Incidental Mutation 'IGL01143:Spata31'
ID 52613
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Spata31
Ensembl Gene ENSMUSG00000056223
Gene Name spermatogenesis associated 31
Synonyms Fam75a, Spata31a, 4930458L03Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.191) question?
Stock # IGL01143
Quality Score
Status
Chromosome 13
Chromosomal Location 65065220-65071008 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to G at 65068630 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 259 (Y259*)
Ref Sequence ENSEMBL: ENSMUSP00000097025 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000070216] [ENSMUST00000221202]
AlphaFold E9QAF0
Predicted Effect probably null
Transcript: ENSMUST00000070216
AA Change: Y259*
SMART Domains Protein: ENSMUSP00000097025
Gene: ENSMUSG00000056223
AA Change: Y259*

DomainStartEndE-ValueType
low complexity region 35 45 N/A INTRINSIC
low complexity region 91 106 N/A INTRINSIC
Pfam:FAM75 149 431 1.7e-83 PFAM
Pfam:FAM75 426 462 4.5e-9 PFAM
low complexity region 478 491 N/A INTRINSIC
low complexity region 544 555 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000221202
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abtb3 A T 10: 85,490,335 (GRCm39) probably benign Het
Adgrl4 A G 3: 151,205,866 (GRCm39) probably null Het
Adgrv1 A C 13: 81,567,470 (GRCm39) D5234E probably benign Het
Bmp7 G T 2: 172,721,275 (GRCm39) H267N probably benign Het
Ccdc113 T C 8: 96,260,888 (GRCm39) V30A probably damaging Het
Ccdc185 A T 1: 182,575,417 (GRCm39) L424Q probably damaging Het
Cep192 T A 18: 67,937,445 (GRCm39) D58E probably damaging Het
Ces1f C T 8: 93,998,458 (GRCm39) probably null Het
Chaf1a T A 17: 56,370,336 (GRCm39) D600E possibly damaging Het
Cndp2 A G 18: 84,695,442 (GRCm39) probably null Het
Dnah11 T A 12: 117,976,475 (GRCm39) D2727V probably damaging Het
Dync1li2 T C 8: 105,156,085 (GRCm39) D252G probably damaging Het
Ephx2 C T 14: 66,326,971 (GRCm39) R408Q probably damaging Het
Fat1 C A 8: 45,488,569 (GRCm39) T3427K possibly damaging Het
Gal3st4 A G 5: 138,269,664 (GRCm39) M1T probably null Het
Gm5828 T C 1: 16,840,172 (GRCm39) noncoding transcript Het
Gm7694 C T 1: 170,130,394 (GRCm39) M1I probably null Het
Gpatch1 A G 7: 35,000,997 (GRCm39) probably benign Het
Grik1 G T 16: 87,754,488 (GRCm39) probably null Het
Gtf2ird2 A G 5: 134,225,394 (GRCm39) T161A possibly damaging Het
Hk2 T C 6: 82,706,533 (GRCm39) I790V possibly damaging Het
Ints9 G A 14: 65,274,870 (GRCm39) V609I probably benign Het
Kcnq4 T G 4: 120,555,820 (GRCm39) D585A probably damaging Het
Large2 T C 2: 92,196,684 (GRCm39) Y464C probably damaging Het
Lpar6 G A 14: 73,476,077 (GRCm39) D13N probably damaging Het
Morn1 T C 4: 155,176,761 (GRCm39) Y132H probably damaging Het
Nphp1 C T 2: 127,622,056 (GRCm39) V24I probably benign Het
Or5b104 A T 19: 13,072,476 (GRCm39) F179I probably damaging Het
Or5w17 T C 2: 87,584,278 (GRCm39) N20D probably benign Het
Or8b1c G T 9: 38,384,338 (GRCm39) M98I possibly damaging Het
Pcdhb13 T C 18: 37,575,690 (GRCm39) W23R probably benign Het
Plekhg3 T C 12: 76,611,756 (GRCm39) probably null Het
Slx4 T C 16: 3,808,752 (GRCm39) K396R probably benign Het
Snx13 A G 12: 35,182,159 (GRCm39) D736G probably damaging Het
Spag17 A G 3: 99,846,614 (GRCm39) D46G probably benign Het
Synj1 T C 16: 90,748,864 (GRCm39) E1064G probably damaging Het
Tom1 A G 8: 75,785,085 (GRCm39) T81A probably benign Het
Ttc23l A G 15: 10,530,775 (GRCm39) I279T probably damaging Het
Ttc39a T C 4: 109,300,010 (GRCm39) probably null Het
Vmn2r108 C A 17: 20,682,727 (GRCm39) A826S possibly damaging Het
Zyg11b A T 4: 108,102,191 (GRCm39) V510E possibly damaging Het
Other mutations in Spata31
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00663:Spata31 APN 13 65,070,602 (GRCm39) nonsense probably null
IGL01321:Spata31 APN 13 65,069,568 (GRCm39) missense probably benign 0.01
IGL01624:Spata31 APN 13 65,069,399 (GRCm39) missense probably damaging 1.00
IGL01844:Spata31 APN 13 65,068,968 (GRCm39) missense possibly damaging 0.49
IGL02259:Spata31 APN 13 65,069,297 (GRCm39) missense possibly damaging 0.90
IGL02358:Spata31 APN 13 65,069,032 (GRCm39) missense probably benign
IGL02377:Spata31 APN 13 65,068,194 (GRCm39) missense probably damaging 0.98
IGL02723:Spata31 APN 13 65,068,463 (GRCm39) missense probably benign 0.10
IGL03125:Spata31 APN 13 65,068,703 (GRCm39) missense probably benign 0.09
IGL03343:Spata31 APN 13 65,067,587 (GRCm39) missense probably benign 0.41
BB006:Spata31 UTSW 13 65,069,532 (GRCm39) missense probably benign 0.04
BB016:Spata31 UTSW 13 65,069,532 (GRCm39) missense probably benign 0.04
F5770:Spata31 UTSW 13 65,069,462 (GRCm39) missense probably benign 0.18
IGL02991:Spata31 UTSW 13 65,068,533 (GRCm39) missense probably benign 0.05
P0043:Spata31 UTSW 13 65,068,820 (GRCm39) splice site probably null
PIT4366001:Spata31 UTSW 13 65,069,319 (GRCm39) nonsense probably null
PIT4458001:Spata31 UTSW 13 65,069,664 (GRCm39) missense probably benign 0.01
PIT4687001:Spata31 UTSW 13 65,069,151 (GRCm39) missense probably benign 0.02
R0042:Spata31 UTSW 13 65,070,377 (GRCm39) missense probably benign 0.00
R0042:Spata31 UTSW 13 65,070,377 (GRCm39) missense probably benign 0.00
R0064:Spata31 UTSW 13 65,069,912 (GRCm39) missense probably damaging 0.98
R0064:Spata31 UTSW 13 65,069,912 (GRCm39) missense probably damaging 0.98
R0639:Spata31 UTSW 13 65,070,027 (GRCm39) missense probably benign 0.02
R1253:Spata31 UTSW 13 65,069,838 (GRCm39) missense probably benign 0.23
R1536:Spata31 UTSW 13 65,069,196 (GRCm39) missense probably damaging 1.00
R1656:Spata31 UTSW 13 65,068,953 (GRCm39) missense probably benign
R1802:Spata31 UTSW 13 65,070,197 (GRCm39) missense probably benign 0.01
R1813:Spata31 UTSW 13 65,069,612 (GRCm39) missense probably benign 0.32
R1916:Spata31 UTSW 13 65,070,359 (GRCm39) nonsense probably null
R1917:Spata31 UTSW 13 65,068,679 (GRCm39) missense possibly damaging 0.92
R1933:Spata31 UTSW 13 65,068,424 (GRCm39) missense probably benign 0.02
R2910:Spata31 UTSW 13 65,068,250 (GRCm39) missense probably benign 0.12
R3750:Spata31 UTSW 13 65,069,557 (GRCm39) missense probably benign 0.01
R3876:Spata31 UTSW 13 65,068,745 (GRCm39) missense probably benign 0.03
R3980:Spata31 UTSW 13 65,070,468 (GRCm39) missense probably benign 0.24
R4056:Spata31 UTSW 13 65,069,469 (GRCm39) missense probably benign 0.00
R4300:Spata31 UTSW 13 65,067,575 (GRCm39) missense probably benign 0.08
R4797:Spata31 UTSW 13 65,070,556 (GRCm39) nonsense probably null
R4997:Spata31 UTSW 13 65,067,537 (GRCm39) missense probably benign 0.00
R5185:Spata31 UTSW 13 65,065,340 (GRCm39) missense possibly damaging 0.93
R5366:Spata31 UTSW 13 65,068,273 (GRCm39) missense probably damaging 0.98
R5539:Spata31 UTSW 13 65,070,783 (GRCm39) missense probably benign 0.00
R5704:Spata31 UTSW 13 65,069,855 (GRCm39) missense probably benign 0.32
R5748:Spata31 UTSW 13 65,068,127 (GRCm39) makesense probably null
R5834:Spata31 UTSW 13 65,070,480 (GRCm39) missense probably benign 0.19
R5926:Spata31 UTSW 13 65,068,539 (GRCm39) missense possibly damaging 0.82
R6476:Spata31 UTSW 13 65,065,456 (GRCm39) missense possibly damaging 0.68
R6603:Spata31 UTSW 13 65,070,479 (GRCm39) missense probably damaging 1.00
R6620:Spata31 UTSW 13 65,067,571 (GRCm39) missense possibly damaging 0.68
R6965:Spata31 UTSW 13 65,070,648 (GRCm39) missense possibly damaging 0.90
R7086:Spata31 UTSW 13 65,070,043 (GRCm39) missense probably benign 0.02
R7140:Spata31 UTSW 13 65,068,913 (GRCm39) missense probably benign
R7396:Spata31 UTSW 13 65,068,547 (GRCm39) missense probably benign
R7545:Spata31 UTSW 13 65,070,359 (GRCm39) nonsense probably null
R7575:Spata31 UTSW 13 65,070,726 (GRCm39) missense unknown
R7607:Spata31 UTSW 13 65,069,406 (GRCm39) missense probably damaging 1.00
R7929:Spata31 UTSW 13 65,069,532 (GRCm39) missense probably benign 0.04
R8024:Spata31 UTSW 13 65,070,618 (GRCm39) missense probably benign 0.12
R8088:Spata31 UTSW 13 65,068,679 (GRCm39) missense probably benign 0.31
R8323:Spata31 UTSW 13 65,070,065 (GRCm39) missense possibly damaging 0.61
R8362:Spata31 UTSW 13 65,070,044 (GRCm39) missense possibly damaging 0.58
R8870:Spata31 UTSW 13 65,068,818 (GRCm39) missense probably benign
R9429:Spata31 UTSW 13 65,070,336 (GRCm39) missense probably benign 0.43
R9465:Spata31 UTSW 13 65,068,527 (GRCm39) missense probably damaging 1.00
R9542:Spata31 UTSW 13 65,070,077 (GRCm39) missense probably damaging 0.96
R9627:Spata31 UTSW 13 65,065,409 (GRCm39) missense possibly damaging 0.95
V7580:Spata31 UTSW 13 65,069,462 (GRCm39) missense probably benign 0.18
V7581:Spata31 UTSW 13 65,069,462 (GRCm39) missense probably benign 0.18
V7583:Spata31 UTSW 13 65,069,462 (GRCm39) missense probably benign 0.18
Z1176:Spata31 UTSW 13 65,069,786 (GRCm39) nonsense probably null
Z1177:Spata31 UTSW 13 65,069,786 (GRCm39) nonsense probably null
Posted On 2013-06-21