Incidental Mutation 'R8833:Ifna13'
ID 673965
Institutional Source Beutler Lab
Gene Symbol Ifna13
Ensembl Gene ENSMUSG00000063376
Gene Name interferon alpha 13
Synonyms
MMRRC Submission 068661-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # R8833 (G1)
Quality Score 225.009
Status Validated
Chromosome 4
Chromosomal Location 88561878-88562696 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to A at 88562157 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Stop codon at position 156 (E156*)
Ref Sequence ENSEMBL: ENSMUSP00000100780 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000105149]
AlphaFold Q80SU4
Predicted Effect probably null
Transcript: ENSMUST00000105149
AA Change: E156*
SMART Domains Protein: ENSMUSP00000100780
Gene: ENSMUSG00000063376
AA Change: E156*

DomainStartEndE-ValueType
IFabd 50 167 2.2e-71 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.5%
  • 20x: 98.5%
Validation Efficiency 100% (53/53)
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akr1c6 T A 13: 4,496,377 (GRCm39) D132E possibly damaging Het
Armh4 C T 14: 50,011,318 (GRCm39) V130I probably benign Het
Atp10b A G 11: 43,112,986 (GRCm39) E844G probably damaging Het
Bbx T A 16: 50,045,629 (GRCm39) M311L probably benign Het
Bzw2 A T 12: 36,169,069 (GRCm39) M153K probably benign Het
C1qtnf6 G T 15: 78,409,574 (GRCm39) T91K probably benign Het
Cdh4 A G 2: 179,535,828 (GRCm39) D793G possibly damaging Het
Ces4a A G 8: 105,858,614 (GRCm39) I11V probably benign Het
Cpne9 T C 6: 113,281,473 (GRCm39) L518P probably damaging Het
Dip2c T A 13: 9,625,519 (GRCm39) probably null Het
Fam135b T C 15: 71,334,783 (GRCm39) N804D probably benign Het
Frem3 G A 8: 81,339,401 (GRCm39) D565N probably benign Het
Fscb T A 12: 64,519,997 (GRCm39) T490S unknown Het
Fuca1 A G 4: 135,648,206 (GRCm39) D31G probably damaging Het
Gbp8 G T 5: 105,166,668 (GRCm39) N220K possibly damaging Het
Gfra2 T C 14: 71,163,337 (GRCm39) F207L probably damaging Het
Grap2 A G 15: 80,522,684 (GRCm39) N70S probably benign Het
Jmjd1c G A 10: 67,054,162 (GRCm39) R22H probably benign Het
Macf1 A G 4: 123,365,134 (GRCm39) V3209A probably benign Het
Muc5b A G 7: 141,412,105 (GRCm39) T1684A unknown Het
Naip5 T A 13: 100,359,442 (GRCm39) E598V probably damaging Het
Niban1 T A 1: 151,520,681 (GRCm39) V125E probably damaging Het
Notch1 G A 2: 26,371,615 (GRCm39) T278I probably damaging Het
Or4d10c A G 19: 12,065,643 (GRCm39) V171A possibly damaging Het
Or4k5 A T 14: 50,385,823 (GRCm39) C169* probably null Het
Or52z13 T G 7: 103,247,444 (GRCm39) F307C possibly damaging Het
Or5k14 A T 16: 58,692,959 (GRCm39) Y185N probably damaging Het
Orm1 A T 4: 63,262,938 (GRCm39) E35V probably damaging Het
Pak1 T A 7: 97,503,839 (GRCm39) I58N possibly damaging Het
Pard3b A G 1: 62,384,158 (GRCm39) E841G probably benign Het
Pcdhb9 G T 18: 37,534,468 (GRCm39) R154I probably benign Het
Pdpr G A 8: 111,852,312 (GRCm39) V560I probably damaging Het
Pkdcc T C 17: 83,531,355 (GRCm39) F455L probably damaging Het
Potefam3c A T 8: 69,881,982 (GRCm39) D331E probably benign Het
Pus7l A T 15: 94,438,143 (GRCm39) F234Y probably damaging Het
Rab3gap2 T A 1: 184,990,722 (GRCm39) L632Q probably damaging Het
Rarb T A 14: 16,819,015 (GRCm38) probably benign Het
Ro60 T A 1: 143,641,517 (GRCm39) K315* probably null Het
Rom1 A T 19: 8,905,471 (GRCm39) H236Q possibly damaging Het
Secisbp2 T C 13: 51,819,352 (GRCm39) S311P probably benign Het
Slc26a1 T C 5: 108,820,182 (GRCm39) D355G probably benign Het
Slc28a3 C T 13: 58,707,077 (GRCm39) A574T probably damaging Het
Sox11 A G 12: 27,392,313 (GRCm39) V32A possibly damaging Het
Spata17 T C 1: 186,915,436 (GRCm39) Y107C probably damaging Het
Speer1a C A 5: 11,394,205 (GRCm39) Y104* probably null Het
Stxbp5l T C 16: 37,024,814 (GRCm39) T595A probably benign Het
Syt11 T C 3: 88,655,149 (GRCm39) D78G probably damaging Het
Tatdn2 T G 6: 113,684,348 (GRCm39) I674S probably damaging Het
Tex14 T A 11: 87,383,878 (GRCm39) S189R probably benign Het
Tln2 C A 9: 67,128,693 (GRCm39) E1465D possibly damaging Het
Tor3a T C 1: 156,483,373 (GRCm39) T350A probably benign Het
Ttr T G 18: 20,799,550 (GRCm39) V36G probably damaging Het
Vmn1r129 A T 7: 21,095,205 (GRCm39) H4Q probably null Het
Vmn1r32 A G 6: 66,530,623 (GRCm39) M51T possibly damaging Het
Zfp141 T C 7: 42,125,687 (GRCm39) T262A possibly damaging Het
Zfp980 T A 4: 145,427,596 (GRCm39) N108K probably benign Het
Other mutations in Ifna13
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02748:Ifna13 APN 4 88,562,097 (GRCm39) missense probably damaging 0.99
R1691:Ifna13 UTSW 4 88,562,291 (GRCm39) missense probably benign 0.00
R1938:Ifna13 UTSW 4 88,562,412 (GRCm39) missense probably damaging 0.98
R1986:Ifna13 UTSW 4 88,562,588 (GRCm39) missense probably benign 0.00
R2279:Ifna13 UTSW 4 88,562,156 (GRCm39) missense probably benign 0.27
R2435:Ifna13 UTSW 4 88,562,366 (GRCm39) missense probably damaging 1.00
R2445:Ifna13 UTSW 4 88,562,133 (GRCm39) missense probably damaging 1.00
R4041:Ifna13 UTSW 4 88,562,228 (GRCm39) missense probably benign 0.00
R4612:Ifna13 UTSW 4 88,562,113 (GRCm39) missense probably damaging 1.00
R6271:Ifna13 UTSW 4 88,562,082 (GRCm39) missense possibly damaging 0.79
R8783:Ifna13 UTSW 4 88,562,526 (GRCm39) missense probably damaging 1.00
R9433:Ifna13 UTSW 4 88,562,540 (GRCm39) missense probably benign 0.08
RF009:Ifna13 UTSW 4 88,562,145 (GRCm39) missense probably damaging 1.00
Z1177:Ifna13 UTSW 4 88,562,615 (GRCm39) missense probably benign 0.26
Predicted Primers PCR Primer
(F):5'- GAAACATCTAGGCAGGTTGATTG -3'
(R):5'- ACTCATCTGCTGCATGGAATG -3'

Sequencing Primer
(F):5'- ACATCTAGGCAGGTTGATTGTATTC -3'
(R):5'- TGGAATGCAACCCTCCTAGACTC -3'
Posted On 2021-07-15