Incidental Mutation 'R5547:Ifi44l'
ID 436334
Institutional Source Beutler Lab
Gene Symbol Ifi44l
Ensembl Gene ENSMUSG00000039146
Gene Name interferon-induced protein 44 like
Synonyms H-28, NS1178, H28
MMRRC Submission 043105-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # R5547 (G1)
Quality Score 225
Status Not validated
Chromosome 3
Chromosomal Location 151464374-151468528 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 151467142 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Isoleucine at position 63 (V63I)
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000046739
AA Change: V63I
SMART Domains Protein: ENSMUSP00000044765
Gene: ENSMUSG00000039146
AA Change: V63I

DomainStartEndE-ValueType
low complexity region 140 154 N/A INTRINSIC
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 94.8%
Validation Efficiency
MGI Phenotype FUNCTION: This gene encodes a minor histocompatibility antigen that is involved in tissue graft rejection and is polymorphic in different mouse strains. The 5' region of this gene, including the translational start codon and the first 293 amino acids, is absent from the C57BL/6J genome. The encoded antigen is not thought to be expressed in C57BL/6J. [provided by RefSeq, Mar 2013]
Allele List at MGI
Other mutations in this stock
Total: 47 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aldh7a1 A G 18: 56,661,356 (GRCm39) S492P probably damaging Het
Arfgef1 A T 1: 10,231,201 (GRCm39) D1133E probably damaging Het
Avpi1 T C 19: 42,113,382 (GRCm39) K25R probably damaging Het
Bank1 T C 3: 135,772,110 (GRCm39) S708G probably damaging Het
C1qtnf2 A G 11: 43,381,794 (GRCm39) E202G probably damaging Het
C6 T A 15: 4,837,970 (GRCm39) V860E probably benign Het
Cbr1 T A 16: 93,406,698 (GRCm39) V138E probably damaging Het
Cdip1 A G 16: 4,587,988 (GRCm39) S2P probably damaging Het
Cep126 T C 9: 8,100,428 (GRCm39) N702S probably damaging Het
Chek1 T C 9: 36,623,400 (GRCm39) I381V probably benign Het
Clock G A 5: 76,378,185 (GRCm39) P572S probably benign Het
Cryz C T 3: 154,317,194 (GRCm39) R138* probably null Het
Ctsll3 T A 13: 60,948,551 (GRCm39) M103L probably benign Het
Daxx TGATGATGACGATGATGACGATGATGA TGATGATGACGATGATGA 17: 34,131,615 (GRCm39) probably benign Het
Daxx CGATGATGATGA CGA 17: 34,131,633 (GRCm39) probably benign Het
Dsg1a T G 18: 20,469,097 (GRCm39) probably null Het
Eya4 T C 10: 22,985,753 (GRCm39) E583G possibly damaging Het
Flt1 T A 5: 147,591,948 (GRCm39) S505C probably damaging Het
Gpr161 C A 1: 165,133,982 (GRCm39) F81L possibly damaging Het
H2-T15 G A 17: 36,368,796 (GRCm39) H95Y possibly damaging Het
Hmcn1 A G 1: 150,613,257 (GRCm39) V1390A possibly damaging Het
Klhl3 C T 13: 58,250,243 (GRCm39) probably null Het
Lekr1 T A 3: 65,576,601 (GRCm39) probably null Het
Lhx5 A G 5: 120,572,675 (GRCm39) Q98R probably benign Het
Nuggc A G 14: 65,879,330 (GRCm39) K681E possibly damaging Het
Numa1 G T 7: 101,663,137 (GRCm39) A735S probably damaging Het
Oog3 A T 4: 143,884,598 (GRCm39) L446Q probably benign Het
Or5ac19 G A 16: 59,089,479 (GRCm39) L184F probably benign Het
Otogl C T 10: 107,617,909 (GRCm39) E1735K possibly damaging Het
Pcsk5 T C 19: 17,729,488 (GRCm39) D119G probably benign Het
Pgpep1 T C 8: 71,105,069 (GRCm39) K64E probably benign Het
Prr19 A C 7: 25,003,388 (GRCm39) D334A probably damaging Het
Ptprh G T 7: 4,557,221 (GRCm39) S691* probably null Het
Recql4 G A 15: 76,589,994 (GRCm39) R684* probably null Het
Rnf112 C T 11: 61,341,854 (GRCm39) V317I possibly damaging Het
Rnf40 T C 7: 127,188,302 (GRCm39) probably null Het
Secisbp2l C T 2: 125,582,657 (GRCm39) G933D possibly damaging Het
Spag17 T C 3: 99,963,468 (GRCm39) V1062A probably benign Het
Tbc1d1 A G 5: 64,481,887 (GRCm39) D696G possibly damaging Het
Tdo2 T C 3: 81,866,247 (GRCm39) R339G probably damaging Het
Tmem245 C T 4: 56,910,156 (GRCm39) probably null Het
Trim24 A G 6: 37,942,485 (GRCm39) E965G probably damaging Het
Trmt112 T C 19: 6,888,156 (GRCm39) S103P probably damaging Het
Trpv6 A T 6: 41,613,088 (GRCm39) V26D possibly damaging Het
Zfp850 A G 7: 27,688,844 (GRCm39) C455R probably damaging Het
Zfp946 T C 17: 22,673,873 (GRCm39) I209T probably benign Het
Zfp957 T C 14: 79,451,406 (GRCm39) N131S probably benign Het
Other mutations in Ifi44l
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02085:Ifi44l APN 3 151,468,477 (GRCm39) missense unknown
R0638:Ifi44l UTSW 3 151,468,396 (GRCm39) missense probably benign 0.13
R1729:Ifi44l UTSW 3 151,468,456 (GRCm39) missense unknown
R3087:Ifi44l UTSW 3 151,468,494 (GRCm39) missense unknown
R4229:Ifi44l UTSW 3 151,468,514 (GRCm39) nonsense probably null
R4230:Ifi44l UTSW 3 151,468,514 (GRCm39) nonsense probably null
R4812:Ifi44l UTSW 3 151,465,336 (GRCm39) missense probably benign 0.00
R6365:Ifi44l UTSW 3 151,467,142 (GRCm39) missense unknown
R7065:Ifi44l UTSW 3 151,465,429 (GRCm39) missense
R9796:Ifi44l UTSW 3 151,468,419 (GRCm39) missense
Predicted Primers PCR Primer
(F):5'- TGAACCCACCTTGACCTAATTC -3'
(R):5'- TGGTGCAGTAGCCATATTTCTCAC -3'

Sequencing Primer
(F):5'- ACACACACTAAGCTTGAGGAG -3'
(R):5'- ACCAAGTTTTCAGATTTACTGTGAG -3'
Posted On 2016-10-24