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: 0.066) question?
Stock # R5170 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 140387362-140402091 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) G to A at 140392870 bp (GRCm39)
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: 35,745,969 (GRCm39) I51V probably benign Het
Agbl2 A G 2: 90,633,541 (GRCm39) K559R probably benign Het
Arhgap30 A G 1: 171,235,618 (GRCm39) D664G probably benign Het
BC034090 A G 1: 155,089,396 (GRCm39) V798A probably damaging Het
Bdp1 A T 13: 100,167,302 (GRCm39) C2237* probably null Het
C3 C T 17: 57,530,938 (GRCm39) V388M probably damaging Het
Ccdc170 G A 10: 4,464,200 (GRCm39) E60K probably damaging Het
Cdh8 G A 8: 100,006,182 (GRCm39) T135M probably damaging Het
Cep131 G T 11: 119,961,435 (GRCm39) A572E probably damaging Het
Clec16a A G 16: 10,559,655 (GRCm39) Y976C probably benign Het
Cplx3 G A 9: 57,522,902 (GRCm39) R153* probably null Het
Defa41 A T 8: 21,691,696 (GRCm39) D26V probably damaging Het
Dmpk C G 7: 18,821,944 (GRCm39) L301V probably benign Het
Eno3 A G 11: 70,553,040 (GRCm39) I393V probably benign Het
Fbxo47 A G 11: 97,748,520 (GRCm39) V305A probably benign Het
Fry G A 5: 150,353,319 (GRCm39) V1779M probably benign Het
Gtse1 T C 15: 85,748,465 (GRCm39) probably null Het
Gucy2e A T 11: 69,126,396 (GRCm39) L328Q probably damaging Het
Ifi207 T C 1: 173,558,064 (GRCm39) T225A unknown Het
Igkv4-80 A C 6: 68,993,649 (GRCm39) S81A probably benign Het
Lamc3 A T 2: 31,777,356 (GRCm39) M1L probably benign Het
Myo16 A G 8: 10,619,745 (GRCm39) D1432G probably benign Het
Nwd2 A T 5: 63,963,380 (GRCm39) N988I probably damaging Het
Otx1 C A 11: 21,947,037 (GRCm39) A91S probably damaging Het
Parp14 T C 16: 35,677,649 (GRCm39) E773G probably benign Het
Psen1 T A 12: 83,761,636 (GRCm39) M146K probably damaging Het
Ptx4 G A 17: 25,342,152 (GRCm39) R209Q probably benign Het
Slc13a2 T C 11: 78,291,634 (GRCm39) T340A probably damaging Het
St8sia1 T C 6: 142,909,434 (GRCm39) K21E probably damaging Het
Stxbp1 T C 2: 32,684,686 (GRCm39) D581G probably benign Het
Sumo2 G A 11: 115,425,486 (GRCm39) probably benign Het
Supt5 G A 7: 28,015,508 (GRCm39) P910S probably benign Het
Tbc1d30 T C 10: 121,142,743 (GRCm39) Q158R possibly damaging Het
Tenm2 T A 11: 35,915,633 (GRCm39) H1968L probably damaging Het
Trmt1 T C 8: 85,421,861 (GRCm39) Y220H probably damaging Het
Trp73 C T 4: 154,189,295 (GRCm39) E60K possibly damaging Het
Ttn A G 2: 76,617,413 (GRCm39) Y8026H probably damaging Het
Zar1l A G 5: 150,441,050 (GRCm39) probably null Het
Zfp740 T C 15: 102,117,640 (GRCm39) Y117H probably damaging Het
Zp1 C A 19: 10,897,918 (GRCm39) V8F possibly damaging Het
Other mutations in Zfp941
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01393:Zfp941 APN 7 140,391,841 (GRCm39) missense probably damaging 1.00
IGL02399:Zfp941 APN 7 140,392,612 (GRCm39) missense probably benign 0.37
IGL03202:Zfp941 APN 7 140,392,966 (GRCm39) missense probably benign 0.02
R0025:Zfp941 UTSW 7 140,393,185 (GRCm39) missense probably benign 0.01
R0025:Zfp941 UTSW 7 140,393,185 (GRCm39) missense probably benign 0.01
R0226:Zfp941 UTSW 7 140,393,188 (GRCm39) missense probably damaging 1.00
R0945:Zfp941 UTSW 7 140,391,577 (GRCm39) missense probably damaging 0.99
R1455:Zfp941 UTSW 7 140,392,687 (GRCm39) missense probably benign 0.29
R1581:Zfp941 UTSW 7 140,392,033 (GRCm39) missense probably benign 0.03
R2474:Zfp941 UTSW 7 140,391,384 (GRCm39) missense probably damaging 1.00
R4052:Zfp941 UTSW 7 140,392,340 (GRCm39) missense possibly damaging 0.81
R4576:Zfp941 UTSW 7 140,391,503 (GRCm39) nonsense probably null
R4604:Zfp941 UTSW 7 140,392,124 (GRCm39) missense probably damaging 1.00
R5311:Zfp941 UTSW 7 140,391,872 (GRCm39) nonsense probably null
R5505:Zfp941 UTSW 7 140,391,830 (GRCm39) missense probably benign 0.03
R5549:Zfp941 UTSW 7 140,388,021 (GRCm39) missense possibly damaging 0.46
R5566:Zfp941 UTSW 7 140,392,679 (GRCm39) missense probably benign 0.01
R5723:Zfp941 UTSW 7 140,392,763 (GRCm39) unclassified probably benign
R5736:Zfp941 UTSW 7 140,392,973 (GRCm39) missense probably benign 0.01
R5861:Zfp941 UTSW 7 140,392,052 (GRCm39) missense probably damaging 1.00
R6041:Zfp941 UTSW 7 140,392,158 (GRCm39) nonsense probably null
R6058:Zfp941 UTSW 7 140,392,010 (GRCm39) missense probably damaging 1.00
R6226:Zfp941 UTSW 7 140,392,398 (GRCm39) missense probably benign 0.01
R6488:Zfp941 UTSW 7 140,392,663 (GRCm39) missense probably benign 0.37
R6824:Zfp941 UTSW 7 140,392,612 (GRCm39) missense probably benign 0.37
R7356:Zfp941 UTSW 7 140,392,028 (GRCm39) missense possibly damaging 0.66
R7554:Zfp941 UTSW 7 140,391,970 (GRCm39) missense possibly damaging 0.69
Z1177:Zfp941 UTSW 7 140,392,099 (GRCm39) missense possibly damaging 0.53
Predicted Primers
Posted On 2016-07-06