olfr39 T C 9: 20,286,395 V240A probably benign Het
Olfr394 A G 11: 73,888,123 M83T possibly damaging Het
Olfr639 G A 7: 104,011,830 P291S probably damaging Het
Otog T C 7: 46,276,741 probably benign Het
Pcbd1 A G 10: 61,092,204 probably benign Het
Pced1a A G 2: 130,422,328 V164A possibly damaging Het
Pgd A G 4: 149,156,753 I233T probably damaging Het
Ror2 C T 13: 53,110,728 S764N probably damaging Het
Sec24d A T 3: 123,353,681 H733L probably damaging Het
Slc1a2 T A 2: 102,743,861 N205K probably benign Het
Sstr2 G T 11: 113,625,016 V254L probably damaging Het
Tm9sf2 G T 14: 122,143,423 V308F probably benign Het
Tor3a T C 1: 156,674,206 K34E probably benign Het
Tsta3 A G 15: 75,926,185 S233P probably damaging Het
Ubr4 T A 4: 139,437,070 probably null Het
Vmn1r56 A G 7: 5,196,118 S167P probably damaging Het
Zswim3 T A 2: 164,820,839 I413N probably damaging Het
Other mutations in 4930533K18Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00499:4930533K18Rik APN 10 70875308 unclassified noncoding transcript
IGL01538:4930533K18Rik APN 10 70872202 unclassified noncoding transcript
R0656:4930533K18Rik UTSW 10 70868800 unclassified noncoding transcript
R1776:4930533K18Rik UTSW 10 70875228 unclassified noncoding transcript
R1824:4930533K18Rik UTSW 10 70872256 unclassified noncoding transcript
R5690:4930533K18Rik UTSW 10 70923314 utr 3 prime probably benign
R8314:4930533K18Rik UTSW 10 70875276 missense noncoding transcript
X0024:4930533K18Rik UTSW 10 70872166 unclassified noncoding transcript
Posted On2015-04-16