Incidental Mutation 'R1403:Zfp937'
ID 262766
Institutional Source Beutler Lab
Gene Symbol Zfp937
Ensembl Gene ENSMUSG00000060336
Gene Name zinc finger protein 937
Synonyms Gm4979
MMRRC Submission 039465-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.096) question?
Stock # R1403 (G1)
Quality Score 95
Status Not validated
Chromosome 2
Chromosomal Location 150059993-150082645 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 150080868 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 299 (Y299*)
Ref Sequence ENSEMBL: ENSMUSP00000073454 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073782]
AlphaFold A2ANU7
Predicted Effect probably null
Transcript: ENSMUST00000073782
AA Change: Y299*
SMART Domains Protein: ENSMUSP00000073454
Gene: ENSMUSG00000060336
AA Change: Y299*

DomainStartEndE-ValueType
KRAB 4 66 8.19e-20 SMART
ZnF_C2H2 103 125 1.28e-3 SMART
ZnF_C2H2 131 153 2.53e-2 SMART
ZnF_C2H2 159 181 9.58e-3 SMART
ZnF_C2H2 187 209 2.09e-3 SMART
ZnF_C2H2 215 237 2.2e-2 SMART
ZnF_C2H2 243 265 2.2e-2 SMART
ZnF_C2H2 271 293 2.2e-2 SMART
ZnF_C2H2 299 321 1.82e-3 SMART
ZnF_C2H2 327 349 3.69e-4 SMART
ZnF_C2H2 355 377 4.47e-3 SMART
ZnF_C2H2 383 405 3.89e-3 SMART
ZnF_C2H2 411 433 4.79e-3 SMART
ZnF_C2H2 439 461 8.47e-4 SMART
ZnF_C2H2 467 490 7.26e-3 SMART
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 97.5%
  • 10x: 88.5%
  • 20x: 65.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 43 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsf2 G T 11: 94,453,700 (GRCm39) N420K probably benign Het
Adam26a A T 8: 44,022,229 (GRCm39) C420* probably null Het
Afap1l1 T C 18: 61,874,909 (GRCm39) Y424C probably damaging Het
Agl A G 3: 116,576,246 (GRCm39) V553A probably benign Het
Akr7a5 T A 4: 139,045,434 (GRCm39) M325K probably damaging Het
Aldh7a1 C A 18: 56,692,341 (GRCm39) E87* probably null Het
Arhgap29 A G 3: 121,767,578 (GRCm39) K7E probably damaging Het
Brca2 T A 5: 150,466,114 (GRCm39) D1959E probably benign Het
Cdh20 G A 1: 109,988,862 (GRCm39) V255I probably benign Het
Chil5 G T 3: 105,925,409 (GRCm39) Q171K probably benign Het
Cul9 C G 17: 46,833,101 (GRCm39) A1326P probably damaging Het
Dhrs7c A T 11: 67,702,476 (GRCm39) I155F probably damaging Het
Dip2c A G 13: 9,603,300 (GRCm39) probably null Het
Fam124b T C 1: 80,191,056 (GRCm39) Y109C possibly damaging Het
Gak T A 5: 108,739,011 (GRCm39) K156M probably damaging Het
Gm17535 A G 9: 3,035,804 (GRCm39) Y224C probably null Het
Got1l1 C G 8: 27,690,745 (GRCm39) probably null Het
Grm1 T C 10: 10,955,879 (GRCm39) D135G probably benign Het
Hrh3 T G 2: 179,744,547 (GRCm39) D131A probably damaging Het
Hspg2 C T 4: 137,267,411 (GRCm39) L2042F possibly damaging Het
Itpr1 A T 6: 108,366,514 (GRCm39) Q979L probably null Het
Klb G C 5: 65,506,089 (GRCm39) R112P possibly damaging Het
Lingo2 A T 4: 35,709,420 (GRCm39) C187S possibly damaging Het
Lrp1 T A 10: 127,417,760 (GRCm39) probably null Het
Ltbp4 T C 7: 27,028,464 (GRCm39) N266S unknown Het
Mgam G A 6: 40,643,815 (GRCm39) S581N possibly damaging Het
Mrgpra9 T A 7: 46,885,386 (GRCm39) I94L probably benign Het
Msantd4 A T 9: 4,384,023 (GRCm39) I115F probably benign Het
Nrxn1 A C 17: 90,950,481 (GRCm39) L566R probably benign Het
Or5p59 T A 7: 107,702,822 (GRCm39) I102N probably benign Het
Prl7d1 A T 13: 27,893,180 (GRCm39) F243I possibly damaging Het
Rbm27 T C 18: 42,450,746 (GRCm39) S509P probably damaging Het
Rnf44 C T 13: 54,829,821 (GRCm39) E306K probably damaging Het
Rp1 T C 1: 4,416,520 (GRCm39) R1531G possibly damaging Het
Sf3b4 A G 3: 96,080,953 (GRCm39) probably null Het
Sfi1 TCGC TC 11: 3,096,254 (GRCm39) probably null Het
Sfi1 CCTCTC CCTCTCTC 11: 3,127,419 (GRCm39) probably benign Het
Sp110 T G 1: 85,506,800 (GRCm39) E421A probably benign Het
Stk4 C T 2: 163,942,448 (GRCm39) T360M probably benign Het
Vcan T A 13: 89,836,603 (GRCm39) E2980D probably benign Het
Vwa2 C T 19: 56,869,570 (GRCm39) P2S unknown Het
Wdr77 G A 3: 105,874,573 (GRCm39) V322I possibly damaging Het
Zfp12 C A 5: 143,230,535 (GRCm39) Y287* probably null Het
Other mutations in Zfp937
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0350:Zfp937 UTSW 2 150,081,222 (GRCm39) missense possibly damaging 0.91
R0449:Zfp937 UTSW 2 150,081,466 (GRCm39) missense probably benign 0.13
R1403:Zfp937 UTSW 2 150,080,868 (GRCm39) nonsense probably null
R1465:Zfp937 UTSW 2 150,080,967 (GRCm39) nonsense probably null
R1465:Zfp937 UTSW 2 150,080,967 (GRCm39) nonsense probably null
R4510:Zfp937 UTSW 2 150,080,431 (GRCm39) missense probably damaging 0.98
R4511:Zfp937 UTSW 2 150,080,431 (GRCm39) missense probably damaging 0.98
R4689:Zfp937 UTSW 2 150,078,706 (GRCm39) missense probably damaging 1.00
R5290:Zfp937 UTSW 2 150,080,229 (GRCm39) nonsense probably null
R6287:Zfp937 UTSW 2 150,080,261 (GRCm39) missense possibly damaging 0.89
R6701:Zfp937 UTSW 2 150,081,136 (GRCm39) missense probably damaging 1.00
R6746:Zfp937 UTSW 2 150,081,343 (GRCm39) nonsense probably null
R6838:Zfp937 UTSW 2 150,081,266 (GRCm39) missense probably benign 0.01
R7162:Zfp937 UTSW 2 150,081,439 (GRCm39) missense probably benign 0.35
R7213:Zfp937 UTSW 2 150,081,385 (GRCm39) missense probably damaging 1.00
R7441:Zfp937 UTSW 2 150,080,630 (GRCm39) frame shift probably null
R7481:Zfp937 UTSW 2 150,081,266 (GRCm39) missense probably benign 0.01
R7694:Zfp937 UTSW 2 150,081,268 (GRCm39) missense probably damaging 1.00
R7856:Zfp937 UTSW 2 150,081,467 (GRCm39) missense probably benign 0.23
R7902:Zfp937 UTSW 2 150,080,681 (GRCm39) missense probably damaging 1.00
R7956:Zfp937 UTSW 2 150,081,076 (GRCm39) missense probably benign 0.03
R8058:Zfp937 UTSW 2 150,081,421 (GRCm39) missense probably benign 0.00
R8468:Zfp937 UTSW 2 150,080,634 (GRCm39) missense probably benign 0.02
R9514:Zfp937 UTSW 2 150,080,890 (GRCm39) missense possibly damaging 0.95
R9617:Zfp937 UTSW 2 150,080,452 (GRCm39) missense probably damaging 1.00
X0017:Zfp937 UTSW 2 150,060,081 (GRCm39) splice site probably null
Predicted Primers
Posted On 2015-02-04