Incidental Mutation 'R4038:Zfp931'
ID 359708
Institutional Source Beutler Lab
Gene Symbol Zfp931
Ensembl Gene ENSMUSG00000078861
Gene Name zinc finger protein 931
Synonyms 2810021G02Rik
MMRRC Submission 040965-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.113) question?
Stock # R4038 (G1)
Quality Score 30
Status Validated
Chromosome 2
Chromosomal Location 177709488-177720269 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 177709777 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamine to Leucine at position 203 (Q203L)
Ref Sequence ENSEMBL: ENSMUSP00000104552 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000108923] [ENSMUST00000108924] [ENSMUST00000131702]
AlphaFold A2AHM2
Predicted Effect probably benign
Transcript: ENSMUST00000108923
SMART Domains Protein: ENSMUSP00000104551
Gene: ENSMUSG00000078861

DomainStartEndE-ValueType
KRAB 4 64 2.27e-13 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000108924
AA Change: Q203L

PolyPhen 2 Score 0.529 (Sensitivity: 0.88; Specificity: 0.90)
SMART Domains Protein: ENSMUSP00000104552
Gene: ENSMUSG00000078861
AA Change: Q203L

DomainStartEndE-ValueType
KRAB 4 66 3.04e-14 SMART
ZnF_C2H2 78 97 2.63e2 SMART
ZnF_C2H2 103 125 1.2e-3 SMART
ZnF_C2H2 131 153 8.02e-5 SMART
ZnF_C2H2 159 181 2.12e-4 SMART
ZnF_C2H2 187 209 1.4e-4 SMART
ZnF_C2H2 215 237 2.99e-4 SMART
ZnF_C2H2 243 265 4.87e-4 SMART
ZnF_C2H2 271 293 7.49e-5 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000123265
Predicted Effect probably benign
Transcript: ENSMUST00000131702
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.4%
  • 10x: 96.7%
  • 20x: 93.1%
Validation Efficiency 93% (39/42)
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ate1 A G 7: 130,106,495 (GRCm39) S282P probably damaging Het
Cacna1d T A 14: 29,788,040 (GRCm39) Q1610L probably damaging Het
Carmil2 C A 8: 106,422,039 (GRCm39) R1103S probably damaging Het
Clca3a1 T A 3: 144,460,994 (GRCm39) Y219F probably benign Het
Creb3l3 A G 10: 80,925,172 (GRCm39) V224A probably benign Het
Crnkl1 T A 2: 145,774,247 (GRCm39) D72V possibly damaging Het
Dhcr24 T C 4: 106,431,075 (GRCm39) F255L probably benign Het
Eef2kmt A T 16: 5,063,135 (GRCm39) V335D probably damaging Het
Elp2 T A 18: 24,767,405 (GRCm39) W696R probably damaging Het
Glb1l3 A C 9: 26,740,343 (GRCm39) M329R probably damaging Het
Gm4787 A T 12: 81,425,132 (GRCm39) F342Y probably damaging Het
Gpr137c C A 14: 45,457,687 (GRCm39) L80I probably damaging Het
Gpr83 A G 9: 14,772,073 (GRCm39) I82V possibly damaging Het
Greb1l C T 18: 10,515,209 (GRCm39) T558I possibly damaging Het
Hnrnpul2 T A 19: 8,800,591 (GRCm39) probably benign Het
Hspa2 T C 12: 76,452,542 (GRCm39) V412A probably damaging Het
Iqcd T C 5: 120,740,587 (GRCm39) V306A probably damaging Het
Lmod3 T C 6: 97,225,275 (GRCm39) N182S probably benign Het
Metrn T C 17: 26,013,984 (GRCm39) T281A probably benign Het
Mid1-ps1 G A Y: 90,773,563 (GRCm39) noncoding transcript Het
Mmachc T A 4: 116,563,215 (GRCm39) T47S probably damaging Het
Nfia C A 4: 97,909,074 (GRCm39) R277S probably damaging Het
Or9m2 T A 2: 87,821,262 (GRCm39) I269N possibly damaging Het
Pcdha8 T C 18: 37,125,914 (GRCm39) M132T probably benign Het
Prkaa2 T C 4: 104,908,444 (GRCm39) N144D probably damaging Het
Ptprf C T 4: 118,114,805 (GRCm39) R150H probably damaging Het
Sfmbt1 T G 14: 30,509,449 (GRCm39) D309E probably damaging Het
Skint5 G T 4: 113,743,011 (GRCm39) T352K unknown Het
Slc16a10 G C 10: 39,932,620 (GRCm39) H314D possibly damaging Het
Slc28a2 C A 2: 122,284,996 (GRCm39) A328E probably benign Het
Ssc4d C A 5: 135,999,170 (GRCm39) W11L possibly damaging Het
Sycp2 C A 2: 178,022,720 (GRCm39) M470I possibly damaging Het
Tfap2c A T 2: 172,398,110 (GRCm39) S413C probably damaging Het
Unc13c A G 9: 73,441,188 (GRCm39) probably null Het
Vmn1r218 T C 13: 23,320,971 (GRCm39) V26A possibly damaging Het
Wipf3 G A 6: 54,458,813 (GRCm39) G56D probably damaging Het
Wiz T C 17: 32,578,198 (GRCm39) E429G probably damaging Het
Zer1 T C 2: 29,997,535 (GRCm39) N457S probably damaging Het
Other mutations in Zfp931
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02980:Zfp931 APN 2 177,711,409 (GRCm39) critical splice acceptor site probably null
R1391:Zfp931 UTSW 2 177,709,984 (GRCm39) missense probably benign 0.01
R1907:Zfp931 UTSW 2 177,711,684 (GRCm39) missense probably damaging 1.00
R2109:Zfp931 UTSW 2 177,711,651 (GRCm39) missense probably null 1.00
R2283:Zfp931 UTSW 2 177,711,714 (GRCm39) missense possibly damaging 0.93
R4039:Zfp931 UTSW 2 177,709,777 (GRCm39) missense possibly damaging 0.53
R4867:Zfp931 UTSW 2 177,709,855 (GRCm39) missense probably damaging 1.00
R4893:Zfp931 UTSW 2 177,709,996 (GRCm39) missense probably damaging 0.99
R5593:Zfp931 UTSW 2 177,709,595 (GRCm39) missense possibly damaging 0.47
R7295:Zfp931 UTSW 2 177,709,824 (GRCm39) nonsense probably null
R8050:Zfp931 UTSW 2 177,709,889 (GRCm39) missense probably damaging 1.00
R8069:Zfp931 UTSW 2 177,709,709 (GRCm39) missense probably benign 0.00
R8432:Zfp931 UTSW 2 177,711,346 (GRCm39) makesense probably null
R8806:Zfp931 UTSW 2 177,709,589 (GRCm39) missense possibly damaging 0.66
R8866:Zfp931 UTSW 2 177,710,178 (GRCm39) nonsense probably null
R8987:Zfp931 UTSW 2 177,709,592 (GRCm39) missense probably damaging 1.00
R8987:Zfp931 UTSW 2 177,709,591 (GRCm39) missense probably damaging 1.00
R9088:Zfp931 UTSW 2 177,709,594 (GRCm39) missense probably damaging 1.00
R9538:Zfp931 UTSW 2 177,709,605 (GRCm39) missense probably benign 0.04
Predicted Primers PCR Primer
(F):5'- GTGTGTAAAGACTATTGGTTTTCGA -3'
(R):5'- GAGTCATAGTCAAAGGCATGAAATA -3'

Sequencing Primer
(F):5'- CTGCAAAGGCTTTACCACATTGG -3'
(R):5'- GCTTTTAAAAGAAGGCGTGACCTCC -3'
Posted On 2015-12-08