Incidental Mutation 'IGL03075:Il1f10'
ID 417653
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Il1f10
Ensembl Gene ENSMUSG00000046845
Gene Name interleukin 1 family, member 10
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL03075
Quality Score
Status
Chromosome 2
Chromosomal Location 24181208-24183832 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 24183188 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Asparagine at position 44 (I44N)
Ref Sequence ENSEMBL: ENSMUSP00000063004 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000058056]
AlphaFold Q8R459
Predicted Effect possibly damaging
Transcript: ENSMUST00000058056
AA Change: I44N

PolyPhen 2 Score 0.791 (Sensitivity: 0.85; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000063004
Gene: ENSMUSG00000046845
AA Change: I44N

DomainStartEndE-ValueType
IL1 5 149 1.11e-21 SMART
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a member of the interleukin 1 cytokine family. This gene and eight other interleukin 1 family genes form a cytokine gene cluster on chromosome 2. This cytokine is thought to participate in a network of interleukin 1 family members to regulate adapted and innate immune responses. Two alternatively spliced transcript variants encoding the same protein have been reported. [provided by RefSeq, Jul 2008]
Allele List at MGI
Other mutations in this stock
Total: 32 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akr1c12 G A 13: 4,322,254 (GRCm39) R263C probably damaging Het
Axdnd1 A T 1: 156,223,012 (GRCm39) S217T probably damaging Het
Crtc3 G A 7: 80,254,151 (GRCm39) probably benign Het
Ctnna2 A T 6: 76,931,713 (GRCm39) M642K probably benign Het
Ddx56 A T 11: 6,211,632 (GRCm39) H491Q probably benign Het
Dvl1 A G 4: 155,939,040 (GRCm39) E208G probably damaging Het
Fam135a A G 1: 24,069,987 (GRCm39) probably benign Het
Gabpa T A 16: 84,649,495 (GRCm39) V234D possibly damaging Het
Gjb4 A G 4: 127,245,386 (GRCm39) V185A possibly damaging Het
Hlcs C T 16: 93,939,706 (GRCm39) A149T probably damaging Het
Itih4 A G 14: 30,614,240 (GRCm39) I397V probably benign Het
Kat6b C T 14: 21,711,638 (GRCm39) R820* probably null Het
Mmp17 T C 5: 129,672,138 (GRCm39) L137P probably damaging Het
Myh2 A G 11: 67,071,662 (GRCm39) N493S probably benign Het
Myo9b A T 8: 71,807,171 (GRCm39) Q1589L probably damaging Het
Or1e29 A T 11: 73,667,298 (GRCm39) L285Q probably damaging Het
Or5ac20 T A 16: 59,104,291 (GRCm39) T190S possibly damaging Het
Osbpl8 A G 10: 111,127,417 (GRCm39) I834V probably benign Het
P2ry12 A T 3: 59,125,579 (GRCm39) V32D probably damaging Het
Polg A G 7: 79,101,660 (GRCm39) V1052A probably damaging Het
Prss38 A C 11: 59,263,881 (GRCm39) V277G probably damaging Het
Rell2 G T 18: 38,090,734 (GRCm39) R137L probably damaging Het
Ro60 A C 1: 143,646,509 (GRCm39) S79A probably benign Het
Scara3 C T 14: 66,168,603 (GRCm39) R338H probably damaging Het
Skint4 T C 4: 111,944,239 (GRCm39) L17P probably damaging Het
Slco1a6 C T 6: 142,048,875 (GRCm39) probably benign Het
Smyd2 T A 1: 189,621,029 (GRCm39) I230F probably damaging Het
Sv2b G T 7: 74,786,068 (GRCm39) H451N probably benign Het
Tbpl2 A T 2: 23,961,997 (GRCm39) probably benign Het
Tmprss9 A G 10: 80,719,863 (GRCm39) D144G possibly damaging Het
Vwa8 T C 14: 79,171,196 (GRCm39) Y247H probably damaging Het
Zc3h15 T C 2: 83,492,535 (GRCm39) Y337H possibly damaging Het
Other mutations in Il1f10
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1857:Il1f10 UTSW 2 24,182,817 (GRCm39) missense possibly damaging 0.90
R7084:Il1f10 UTSW 2 24,183,682 (GRCm39) nonsense probably null
R7492:Il1f10 UTSW 2 24,182,829 (GRCm39) missense probably benign 0.08
R8158:Il1f10 UTSW 2 24,181,267 (GRCm39) missense possibly damaging 0.68
R8698:Il1f10 UTSW 2 24,183,197 (GRCm39) missense probably damaging 1.00
Posted On 2016-08-02