Incidental Mutation 'R6491:Zfp938'
ID 522883
Institutional Source Beutler Lab
Gene Symbol Zfp938
Ensembl Gene ENSMUSG00000062931
Gene Name zinc finger protein 938
Synonyms B230315N10Rik
MMRRC Submission 044623-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.075) question?
Stock # R6491 (G1)
Quality Score 225.009
Status Validated
Chromosome 10
Chromosomal Location 82060684-82077114 bp(-) (GRCm39)
Type of Mutation makesense
DNA Base Change (assembly) A to G at 82063363 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Stop codon to Glutamine at position 65 (*65Q)
Ref Sequence ENSEMBL: ENSMUSP00000121613 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000041264] [ENSMUST00000041264] [ENSMUST00000156218]
AlphaFold E9Q9G3
Predicted Effect probably null
Transcript: ENSMUST00000041264
SMART Domains Protein: ENSMUSP00000047110
Gene: ENSMUSG00000062931

DomainStartEndE-ValueType
KRAB 4 64 5.28e-14 SMART
ZnF_C2H2 161 188 2.82e1 SMART
ZnF_C2H2 267 289 1.23e0 SMART
ZnF_C2H2 295 317 2.91e-2 SMART
ZnF_C2H2 323 345 2.4e-3 SMART
ZnF_C2H2 351 373 7.26e-3 SMART
ZnF_C2H2 379 401 4.65e-1 SMART
ZnF_C2H2 407 429 1.47e-3 SMART
ZnF_C2H2 435 457 5.59e-4 SMART
ZnF_C2H2 463 485 1.82e-3 SMART
ZnF_C2H2 491 513 3.63e-3 SMART
ZnF_C2H2 519 541 7.67e-2 SMART
ZnF_C2H2 547 569 2.4e-3 SMART
Predicted Effect probably null
Transcript: ENSMUST00000041264
SMART Domains Protein: ENSMUSP00000047110
Gene: ENSMUSG00000062931

DomainStartEndE-ValueType
KRAB 4 64 5.28e-14 SMART
ZnF_C2H2 161 188 2.82e1 SMART
ZnF_C2H2 267 289 1.23e0 SMART
ZnF_C2H2 295 317 2.91e-2 SMART
ZnF_C2H2 323 345 2.4e-3 SMART
ZnF_C2H2 351 373 7.26e-3 SMART
ZnF_C2H2 379 401 4.65e-1 SMART
ZnF_C2H2 407 429 1.47e-3 SMART
ZnF_C2H2 435 457 5.59e-4 SMART
ZnF_C2H2 463 485 1.82e-3 SMART
ZnF_C2H2 491 513 3.63e-3 SMART
ZnF_C2H2 519 541 7.67e-2 SMART
ZnF_C2H2 547 569 2.4e-3 SMART
Predicted Effect probably null
Transcript: ENSMUST00000156218
AA Change: *65Q
SMART Domains Protein: ENSMUSP00000121613
Gene: ENSMUSG00000062931
AA Change: *65Q

DomainStartEndE-ValueType
KRAB 4 64 5.28e-14 SMART
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.1%
  • 20x: 94.5%
Validation Efficiency 100% (35/35)
Allele List at MGI
Other mutations in this stock
Total: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4833420G17Rik T C 13: 119,612,508 (GRCm39) L431P probably damaging Het
Acad10 A C 5: 121,768,220 (GRCm39) W779G probably damaging Het
Acrbp A G 6: 125,028,442 (GRCm39) probably benign Het
Ank3 G A 10: 69,827,459 (GRCm39) A565T probably benign Het
Ap2a1 A T 7: 44,565,588 (GRCm39) I93K probably damaging Het
Arnt T A 3: 95,383,454 (GRCm39) M240K probably damaging Het
Ceacam12 A T 7: 17,803,185 (GRCm39) K197M probably damaging Het
Cep41 T C 6: 30,656,483 (GRCm39) N323S probably benign Het
Dst A G 1: 34,232,093 (GRCm39) T2904A probably benign Het
Eml1 G A 12: 108,479,330 (GRCm39) probably null Het
Fbln2 A G 6: 91,236,732 (GRCm39) N749S possibly damaging Het
Irf2bpl A G 12: 86,930,238 (GRCm39) V145A probably benign Het
Itga2b T C 11: 102,350,695 (GRCm39) probably null Het
Itga8 T C 2: 12,209,587 (GRCm39) D466G probably damaging Het
Kdm4c G T 4: 74,291,873 (GRCm39) C830F probably damaging Het
Mrps27 T C 13: 99,499,538 (GRCm39) S73P probably damaging Het
Mtdh T G 15: 34,116,473 (GRCm39) N17K probably damaging Het
Muc3a A G 5: 137,246,591 (GRCm39) S9P probably benign Het
Or8b46 A G 9: 38,558,751 (GRCm39) L23P probably damaging Het
Oxgr1 T A 14: 120,259,419 (GRCm39) I263F probably benign Het
Phc1 A G 6: 122,311,923 (GRCm39) Het
Ppp2r5d A G 17: 46,996,509 (GRCm39) F388S probably damaging Het
Pxmp4 A G 2: 154,434,083 (GRCm39) probably null Het
Rnd2 C T 11: 101,359,825 (GRCm39) L57F probably damaging Het
Ror1 A G 4: 100,267,109 (GRCm39) N270S possibly damaging Het
Slc7a14 T C 3: 31,278,093 (GRCm39) Y504C probably damaging Het
Snx9 A G 17: 5,970,437 (GRCm39) D391G probably benign Het
St18 T A 1: 6,898,209 (GRCm39) Y670* probably null Het
Tjp1 A T 7: 64,986,865 (GRCm39) F207I possibly damaging Het
Trappc3 A G 4: 126,169,022 (GRCm39) I171V probably benign Het
Ugt2b5 A T 5: 87,273,328 (GRCm39) L446* probably null Het
Vmn2r105 A T 17: 20,447,992 (GRCm39) Y277* probably null Het
Vmn2r11 A T 5: 109,196,800 (GRCm39) N557K possibly damaging Het
Yod1 G A 1: 130,645,275 (GRCm39) G19S probably damaging Het
Other mutations in Zfp938
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00659:Zfp938 APN 10 82,063,355 (GRCm39) utr 3 prime probably benign
IGL00743:Zfp938 APN 10 82,062,317 (GRCm39) missense probably benign
IGL01764:Zfp938 APN 10 82,063,624 (GRCm39) splice site probably benign
IGL01814:Zfp938 APN 10 82,062,052 (GRCm39) missense probably benign
IGL02244:Zfp938 APN 10 82,061,906 (GRCm39) missense possibly damaging 0.86
IGL02865:Zfp938 APN 10 82,062,026 (GRCm39) missense probably benign 0.33
R0372:Zfp938 UTSW 10 82,063,662 (GRCm39) missense probably damaging 1.00
R0666:Zfp938 UTSW 10 82,061,606 (GRCm39) missense probably damaging 1.00
R0964:Zfp938 UTSW 10 82,061,253 (GRCm39) missense probably benign 0.00
R1453:Zfp938 UTSW 10 82,063,632 (GRCm39) critical splice donor site probably null
R1672:Zfp938 UTSW 10 82,060,982 (GRCm39) missense probably benign
R1929:Zfp938 UTSW 10 82,061,381 (GRCm39) missense probably damaging 1.00
R1959:Zfp938 UTSW 10 82,061,465 (GRCm39) missense probably damaging 1.00
R2127:Zfp938 UTSW 10 82,061,876 (GRCm39) missense probably benign
R2271:Zfp938 UTSW 10 82,061,381 (GRCm39) missense probably damaging 1.00
R2900:Zfp938 UTSW 10 82,061,340 (GRCm39) missense possibly damaging 0.92
R4502:Zfp938 UTSW 10 82,062,105 (GRCm39) missense possibly damaging 0.73
R4503:Zfp938 UTSW 10 82,062,105 (GRCm39) missense possibly damaging 0.73
R4886:Zfp938 UTSW 10 82,061,957 (GRCm39) missense probably benign 0.33
R4934:Zfp938 UTSW 10 82,062,012 (GRCm39) missense possibly damaging 0.86
R5174:Zfp938 UTSW 10 82,061,838 (GRCm39) missense possibly damaging 0.53
R5410:Zfp938 UTSW 10 82,061,092 (GRCm39) missense possibly damaging 0.89
R6284:Zfp938 UTSW 10 82,063,400 (GRCm39) missense possibly damaging 0.73
R6575:Zfp938 UTSW 10 82,061,160 (GRCm39) nonsense probably null
R6649:Zfp938 UTSW 10 82,061,232 (GRCm39) missense probably damaging 0.99
R7992:Zfp938 UTSW 10 82,061,777 (GRCm39) missense possibly damaging 0.53
R8211:Zfp938 UTSW 10 82,062,419 (GRCm39) missense possibly damaging 0.53
R8313:Zfp938 UTSW 10 82,061,422 (GRCm39) missense possibly damaging 0.75
R8963:Zfp938 UTSW 10 82,061,287 (GRCm39) missense possibly damaging 0.61
X0066:Zfp938 UTSW 10 82,061,931 (GRCm39) missense probably benign 0.33
Predicted Primers PCR Primer
(F):5'- CCATCTCTGGGCTGGTAGTCT -3'
(R):5'- CAAACCTTTCTTAGAAATGAGTGCTC -3'

Sequencing Primer
(F):5'- ACTTCCTTTGGTGATGAACAGC -3'
(R):5'- CTTTCTTAGAAATGAGTGCTCTTCTG -3'
Posted On 2018-06-06