Incidental Mutation 'R4959:Zswim4'
ID 382162
Institutional Source Beutler Lab
Gene Symbol Zswim4
Ensembl Gene ENSMUSG00000035671
Gene Name zinc finger SWIM-type containing 4
Synonyms E130119J17Rik
MMRRC Submission 042556-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.202) question?
Stock # R4959 (G1)
Quality Score 225
Status Not validated
Chromosome 8
Chromosomal Location 84937571-84963671 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 84938852 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Aspartic acid at position 1010 (A1010D)
Ref Sequence ENSEMBL: ENSMUSP00000040078 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039480]
AlphaFold Q8C7B8
Predicted Effect probably benign
Transcript: ENSMUST00000039480
AA Change: A1010D

PolyPhen 2 Score 0.223 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000040078
Gene: ENSMUSG00000035671
AA Change: A1010D

DomainStartEndE-ValueType
low complexity region 531 545 N/A INTRINSIC
low complexity region 576 588 N/A INTRINSIC
low complexity region 607 628 N/A INTRINSIC
low complexity region 672 683 N/A INTRINSIC
low complexity region 907 917 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000083510
Predicted Effect noncoding transcript
Transcript: ENSMUST00000083607
Predicted Effect noncoding transcript
Transcript: ENSMUST00000083677
Predicted Effect noncoding transcript
Transcript: ENSMUST00000180630
Predicted Effect noncoding transcript
Transcript: ENSMUST00000199621
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.2%
  • 10x: 95.6%
  • 20x: 89.7%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 99 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2700049A03Rik A T 12: 71,211,321 (GRCm39) E685V possibly damaging Het
2700049A03Rik G T 12: 71,211,320 (GRCm39) E685* probably null Het
6820408C15Rik T A 2: 152,282,808 (GRCm39) I221K possibly damaging Het
Aadacl3 A T 4: 144,183,656 (GRCm39) C136S probably benign Het
Abhd16a T A 17: 35,321,318 (GRCm39) S498T probably benign Het
Acrv1 G A 9: 36,605,996 (GRCm39) probably null Het
Adamts18 G A 8: 114,463,357 (GRCm39) R830* probably null Het
Art3 A G 5: 92,551,478 (GRCm39) Y279C probably damaging Het
Atm A T 9: 53,426,601 (GRCm39) D552E probably benign Het
Ccdc154 T C 17: 25,389,888 (GRCm39) L508P probably damaging Het
Ccser2 A T 14: 36,662,753 (GRCm39) S144T probably benign Het
Cgn C T 3: 94,685,564 (GRCm39) A320T probably benign Het
Cklf A G 8: 104,988,184 (GRCm39) K106E probably benign Het
Clec12a C A 6: 129,330,628 (GRCm39) T70K probably benign Het
CN725425 G A 15: 91,129,904 (GRCm39) A256T possibly damaging Het
Crb2 G T 2: 37,680,482 (GRCm39) R470L probably damaging Het
Csn1s1 T G 5: 87,821,120 (GRCm39) S33A probably benign Het
D630045J12Rik C T 6: 38,125,302 (GRCm39) V1571M possibly damaging Het
Deup1 G A 9: 15,523,310 (GRCm39) Q58* probably null Het
Dph2 T A 4: 117,748,527 (GRCm39) D82V probably damaging Het
Dsp C T 13: 38,375,686 (GRCm39) A1157V probably benign Het
Evi5l G T 8: 4,255,406 (GRCm39) V477L probably benign Het
Fam187b T A 7: 30,681,687 (GRCm39) H131Q probably damaging Het
Fam193b A G 13: 55,691,097 (GRCm39) I259T probably damaging Het
Fam91a1 A G 15: 58,303,059 (GRCm39) T323A probably benign Het
Fat4 T G 3: 39,037,195 (GRCm39) S3616A probably benign Het
Fbxo38 A T 18: 62,655,578 (GRCm39) N369K probably benign Het
Fitm1 T A 14: 55,813,831 (GRCm39) probably null Het
Fkbp5 T C 17: 28,647,343 (GRCm39) E164G probably damaging Het
Fpr-rs3 T C 17: 20,844,211 (GRCm39) Y310C possibly damaging Het
Fryl A T 5: 73,192,401 (GRCm39) M2678K probably benign Het
Fsip2 T C 2: 82,815,169 (GRCm39) I3634T probably benign Het
Gm3233 T C 10: 77,595,399 (GRCm39) probably benign Het
Gzmd T G 14: 56,369,955 (GRCm39) T9P unknown Het
Htr2b A T 1: 86,027,813 (GRCm39) I231N probably damaging Het
Il2ra A G 2: 11,681,664 (GRCm39) T90A possibly damaging Het
Kbtbd2 A G 6: 56,758,943 (GRCm39) F60S probably benign Het
Kif21b G A 1: 136,076,108 (GRCm39) C299Y possibly damaging Het
Lsm5 A T 6: 56,680,309 (GRCm39) D44E probably damaging Het
Mapk1 T A 16: 16,836,170 (GRCm39) M106K probably damaging Het
Mpp2 A G 11: 101,954,117 (GRCm39) V193A probably damaging Het
Muc4 T C 16: 32,575,437 (GRCm39) S1398P possibly damaging Het
Ndufs2 A G 1: 171,065,578 (GRCm39) Y282H probably damaging Het
Nes T A 3: 87,882,983 (GRCm39) L414Q probably damaging Het
Neurl2 T A 2: 164,675,122 (GRCm39) probably null Het
Ngef A G 1: 87,431,070 (GRCm39) F159S possibly damaging Het
Nlrx1 T C 9: 44,165,448 (GRCm39) H816R possibly damaging Het
Or10v5 A G 19: 11,806,300 (GRCm39) L30P probably benign Het
Or1e22 A T 11: 73,376,893 (GRCm39) Y252* probably null Het
Or2f1 T C 6: 42,721,621 (GRCm39) S217P probably damaging Het
Or4c106 T C 2: 88,682,516 (GRCm39) V74A possibly damaging Het
Or4f17-ps1 T A 2: 111,357,969 (GRCm39) F103L probably damaging Het
Or4p7 T A 2: 88,221,674 (GRCm39) L28I probably benign Het
Or7g35 A G 9: 19,496,504 (GRCm39) T224A probably benign Het
Pcgf2 A T 11: 97,582,515 (GRCm39) Y7N possibly damaging Het
Pdlim5 G A 3: 142,017,740 (GRCm39) probably benign Het
Pdzd2 A G 15: 12,375,734 (GRCm39) V1467A probably damaging Het
Pigp C A 16: 94,160,006 (GRCm39) G134V probably benign Het
Pik3c2g T C 6: 139,789,657 (GRCm39) Y385H possibly damaging Het
Pnliprp2 G A 19: 58,754,750 (GRCm39) E265K probably benign Het
Prl3c1 G T 13: 27,386,471 (GRCm39) probably null Het
Ptpn4 A T 1: 119,692,826 (GRCm39) Y110* probably null Het
Ptprq C T 10: 107,522,416 (GRCm39) V546I probably damaging Het
Rd3l C T 12: 111,946,578 (GRCm39) probably null Het
Rpl37 G A 15: 5,147,128 (GRCm39) R56Q possibly damaging Het
Rttn A T 18: 89,060,292 (GRCm39) H998L probably damaging Het
Rufy1 A T 11: 50,292,315 (GRCm39) F491L probably benign Het
Simc1 T G 13: 54,673,131 (GRCm39) V493G possibly damaging Het
Slc22a14 CTTTCCTGAA C 9: 119,003,101 (GRCm39) probably benign Het
Slc25a46 A T 18: 31,735,807 (GRCm39) I144N possibly damaging Het
Smtn A T 11: 3,477,825 (GRCm39) M1K probably null Het
Snd1 C A 6: 28,884,250 (GRCm39) Y766* probably null Het
Spata31d1d C T 13: 59,875,102 (GRCm39) G811D probably damaging Het
Spta1 A C 1: 174,074,174 (GRCm39) D2371A probably damaging Het
Stard6 A C 18: 70,631,631 (GRCm39) D74A possibly damaging Het
Stim2 G T 5: 54,262,712 (GRCm39) R318L probably benign Het
Sufu C T 19: 46,463,991 (GRCm39) T401I possibly damaging Het
Suz12 G A 11: 79,920,057 (GRCm39) G539D probably damaging Het
Sytl2 C G 7: 90,025,245 (GRCm39) S411C probably damaging Het
Taf6 G A 5: 138,181,465 (GRCm39) Q156* probably null Het
Tead4 T C 6: 128,247,950 (GRCm39) D29G probably damaging Het
Thada T C 17: 84,751,611 (GRCm39) Y455C probably damaging Het
Tlr6 G C 5: 65,111,002 (GRCm39) T635S possibly damaging Het
Tlr9 A G 9: 106,101,876 (GRCm39) D389G probably benign Het
Tmem54 A T 4: 129,002,073 (GRCm39) H40L probably damaging Het
Trappc9 G T 15: 72,808,905 (GRCm39) N540K probably damaging Het
Trbv28 C T 6: 41,248,788 (GRCm39) S106F probably damaging Het
Trrap A T 5: 144,793,770 (GRCm39) H3384L probably damaging Het
Usp16 T A 16: 87,277,802 (GRCm39) M684K probably damaging Het
Vat1 G A 11: 101,351,426 (GRCm39) T305M probably damaging Het
Vmn2r85 A G 10: 130,257,302 (GRCm39) S544P probably damaging Het
Vps8 T C 16: 21,278,536 (GRCm39) S267P probably damaging Het
Ylpm1 T A 12: 85,096,719 (GRCm39) V1242E probably damaging Het
Zfp267 C T 3: 36,218,285 (GRCm39) R102C possibly damaging Het
Zfp322a T C 13: 23,541,052 (GRCm39) Y230C probably damaging Het
Zfp352 T A 4: 90,112,376 (GRCm39) V172E probably benign Het
Zfp936 A T 7: 42,839,034 (GRCm39) H167L probably damaging Het
Zkscan14 A G 5: 145,132,302 (GRCm39) Y410H probably benign Het
Zkscan17 A G 11: 59,394,538 (GRCm39) M21T probably damaging Het
Other mutations in Zswim4
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00493:Zswim4 APN 8 84,938,769 (GRCm39) missense probably damaging 1.00
IGL03048:Zswim4 UTSW 8 84,938,604 (GRCm39) missense possibly damaging 0.95
R0217:Zswim4 UTSW 8 84,939,293 (GRCm39) missense probably damaging 1.00
R0688:Zswim4 UTSW 8 84,955,517 (GRCm39) missense possibly damaging 0.93
R1217:Zswim4 UTSW 8 84,946,601 (GRCm39) missense possibly damaging 0.89
R1853:Zswim4 UTSW 8 84,950,829 (GRCm39) missense probably damaging 1.00
R1878:Zswim4 UTSW 8 84,939,405 (GRCm39) missense possibly damaging 0.55
R2205:Zswim4 UTSW 8 84,952,498 (GRCm39) missense possibly damaging 0.70
R2940:Zswim4 UTSW 8 84,950,377 (GRCm39) missense probably damaging 1.00
R3747:Zswim4 UTSW 8 84,938,676 (GRCm39) missense possibly damaging 0.86
R3748:Zswim4 UTSW 8 84,938,676 (GRCm39) missense possibly damaging 0.86
R3750:Zswim4 UTSW 8 84,938,676 (GRCm39) missense possibly damaging 0.86
R4777:Zswim4 UTSW 8 84,963,586 (GRCm39) missense probably benign
R4831:Zswim4 UTSW 8 84,938,948 (GRCm39) missense probably damaging 1.00
R4968:Zswim4 UTSW 8 84,944,001 (GRCm39) missense probably benign 0.37
R4973:Zswim4 UTSW 8 84,938,852 (GRCm39) missense probably benign 0.22
R4977:Zswim4 UTSW 8 84,953,296 (GRCm39) splice site probably null
R4978:Zswim4 UTSW 8 84,953,296 (GRCm39) splice site probably null
R4980:Zswim4 UTSW 8 84,953,296 (GRCm39) splice site probably null
R4981:Zswim4 UTSW 8 84,953,296 (GRCm39) splice site probably null
R4982:Zswim4 UTSW 8 84,953,296 (GRCm39) splice site probably null
R4983:Zswim4 UTSW 8 84,953,296 (GRCm39) splice site probably null
R5248:Zswim4 UTSW 8 84,946,561 (GRCm39) missense probably benign 0.13
R5337:Zswim4 UTSW 8 84,961,708 (GRCm39) missense probably damaging 1.00
R5366:Zswim4 UTSW 8 84,939,419 (GRCm39) missense probably benign 0.39
R5646:Zswim4 UTSW 8 84,957,739 (GRCm39) splice site probably null
R5845:Zswim4 UTSW 8 84,943,871 (GRCm39) splice site probably null
R6193:Zswim4 UTSW 8 84,952,774 (GRCm39) missense probably benign
R6270:Zswim4 UTSW 8 84,957,580 (GRCm39) missense probably damaging 1.00
R6648:Zswim4 UTSW 8 84,957,543 (GRCm39) missense probably benign 0.22
R6920:Zswim4 UTSW 8 84,940,714 (GRCm39) missense probably benign 0.01
R7117:Zswim4 UTSW 8 84,940,681 (GRCm39) missense probably damaging 1.00
R7155:Zswim4 UTSW 8 84,946,556 (GRCm39) missense probably damaging 1.00
R7344:Zswim4 UTSW 8 84,950,327 (GRCm39) nonsense probably null
R7354:Zswim4 UTSW 8 84,955,478 (GRCm39) missense probably damaging 1.00
R8036:Zswim4 UTSW 8 84,949,918 (GRCm39) missense probably benign 0.22
R8408:Zswim4 UTSW 8 84,939,014 (GRCm39) missense possibly damaging 0.82
R8518:Zswim4 UTSW 8 84,938,586 (GRCm39) missense probably damaging 1.00
R8750:Zswim4 UTSW 8 84,939,313 (GRCm39) missense possibly damaging 0.82
R8830:Zswim4 UTSW 8 84,949,945 (GRCm39) missense possibly damaging 0.92
R8838:Zswim4 UTSW 8 84,940,699 (GRCm39) missense probably damaging 1.00
R8840:Zswim4 UTSW 8 84,940,699 (GRCm39) missense probably damaging 1.00
R8842:Zswim4 UTSW 8 84,940,699 (GRCm39) missense probably damaging 1.00
R9185:Zswim4 UTSW 8 84,963,633 (GRCm39) start codon destroyed probably null 0.94
R9355:Zswim4 UTSW 8 84,955,687 (GRCm39) missense probably damaging 1.00
R9432:Zswim4 UTSW 8 84,963,539 (GRCm39) missense probably damaging 1.00
R9635:Zswim4 UTSW 8 84,939,354 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- AACTGTGCGAACTGGAGGTG -3'
(R):5'- GCATTGCCTTCAACCAAGAC -3'

Sequencing Primer
(F):5'- AACTGGAGGTGCCCGTCTG -3'
(R):5'- GACAGCCACCCTGCAGTC -3'
Posted On 2016-04-27