Incidental Mutation 'IGL02642:Amer3'
ID 301799
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Amer3
Ensembl Gene ENSMUSG00000045174
Gene Name APC membrane recruitment 3
Synonyms 9430069J07Rik, Fam123c
Accession Numbers
Essential gene? Probably non essential (E-score: 0.062) question?
Stock # IGL02642
Quality Score
Status
Chromosome 1
Chromosomal Location 34618738-34630025 bp(+) (GRCm39)
Type of Mutation utr 5 prime
DNA Base Change (assembly) A to G at 34625761 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000054748 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000052670]
AlphaFold Q6NS69
Predicted Effect probably benign
Transcript: ENSMUST00000052670
SMART Domains Protein: ENSMUSP00000054748
Gene: ENSMUSG00000045174

DomainStartEndE-ValueType
Pfam:WTX 138 444 1.6e-37 PFAM
low complexity region 506 523 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acadm T C 3: 153,644,720 (GRCm39) D68G probably damaging Het
Ankrd11 A G 8: 123,617,390 (GRCm39) L2133P probably damaging Het
Bcdin3d G T 15: 99,368,673 (GRCm39) H175Q probably damaging Het
Brd8 C A 18: 34,741,117 (GRCm39) probably benign Het
C1rl C A 6: 124,470,806 (GRCm39) T38N possibly damaging Het
Cd160 T C 3: 96,707,927 (GRCm39) T140A probably benign Het
Cdk16 T G X: 20,563,167 (GRCm39) D381E probably benign Het
Cpq G A 15: 33,381,546 (GRCm39) G303D probably damaging Het
Dmp1 T C 5: 104,359,536 (GRCm39) S71P probably damaging Het
Enc1 A C 13: 97,382,042 (GRCm39) D184A possibly damaging Het
Enkur T C 2: 21,199,198 (GRCm39) D112G probably benign Het
Esrra A T 19: 6,890,218 (GRCm39) V59E possibly damaging Het
F830016B08Rik A G 18: 60,433,058 (GRCm39) N47S probably benign Het
Fads1 T A 19: 10,163,785 (GRCm39) V189D probably damaging Het
Fam167a T A 14: 63,689,721 (GRCm39) I6N probably damaging Het
Fam98b A G 2: 117,090,793 (GRCm39) T164A probably benign Het
Fhip2a A G 19: 57,373,782 (GRCm39) N681D possibly damaging Het
Fryl T A 5: 73,252,809 (GRCm39) I953L probably benign Het
Gm10610 T A 7: 83,198,813 (GRCm39) noncoding transcript Het
Grik5 G T 7: 24,758,408 (GRCm39) N338K possibly damaging Het
Gstt2 A G 10: 75,668,652 (GRCm39) I72T probably benign Het
Gusb T C 5: 130,029,376 (GRCm39) probably null Het
Hccs A G X: 168,098,588 (GRCm39) probably benign Het
Hoxb4 A G 11: 96,211,050 (GRCm39) K217E probably damaging Het
Hpd C T 5: 123,319,503 (GRCm39) V22I possibly damaging Het
Ighv1-47 A G 12: 114,954,844 (GRCm39) Y79H probably damaging Het
Il7r C A 15: 9,513,133 (GRCm39) probably benign Het
Lama1 A T 17: 68,119,361 (GRCm39) M2613L probably benign Het
Lama2 G A 10: 27,343,269 (GRCm39) H68Y probably damaging Het
Lce1c C A 3: 92,587,845 (GRCm39) probably benign Het
Lmx1a G T 1: 167,672,192 (GRCm39) probably benign Het
Lrfn1 T C 7: 28,158,113 (GRCm39) probably benign Het
Lrriq1 T A 10: 103,057,322 (GRCm39) probably null Het
Mri1 A T 8: 84,983,702 (GRCm39) L63Q probably damaging Het
Mrps11 G T 7: 78,438,522 (GRCm39) probably null Het
Mtif2 C A 11: 29,494,395 (GRCm39) Q666K probably benign Het
Mtr A T 13: 12,210,118 (GRCm39) probably benign Het
Mug1 A G 6: 121,859,544 (GRCm39) N1181S probably benign Het
Myom1 A T 17: 71,408,093 (GRCm39) E1209V possibly damaging Het
Nhsl1 A G 10: 18,284,138 (GRCm39) I26M possibly damaging Het
Nlrp1a T A 11: 71,014,358 (GRCm39) K297N probably benign Het
Obox5 T C 7: 15,491,972 (GRCm39) V129A probably benign Het
Pex16 C T 2: 92,206,981 (GRCm39) A53V probably damaging Het
Pfpl T C 19: 12,407,107 (GRCm39) F453L probably damaging Het
Pip5k1b G T 19: 24,323,731 (GRCm39) H406N probably benign Het
Pip5k1c C A 10: 81,153,155 (GRCm39) probably null Het
Plcxd3 T C 15: 4,546,122 (GRCm39) F42S possibly damaging Het
Pnpla7 T C 2: 24,940,288 (GRCm39) F1056L probably benign Het
Rapgef1 T C 2: 29,590,872 (GRCm39) probably benign Het
Rdh11 G A 12: 79,232,110 (GRCm39) probably benign Het
Serac1 A G 17: 6,096,021 (GRCm39) F576S possibly damaging Het
Slc45a4 A T 15: 73,458,664 (GRCm39) M295K probably benign Het
Taf1c T C 8: 120,325,796 (GRCm39) T689A probably benign Het
Timm10b G T 7: 105,317,645 (GRCm39) probably benign Het
Tle5 A T 10: 81,397,126 (GRCm39) Q34L possibly damaging Het
Tnc A T 4: 63,883,816 (GRCm39) probably benign Het
Toporsl T C 4: 52,611,114 (GRCm39) W336R probably benign Het
Usp54 C A 14: 20,615,140 (GRCm39) probably benign Het
Vmn1r233 T C 17: 21,214,291 (GRCm39) R220G probably damaging Het
Other mutations in Amer3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00494:Amer3 APN 1 34,627,608 (GRCm39) missense probably benign 0.26
IGL01062:Amer3 APN 1 34,625,820 (GRCm39) missense probably damaging 0.96
IGL01501:Amer3 APN 1 34,627,398 (GRCm39) missense probably benign
IGL02861:Amer3 APN 1 34,627,206 (GRCm39) missense probably damaging 1.00
IGL02953:Amer3 APN 1 34,626,877 (GRCm39) missense probably damaging 0.98
R0183:Amer3 UTSW 1 34,626,838 (GRCm39) missense probably damaging 0.99
R0335:Amer3 UTSW 1 34,618,381 (GRCm39) unclassified probably benign
R0639:Amer3 UTSW 1 34,626,902 (GRCm39) nonsense probably null
R1391:Amer3 UTSW 1 34,627,470 (GRCm39) missense probably benign 0.09
R1514:Amer3 UTSW 1 34,618,408 (GRCm39) unclassified probably benign
R1615:Amer3 UTSW 1 34,627,252 (GRCm39) missense probably damaging 0.99
R2014:Amer3 UTSW 1 34,618,525 (GRCm39) unclassified probably benign
R2104:Amer3 UTSW 1 34,627,759 (GRCm39) missense probably benign 0.00
R3080:Amer3 UTSW 1 34,627,503 (GRCm39) missense probably benign 0.23
R4508:Amer3 UTSW 1 34,627,380 (GRCm39) missense probably benign 0.00
R4635:Amer3 UTSW 1 34,626,958 (GRCm39) missense probably damaging 1.00
R4978:Amer3 UTSW 1 34,618,381 (GRCm39) unclassified probably benign
R4990:Amer3 UTSW 1 34,627,822 (GRCm39) missense probably benign 0.17
R4991:Amer3 UTSW 1 34,627,822 (GRCm39) missense probably benign 0.17
R5112:Amer3 UTSW 1 34,626,157 (GRCm39) missense possibly damaging 0.94
R5645:Amer3 UTSW 1 34,627,462 (GRCm39) missense possibly damaging 0.76
R6483:Amer3 UTSW 1 34,626,771 (GRCm39) missense probably damaging 0.97
R6769:Amer3 UTSW 1 34,627,330 (GRCm39) missense possibly damaging 0.93
R7097:Amer3 UTSW 1 34,627,869 (GRCm39) missense probably benign
R7246:Amer3 UTSW 1 34,625,809 (GRCm39) missense possibly damaging 0.82
R7347:Amer3 UTSW 1 34,626,983 (GRCm39) missense probably damaging 1.00
R7466:Amer3 UTSW 1 34,627,074 (GRCm39) missense probably damaging 1.00
R7719:Amer3 UTSW 1 34,628,083 (GRCm39) missense possibly damaging 0.55
R8158:Amer3 UTSW 1 34,626,741 (GRCm39) missense possibly damaging 0.68
R8862:Amer3 UTSW 1 34,626,465 (GRCm39) missense probably damaging 1.00
R9028:Amer3 UTSW 1 34,627,758 (GRCm39) missense probably benign 0.28
R9287:Amer3 UTSW 1 34,627,900 (GRCm39) missense possibly damaging 0.69
R9567:Amer3 UTSW 1 34,627,836 (GRCm39) missense probably benign 0.09
R9620:Amer3 UTSW 1 34,628,043 (GRCm39) missense probably benign 0.09
RF016:Amer3 UTSW 1 34,626,201 (GRCm39) missense probably damaging 1.00
X0020:Amer3 UTSW 1 34,627,917 (GRCm39) missense probably benign 0.00
Z1176:Amer3 UTSW 1 34,628,094 (GRCm39) missense probably benign
Z1177:Amer3 UTSW 1 34,626,277 (GRCm39) nonsense probably null
Posted On 2015-04-16