Incidental Mutation 'IGL02598:Kics2'
ID 299978
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Kics2
Ensembl Gene ENSMUSG00000053684
Gene Name KICSTOR subunit 2
Synonyms BC048403
Accession Numbers
Essential gene? Probably non essential (E-score: 0.185) question?
Stock # IGL02598
Quality Score
Status
Chromosome 10
Chromosomal Location 121575835-121588770 bp(+) (GRCm39)
Type of Mutation utr 5 prime
DNA Base Change (assembly) G to A at 121575876 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000117249 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000065600] [ENSMUST00000136432]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000065600
SMART Domains Protein: ENSMUSP00000070834
Gene: ENSMUSG00000053684

DomainStartEndE-ValueType
Pfam:DUF2003 7 444 3.8e-252 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000136432
SMART Domains Protein: ENSMUSP00000117249
Gene: ENSMUSG00000053684

DomainStartEndE-ValueType
Pfam:DUF2003 1 309 1.1e-205 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4933414I15Rik A T 11: 50,834,448 (GRCm39) M1K probably null Het
Abca13 C T 11: 9,381,898 (GRCm39) T3850I probably damaging Het
Abcc4 A T 14: 118,905,781 (GRCm39) L95* probably null Het
Acacb A G 5: 114,384,098 (GRCm39) Y2209C probably damaging Het
Acadm A G 3: 153,644,181 (GRCm39) probably benign Het
Arid2 G A 15: 96,269,417 (GRCm39) V1177M probably damaging Het
Atp8a1 A T 5: 67,840,099 (GRCm39) probably null Het
Catsperd A G 17: 56,954,815 (GRCm39) probably null Het
Cd28 A G 1: 60,802,498 (GRCm39) probably benign Het
Cep164 A G 9: 45,682,002 (GRCm39) Y1934H probably damaging Het
Cep350 T C 1: 155,738,713 (GRCm39) I2377V probably benign Het
Csmd3 T C 15: 47,533,086 (GRCm39) K1581E probably damaging Het
Dab2 A T 15: 6,458,847 (GRCm39) N232I probably damaging Het
Dyrk4 G A 6: 126,860,982 (GRCm39) probably benign Het
Efcab14 T A 4: 115,597,631 (GRCm39) C75* probably null Het
Elovl1 T C 4: 118,288,616 (GRCm39) probably null Het
Eps8l2 T G 7: 140,934,849 (GRCm39) probably benign Het
Grik1 A T 16: 87,744,872 (GRCm39) V460E probably damaging Het
Gtf2f2 A G 14: 76,245,182 (GRCm39) S35P probably benign Het
Ifi203 A G 1: 173,762,568 (GRCm39) probably benign Het
Ifi209 T C 1: 173,472,281 (GRCm39) V374A probably damaging Het
Lars1 A G 18: 42,360,342 (GRCm39) S705P possibly damaging Het
Lcmt1 A G 7: 123,020,871 (GRCm39) probably benign Het
Limd1 T C 9: 123,345,933 (GRCm39) S571P probably benign Het
Limd1 T A 9: 123,309,236 (GRCm39) Y312N probably benign Het
Lin28b A T 10: 45,296,622 (GRCm39) D125E possibly damaging Het
Lmtk3 T C 7: 45,442,564 (GRCm39) S416P probably damaging Het
Map7d3 T C X: 55,855,146 (GRCm39) T446A probably benign Het
Masp1 T A 16: 23,278,381 (GRCm39) M523L probably benign Het
Mroh4 C A 15: 74,483,092 (GRCm39) probably null Het
Mtmr6 G A 14: 60,537,953 (GRCm39) A651T probably damaging Het
Myocd A G 11: 65,074,296 (GRCm39) S738P probably benign Het
Or10a2 A T 7: 106,673,923 (GRCm39) N296I possibly damaging Het
Or4d5 A T 9: 40,011,861 (GRCm39) F308L probably benign Het
Or52l1 A G 7: 104,830,163 (GRCm39) V134A probably damaging Het
Or5d46 A T 2: 88,170,595 (GRCm39) I229F possibly damaging Het
Or6c3b A T 10: 129,527,142 (GRCm39) I256N possibly damaging Het
Parg G T 14: 31,936,281 (GRCm39) V479L probably damaging Het
Pcdhb10 C A 18: 37,546,834 (GRCm39) H637N possibly damaging Het
Plekhg2 G A 7: 28,059,900 (GRCm39) T1118I possibly damaging Het
Podxl T C 6: 31,501,355 (GRCm39) E400G probably damaging Het
Prss54 C A 8: 96,292,337 (GRCm39) V81F probably damaging Het
Pzp A G 6: 128,464,420 (GRCm39) L1369P probably benign Het
Rfx8 A T 1: 39,735,128 (GRCm39) probably benign Het
Rgs6 C T 12: 83,138,571 (GRCm39) P302S probably benign Het
Rnf148 A C 6: 23,654,456 (GRCm39) I180S probably damaging Het
Sacm1l A G 9: 123,408,061 (GRCm39) D350G probably benign Het
Slc33a1 C T 3: 63,850,753 (GRCm39) G524S probably benign Het
Slc5a7 A G 17: 54,591,221 (GRCm39) V237A probably benign Het
Spink7 T C 18: 62,727,356 (GRCm39) D56G probably damaging Het
Syn3 A G 10: 86,303,063 (GRCm39) S31P probably damaging Het
Tesl1 A T X: 23,773,710 (GRCm39) T404S probably benign Het
Thrb C A 14: 18,008,606 (GRCm38) P110Q possibly damaging Het
Vmn2r76 G T 7: 85,877,879 (GRCm39) T506K probably benign Het
Vps45 A G 3: 95,938,354 (GRCm39) L486P probably benign Het
Zan G A 5: 137,444,473 (GRCm39) T1823M unknown Het
Zdhhc6 T A 19: 55,302,959 (GRCm39) Q14L probably benign Het
Zfp990 A T 4: 145,263,533 (GRCm39) N177I possibly damaging Het
Other mutations in Kics2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02164:Kics2 APN 10 121,586,675 (GRCm39) missense probably damaging 1.00
IGL02747:Kics2 APN 10 121,581,455 (GRCm39) missense possibly damaging 0.94
R0381:Kics2 UTSW 10 121,581,280 (GRCm39) missense probably damaging 1.00
R0732:Kics2 UTSW 10 121,586,852 (GRCm39) missense possibly damaging 0.55
R2383:Kics2 UTSW 10 121,586,554 (GRCm39) missense possibly damaging 0.69
R4299:Kics2 UTSW 10 121,581,351 (GRCm39) missense probably benign 0.01
R4760:Kics2 UTSW 10 121,575,912 (GRCm39) missense probably damaging 1.00
R5595:Kics2 UTSW 10 121,576,052 (GRCm39) start gained probably benign
R6184:Kics2 UTSW 10 121,586,810 (GRCm39) missense probably damaging 1.00
R6487:Kics2 UTSW 10 121,581,446 (GRCm39) missense probably damaging 1.00
R6977:Kics2 UTSW 10 121,581,371 (GRCm39) missense probably damaging 0.98
R7094:Kics2 UTSW 10 121,576,098 (GRCm39) missense possibly damaging 0.95
R7250:Kics2 UTSW 10 121,581,376 (GRCm39) missense possibly damaging 0.82
R8186:Kics2 UTSW 10 121,581,247 (GRCm39) missense possibly damaging 0.79
R8554:Kics2 UTSW 10 121,575,960 (GRCm39) missense probably benign
R9005:Kics2 UTSW 10 121,586,501 (GRCm39) missense probably damaging 1.00
R9124:Kics2 UTSW 10 121,586,416 (GRCm39) nonsense probably null
R9245:Kics2 UTSW 10 121,586,273 (GRCm39) missense probably damaging 0.98
Posted On 2015-04-16