Incidental Mutation 'IGL02259:Ang6'
ID 286661
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ang6
Ensembl Gene ENSMUSG00000072598
Gene Name angiogenin, ribonuclease A family, member 6
Synonyms EG630952
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02259
Quality Score
Status
Chromosome 14
Chromosomal Location 44239121-44243875 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 44239363 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Phenylalanine to Leucine at position 122 (F122L)
Ref Sequence ENSEMBL: ENSMUSP00000094632 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000096869] [ENSMUST00000160223]
AlphaFold Q5GAN0
Predicted Effect probably benign
Transcript: ENSMUST00000096869
AA Change: F122L

PolyPhen 2 Score 0.251 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000094632
Gene: ENSMUSG00000072598
AA Change: F122L

DomainStartEndE-ValueType
low complexity region 7 20 N/A INTRINSIC
RNAse_Pc 26 144 3.87e-49 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000160223
SMART Domains Protein: ENSMUSP00000125045
Gene: ENSMUSG00000072598

DomainStartEndE-ValueType
low complexity region 7 20 N/A INTRINSIC
RNAse_Pc 26 144 3.87e-49 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Atm A T 9: 53,429,794 (GRCm39) probably benign Het
Ccsap G A 8: 124,572,166 (GRCm39) T112M possibly damaging Het
Cd63 T C 10: 128,747,843 (GRCm39) S113P probably benign Het
Cntnap5c T C 17: 58,341,857 (GRCm39) F183L probably damaging Het
Cux1 T A 5: 136,355,687 (GRCm39) S321C probably damaging Het
Cyp2ab1 G A 16: 20,131,897 (GRCm39) T281I probably damaging Het
Cyp2c40 A C 19: 39,792,246 (GRCm39) C233G probably benign Het
Dnah8 T C 17: 30,978,588 (GRCm39) I2955T probably benign Het
Drc7 A G 8: 95,782,733 (GRCm39) T33A probably benign Het
Gigyf2 T A 1: 87,339,559 (GRCm39) Y481N probably damaging Het
Gsap A T 5: 21,391,398 (GRCm39) E13V probably benign Het
Ifna4 A G 4: 88,760,293 (GRCm39) K66E probably damaging Het
Kif14 T A 1: 136,427,840 (GRCm39) M1103K probably benign Het
Kif6 A T 17: 50,202,919 (GRCm39) probably benign Het
Lsm14a G T 7: 34,070,558 (GRCm39) P113T probably damaging Het
Med12l T A 3: 59,153,264 (GRCm39) N1096K probably damaging Het
Med13 C A 11: 86,248,327 (GRCm39) G9W possibly damaging Het
Minar1 A T 9: 89,484,412 (GRCm39) H328Q possibly damaging Het
Nbr1 G A 11: 101,468,816 (GRCm39) A639T probably damaging Het
Nid2 G T 14: 19,818,277 (GRCm39) probably null Het
Numa1 A G 7: 101,636,955 (GRCm39) D22G possibly damaging Het
Or13p10 G A 4: 118,523,634 (GRCm39) V307I probably benign Het
Or2n1 G T 17: 38,486,577 (GRCm39) V201L probably benign Het
Phkg2 A G 7: 127,181,458 (GRCm39) probably benign Het
Plcb4 T C 2: 135,752,166 (GRCm39) probably null Het
Plch1 C T 3: 63,630,170 (GRCm39) probably null Het
Prb1b A T 6: 132,289,637 (GRCm39) D62E unknown Het
Prl8a1 A C 13: 27,766,089 (GRCm39) V2G probably benign Het
Spata31 T C 13: 65,069,297 (GRCm39) S482P possibly damaging Het
Tbc1d4 A G 14: 101,703,166 (GRCm39) C760R probably damaging Het
Tgs1 A G 4: 3,604,743 (GRCm39) N722D probably damaging Het
Tmcc2 T C 1: 132,288,898 (GRCm39) D28G probably benign Het
Zfp457 C T 13: 67,444,471 (GRCm39) A11T possibly damaging Het
Zfp879 T C 11: 50,729,255 (GRCm39) S48G probably benign Het
Other mutations in Ang6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00577:Ang6 APN 14 44,239,458 (GRCm39) missense probably benign 0.36
IGL02589:Ang6 APN 14 44,239,419 (GRCm39) missense possibly damaging 0.92
R1844:Ang6 UTSW 14 44,239,330 (GRCm39) missense possibly damaging 0.87
R1926:Ang6 UTSW 14 44,239,695 (GRCm39) missense possibly damaging 0.91
R7545:Ang6 UTSW 14 44,239,636 (GRCm39) missense probably benign 0.00
R8483:Ang6 UTSW 14 44,239,285 (GRCm39) makesense probably null
R9210:Ang6 UTSW 14 44,239,407 (GRCm39) missense probably benign 0.10
Posted On 2015-04-16