Incidental Mutation 'IGL02491:Zfp983'
ID 295669
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp983
Ensembl Gene ENSMUSG00000035868
Gene Name zinc finger protein 983
Synonyms 3110052M02Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.093) question?
Stock # IGL02491
Quality Score
Status
Chromosome 17
Chromosomal Location 21869545-21883882 bp(+) (GRCm39)
Type of Mutation critical splice donor site (1 bp from exon)
DNA Base Change (assembly) G to A at 21876528 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000039392 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039726]
AlphaFold E9PUT0
Predicted Effect probably null
Transcript: ENSMUST00000039726
SMART Domains Protein: ENSMUSP00000039392
Gene: ENSMUSG00000035868

DomainStartEndE-ValueType
KRAB 13 73 2.42e-22 SMART
ZnF_C2H2 185 207 5.5e-3 SMART
ZnF_C2H2 213 235 5.14e-3 SMART
ZnF_C2H2 241 263 4.54e-4 SMART
ZnF_C2H2 269 291 7.9e-4 SMART
ZnF_C2H2 297 319 2.86e-1 SMART
ZnF_C2H2 325 347 6.88e-4 SMART
ZnF_C2H2 353 375 1.95e-3 SMART
ZnF_C2H2 381 403 1.04e-3 SMART
ZnF_C2H2 409 431 2.79e-4 SMART
ZnF_C2H2 437 459 3.63e-3 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 55 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca6 T C 11: 110,067,794 (GRCm39) probably benign Het
Acacb T A 5: 114,330,166 (GRCm39) I443N probably damaging Het
C1qtnf3 A T 15: 10,972,067 (GRCm39) I118F possibly damaging Het
Carmil3 C T 14: 55,741,974 (GRCm39) A1148V probably benign Het
Ccdc62 A T 5: 124,099,378 (GRCm39) S677C probably damaging Het
Cdc45 C T 16: 18,617,479 (GRCm39) M200I probably benign Het
Col11a2 C A 17: 34,283,181 (GRCm39) probably benign Het
Cpsf7 A G 19: 10,517,001 (GRCm39) I368V possibly damaging Het
Csmd2 T C 4: 128,428,050 (GRCm39) S2934P probably benign Het
Csmd3 A G 15: 47,777,511 (GRCm39) probably benign Het
Cubn A G 2: 13,326,039 (GRCm39) Y2709H probably damaging Het
Cyp2d12 T A 15: 82,442,682 (GRCm39) L375Q possibly damaging Het
Etv4 A T 11: 101,674,791 (GRCm39) probably null Het
Exph5 T A 9: 53,286,343 (GRCm39) D1141E possibly damaging Het
Fbxo16 T A 14: 65,558,736 (GRCm39) H298Q probably benign Het
Fbxw21 T A 9: 108,972,887 (GRCm39) Y349F probably benign Het
Foxs1 G A 2: 152,774,721 (GRCm39) R111C probably damaging Het
Galnt15 T A 14: 31,778,273 (GRCm39) L436Q probably damaging Het
Gbf1 T C 19: 46,250,979 (GRCm39) probably benign Het
Gm8237 A T 14: 5,863,577 (GRCm38) C29* probably null Het
Hcn1 A G 13: 117,946,576 (GRCm39) D317G unknown Het
Itgam A G 7: 127,715,190 (GRCm39) N877D possibly damaging Het
Kcnma1 T C 14: 23,361,757 (GRCm39) R1047G probably damaging Het
Klhdc3 T C 17: 46,988,226 (GRCm39) R180G possibly damaging Het
Lpcat2 T C 8: 93,600,879 (GRCm39) V241A probably damaging Het
Mnat1 A G 12: 73,170,682 (GRCm39) N24S probably null Het
Mprip A G 11: 59,660,857 (GRCm39) T967A probably benign Het
Mtf1 T C 4: 124,732,372 (GRCm39) F477L probably benign Het
Naaladl1 A G 19: 6,159,748 (GRCm39) E393G possibly damaging Het
Or10ak7 A T 4: 118,791,358 (GRCm39) L229H probably damaging Het
Or2at1 A G 7: 99,416,540 (GRCm39) E57G possibly damaging Het
Or5e1 A G 7: 108,354,321 (GRCm39) K86R probably damaging Het
Pcdhb6 A T 18: 37,468,735 (GRCm39) D552V probably damaging Het
Pglyrp3 C T 3: 91,921,944 (GRCm39) S4F possibly damaging Het
Pramel13 A T 4: 144,121,322 (GRCm39) M234K probably damaging Het
Prss27 A T 17: 24,263,229 (GRCm39) probably benign Het
Slc5a9 A G 4: 111,753,549 (GRCm39) S51P probably damaging Het
Slc6a4 A G 11: 76,918,034 (GRCm39) Y592C probably damaging Het
Slc7a13 T A 4: 19,841,404 (GRCm39) V417D probably damaging Het
Spring1 T C 5: 118,397,160 (GRCm39) Y130H probably benign Het
Syne2 A G 12: 76,118,953 (GRCm39) T5857A probably benign Het
Thap1 A C 8: 26,650,885 (GRCm39) S52R probably damaging Het
Thsd4 T C 9: 59,907,301 (GRCm39) N158S probably damaging Het
Tmem147 A T 7: 30,427,626 (GRCm39) probably benign Het
Trdmt1 G A 2: 13,521,483 (GRCm39) A311V probably benign Het
U2surp T A 9: 95,372,273 (GRCm39) R296S probably damaging Het
Upf2 A G 2: 6,030,975 (GRCm39) D805G unknown Het
Usp34 T A 11: 23,382,630 (GRCm39) H2057Q probably damaging Het
Vmn2r110 T A 17: 20,816,400 (GRCm39) D41V probably damaging Het
Vmn2r16 T A 5: 109,487,703 (GRCm39) L192* probably null Het
Vnn3 T A 10: 23,741,816 (GRCm39) S374T probably benign Het
Wdr62 A C 7: 29,942,184 (GRCm39) D1089E probably benign Het
Xdh T A 17: 74,193,459 (GRCm39) D1279V probably damaging Het
Zfp13 C T 17: 23,795,072 (GRCm39) A493T probably benign Het
Zfp518b A G 5: 38,831,123 (GRCm39) I294T possibly damaging Het
Other mutations in Zfp983
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02492:Zfp983 APN 17 21,876,528 (GRCm39) critical splice donor site probably null
IGL03145:Zfp983 APN 17 21,877,924 (GRCm39) missense probably damaging 0.99
R0257:Zfp983 UTSW 17 21,880,356 (GRCm39) missense probably benign 0.35
R1518:Zfp983 UTSW 17 21,881,269 (GRCm39) missense probably damaging 1.00
R1925:Zfp983 UTSW 17 21,880,933 (GRCm39) missense probably damaging 1.00
R2504:Zfp983 UTSW 17 21,877,883 (GRCm39) missense probably damaging 1.00
R3701:Zfp983 UTSW 17 21,880,455 (GRCm39) missense probably damaging 1.00
R4308:Zfp983 UTSW 17 21,881,124 (GRCm39) missense probably benign 0.05
R5648:Zfp983 UTSW 17 21,877,947 (GRCm39) missense probably damaging 1.00
R6029:Zfp983 UTSW 17 21,881,401 (GRCm39) missense probably benign 0.03
R6188:Zfp983 UTSW 17 21,877,935 (GRCm39) missense probably damaging 1.00
R6662:Zfp983 UTSW 17 21,881,001 (GRCm39) missense probably damaging 1.00
R7313:Zfp983 UTSW 17 21,880,413 (GRCm39) missense probably damaging 0.97
R7361:Zfp983 UTSW 17 21,880,850 (GRCm39) missense probably damaging 1.00
R8710:Zfp983 UTSW 17 21,880,234 (GRCm39) missense probably damaging 0.99
R9153:Zfp983 UTSW 17 21,876,522 (GRCm39) missense probably benign 0.08
R9285:Zfp983 UTSW 17 21,876,520 (GRCm39) missense possibly damaging 0.76
Posted On 2015-04-16