Incidental Mutation 'R1403:Zfp937'
ID188590
Institutional Source Beutler Lab
Gene Symbol Zfp937
Ensembl Gene ENSMUSG00000060336
Gene Namezinc finger protein 937
SynonymsGm4979
MMRRC Submission 039465-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.074) question?
Stock #R1403 (G1)
Quality Score225
Status Validated
Chromosome2
Chromosomal Location150218073-150240725 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 150238948 bp
ZygosityHeterozygous
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]
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: 98.6%
  • 10x: 97.0%
  • 20x: 94.5%
Validation Efficiency 94% (51/54)
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca1 G A 4: 53,059,253 probably benign Het
AC238840.3 T G 7: 38,867,921 I28L probably benign Het
Acsf2 G T 11: 94,562,874 N420K probably benign Het
Adam26a A T 8: 43,569,192 C420* probably null Het
Afap1l1 T C 18: 61,741,838 Y424C probably damaging Het
Agl A G 3: 116,782,597 V553A probably benign Het
Akr7a5 T A 4: 139,318,123 M325K probably damaging Het
Akt3 C T 1: 177,131,110 probably benign Het
Aldh7a1 C A 18: 56,559,269 E87* probably null Het
Arhgap29 A G 3: 121,973,929 K7E probably damaging Het
Brca2 T A 5: 150,542,649 D1959E probably benign Het
Cdc42se2 A G 11: 54,720,366 probably benign Het
Cdh7 G A 1: 110,061,132 V255I probably benign Het
Chil5 G T 3: 106,018,093 Q171K probably benign Het
Cul9 C G 17: 46,522,175 A1326P probably damaging Het
Dhrs7c A T 11: 67,811,650 I155F probably damaging Het
Dip2c A G 13: 9,553,264 probably null Het
Ell T A 8: 70,591,488 probably benign Het
Fam124b T C 1: 80,213,339 Y109C possibly damaging Het
Gak T A 5: 108,591,145 K156M probably damaging Het
Gm9797 C A 10: 11,609,550 noncoding transcript Het
Got1l1 C G 8: 27,200,717 probably null Het
Grm1 T C 10: 11,080,135 D135G probably benign Het
Hrh3 T G 2: 180,102,754 D131A probably damaging Het
Itpr1 A T 6: 108,389,553 Q979L probably null Het
Kdm7a C A 6: 39,151,253 probably benign Het
Klb G C 5: 65,348,746 R112P possibly damaging Het
Lingo2 A T 4: 35,709,420 C187S possibly damaging Het
Lrp1 T A 10: 127,581,891 probably null Het
Ltbp4 T C 7: 27,329,039 N266S unknown Het
Mgam G A 6: 40,666,881 S581N possibly damaging Het
Mrgpra9 T A 7: 47,235,638 I94L probably benign Het
Msantd4 A T 9: 4,384,023 I115F probably benign Het
Mterf3 A G 13: 66,929,880 probably benign Het
Neurl1a C A 19: 47,253,711 N414K probably damaging Het
Nfkbiz A G 16: 55,816,470 probably benign Het
Nrxn1 A C 17: 90,643,053 L566R probably benign Het
Nsmce1 A G 7: 125,467,855 probably benign Het
Olfr483 T A 7: 108,103,615 I102N probably benign Het
Prl7d1 A T 13: 27,709,197 F243I possibly damaging Het
Rbm27 T C 18: 42,317,681 S509P probably damaging Het
Rnf126 C T 10: 79,760,868 A239T probably benign Het
Rnf44 C T 13: 54,682,008 E306K probably damaging Het
Rp1 T C 1: 4,346,297 R1531G possibly damaging Het
Sf3b4 A G 3: 96,173,637 probably null Het
Stk4 C T 2: 164,100,528 T360M probably benign Het
Syt15 C A 14: 34,221,202 probably benign Het
Vcan T A 13: 89,688,484 E2980D probably benign Het
Vps13b A G 15: 35,709,122 probably benign Het
Vwa2 C T 19: 56,881,138 P2S unknown Het
Wdr77 G A 3: 105,967,257 V322I possibly damaging Het
Zfp12 C A 5: 143,244,780 Y287* probably null Het
Other mutations in Zfp937
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0350:Zfp937 UTSW 2 150239302 missense possibly damaging 0.91
R0449:Zfp937 UTSW 2 150239546 missense probably benign 0.13
R1403:Zfp937 UTSW 2 150238948 nonsense probably null
R1465:Zfp937 UTSW 2 150239047 nonsense probably null
R1465:Zfp937 UTSW 2 150239047 nonsense probably null
R4510:Zfp937 UTSW 2 150238511 missense probably damaging 0.98
R4511:Zfp937 UTSW 2 150238511 missense probably damaging 0.98
R4689:Zfp937 UTSW 2 150236786 missense probably damaging 1.00
R5290:Zfp937 UTSW 2 150238309 nonsense probably null
R6287:Zfp937 UTSW 2 150238341 missense possibly damaging 0.89
R6701:Zfp937 UTSW 2 150239216 missense probably damaging 1.00
R6746:Zfp937 UTSW 2 150239423 nonsense probably null
R6838:Zfp937 UTSW 2 150239346 missense probably benign 0.01
R7162:Zfp937 UTSW 2 150239519 missense probably benign 0.35
R7213:Zfp937 UTSW 2 150239465 missense probably damaging 1.00
R7441:Zfp937 UTSW 2 150238710 frame shift probably null
R7481:Zfp937 UTSW 2 150239346 missense probably benign 0.01
R7694:Zfp937 UTSW 2 150239348 missense probably damaging 1.00
R7856:Zfp937 UTSW 2 150239547 missense probably benign 0.23
R7902:Zfp937 UTSW 2 150238761 missense probably damaging 1.00
R7939:Zfp937 UTSW 2 150239547 missense probably benign 0.23
R7985:Zfp937 UTSW 2 150238761 missense probably damaging 1.00
R8058:Zfp937 UTSW 2 150239501 missense not run
X0017:Zfp937 UTSW 2 150218161 utr 5 prime probably null
Predicted Primers
Posted On2014-05-09