Incidental Mutation 'PIT4366001:Spata31'
ID 554788
Institutional Source Beutler Lab
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 # PIT4366001 (G1)
Quality Score 225.009
Status Not validated
Chromosome 13
Chromosomal Location 65065220-65071008 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to A at 65069319 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Stop codon at position 489 (S489*)
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: S489*
SMART Domains Protein: ENSMUSP00000097025
Gene: ENSMUSG00000056223
AA Change: S489*

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
  • 1x: 93.0%
  • 3x: 90.7%
  • 10x: 85.5%
  • 20x: 73.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 68 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aatk C A 11: 119,901,786 (GRCm39) S870I possibly damaging Het
Abca13 T C 11: 9,244,962 (GRCm39) V2275A probably benign Het
Abcb5 T C 12: 118,899,833 (GRCm39) K278R probably damaging Het
Adcy2 TA TAA 13: 68,858,109 (GRCm39) probably benign Het
Add3 C T 19: 53,205,298 (GRCm39) P16L unknown Het
Akap9 T A 5: 4,096,221 (GRCm39) D2365E probably benign Het
Asah1 A G 8: 41,796,783 (GRCm39) S300P possibly damaging Het
Astn1 A T 1: 158,424,779 (GRCm39) H655L probably benign Het
Astn1 A T 1: 158,424,781 (GRCm39) I656F probably benign Het
Bmpr1b T A 3: 141,586,224 (GRCm39) T13S probably benign Het
Camsap2 A G 1: 136,208,055 (GRCm39) F478L Het
Card10 G A 15: 78,671,631 (GRCm39) S611L probably benign Het
Cep68 T C 11: 20,190,007 (GRCm39) N335S probably benign Het
Chac1 T C 2: 119,181,986 (GRCm39) W35R probably damaging Het
Cntn6 T C 6: 104,809,498 (GRCm39) V511A probably benign Het
Cpne9 G T 6: 113,271,707 (GRCm39) G356W probably damaging Het
Dnah10 C A 5: 124,852,588 (GRCm39) T1939K possibly damaging Het
Dock10 T C 1: 80,573,438 (GRCm39) N239D probably benign Het
Dock5 T C 14: 68,062,123 (GRCm39) K415R possibly damaging Het
Dtd2 C A 12: 52,046,582 (GRCm39) D86Y probably damaging Het
Efcab9 A G 11: 32,473,608 (GRCm39) F127S probably damaging Het
Ermp1 T C 19: 29,606,189 (GRCm39) H375R probably benign Het
Frem2 A T 3: 53,560,622 (GRCm39) M1295K probably damaging Het
Gbp7 T G 3: 142,248,712 (GRCm39) I325R probably benign Het
Gpr179 T C 11: 97,227,677 (GRCm39) K1493E probably benign Het
Gucy2g T A 19: 55,226,214 (GRCm39) E234V probably null Het
Itpr1 T A 6: 108,470,718 (GRCm39) C2215* probably null Het
Ltn1 G A 16: 87,177,728 (GRCm39) R1634* probably null Het
Lynx1 A T 15: 74,623,258 (GRCm39) M58K possibly damaging Het
Macc1 T C 12: 119,410,684 (GRCm39) V484A probably benign Het
Map3k9 C T 12: 81,819,535 (GRCm39) V240M possibly damaging Het
Mars1 A G 10: 127,135,267 (GRCm39) M608T possibly damaging Het
Mc2r T C 18: 68,540,826 (GRCm39) M156V probably benign Het
Mchr1 G T 15: 81,121,417 (GRCm39) V56L probably benign Het
Mlxip C T 5: 123,533,173 (GRCm39) P61S probably benign Het
Mtarc1 A G 1: 184,539,383 (GRCm39) F96S probably benign Het
Muc4 A G 16: 32,575,542 (GRCm39) T1557A unknown Het
Myt1 T C 2: 181,467,731 (GRCm39) V1135A probably damaging Het
Ndufaf6 A T 4: 11,073,215 (GRCm39) S76T probably benign Het
Ntrk2 A G 13: 59,208,149 (GRCm39) Y665C probably damaging Het
Oaz3 T G 3: 94,340,901 (GRCm39) R215S unknown Het
Or10x1 T C 1: 174,196,656 (GRCm39) Y58H probably damaging Het
Or5m10b T C 2: 85,699,226 (GRCm39) C97R probably damaging Het
Or5m8 A T 2: 85,822,385 (GRCm39) N75Y probably damaging Het
Or5w1b C T 2: 87,475,534 (GRCm39) W311* probably null Het
Perm1 G T 4: 156,303,192 (GRCm39) V579L probably benign Het
Phyhipl A G 10: 70,404,788 (GRCm39) V140A probably benign Het
Pip5k1c T A 10: 81,144,842 (GRCm39) S228T probably damaging Het
Plekhn1 T G 4: 156,309,268 (GRCm39) T213P probably damaging Het
Pomt2 A T 12: 87,163,303 (GRCm39) probably null Het
Ptcd1 A G 5: 145,088,145 (GRCm39) V622A probably benign Het
Ptn T A 6: 36,718,284 (GRCm39) H127L probably benign Het
Ptprk A T 10: 28,462,015 (GRCm39) M1193L probably benign Het
Ptpru G A 4: 131,527,023 (GRCm39) P650S probably benign Het
Pum2 T A 12: 8,783,390 (GRCm39) L613Q probably damaging Het
Rapgef6 A G 11: 54,582,446 (GRCm39) T1458A probably damaging Het
Sap130 C T 18: 31,810,462 (GRCm39) A470V probably benign Het
Sertad2 C A 11: 20,598,116 (GRCm39) P104Q probably benign Het
Sfrp4 A T 13: 19,814,414 (GRCm39) M324L unknown Het
Sh3bp4 A G 1: 89,073,156 (GRCm39) N668S probably benign Het
Snx30 C A 4: 59,894,653 (GRCm39) D410E probably benign Het
Taok3 T A 5: 117,366,050 (GRCm39) M367K probably benign Het
Tfap2a T C 13: 40,874,850 (GRCm39) N254D possibly damaging Het
Tgtp1 T G 11: 48,877,867 (GRCm39) L279F possibly damaging Het
Tmpo A G 10: 90,999,172 (GRCm39) F205S probably damaging Het
Tmprss5 A T 9: 49,023,517 (GRCm39) I218L probably benign Het
Tti2 A G 8: 31,641,224 (GRCm39) E116G probably benign Het
Vmn2r59 A T 7: 41,695,205 (GRCm39) N402K possibly damaging Het
Other mutations in Spata31
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00663:Spata31 APN 13 65,070,602 (GRCm39) nonsense probably null
IGL01143:Spata31 APN 13 65,068,630 (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
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
Predicted Primers PCR Primer
(F):5'- AGATCCAATCAGGGGCTTGG -3'
(R):5'- CCTATGTACAGAAGTGGTTGAGGAG -3'

Sequencing Primer
(F):5'- CCCTCTAAGTATGCGACA -3'
(R):5'- TGAGGAGGTCTGGGCAC -3'
Posted On 2019-06-07