Incidental Mutation 'IGL02353:8030411F24Rik'
ID289581
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol 8030411F24Rik
Ensembl Gene ENSMUSG00000027444
Gene NameRIKEN cDNA 8030411F24 gene
Synonymscystatin SC
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.034) question?
Stock #IGL02353
Quality Score
Status
Chromosome2
Chromosomal Location148782009-148785937 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) A to G at 148783467 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000028933 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000028933]
Predicted Effect probably benign
Transcript: ENSMUST00000028933
SMART Domains Protein: ENSMUSP00000028933
Gene: ENSMUSG00000027444

DomainStartEndE-ValueType
CY 20 128 2.25e-3 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aldh18a1 A T 19: 40,577,920 V102D probably damaging Het
Car4 C T 11: 84,965,767 P294S probably damaging Het
Casp6 C T 3: 129,910,526 S87L probably damaging Het
Ccdc121 T C 1: 181,510,625 E254G possibly damaging Het
Ccnl1 A C 3: 65,948,720 C255G probably damaging Het
Celf4 T C 18: 25,486,898 I485M probably damaging Het
Cntln A G 4: 85,049,850 R769G probably damaging Het
Cyp2d12 T C 15: 82,558,970 V360A probably benign Het
Dgki T C 6: 36,847,389 E1068G probably damaging Het
Fbxl4 A G 4: 22,433,684 N607S probably benign Het
Fgd4 T C 16: 16,462,045 I383V probably damaging Het
Fgd6 C T 10: 94,138,396 T1333I possibly damaging Het
Got1 A G 19: 43,524,443 S5P probably damaging Het
Herc2 T A 7: 56,114,812 N995K probably damaging Het
Kcnma1 A G 14: 23,591,613 F159S probably damaging Het
Krt83 T C 15: 101,485,458 S456G probably benign Het
Lhb T C 7: 45,421,294 V32A possibly damaging Het
Mau2 A T 8: 70,019,638 V602E probably damaging Het
Mpst C T 15: 78,410,085 L6F probably damaging Het
Nlrp2 G A 7: 5,337,599 T72I probably damaging Het
Olfr44 A G 9: 39,485,148 I32T probably benign Het
Phldb2 T C 16: 45,748,779 Y1239C probably damaging Het
Slc22a8 T C 19: 8,608,255 F328S possibly damaging Het
Spns1 C T 7: 126,375,140 R94Q probably damaging Het
Sult2a3 G A 7: 14,121,650 R94* probably null Het
Syt16 A G 12: 74,129,471 N38S probably damaging Het
Tbc1d1 G A 5: 64,256,836 R180Q probably damaging Het
Ush2a T C 1: 188,728,438 I2632T probably benign Het
Vcam1 T A 3: 116,115,894 I595F possibly damaging Het
Other mutations in 8030411F24Rik
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00857:8030411F24Rik APN 2 148782250 missense possibly damaging 0.93
IGL00936:8030411F24Rik APN 2 148785804 missense probably benign 0.05
IGL03088:8030411F24Rik APN 2 148783407 missense possibly damaging 0.81
R0078:8030411F24Rik UTSW 2 148785825 makesense probably null
R0465:8030411F24Rik UTSW 2 148783425 missense probably benign 0.14
R0542:8030411F24Rik UTSW 2 148782172 missense probably benign
R0723:8030411F24Rik UTSW 2 148783362 missense probably damaging 0.98
R2025:8030411F24Rik UTSW 2 148782228 missense probably damaging 0.98
R5153:8030411F24Rik UTSW 2 148783440 missense probably benign 0.12
R5360:8030411F24Rik UTSW 2 148783378 missense probably damaging 1.00
R5362:8030411F24Rik UTSW 2 148783378 missense probably damaging 1.00
R5363:8030411F24Rik UTSW 2 148783378 missense probably damaging 1.00
Posted On2015-04-16