Incidental Mutation 'IGL01107:Defa22'
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ID278180
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Defa22
Ensembl Gene ENSMUSG00000074443
Gene Namedefensin, alpha, 22
SynonymsDefcr22
Accession Numbers

Ncbi RefSeq: NM_207658.4; MGI:3639039

Is this an essential gene? Probably non essential (E-score: 0.046) question?
Stock #IGL01107
Quality Score
Status
Chromosome8
Chromosomal Location21162277-21163249 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) T to A at 21163037 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000096496 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000098897] [ENSMUST00000098897] [ENSMUST00000098897] [ENSMUST00000098897]
Predicted Effect probably null
Transcript: ENSMUST00000098897
SMART Domains Protein: ENSMUSP00000096496
Gene: ENSMUSG00000074443

DomainStartEndE-ValueType
Pfam:Defensin_propep 1 51 4.1e-26 PFAM
DEFSN 64 89 1.46e-3 SMART
Predicted Effect probably null
Transcript: ENSMUST00000098897
SMART Domains Protein: ENSMUSP00000096496
Gene: ENSMUSG00000074443

DomainStartEndE-ValueType
Pfam:Defensin_propep 1 51 4.1e-26 PFAM
DEFSN 64 89 1.46e-3 SMART
Predicted Effect probably null
Transcript: ENSMUST00000098897
SMART Domains Protein: ENSMUSP00000096496
Gene: ENSMUSG00000074443

DomainStartEndE-ValueType
Pfam:Defensin_propep 1 51 4.1e-26 PFAM
DEFSN 64 89 1.46e-3 SMART
Predicted Effect probably null
Transcript: ENSMUST00000098897
SMART Domains Protein: ENSMUSP00000096496
Gene: ENSMUSG00000074443

DomainStartEndE-ValueType
Pfam:Defensin_propep 1 51 4.1e-26 PFAM
DEFSN 64 89 1.46e-3 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700001O22Rik A T 2: 30,797,936 F215Y probably damaging Het
2700049A03Rik T C 12: 71,194,468 probably null Het
Akip1 C T 7: 109,711,838 T195M probably damaging Het
Arhgef16 T C 4: 154,280,244 N631S probably benign Het
Brat1 C T 5: 140,717,177 S544L probably damaging Het
Cfap65 C T 1: 74,919,183 probably null Het
D17Wsu92e A T 17: 27,786,069 probably null Het
Dnajc4 C T 19: 6,989,501 R153H probably benign Het
Dusp11 A G 6: 85,952,370 probably benign Het
E2f4 T A 8: 105,304,177 probably benign Het
Ece1 T A 4: 137,938,658 L271Q probably damaging Het
Fcgrt T C 7: 45,093,328 D343G probably damaging Het
Igsf10 T C 3: 59,331,524 E412G probably damaging Het
Il4ra G T 7: 125,575,914 L431F possibly damaging Het
Krt86 T A 15: 101,475,425 L200Q probably damaging Het
Lpcat1 T A 13: 73,494,828 F126I probably damaging Het
Prag1 A G 8: 36,099,931 T79A probably benign Het
Pramef12 A T 4: 144,393,094 I301N probably benign Het
Psg29 G T 7: 17,204,925 L41F probably benign Het
Rai14 C T 15: 10,599,711 probably benign Het
Reg3a A G 6: 78,383,245 D136G probably benign Het
Rif1 A G 2: 52,111,303 T1590A probably benign Het
Rorb A T 19: 18,957,328 L300* probably null Het
Sin3b T C 8: 72,731,105 C150R possibly damaging Het
Smarcc1 C A 9: 110,221,937 H942N probably damaging Het
Tas2r105 A G 6: 131,687,111 V118A probably benign Het
Tmem131 T C 1: 36,829,581 S388G probably damaging Het
Ttll9 C A 2: 153,002,889 probably benign Het
Ush1c A G 7: 46,209,901 L498P probably damaging Het
Vmn2r100 A G 17: 19,521,356 Y110C probably damaging Het
Zbtb11 T C 16: 56,006,007 Y800H probably damaging Het
Zdhhc20 T A 14: 57,865,589 E101V probably damaging Het
Other mutations in Defa22
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01154:Defa22 APN 8 21163037 splice site probably null
IGL01155:Defa22 APN 8 21163037 splice site probably null
IGL02142:Defa22 APN 8 21163114 missense possibly damaging 0.93
P0047:Defa22 UTSW 8 21163086 nonsense probably null
PIT4696001:Defa22 UTSW 8 21162336 missense probably damaging 0.99
R0738:Defa22 UTSW 8 21162375 missense probably benign 0.00
R1266:Defa22 UTSW 8 21162368 missense probably damaging 0.97
Posted On2015-04-16