Incidental Mutation 'R5170:Zfp941'
ID 397504
Institutional Source Beutler Lab
Gene Symbol Zfp941
Ensembl Gene ENSMUSG00000060314
Gene Name zinc finger protein 941
Synonyms BC066028
MMRRC Submission 042750-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.068) question?
Stock # R5170 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 140807449-140822178 bp(-) (GRCm38)
Type of Mutation unclassified
DNA Base Change (assembly) G to A at 140812957 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147965 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080651] [ENSMUST00000106052] [ENSMUST00000150053]
AlphaFold Q3URY5
Predicted Effect unknown
Transcript: ENSMUST00000080651
AA Change: P163L
SMART Domains Protein: ENSMUSP00000079482
Gene: ENSMUSG00000060314
AA Change: P163L

DomainStartEndE-ValueType
KRAB 4 65 3.88e-21 SMART
ZnF_C2H2 339 361 1.26e-2 SMART
ZnF_C2H2 367 389 1.12e-3 SMART
ZnF_C2H2 395 417 7.78e-3 SMART
ZnF_C2H2 423 445 1.12e-3 SMART
ZnF_C2H2 451 471 1.16e1 SMART
ZnF_C2H2 500 522 2.57e-3 SMART
ZnF_C2H2 528 550 7.9e-4 SMART
ZnF_C2H2 556 578 6.42e-4 SMART
ZnF_C2H2 584 606 1.38e-3 SMART
ZnF_C2H2 612 634 3.69e-4 SMART
Predicted Effect unknown
Transcript: ENSMUST00000106052
AA Change: P163L
SMART Domains Protein: ENSMUSP00000101667
Gene: ENSMUSG00000060314
AA Change: P163L

DomainStartEndE-ValueType
KRAB 4 65 3.88e-21 SMART
ZnF_C2H2 339 361 1.26e-2 SMART
ZnF_C2H2 367 389 1.12e-3 SMART
ZnF_C2H2 395 417 7.78e-3 SMART
ZnF_C2H2 423 445 1.12e-3 SMART
ZnF_C2H2 451 471 1.16e1 SMART
ZnF_C2H2 500 522 2.57e-3 SMART
ZnF_C2H2 528 550 7.9e-4 SMART
ZnF_C2H2 556 578 6.42e-4 SMART
ZnF_C2H2 584 606 1.38e-3 SMART
ZnF_C2H2 612 634 3.69e-4 SMART
ZnF_C2H2 640 662 2.99e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000150053
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.3%
  • 20x: 95.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acox3 A G 5: 35,588,625 (GRCm38) I51V probably benign Het
Agbl2 A G 2: 90,803,197 (GRCm38) K559R probably benign Het
Arhgap30 A G 1: 171,408,050 (GRCm38) D664G probably benign Het
BC034090 A G 1: 155,213,650 (GRCm38) V798A probably damaging Het
Bdp1 A T 13: 100,030,794 (GRCm38) C2237* probably null Het
C3 C T 17: 57,223,938 (GRCm38) V388M probably damaging Het
Ccdc170 G A 10: 4,514,200 (GRCm38) E60K probably damaging Het
Cdh8 G A 8: 99,279,550 (GRCm38) T135M probably damaging Het
Cep131 G T 11: 120,070,609 (GRCm38) A572E probably damaging Het
Clec16a A G 16: 10,741,791 (GRCm38) Y976C probably benign Het
Dmpk C G 7: 19,088,019 (GRCm38) L301V probably benign Het
Eno3 A G 11: 70,662,214 (GRCm38) I393V probably benign Het
Fbxo47 A G 11: 97,857,694 (GRCm38) V305A probably benign Het
Fry G A 5: 150,429,854 (GRCm38) V1779M probably benign Het
Gm15293 A T 8: 21,201,680 (GRCm38) D26V probably damaging Het
Gtse1 T C 15: 85,864,264 (GRCm38) probably null Het
Gucy2e A T 11: 69,235,570 (GRCm38) L328Q probably damaging Het
Ifi207 T C 1: 173,730,498 (GRCm38) T225A unknown Het
Igkv4-80 A C 6: 69,016,665 (GRCm38) S81A probably benign Het
Lamc3 A T 2: 31,887,344 (GRCm38) M1L probably benign Het
Lman1l G A 9: 57,615,619 (GRCm38) R153* probably null Het
Myo16 A G 8: 10,569,745 (GRCm38) D1432G probably benign Het
Nwd2 A T 5: 63,806,037 (GRCm38) N988I probably damaging Het
Otx1 C A 11: 21,997,037 (GRCm38) A91S probably damaging Het
Parp14 T C 16: 35,857,279 (GRCm38) E773G probably benign Het
Psen1 T A 12: 83,714,862 (GRCm38) M146K probably damaging Het
Ptx4 G A 17: 25,123,178 (GRCm38) R209Q probably benign Het
Slc13a2 T C 11: 78,400,808 (GRCm38) T340A probably damaging Het
St8sia1 T C 6: 142,963,708 (GRCm38) K21E probably damaging Het
Stxbp1 T C 2: 32,794,674 (GRCm38) D581G probably benign Het
Sumo2 G A 11: 115,534,660 (GRCm38) probably benign Het
Supt5 G A 7: 28,316,083 (GRCm38) P910S probably benign Het
Tbc1d30 T C 10: 121,306,838 (GRCm38) Q158R possibly damaging Het
Tenm2 T A 11: 36,024,806 (GRCm38) H1968L probably damaging Het
Trmt1 T C 8: 84,695,232 (GRCm38) Y220H probably damaging Het
Trp73 C T 4: 154,104,838 (GRCm38) E60K possibly damaging Het
Ttn A G 2: 76,787,069 (GRCm38) Y8026H probably damaging Het
Zar1l A G 5: 150,517,585 (GRCm38) probably null Het
Zfp740 T C 15: 102,209,205 (GRCm38) Y117H probably damaging Het
Zp1 C A 19: 10,920,554 (GRCm38) V8F possibly damaging Het
Other mutations in Zfp941
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01393:Zfp941 APN 7 140,811,928 (GRCm38) missense probably damaging 1.00
IGL02399:Zfp941 APN 7 140,812,699 (GRCm38) missense probably benign 0.37
IGL03202:Zfp941 APN 7 140,813,053 (GRCm38) missense probably benign 0.02
R0025:Zfp941 UTSW 7 140,813,272 (GRCm38) missense probably benign 0.01
R0025:Zfp941 UTSW 7 140,813,272 (GRCm38) missense probably benign 0.01
R0226:Zfp941 UTSW 7 140,813,275 (GRCm38) missense probably damaging 1.00
R0945:Zfp941 UTSW 7 140,811,664 (GRCm38) missense probably damaging 0.99
R1455:Zfp941 UTSW 7 140,812,774 (GRCm38) missense probably benign 0.29
R1581:Zfp941 UTSW 7 140,812,120 (GRCm38) missense probably benign 0.03
R2474:Zfp941 UTSW 7 140,811,471 (GRCm38) missense probably damaging 1.00
R4052:Zfp941 UTSW 7 140,812,427 (GRCm38) missense possibly damaging 0.81
R4576:Zfp941 UTSW 7 140,811,590 (GRCm38) nonsense probably null
R4604:Zfp941 UTSW 7 140,812,211 (GRCm38) missense probably damaging 1.00
R5311:Zfp941 UTSW 7 140,811,959 (GRCm38) nonsense probably null
R5505:Zfp941 UTSW 7 140,811,917 (GRCm38) missense probably benign 0.03
R5549:Zfp941 UTSW 7 140,808,108 (GRCm38) missense possibly damaging 0.46
R5566:Zfp941 UTSW 7 140,812,766 (GRCm38) missense probably benign 0.01
R5723:Zfp941 UTSW 7 140,812,850 (GRCm38) unclassified probably benign
R5736:Zfp941 UTSW 7 140,813,060 (GRCm38) missense probably benign 0.01
R5861:Zfp941 UTSW 7 140,812,139 (GRCm38) missense probably damaging 1.00
R6041:Zfp941 UTSW 7 140,812,245 (GRCm38) nonsense probably null
R6058:Zfp941 UTSW 7 140,812,097 (GRCm38) missense probably damaging 1.00
R6226:Zfp941 UTSW 7 140,812,485 (GRCm38) missense probably benign 0.01
R6488:Zfp941 UTSW 7 140,812,750 (GRCm38) missense probably benign 0.37
R6824:Zfp941 UTSW 7 140,812,699 (GRCm38) missense probably benign 0.37
R7356:Zfp941 UTSW 7 140,812,115 (GRCm38) missense possibly damaging 0.66
R7554:Zfp941 UTSW 7 140,812,057 (GRCm38) missense possibly damaging 0.69
Z1177:Zfp941 UTSW 7 140,812,186 (GRCm38) missense possibly damaging 0.53
Predicted Primers
Posted On 2016-07-06