Incidental Mutation 'R5290:Slfn10-ps'
ID 424669
Institutional Source Beutler Lab
Gene Symbol Slfn10-ps
Ensembl Gene ENSMUSG00000072621
Gene Name schlafen 10, pseudogene
Synonyms
MMRRC Submission 042873-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.073) question?
Stock # R5290 (G1)
Quality Score 225
Status Validated
Chromosome 11
Chromosomal Location 82919681-82926992 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to A at 82919851 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s):
AlphaFold no structure available at present
Predicted Effect noncoding transcript
Transcript: ENSMUST00000100716
SMART Domains Protein: ENSMUSP00000098282
Gene: ENSMUSG00000072621

DomainStartEndE-ValueType
Pfam:AlbA_2 142 278 1.3e-13 PFAM
Pfam:DUF2075 529 697 1.6e-7 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000119608
Predicted Effect noncoding transcript
Transcript: ENSMUST00000152760
SMART Domains Protein: ENSMUSP00000130353
Gene: ENSMUSG00000072621

DomainStartEndE-ValueType
Pfam:AAA_4 142 280 1.8e-14 PFAM
Pfam:DUF2075 529 693 1.8e-8 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185158
Meta Mutation Damage Score 0.0869 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.1%
  • 20x: 94.8%
Validation Efficiency 97% (70/72)
Allele List at MGI
Other mutations in this stock
Total: 62 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110008E08Rik A T 16: 90,351,098 (GRCm39) noncoding transcript Het
2700049A03Rik C A 12: 71,235,565 (GRCm39) P1172T probably benign Het
Abi3bp T A 16: 56,462,838 (GRCm39) probably null Het
Apod T A 16: 31,129,884 (GRCm39) H24L probably damaging Het
Arfgef3 T C 10: 18,476,208 (GRCm39) E1537G probably damaging Het
B020004C17Rik T C 14: 57,254,036 (GRCm39) V53A possibly damaging Het
Ccdc113 C A 8: 96,267,424 (GRCm39) probably null Het
Cd7 T G 11: 120,928,936 (GRCm39) D105A probably damaging Het
Celsr3 C T 9: 108,720,357 (GRCm39) T2550M probably benign Het
Cibar1 T C 4: 12,171,195 (GRCm39) Q86R probably benign Het
Col6a5 C T 9: 105,823,282 (GRCm39) G25D unknown Het
Cps1 A G 1: 67,211,868 (GRCm39) M679V probably benign Het
Dnai4 A T 4: 102,906,730 (GRCm39) D694E probably benign Het
Dync1h1 A T 12: 110,581,502 (GRCm39) T316S probably benign Het
Edrf1 T C 7: 133,252,295 (GRCm39) Y449H probably damaging Het
Fkbpl G A 17: 34,864,303 (GRCm39) A24T probably benign Het
Flg2 A T 3: 93,127,873 (GRCm39) I2262L unknown Het
Flnc T C 6: 29,457,553 (GRCm39) L2417P probably damaging Het
Gabrp A T 11: 33,517,310 (GRCm39) Y121N probably damaging Het
Gdpd4 A G 7: 97,615,543 (GRCm39) T123A possibly damaging Het
Gpr162 C A 6: 124,838,232 (GRCm39) M139I probably benign Het
Greb1l G A 18: 10,542,427 (GRCm39) E1341K probably damaging Het
Gsn G A 2: 35,186,484 (GRCm39) S410N probably benign Het
Gtf2f2 T C 14: 76,135,089 (GRCm39) Y212C probably damaging Het
Hao2 C T 3: 98,784,493 (GRCm39) A291T probably damaging Het
Igkv1-133 A G 6: 67,702,563 (GRCm39) T94A possibly damaging Het
Irf2bp1 G A 7: 18,738,923 (GRCm39) A188T possibly damaging Het
Itpr1 T C 6: 108,383,106 (GRCm39) V1478A possibly damaging Het
Kdm5b T C 1: 134,549,837 (GRCm39) probably null Het
Kif5b A T 18: 6,234,882 (GRCm39) D49E probably damaging Het
Lmbr1l A G 15: 98,810,123 (GRCm39) W113R probably damaging Het
Lrp2 T C 2: 69,343,698 (GRCm39) D887G probably damaging Het
Lrrc14 T A 15: 76,598,143 (GRCm39) M291K probably benign Het
Lypd11 T C 7: 24,422,836 (GRCm39) E79G probably benign Het
Mgarp G A 3: 51,296,387 (GRCm39) A205V possibly damaging Het
Msl2 T C 9: 100,978,606 (GRCm39) probably null Het
Nfix G A 8: 85,440,406 (GRCm39) Q487* probably null Het
Notch4 T C 17: 34,784,263 (GRCm39) V22A probably benign Het
Npc1l1 T A 11: 6,172,221 (GRCm39) Q823L probably benign Het
Obox3 T C 7: 15,360,774 (GRCm39) K122E probably benign Het
Or10ab5 C T 7: 108,245,755 (GRCm39) M9I probably benign Het
Or2a12 A G 6: 42,904,972 (GRCm39) K269R probably damaging Het
Or8s10 T C 15: 98,336,213 (GRCm39) Y288H probably damaging Het
Plekhh3 T A 11: 101,057,397 (GRCm39) M287L possibly damaging Het
Prpf3 A T 3: 95,760,857 (GRCm39) I15K probably benign Het
Rpl12-ps1 G T 1: 36,997,423 (GRCm39) noncoding transcript Het
Rps8 G C 4: 117,012,352 (GRCm39) probably benign Het
Setd2 T C 9: 110,446,899 (GRCm39) V2489A probably damaging Het
Smad2 C T 18: 76,395,795 (GRCm39) P78L probably damaging Het
Spen G A 4: 141,201,127 (GRCm39) T2500I probably damaging Het
Stmnd1 A G 13: 46,453,074 (GRCm39) D250G probably benign Het
Tjp2 T G 19: 24,108,568 (GRCm39) E181D probably benign Het
Tmem131l T C 3: 83,806,572 (GRCm39) D1478G probably benign Het
Trim72 G T 7: 127,609,176 (GRCm39) R326L probably benign Het
Ttn A T 2: 76,727,584 (GRCm39) probably benign Het
Vmn1r177 A T 7: 23,565,498 (GRCm39) M126K probably damaging Het
Vmn1r57 A G 7: 5,224,319 (GRCm39) I281M probably damaging Het
Vmn2r108 C A 17: 20,691,665 (GRCm39) R286L probably benign Het
Wdr25 T C 12: 108,863,968 (GRCm39) S38P probably benign Het
Zfp937 T A 2: 150,080,229 (GRCm39) Y86* probably null Het
Zfr2 CTCAGACTGGTGTCAGAC CTCAGAC 10: 81,082,544 (GRCm39) probably null Het
Zswim1 C T 2: 164,667,845 (GRCm39) H366Y probably damaging Het
Other mutations in Slfn10-ps
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00773:Slfn10-ps APN 11 82,926,355 (GRCm39) unclassified noncoding transcript
IGL00826:Slfn10-ps APN 11 82,926,085 (GRCm39) unclassified noncoding transcript
IGL01022:Slfn10-ps APN 11 82,926,353 (GRCm39) unclassified noncoding transcript
IGL01409:Slfn10-ps APN 11 82,926,322 (GRCm39) unclassified noncoding transcript
IGL01664:Slfn10-ps APN 11 82,926,761 (GRCm39) unclassified noncoding transcript
IGL01700:Slfn10-ps APN 11 82,919,938 (GRCm39) unclassified noncoding transcript
IGL02093:Slfn10-ps APN 11 82,923,016 (GRCm39) unclassified noncoding transcript
IGL02253:Slfn10-ps APN 11 82,919,890 (GRCm39) unclassified noncoding transcript
IGL02364:Slfn10-ps APN 11 82,923,117 (GRCm39) unclassified noncoding transcript
IGL02466:Slfn10-ps APN 11 82,921,090 (GRCm39) unclassified noncoding transcript
IGL02636:Slfn10-ps APN 11 82,920,971 (GRCm39) unclassified noncoding transcript
R0055:Slfn10-ps UTSW 11 82,921,126 (GRCm39) unclassified noncoding transcript
R0055:Slfn10-ps UTSW 11 82,921,126 (GRCm39) unclassified noncoding transcript
R0069:Slfn10-ps UTSW 11 82,926,368 (GRCm39) unclassified noncoding transcript
R0069:Slfn10-ps UTSW 11 82,926,368 (GRCm39) unclassified noncoding transcript
R0164:Slfn10-ps UTSW 11 82,926,128 (GRCm39) unclassified noncoding transcript
R0362:Slfn10-ps UTSW 11 82,926,600 (GRCm39) unclassified noncoding transcript
R0382:Slfn10-ps UTSW 11 82,920,360 (GRCm39) unclassified noncoding transcript
R0597:Slfn10-ps UTSW 11 82,926,479 (GRCm39) unclassified noncoding transcript
R0812:Slfn10-ps UTSW 11 82,926,388 (GRCm39) unclassified noncoding transcript
R0904:Slfn10-ps UTSW 11 82,926,235 (GRCm39) unclassified noncoding transcript
R1552:Slfn10-ps UTSW 11 82,920,676 (GRCm39) unclassified noncoding transcript
R1703:Slfn10-ps UTSW 11 82,920,869 (GRCm39) unclassified noncoding transcript
R2127:Slfn10-ps UTSW 11 82,921,168 (GRCm39) unclassified noncoding transcript
R2151:Slfn10-ps UTSW 11 82,926,511 (GRCm39) unclassified noncoding transcript
R2302:Slfn10-ps UTSW 11 82,919,756 (GRCm39) unclassified noncoding transcript
R3114:Slfn10-ps UTSW 11 82,919,955 (GRCm39) unclassified noncoding transcript
R4293:Slfn10-ps UTSW 11 82,926,260 (GRCm39) unclassified noncoding transcript
R4929:Slfn10-ps UTSW 11 82,920,345 (GRCm39) unclassified noncoding transcript
R4970:Slfn10-ps UTSW 11 82,921,207 (GRCm39) unclassified noncoding transcript
R5083:Slfn10-ps UTSW 11 82,921,341 (GRCm39) unclassified noncoding transcript
R5306:Slfn10-ps UTSW 11 82,926,355 (GRCm39) unclassified noncoding transcript
R5444:Slfn10-ps UTSW 11 82,926,113 (GRCm39) unclassified noncoding transcript
Predicted Primers PCR Primer
(F):5'- ACTGTTGAGCTATACCCCTCAGG -3'
(R):5'- GTGTATCAGGCACCCATGAG -3'

Sequencing Primer
(F):5'- TGAGCTATACCCCTCAGGAGTTG -3'
(R):5'- GTGTATCAGGCACCCATGAGATTAC -3'
Posted On 2016-08-04