Incidental Mutation 'R0123:Zswim8'
ID 21186
Institutional Source Beutler Lab
Gene Symbol Zswim8
Ensembl Gene ENSMUSG00000021819
Gene Name zinc finger SWIM-type containing 8
Synonyms 2310021P13Rik, 4832404P21Rik
MMRRC Submission 038408-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.965) question?
Stock # R0123 (G1)
Quality Score 225
Status Validated
Chromosome 14
Chromosomal Location 20757620-20773687 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 20766558 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000153285 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000022358] [ENSMUST00000223840] [ENSMUST00000224129] [ENSMUST00000224751]
AlphaFold Q3UHH1
Predicted Effect probably benign
Transcript: ENSMUST00000022358
SMART Domains Protein: ENSMUSP00000022358
Gene: ENSMUSG00000021819

DomainStartEndE-ValueType
low complexity region 50 66 N/A INTRINSIC
low complexity region 89 102 N/A INTRINSIC
low complexity region 390 405 N/A INTRINSIC
low complexity region 578 612 N/A INTRINSIC
low complexity region 736 751 N/A INTRINSIC
low complexity region 1000 1015 N/A INTRINSIC
low complexity region 1120 1135 N/A INTRINSIC
low complexity region 1176 1211 N/A INTRINSIC
low complexity region 1259 1270 N/A INTRINSIC
low complexity region 1343 1355 N/A INTRINSIC
low complexity region 1470 1487 N/A INTRINSIC
low complexity region 1491 1511 N/A INTRINSIC
low complexity region 1527 1542 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223561
Predicted Effect noncoding transcript
Transcript: ENSMUST00000223782
Predicted Effect probably benign
Transcript: ENSMUST00000223840
Predicted Effect probably benign
Transcript: ENSMUST00000224129
Predicted Effect noncoding transcript
Transcript: ENSMUST00000224485
Predicted Effect probably benign
Transcript: ENSMUST00000224751
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225743
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225332
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225010
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225715
Predicted Effect noncoding transcript
Transcript: ENSMUST00000225187
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.1%
  • 10x: 95.8%
  • 20x: 91.1%
Validation Efficiency 99% (71/72)
Allele List at MGI
Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110059E24Rik T C 19: 21,575,565 (GRCm39) probably benign Het
Abca16 T A 7: 120,139,378 (GRCm39) L1470Q probably damaging Het
Abraxas2 G A 7: 132,476,584 (GRCm39) R105Q probably damaging Het
Becn1 A G 11: 101,181,324 (GRCm39) Y326H probably damaging Het
Bicd1 T C 6: 149,414,448 (GRCm39) I387T probably benign Het
Btbd9 C T 17: 30,493,916 (GRCm39) D492N possibly damaging Het
Cacna1g T A 11: 94,300,302 (GRCm39) H2156L probably damaging Het
Cd22 A G 7: 30,566,533 (GRCm39) probably benign Het
Cd59b G A 2: 103,909,286 (GRCm39) probably null Het
Chn2 T C 6: 54,267,436 (GRCm39) probably benign Het
Cmya5 A G 13: 93,232,412 (GRCm39) L892P possibly damaging Het
Col5a2 A G 1: 45,446,195 (GRCm39) I461T probably benign Het
Cts8 T A 13: 61,401,391 (GRCm39) M75L probably benign Het
Ddx50 A T 10: 62,457,156 (GRCm39) probably benign Het
Dlg5 T C 14: 24,197,274 (GRCm39) M1558V probably benign Het
Dnlz T C 2: 26,241,380 (GRCm39) N116S probably damaging Het
Efcab14 T C 4: 115,597,728 (GRCm39) F108L probably damaging Het
Ell2 T C 13: 75,910,259 (GRCm39) probably benign Het
Fam234b T G 6: 135,194,072 (GRCm39) S242A possibly damaging Het
Fhip2a G A 19: 57,369,839 (GRCm39) D461N probably benign Het
Garnl3 T C 2: 32,896,816 (GRCm39) T608A possibly damaging Het
Gata3 T C 2: 9,879,620 (GRCm39) T119A probably benign Het
Hdac2 T A 10: 36,865,180 (GRCm39) D131E probably benign Het
Hira T A 16: 18,774,921 (GRCm39) F949I probably benign Het
Il3 A G 11: 54,156,506 (GRCm39) probably null Het
Itgb3 A T 11: 104,527,914 (GRCm39) K216N probably damaging Het
Jkampl A G 6: 73,446,402 (GRCm39) L49P possibly damaging Het
Kctd21 T A 7: 96,997,298 (GRCm39) I257N probably benign Het
Kif16b A T 2: 142,514,295 (GRCm39) S1215T probably benign Het
Lhx9 A T 1: 138,766,417 (GRCm39) C124S probably damaging Het
Lrch3 T A 16: 32,782,124 (GRCm39) probably benign Het
Lrp1b T C 2: 40,486,995 (GRCm39) E142G probably damaging Het
Macf1 T C 4: 123,326,636 (GRCm39) M2835V possibly damaging Het
Mndal A T 1: 173,685,079 (GRCm39) probably benign Het
Mug2 G T 6: 122,051,673 (GRCm39) V952L possibly damaging Het
Nepn A T 10: 52,276,533 (GRCm39) T29S probably damaging Het
Nlgn1 C T 3: 25,490,089 (GRCm39) C546Y probably damaging Het
Notch4 C T 17: 34,784,337 (GRCm39) R43W possibly damaging Het
Nrxn1 A T 17: 91,302,915 (GRCm39) probably null Het
Or14a260 A G 7: 85,984,803 (GRCm39) I267T probably benign Het
Or8k53 T C 2: 86,178,072 (GRCm39) I13V possibly damaging Het
Phf3 A T 1: 30,844,146 (GRCm39) D1604E probably benign Het
Plekhn1 T C 4: 156,312,700 (GRCm39) R53G probably benign Het
Pnp2 T C 14: 51,200,634 (GRCm39) F100S probably damaging Het
Rimoc1 T C 15: 4,015,776 (GRCm39) K263E probably damaging Het
Rxfp1 A G 3: 79,564,783 (GRCm39) S327P probably damaging Het
Siah2 A G 3: 58,583,536 (GRCm39) V250A probably damaging Het
Slc10a7 T A 8: 79,423,787 (GRCm39) probably null Het
Slc9a1 A G 4: 133,147,916 (GRCm39) K645E probably benign Het
Smarca4 T C 9: 21,548,620 (GRCm39) L302P probably damaging Het
Tas2r120 T A 6: 132,634,552 (GRCm39) Y211* probably null Het
Tenm3 A T 8: 49,127,507 (GRCm39) L57Q probably damaging Het
Tep1 C T 14: 51,067,150 (GRCm39) V2269I possibly damaging Het
Tpd52l1 A G 10: 31,255,252 (GRCm39) S32P probably damaging Het
Tsfm A G 10: 126,858,798 (GRCm39) probably benign Het
Ttn T A 2: 76,540,468 (GRCm39) R34173W probably damaging Het
Ttn C A 2: 76,623,474 (GRCm39) V15368L possibly damaging Het
Upk1a A T 7: 30,311,819 (GRCm39) I25N possibly damaging Het
Vmn1r45 A T 6: 89,910,492 (GRCm39) Y159* probably null Het
Vmn2r13 C A 5: 109,322,915 (GRCm39) V125L probably benign Het
Vps13b T C 15: 35,887,407 (GRCm39) I3272T probably benign Het
Zfp108 A G 7: 23,959,892 (GRCm39) H161R probably benign Het
Zfp982 A T 4: 147,597,093 (GRCm39) K150I probably benign Het
Zfyve1 A G 12: 83,601,847 (GRCm39) probably benign Het
Other mutations in Zswim8
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00418:Zswim8 APN 14 20,768,543 (GRCm39) missense probably damaging 0.99
IGL00470:Zswim8 APN 14 20,773,249 (GRCm39) missense probably damaging 1.00
IGL00675:Zswim8 APN 14 20,766,969 (GRCm39) unclassified probably benign
IGL00896:Zswim8 APN 14 20,766,069 (GRCm39) missense probably damaging 1.00
IGL01343:Zswim8 APN 14 20,763,409 (GRCm39) missense probably damaging 1.00
IGL01736:Zswim8 APN 14 20,764,780 (GRCm39) missense probably benign 0.11
IGL01961:Zswim8 APN 14 20,762,402 (GRCm39) missense possibly damaging 0.76
IGL02331:Zswim8 APN 14 20,773,325 (GRCm39) missense probably damaging 1.00
IGL02485:Zswim8 APN 14 20,761,955 (GRCm39) missense probably damaging 0.98
IGL02662:Zswim8 APN 14 20,763,142 (GRCm39) missense probably benign 0.14
IGL03001:Zswim8 APN 14 20,764,459 (GRCm39) missense probably damaging 1.00
pool UTSW 14 20,764,641 (GRCm39) splice site probably null
R0362:Zswim8 UTSW 14 20,772,013 (GRCm39) missense possibly damaging 0.58
R0402:Zswim8 UTSW 14 20,760,834 (GRCm39) missense probably damaging 1.00
R0458:Zswim8 UTSW 14 20,768,965 (GRCm39) missense probably damaging 1.00
R1087:Zswim8 UTSW 14 20,767,933 (GRCm39) splice site probably null
R1158:Zswim8 UTSW 14 20,771,736 (GRCm39) splice site probably benign
R1171:Zswim8 UTSW 14 20,763,181 (GRCm39) missense possibly damaging 0.94
R1389:Zswim8 UTSW 14 20,760,816 (GRCm39) missense probably damaging 1.00
R1773:Zswim8 UTSW 14 20,761,598 (GRCm39) missense probably damaging 0.96
R1780:Zswim8 UTSW 14 20,766,395 (GRCm39) missense probably damaging 0.99
R1850:Zswim8 UTSW 14 20,760,815 (GRCm39) nonsense probably null
R2421:Zswim8 UTSW 14 20,769,525 (GRCm39) missense probably damaging 1.00
R3826:Zswim8 UTSW 14 20,761,157 (GRCm39) nonsense probably null
R3965:Zswim8 UTSW 14 20,763,141 (GRCm39) missense probably benign
R4301:Zswim8 UTSW 14 20,763,977 (GRCm39) missense possibly damaging 0.91
R4499:Zswim8 UTSW 14 20,764,365 (GRCm39) missense probably benign 0.05
R4633:Zswim8 UTSW 14 20,768,891 (GRCm39) missense probably damaging 1.00
R4675:Zswim8 UTSW 14 20,764,681 (GRCm39) missense probably benign
R4958:Zswim8 UTSW 14 20,763,533 (GRCm39) missense probably damaging 1.00
R5255:Zswim8 UTSW 14 20,771,719 (GRCm39) missense probably damaging 1.00
R5288:Zswim8 UTSW 14 20,768,939 (GRCm39) missense possibly damaging 0.92
R5341:Zswim8 UTSW 14 20,766,122 (GRCm39) missense probably damaging 1.00
R5495:Zswim8 UTSW 14 20,772,354 (GRCm39) missense probably damaging 0.97
R5652:Zswim8 UTSW 14 20,763,495 (GRCm39) missense possibly damaging 0.62
R6273:Zswim8 UTSW 14 20,763,521 (GRCm39) missense probably benign 0.06
R6281:Zswim8 UTSW 14 20,764,708 (GRCm39) missense probably benign 0.02
R6364:Zswim8 UTSW 14 20,763,079 (GRCm39) missense probably damaging 1.00
R6426:Zswim8 UTSW 14 20,768,594 (GRCm39) missense probably damaging 0.99
R6576:Zswim8 UTSW 14 20,771,942 (GRCm39) missense probably benign 0.41
R6798:Zswim8 UTSW 14 20,766,060 (GRCm39) missense probably damaging 1.00
R7059:Zswim8 UTSW 14 20,764,641 (GRCm39) splice site probably null
R7243:Zswim8 UTSW 14 20,764,436 (GRCm39) missense probably damaging 1.00
R7250:Zswim8 UTSW 14 20,770,036 (GRCm39) missense probably damaging 1.00
R7311:Zswim8 UTSW 14 20,771,552 (GRCm39) missense probably damaging 1.00
R7567:Zswim8 UTSW 14 20,770,001 (GRCm39) missense probably damaging 1.00
R7635:Zswim8 UTSW 14 20,766,368 (GRCm39) missense probably damaging 0.99
R7771:Zswim8 UTSW 14 20,763,048 (GRCm39) missense probably damaging 1.00
R7874:Zswim8 UTSW 14 20,773,217 (GRCm39) missense probably damaging 0.98
R7994:Zswim8 UTSW 14 20,758,072 (GRCm39) missense possibly damaging 0.95
R8466:Zswim8 UTSW 14 20,760,744 (GRCm39) missense possibly damaging 0.93
R9019:Zswim8 UTSW 14 20,761,119 (GRCm39) missense probably damaging 1.00
R9177:Zswim8 UTSW 14 20,761,908 (GRCm39) missense probably damaging 1.00
R9192:Zswim8 UTSW 14 20,769,588 (GRCm39) missense probably damaging 1.00
R9229:Zswim8 UTSW 14 20,766,393 (GRCm39) missense probably benign 0.45
R9268:Zswim8 UTSW 14 20,761,908 (GRCm39) missense probably damaging 1.00
R9562:Zswim8 UTSW 14 20,762,150 (GRCm39) nonsense probably null
R9589:Zswim8 UTSW 14 20,763,171 (GRCm39) missense probably damaging 0.99
R9621:Zswim8 UTSW 14 20,772,231 (GRCm39) missense probably benign 0.00
X0026:Zswim8 UTSW 14 20,760,700 (GRCm39) splice site probably null
X0028:Zswim8 UTSW 14 20,764,725 (GRCm39) missense probably benign 0.19
X0058:Zswim8 UTSW 14 20,763,058 (GRCm39) missense probably damaging 0.99
Z1177:Zswim8 UTSW 14 20,763,112 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TTGCACTTCCCATGTAGGGCAAG -3'
(R):5'- AGGGCATTATACCTGGAGCACAGAG -3'

Sequencing Primer
(F):5'- AAGGTGTCCACAAGCCGTC -3'
(R):5'- TTATACCTGGAGCACAGAGAACATC -3'
Posted On 2013-04-11