Incidental Mutation 'IGL02962:Ear10'
ID365376
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ear10
Ensembl Gene ENSMUSG00000090166
Gene Nameeosinophil-associated, ribonuclease A family, member 10
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.149) question?
Stock #IGL02962
Quality Score
Status
Chromosome14
Chromosomal Location43922720-43923559 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 43923317 bp
ZygosityHeterozygous
Amino Acid Change Leucine to Isoleucine at position 18 (L18I)
Ref Sequence ENSEMBL: ENSMUSP00000130933 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000159175] [ENSMUST00000160298] [ENSMUST00000163652]
Predicted Effect probably damaging
Transcript: ENSMUST00000159175
AA Change: L18I

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000123872
Gene: ENSMUSG00000090166
AA Change: L18I

DomainStartEndE-ValueType
low complexity region 5 22 N/A INTRINSIC
RNAse_Pc 27 156 9.52e-58 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000160298
SMART Domains Protein: ENSMUSP00000125038
Gene: ENSMUSG00000089901

DomainStartEndE-ValueType
transmembrane domain 12 34 N/A INTRINSIC
low complexity region 365 404 N/A INTRINSIC
transmembrane domain 530 552 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000163652
AA Change: L18I

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000130933
Gene: ENSMUSG00000090166
AA Change: L18I

DomainStartEndE-ValueType
low complexity region 5 22 N/A INTRINSIC
RNAse_Pc 27 156 9.52e-58 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017N19Rik T A 10: 100,610,593 probably null Het
9530068E07Rik T C 11: 52,403,535 V209A possibly damaging Het
Abca3 T A 17: 24,400,409 V907E probably damaging Het
Acvrl1 T C 15: 101,135,501 Y90H probably benign Het
Aff3 T C 1: 38,535,656 D81G probably damaging Het
Amn G T 12: 111,274,517 V152L probably damaging Het
Arhgap44 A G 11: 65,067,161 probably benign Het
Atad5 T A 11: 80,108,579 V895D possibly damaging Het
Card9 T G 2: 26,358,017 probably null Het
Ccer1 T C 10: 97,693,840 S122P unknown Het
Ccr2 A G 9: 124,105,675 probably benign Het
Dsg1a T A 18: 20,340,324 I818N possibly damaging Het
Gm13089 T A 4: 143,697,340 E293V probably benign Het
Mertk A G 2: 128,777,454 Y544C probably damaging Het
Miga1 A T 3: 152,285,341 probably benign Het
Myo18a T C 11: 77,778,235 V307A probably damaging Het
Olfr1354 T A 10: 78,916,939 L33H probably damaging Het
Olfr488 A T 7: 108,255,703 I145N possibly damaging Het
Pou2f3 T C 9: 43,125,089 probably benign Het
Prickle2 A C 6: 92,376,422 S744A probably benign Het
Prkcb T A 7: 122,425,047 probably null Het
Prkd2 A G 7: 16,869,832 T813A probably benign Het
Prkra G A 2: 76,633,547 T257M probably damaging Het
Rbm18 C T 2: 36,122,874 R102Q probably damaging Het
Rbsn A G 6: 92,190,326 S446P probably benign Het
Rpgrip1l A T 8: 91,270,362 V28D possibly damaging Het
Sdccag8 A T 1: 176,948,362 K613I probably damaging Het
Serbp1 G A 6: 67,267,119 G8D probably damaging Het
Slc6a2 T A 8: 92,972,762 Y139* probably null Het
Slc7a2 T A 8: 40,905,584 F321L probably damaging Het
Slco1b2 G A 6: 141,648,553 S48N probably damaging Het
Ssbp2 G T 13: 91,642,371 V118L possibly damaging Het
Sugp1 T A 8: 70,059,862 probably benign Het
Taar5 C A 10: 23,970,985 R94S possibly damaging Het
Tgs1 G T 4: 3,586,181 A353S probably benign Het
Trav1 A G 14: 52,428,642 E32G probably damaging Het
Trp53bp2 T C 1: 182,431,595 V71A probably benign Het
Vmn2r50 T C 7: 10,050,325 Y74C probably damaging Het
Wars A T 12: 108,875,780 M147K probably damaging Het
Other mutations in Ear10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01866:Ear10 APN 14 43923328 missense probably damaging 0.99
IGL02867:Ear10 APN 14 43923269 missense probably damaging 0.99
IGL02889:Ear10 APN 14 43923269 missense probably damaging 0.99
R0636:Ear10 UTSW 14 43922994 synonymous probably null
R1924:Ear10 UTSW 14 43922900 makesense probably null
R4289:Ear10 UTSW 14 43922947 missense probably benign 0.00
R6351:Ear10 UTSW 14 43923055 missense probably damaging 1.00
Posted On2015-12-18