Incidental Mutation 'R3087:Ifi44l'
ID 262857
Institutional Source Beutler Lab
Gene Symbol Ifi44l
Ensembl Gene ENSMUSG00000039146
Gene Name interferon-induced protein 44 like
Synonyms H-28, NS1178, H28
MMRRC Submission 040576-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # R3087 (G1)
Quality Score 225
Status Validated
Chromosome 3
Chromosomal Location 151464374-151468528 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 151468494 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Arginine at position 12 (H12R)
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect unknown
Transcript: ENSMUST00000046739
AA Change: H12R
SMART Domains Protein: ENSMUSP00000044765
Gene: ENSMUSG00000039146
AA Change: H12R

DomainStartEndE-ValueType
low complexity region 140 154 N/A INTRINSIC
Meta Mutation Damage Score 0.1293 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.1%
  • 20x: 94.6%
Validation Efficiency 97% (29/30)
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: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aknad1 C T 3: 108,664,179 (GRCm39) Q381* probably null Het
Arhgef39 C T 4: 43,497,581 (GRCm39) probably null Het
Cblif A T 19: 11,737,737 (GRCm39) K383* probably null Het
Ccdc85a G T 11: 28,342,857 (GRCm39) C113* probably null Het
Cdc16 T C 8: 13,809,004 (GRCm39) Y19H probably damaging Het
Ces2e T A 8: 105,657,347 (GRCm39) M289K probably benign Het
Cyp2u1 G A 3: 131,096,676 (GRCm39) A34V probably benign Het
Dkk2 A C 3: 131,791,900 (GRCm39) N36T probably damaging Het
Fam222a A G 5: 114,750,015 (GRCm39) S404G probably damaging Het
Fbll1 A T 11: 35,689,017 (GRCm39) V82E probably damaging Het
Flt3 A G 5: 147,284,856 (GRCm39) S754P probably benign Het
Fmo5 T C 3: 97,549,011 (GRCm39) W220R probably damaging Het
Gm7275 A G 16: 47,894,098 (GRCm39) noncoding transcript Het
Gmeb2 G T 2: 180,897,433 (GRCm39) probably benign Het
Itsn2 T C 12: 4,716,303 (GRCm39) Y1021H probably damaging Het
Map4 T C 9: 109,882,257 (GRCm39) S374P possibly damaging Het
Map4k4 A T 1: 40,060,242 (GRCm39) probably null Het
Mast4 G T 13: 102,990,434 (GRCm39) probably benign Het
Mdfic T A 6: 15,799,668 (GRCm39) L265H probably damaging Het
Pabpc2 A G 18: 39,907,319 (GRCm39) I195V probably benign Het
Pramel25 A G 4: 143,520,416 (GRCm39) D56G probably benign Het
Prdm1 T C 10: 44,322,823 (GRCm39) Y224C probably damaging Het
Spidr T C 16: 15,786,483 (GRCm39) Y420C probably damaging Het
Tlr6 A T 5: 65,111,668 (GRCm39) M413K probably damaging Het
Ttn T A 2: 76,585,168 (GRCm39) I22042F probably damaging Het
Vmn1r11 A C 6: 57,114,691 (GRCm39) K81N possibly damaging Het
Vmn2r107 G A 17: 20,580,607 (GRCm39) E515K probably benign Het
Vstm4 T C 14: 32,614,592 (GRCm39) V178A possibly damaging 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
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
R5547:Ifi44l UTSW 3 151,467,142 (GRCm39) missense unknown
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'- ACCTTTGCCAAAGTCCCAGG -3'
(R):5'- AGATCTTGGCAACCAGCTGG -3'

Sequencing Primer
(F):5'- AAAGTCCCAGGGCTTGTG -3'
(R):5'- CTGGGAAGAACCTTTAACTAAGC -3'
Posted On 2015-02-05