Incidental Mutation 'R7441:Zfp937'
ID 576942
Institutional Source Beutler Lab
Gene Symbol Zfp937
Ensembl Gene ENSMUSG00000060336
Gene Name zinc finger protein 937
Synonyms Gm4979
MMRRC Submission 045517-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.096) question?
Stock # R7441 (G1)
Quality Score 184.468
Status Not validated
Chromosome 2
Chromosomal Location 150059993-150082645 bp(+) (GRCm39)
Type of Mutation frame shift
DNA Base Change (assembly) GTGATAAGGCATTTGCACAAAACAGTCATCTCCTAACACATAAAAGAACACAT to G at 150080630 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000073454 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000073782]
AlphaFold A2ANU7
Predicted Effect probably null
Transcript: ENSMUST00000073782
SMART Domains Protein: ENSMUSP00000073454
Gene: ENSMUSG00000060336

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
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4921509C19Rik A C 2: 151,314,845 (GRCm39) S278A possibly damaging Het
Adamts20 T C 15: 94,251,554 (GRCm39) D411G probably damaging Het
Adgrl3 A G 5: 81,871,987 (GRCm39) I894V possibly damaging Het
Adprhl1 C T 8: 13,273,069 (GRCm39) V1230I probably benign Het
Agpat1 T A 17: 34,829,883 (GRCm39) Y77N probably damaging Het
Anpep A G 7: 79,477,392 (GRCm39) V725A possibly damaging Het
Apc T A 18: 34,445,126 (GRCm39) I674K probably damaging Het
Arhgef2 A G 3: 88,551,262 (GRCm39) R808G probably damaging Het
Asap1 A G 15: 64,002,105 (GRCm39) V402A probably damaging Het
Aspg T C 12: 112,091,255 (GRCm39) V479A possibly damaging Het
B3galnt2 G A 13: 14,169,070 (GRCm39) V368M probably benign Het
Bahcc1 T C 11: 120,177,132 (GRCm39) S2007P probably damaging Het
Cyfip2 A T 11: 46,087,254 (GRCm39) I1212N possibly damaging Het
Dnajc16 A T 4: 141,491,124 (GRCm39) D675E probably damaging Het
Dram2 T C 3: 106,462,503 (GRCm39) F4L probably damaging Het
Dsp A G 13: 38,379,425 (GRCm39) T2057A probably benign Het
Dync1h1 T G 12: 110,602,887 (GRCm39) L2176R probably damaging Het
Efhb A T 17: 53,708,549 (GRCm39) I707N possibly damaging Het
Eif2ak4 A G 2: 118,302,377 (GRCm39) T1555A probably benign Het
Erc1 G A 6: 119,801,912 (GRCm39) T35I possibly damaging Het
Esr2 C A 12: 76,188,168 (GRCm39) M363I probably benign Het
Etl4 A T 2: 20,749,000 (GRCm39) N446I possibly damaging Het
Evpl T A 11: 116,113,782 (GRCm39) K1303* probably null Het
Fam135b A T 15: 71,335,529 (GRCm39) V555E probably damaging Het
Fam186b A G 15: 99,177,970 (GRCm39) L452P probably benign Het
Fmn1 A T 2: 113,271,956 (GRCm39) Q108L unknown Het
Gcc2 A G 10: 58,092,723 (GRCm39) T48A probably benign Het
Gm6619 T G 6: 131,467,354 (GRCm39) I73S possibly damaging Het
Gm8267 T A 14: 44,960,397 (GRCm39) D116V probably damaging Het
Gtf3c3 G A 1: 54,459,607 (GRCm39) T385M probably benign Het
Iqgap2 C A 13: 95,764,584 (GRCm39) M1553I probably benign Het
Kcnk1 G T 8: 126,722,307 (GRCm39) G37C probably damaging Het
Kifc3 T C 8: 95,864,615 (GRCm39) M32V probably benign Het
Krt81 C A 15: 101,359,251 (GRCm39) K222N possibly damaging Het
Lrrc63 A G 14: 75,363,697 (GRCm39) S145P possibly damaging Het
Mybbp1a T A 11: 72,342,101 (GRCm39) V1279E probably benign Het
Niban3 A G 8: 72,052,808 (GRCm39) D94G probably benign Het
Or11g26 A T 14: 50,752,853 (GRCm39) Y64F probably damaging Het
Or8u9 T A 2: 86,001,354 (GRCm39) D269V probably damaging Het
Pierce1 TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC 2: 28,356,122 (GRCm39) probably benign Het
Pramel12 A G 4: 143,145,410 (GRCm39) Y293C probably benign Het
Ptpn18 T C 1: 34,512,416 (GRCm39) V407A probably benign Het
Ptpn9 T A 9: 56,934,717 (GRCm39) Y160* probably null Het
Ptprj T C 2: 90,280,163 (GRCm39) K1045R possibly damaging Het
Rundc3a G T 11: 102,290,872 (GRCm39) probably null Het
Scn11a C T 9: 119,587,692 (GRCm39) V1351I probably benign Het
Slc26a9 A G 1: 131,690,556 (GRCm39) Y520C probably damaging Het
Spata20 G A 11: 94,374,867 (GRCm39) A245V probably benign Het
Steap3 A C 1: 120,169,248 (GRCm39) F350V probably benign Het
Swt1 A T 1: 151,286,815 (GRCm39) F226I probably benign Het
Taar7f A G 10: 23,925,885 (GRCm39) T160A possibly damaging Het
Timd5 G A 11: 46,419,382 (GRCm39) W66* probably null Het
Upf2 A T 2: 6,023,743 (GRCm39) I698F unknown Het
Vmn2r84 T C 10: 130,227,982 (GRCm39) T85A possibly damaging Het
Zfp426 T C 9: 20,382,147 (GRCm39) E280G possibly damaging Het
Zfp810 C A 9: 22,190,568 (GRCm39) E78* 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
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
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 PCR Primer
(F):5'- AGCCATCCTCAAGGGCATC -3'
(R):5'- TAGGAGATGACTGTTTTGTGCAAA -3'

Sequencing Primer
(F):5'- CTGTCATCTTCGAGGGCATCAAAG -3'
(R):5'- GTGCAAATGCCTTATCACACTGG -3'
Posted On 2019-10-07