Incidental Mutation 'IGL01402:Dpy19l4'
ID 278379
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Dpy19l4
Ensembl Gene ENSMUSG00000045205
Gene Name dpy-19 like 4
Synonyms Narg3, LOC381510
Accession Numbers
Essential gene? Probably non essential (E-score: 0.105) question?
Stock # IGL01402
Quality Score
Status
Chromosome 4
Chromosomal Location 11261315-11322137 bp(-) (GRCm39)
Type of Mutation critical splice donor site (1 bp from exon)
DNA Base Change (assembly) C to A at 11273006 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000115537 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000084892] [ENSMUST00000128024] [ENSMUST00000139385]
AlphaFold A2AJQ3
Predicted Effect probably null
Transcript: ENSMUST00000084892
SMART Domains Protein: ENSMUSP00000081954
Gene: ENSMUSG00000045205

DomainStartEndE-ValueType
Pfam:Dpy19 59 714 3e-213 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000128024
SMART Domains Protein: ENSMUSP00000122823
Gene: ENSMUSG00000045205

DomainStartEndE-ValueType
Pfam:Dpy19 58 293 1e-89 PFAM
Pfam:Dpy19 291 524 4.8e-51 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000139385
SMART Domains Protein: ENSMUSP00000115537
Gene: ENSMUSG00000045205

DomainStartEndE-ValueType
Pfam:Dpy19 1 258 3.2e-71 PFAM
Pfam:Dpy19 254 488 7e-70 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 65 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921524L21Rik T C 18: 6,638,653 (GRCm39) S351P possibly damaging Het
Abca2 T C 2: 25,332,015 (GRCm39) S1376P probably damaging Het
Ablim3 A G 18: 62,004,754 (GRCm39) Y12H probably damaging Het
Akr1b7 A G 6: 34,398,052 (GRCm39) R294G possibly damaging Het
Aldh3b1 A C 19: 3,971,205 (GRCm39) V153G probably benign Het
Alk A T 17: 72,181,173 (GRCm39) H1372Q probably damaging Het
Ano9 A C 7: 140,681,955 (GRCm39) Y731* probably null Het
Apol11b G A 15: 77,522,219 (GRCm39) T26M probably damaging Het
Asl T C 5: 130,048,645 (GRCm39) E43G probably damaging Het
Cd4 G A 6: 124,856,341 (GRCm39) T50I probably benign Het
Cfap43 T C 19: 47,784,105 (GRCm39) D476G probably benign Het
Cpa1 A G 6: 30,645,275 (GRCm39) H417R possibly damaging Het
Cpeb3 T C 19: 37,065,948 (GRCm39) D407G probably benign Het
Dcaf15 A T 8: 84,825,026 (GRCm39) C469S probably damaging Het
E4f1 A T 17: 24,663,208 (GRCm39) L699Q probably damaging Het
Eif4g2 A G 7: 110,676,234 (GRCm39) F349S possibly damaging Het
Ermap T C 4: 119,044,355 (GRCm39) Y147C probably damaging Het
Frk A C 10: 34,423,381 (GRCm39) E153A probably damaging Het
Fubp3 G A 2: 31,494,733 (GRCm39) probably null Het
Gdi2 A G 13: 3,614,611 (GRCm39) T319A probably benign Het
Gjc3 A G 5: 137,956,120 (GRCm39) F55S probably damaging Het
Gm10762 C T 2: 128,809,005 (GRCm39) probably benign Het
Got1 A G 19: 43,493,048 (GRCm39) I291T possibly damaging Het
Gpr179 C A 11: 97,229,012 (GRCm39) G1048* probably null Het
Hectd3 G T 4: 116,853,262 (GRCm39) R163L probably damaging Het
Hectd4 T C 5: 121,477,480 (GRCm39) probably benign Het
Ifnb1 T C 4: 88,440,480 (GRCm39) R178G probably benign Het
Ino80 T A 2: 119,287,199 (GRCm39) D56V possibly damaging Het
Kctd1 T A 18: 15,102,610 (GRCm39) Q857L probably damaging Het
Kdm5a T A 6: 120,367,640 (GRCm39) L445* probably null Het
Lins1 G A 7: 66,363,676 (GRCm39) V524I probably damaging Het
Lrp1 A T 10: 127,430,901 (GRCm39) Y383N probably damaging Het
Malrd1 G A 2: 16,106,768 (GRCm39) probably null Het
Mgam A C 6: 40,621,879 (GRCm39) K84Q probably benign Het
Mlh3 A T 12: 85,314,703 (GRCm39) F494L probably benign Het
Mpped1 T C 15: 83,676,414 (GRCm39) F60S possibly damaging Het
Myo1e A G 9: 70,245,048 (GRCm39) Y382C probably benign Het
Ncor1 C A 11: 62,231,300 (GRCm39) V836F probably damaging Het
Nktr G A 9: 121,570,218 (GRCm39) probably null Het
Or10al4 A G 17: 38,037,193 (GRCm39) T93A probably benign Het
Or4d5 A G 9: 40,012,558 (GRCm39) I76T probably benign Het
Or5k8 G A 16: 58,644,958 (GRCm39) T38I probably damaging Het
Rnf144a T A 12: 26,377,300 (GRCm39) Y93F probably benign Het
Rubcn G A 16: 32,647,666 (GRCm39) T636M probably damaging Het
Scn5a A C 9: 119,315,536 (GRCm39) L1724R probably damaging Het
Sel1l A G 12: 91,808,607 (GRCm39) S45P possibly damaging Het
Serpina3k A G 12: 104,306,882 (GRCm39) D38G probably benign Het
Sh3bgr A C 16: 96,007,690 (GRCm39) K18N probably damaging Het
Slc28a2 T G 2: 122,282,538 (GRCm39) I287M probably damaging Het
St8sia6 T C 2: 13,670,318 (GRCm39) N214S probably damaging Het
Syt11 A G 3: 88,669,523 (GRCm39) I123T probably benign Het
Tcerg1l A T 7: 137,861,568 (GRCm39) I387N probably damaging Het
Tfg C A 16: 56,514,856 (GRCm39) probably benign Het
Tgm4 A G 9: 122,880,519 (GRCm39) K307E possibly damaging Het
Tmem177 T C 1: 119,837,791 (GRCm39) D296G probably damaging Het
Tmem270 C T 5: 134,930,763 (GRCm39) probably benign Het
Tnrc6b G T 15: 80,764,745 (GRCm39) G749V possibly damaging Het
Trp63 C A 16: 25,639,135 (GRCm39) probably benign Het
Ugt1a8 T C 1: 88,015,617 (GRCm39) L10P probably benign Het
Vmn2r107 A T 17: 20,596,009 (GRCm39) K854M probably damaging Het
Vmn2r45 T C 7: 8,484,467 (GRCm39) N446S probably damaging Het
Vps13c A T 9: 67,820,486 (GRCm39) probably null Het
Wdr91 G A 6: 34,865,998 (GRCm39) P518L probably benign Het
Yap1 G A 9: 7,934,742 (GRCm39) probably benign Het
Zfp282 A C 6: 47,874,770 (GRCm39) D325A probably damaging Het
Other mutations in Dpy19l4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00479:Dpy19l4 APN 4 11,290,411 (GRCm39) missense probably benign 0.00
IGL01404:Dpy19l4 APN 4 11,273,006 (GRCm39) critical splice donor site probably null
IGL01643:Dpy19l4 APN 4 11,290,184 (GRCm39) splice site probably benign
IGL01758:Dpy19l4 APN 4 11,265,846 (GRCm39) missense probably damaging 1.00
IGL01896:Dpy19l4 APN 4 11,267,752 (GRCm39) missense possibly damaging 0.81
IGL02222:Dpy19l4 APN 4 11,281,116 (GRCm39) missense possibly damaging 0.93
IGL02314:Dpy19l4 APN 4 11,267,720 (GRCm39) missense possibly damaging 0.50
IGL02422:Dpy19l4 APN 4 11,265,803 (GRCm39) missense possibly damaging 0.95
IGL02565:Dpy19l4 APN 4 11,309,440 (GRCm39) missense probably benign 0.14
IGL03121:Dpy19l4 APN 4 11,303,334 (GRCm39) missense probably damaging 1.00
IGL03357:Dpy19l4 APN 4 11,267,615 (GRCm39) missense probably damaging 1.00
IGL03368:Dpy19l4 APN 4 11,290,253 (GRCm39) missense possibly damaging 0.53
R0003:Dpy19l4 UTSW 4 11,267,619 (GRCm39) missense probably damaging 1.00
R0481:Dpy19l4 UTSW 4 11,272,993 (GRCm39) splice site probably benign
R0506:Dpy19l4 UTSW 4 11,289,715 (GRCm39) missense probably benign 0.07
R1114:Dpy19l4 UTSW 4 11,287,643 (GRCm39) splice site probably benign
R1332:Dpy19l4 UTSW 4 11,276,901 (GRCm39) missense probably damaging 1.00
R1336:Dpy19l4 UTSW 4 11,276,901 (GRCm39) missense probably damaging 1.00
R1355:Dpy19l4 UTSW 4 11,303,371 (GRCm39) nonsense probably null
R1421:Dpy19l4 UTSW 4 11,304,011 (GRCm39) missense probably benign 0.09
R1422:Dpy19l4 UTSW 4 11,317,168 (GRCm39) missense possibly damaging 0.88
R1465:Dpy19l4 UTSW 4 11,296,034 (GRCm39) missense probably damaging 1.00
R1465:Dpy19l4 UTSW 4 11,296,034 (GRCm39) missense probably damaging 1.00
R1766:Dpy19l4 UTSW 4 11,303,360 (GRCm39) missense probably damaging 1.00
R1803:Dpy19l4 UTSW 4 11,281,020 (GRCm39) missense possibly damaging 0.81
R2090:Dpy19l4 UTSW 4 11,304,344 (GRCm39) missense probably benign 0.34
R2324:Dpy19l4 UTSW 4 11,276,857 (GRCm39) unclassified probably benign
R2446:Dpy19l4 UTSW 4 11,304,143 (GRCm39) splice site probably null
R3769:Dpy19l4 UTSW 4 11,276,868 (GRCm39) splice site probably null
R4151:Dpy19l4 UTSW 4 11,309,485 (GRCm39) missense possibly damaging 0.89
R4472:Dpy19l4 UTSW 4 11,304,053 (GRCm39) missense possibly damaging 0.91
R4609:Dpy19l4 UTSW 4 11,295,999 (GRCm39) nonsense probably null
R4708:Dpy19l4 UTSW 4 11,277,970 (GRCm39) missense probably benign 0.00
R4722:Dpy19l4 UTSW 4 11,290,521 (GRCm39) missense possibly damaging 0.84
R4997:Dpy19l4 UTSW 4 11,287,493 (GRCm39) missense probably benign 0.01
R5085:Dpy19l4 UTSW 4 11,265,943 (GRCm39) critical splice acceptor site probably null
R5088:Dpy19l4 UTSW 4 11,303,357 (GRCm39) missense probably damaging 1.00
R5288:Dpy19l4 UTSW 4 11,304,014 (GRCm39) missense probably damaging 1.00
R5288:Dpy19l4 UTSW 4 11,289,721 (GRCm39) missense probably damaging 1.00
R5413:Dpy19l4 UTSW 4 11,289,700 (GRCm39) missense probably damaging 1.00
R5758:Dpy19l4 UTSW 4 11,276,886 (GRCm39) missense probably damaging 1.00
R6024:Dpy19l4 UTSW 4 11,276,876 (GRCm39) missense probably damaging 1.00
R6312:Dpy19l4 UTSW 4 11,289,671 (GRCm39) nonsense probably null
R6339:Dpy19l4 UTSW 4 11,285,111 (GRCm39) missense probably damaging 0.98
R7055:Dpy19l4 UTSW 4 11,290,291 (GRCm39) critical splice acceptor site probably null
R7359:Dpy19l4 UTSW 4 11,273,125 (GRCm39) missense probably benign 0.00
R7525:Dpy19l4 UTSW 4 11,317,160 (GRCm39) nonsense probably null
R7579:Dpy19l4 UTSW 4 11,265,909 (GRCm39) missense probably benign 0.39
R7913:Dpy19l4 UTSW 4 11,265,859 (GRCm39) nonsense probably null
R8047:Dpy19l4 UTSW 4 11,317,139 (GRCm39) missense probably benign 0.00
R8049:Dpy19l4 UTSW 4 11,303,982 (GRCm39) missense probably benign 0.44
R8495:Dpy19l4 UTSW 4 11,267,659 (GRCm39) missense probably benign
R8911:Dpy19l4 UTSW 4 11,317,078 (GRCm39) missense possibly damaging 0.82
R8928:Dpy19l4 UTSW 4 11,304,674 (GRCm39) intron probably benign
R8955:Dpy19l4 UTSW 4 11,290,195 (GRCm39) missense probably benign 0.00
R9332:Dpy19l4 UTSW 4 11,304,298 (GRCm39) critical splice donor site probably null
R9372:Dpy19l4 UTSW 4 11,303,343 (GRCm39) missense possibly damaging 0.91
R9401:Dpy19l4 UTSW 4 11,265,806 (GRCm39) missense probably benign 0.29
Posted On 2015-04-16