Incidental Mutation 'R1307:Zfp985'
ID 157824
Institutional Source Beutler Lab
Gene Symbol Zfp985
Ensembl Gene ENSMUSG00000065999
Gene Name zinc finger protein 985
Synonyms Gm13154
MMRRC Submission 039373-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.624) question?
Stock # R1307 (G1)
Quality Score 225
Status Not validated
Chromosome 4
Chromosomal Location 147637734-147669655 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to T at 147667704 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Phenylalanine at position 191 (L191F)
Ref Sequence ENSEMBL: ENSMUSP00000080438 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000081742] [ENSMUST00000139784] [ENSMUST00000143885]
AlphaFold A2A7A5
Predicted Effect probably benign
Transcript: ENSMUST00000081742
AA Change: L191F

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000080438
Gene: ENSMUSG00000065999
AA Change: L191F

DomainStartEndE-ValueType
KRAB 13 72 4.36e-15 SMART
ZnF_C2H2 238 260 8.34e-3 SMART
ZnF_C2H2 266 288 1.47e-3 SMART
ZnF_C2H2 294 316 2.36e-2 SMART
ZnF_C2H2 322 344 8.34e-3 SMART
ZnF_C2H2 350 372 7.67e-2 SMART
ZnF_C2H2 378 400 8.6e-5 SMART
ZnF_C2H2 406 428 8.6e-5 SMART
ZnF_C2H2 434 456 7.9e-4 SMART
ZnF_C2H2 462 484 1.95e-3 SMART
ZnF_C2H2 490 512 2.09e-3 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000139784
SMART Domains Protein: ENSMUSP00000123296
Gene: ENSMUSG00000065999

DomainStartEndE-ValueType
KRAB 13 72 4.36e-15 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000143885
SMART Domains Protein: ENSMUSP00000121177
Gene: ENSMUSG00000065999

DomainStartEndE-ValueType
KRAB 13 72 4.36e-15 SMART
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 98.0%
  • 10x: 95.6%
  • 20x: 91.4%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ascc1 A T 10: 59,848,321 (GRCm39) I83L probably benign Het
Bcl2a1b T C 9: 89,081,543 (GRCm39) V44A probably damaging Het
Bdp1 T C 13: 100,186,271 (GRCm39) D1727G possibly damaging Het
Cabp1 A G 5: 115,310,965 (GRCm39) F294L probably damaging Het
Coq8b T A 7: 26,950,016 (GRCm39) M365K probably damaging Het
Gk2 A T 5: 97,603,268 (GRCm39) D523E probably benign Het
Havcr1 C T 11: 46,647,097 (GRCm39) T177I probably damaging Het
Kdm4a T C 4: 118,032,839 (GRCm39) T76A probably benign Het
Lama4 A T 10: 38,946,028 (GRCm39) I804F probably benign Het
Ntn4 C T 10: 93,543,215 (GRCm39) R314W probably damaging Het
Pcdh10 A G 3: 45,336,314 (GRCm39) N876S probably benign Het
Polr3f T C 2: 144,375,113 (GRCm39) V95A probably damaging Het
Ptk2 A G 15: 73,163,895 (GRCm39) V389A probably benign Het
Rhof T C 5: 123,258,378 (GRCm39) E151G probably damaging Het
Slc25a28 T C 19: 43,655,470 (GRCm39) N135S probably benign Het
Sphk1 G A 11: 116,426,928 (GRCm39) V295I probably benign Het
Sv2b G T 7: 74,856,182 (GRCm39) T36K probably damaging Het
Sybu T C 15: 44,538,786 (GRCm39) E291G probably damaging Het
Tnc T C 4: 63,927,096 (GRCm39) E810G probably damaging Het
Uba52 T C 8: 70,961,166 (GRCm39) H68R probably damaging Het
Unc79 A G 12: 103,036,335 (GRCm39) N552S probably damaging Het
Ush2a T C 1: 188,090,164 (GRCm39) C416R probably damaging Het
Ush2a T C 1: 188,184,037 (GRCm39) V1447A probably damaging Het
Other mutations in Zfp985
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0098:Zfp985 UTSW 4 147,661,566 (GRCm39) missense probably damaging 0.97
R0324:Zfp985 UTSW 4 147,667,314 (GRCm39) missense probably benign 0.00
R1594:Zfp985 UTSW 4 147,667,537 (GRCm39) missense probably benign 0.05
R1657:Zfp985 UTSW 4 147,668,567 (GRCm39) missense probably benign 0.01
R1667:Zfp985 UTSW 4 147,668,407 (GRCm39) missense possibly damaging 0.84
R1761:Zfp985 UTSW 4 147,668,502 (GRCm39) missense probably benign 0.00
R1858:Zfp985 UTSW 4 147,667,315 (GRCm39) missense probably benign 0.29
R2509:Zfp985 UTSW 4 147,667,443 (GRCm39) missense possibly damaging 0.75
R2510:Zfp985 UTSW 4 147,667,443 (GRCm39) missense possibly damaging 0.75
R2847:Zfp985 UTSW 4 147,667,468 (GRCm39) nonsense probably null
R2848:Zfp985 UTSW 4 147,667,468 (GRCm39) nonsense probably null
R4245:Zfp985 UTSW 4 147,667,396 (GRCm39) missense probably damaging 0.96
R4260:Zfp985 UTSW 4 147,668,029 (GRCm39) missense probably damaging 1.00
R4434:Zfp985 UTSW 4 147,668,368 (GRCm39) missense probably benign 0.37
R4480:Zfp985 UTSW 4 147,668,536 (GRCm39) missense probably benign 0.07
R4512:Zfp985 UTSW 4 147,668,020 (GRCm39) missense probably damaging 1.00
R4514:Zfp985 UTSW 4 147,668,020 (GRCm39) missense probably damaging 1.00
R4528:Zfp985 UTSW 4 147,667,347 (GRCm39) missense possibly damaging 0.49
R4836:Zfp985 UTSW 4 147,668,612 (GRCm39) missense probably damaging 0.97
R4884:Zfp985 UTSW 4 147,667,801 (GRCm39) missense probably benign 0.04
R5054:Zfp985 UTSW 4 147,667,438 (GRCm39) missense probably damaging 0.98
R5106:Zfp985 UTSW 4 147,668,612 (GRCm39) missense probably damaging 0.97
R5205:Zfp985 UTSW 4 147,667,368 (GRCm39) missense probably damaging 1.00
R5266:Zfp985 UTSW 4 147,667,289 (GRCm39) critical splice acceptor site probably null
R5468:Zfp985 UTSW 4 147,667,702 (GRCm39) missense probably benign
R5533:Zfp985 UTSW 4 147,667,440 (GRCm39) nonsense probably null
R6282:Zfp985 UTSW 4 147,667,805 (GRCm39) missense probably benign 0.00
R6303:Zfp985 UTSW 4 147,668,232 (GRCm39) missense probably benign 0.01
R6609:Zfp985 UTSW 4 147,668,124 (GRCm39) missense probably damaging 1.00
R6609:Zfp985 UTSW 4 147,667,578 (GRCm39) missense probably benign
R6722:Zfp985 UTSW 4 147,667,528 (GRCm39) missense probably benign 0.26
R6858:Zfp985 UTSW 4 147,667,764 (GRCm39) nonsense probably null
R7064:Zfp985 UTSW 4 147,667,573 (GRCm39) missense probably benign 0.20
R7216:Zfp985 UTSW 4 147,667,913 (GRCm39) missense probably damaging 1.00
R7471:Zfp985 UTSW 4 147,667,388 (GRCm39) missense possibly damaging 0.75
R7583:Zfp985 UTSW 4 147,667,946 (GRCm39) nonsense probably null
R7685:Zfp985 UTSW 4 147,667,331 (GRCm39) missense probably benign 0.00
R8242:Zfp985 UTSW 4 147,668,639 (GRCm39) missense possibly damaging 0.52
R8504:Zfp985 UTSW 4 147,667,883 (GRCm39) missense possibly damaging 0.70
R8780:Zfp985 UTSW 4 147,668,412 (GRCm39) missense possibly damaging 0.79
R8785:Zfp985 UTSW 4 147,668,080 (GRCm39) missense probably damaging 1.00
R9485:Zfp985 UTSW 4 147,668,280 (GRCm39) missense probably damaging 1.00
R9513:Zfp985 UTSW 4 147,667,999 (GRCm39) missense probably damaging 1.00
R9631:Zfp985 UTSW 4 147,665,742 (GRCm39) missense probably damaging 1.00
R9722:Zfp985 UTSW 4 147,667,618 (GRCm39) missense possibly damaging 0.63
R9786:Zfp985 UTSW 4 147,668,047 (GRCm39) missense probably benign
X0050:Zfp985 UTSW 4 147,667,728 (GRCm39) frame shift probably null
Predicted Primers
Posted On 2014-02-18