Incidental Mutation 'IGL00087:Spaca7'
ID 1414
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Spaca7
Ensembl Gene ENSMUSG00000010435
Gene Name sperm acrosome associated 7
Synonyms 1700094C09Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.069) question?
Stock # IGL00087
Quality Score
Status
Chromosome 8
Chromosomal Location 12623038-12650744 bp(+) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to T at 12630941 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000147934 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000010579] [ENSMUST00000209428] [ENSMUST00000210276] [ENSMUST00000210424] [ENSMUST00000211182]
AlphaFold Q9D2S4
Predicted Effect probably benign
Transcript: ENSMUST00000010579
SMART Domains Protein: ENSMUSP00000010579
Gene: ENSMUSG00000010435

DomainStartEndE-ValueType
Pfam:SPACA7 19 130 2.2e-47 PFAM
low complexity region 139 150 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000209428
Predicted Effect probably benign
Transcript: ENSMUST00000210276
Predicted Effect probably benign
Transcript: ENSMUST00000210424
Predicted Effect probably benign
Transcript: ENSMUST00000211182
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930432M17Rik C A 3: 121,473,282 (GRCm39) probably benign Het
Actr2 C A 11: 20,044,370 (GRCm39) V79L probably benign Het
Ankrd36 A C 11: 5,570,131 (GRCm39) Y533S probably benign Het
Btnl1 A T 17: 34,600,091 (GRCm39) D198V probably damaging Het
Carmil2 T A 8: 106,418,038 (GRCm39) I684N probably benign Het
Cdk17 T A 10: 93,062,633 (GRCm39) V257D probably damaging Het
Ctsj T G 13: 61,149,232 (GRCm39) S271R possibly damaging Het
Cul9 T A 17: 46,836,635 (GRCm39) Q1130L probably damaging Het
Daam1 G T 12: 71,988,993 (GRCm39) S131I unknown Het
Dab1 G A 4: 104,536,007 (GRCm39) V139M probably damaging Het
Dab1 A T 4: 104,535,950 (GRCm39) I120F possibly damaging Het
Dnah2 A G 11: 69,383,498 (GRCm39) V1142A possibly damaging Het
Dsg1b C T 18: 20,529,533 (GRCm39) T326I probably damaging Het
Eif3k A C 7: 28,674,101 (GRCm39) probably benign Het
Fam76b T C 9: 13,748,180 (GRCm39) V3A possibly damaging Het
Fitm2 A G 2: 163,311,712 (GRCm39) V167A probably benign Het
Gfap T A 11: 102,779,544 (GRCm39) I418F possibly damaging Het
Grm5 T C 7: 87,779,989 (GRCm39) V1143A probably benign Het
Itpr2 A G 6: 146,298,510 (GRCm39) I317T probably damaging Het
Itprid1 T A 6: 55,945,022 (GRCm39) L581Q possibly damaging Het
Kcnn2 A C 18: 45,725,303 (GRCm39) R266S probably damaging Het
Kntc1 T A 5: 123,928,222 (GRCm39) S1240T probably benign Het
Lmnb2 T C 10: 80,739,871 (GRCm39) D490G possibly damaging Het
Muc4 G A 16: 32,754,086 (GRCm38) G1321R probably benign Het
Or3a1b A T 11: 74,012,705 (GRCm39) I197F probably benign Het
Pax9 A G 12: 56,746,860 (GRCm39) N232S probably benign Het
Pdcd6ip A G 9: 113,526,586 (GRCm39) S108P possibly damaging Het
Pitpnc1 T C 11: 107,103,469 (GRCm39) E210G possibly damaging Het
Prdm10 T C 9: 31,272,108 (GRCm39) probably benign Het
Prl4a1 G A 13: 28,205,443 (GRCm39) G136E probably damaging Het
Pstpip2 A G 18: 77,961,994 (GRCm39) S255G probably benign Het
Rimbp3 T G 16: 17,027,607 (GRCm39) S344A probably benign Het
Rint1 A G 5: 23,999,429 (GRCm39) T73A probably benign Het
Rnf145 T C 11: 44,446,039 (GRCm39) V291A possibly damaging Het
Rrm1 T A 7: 102,103,714 (GRCm39) L221* probably null Het
Scn11a A G 9: 119,599,572 (GRCm39) L1114P probably benign Het
Slc44a4 A G 17: 35,149,216 (GRCm39) probably benign Het
Sorl1 A C 9: 41,885,390 (GRCm39) N2070K probably damaging Het
Speer1k C T 5: 10,997,805 (GRCm39) probably benign Het
Speer4c2 C A 5: 15,861,884 (GRCm39) probably benign Het
Srsf6 G T 2: 162,773,627 (GRCm39) V13F probably damaging Het
Stab1 G T 14: 30,883,314 (GRCm39) T336N probably benign Het
Strbp A G 2: 37,476,516 (GRCm39) probably benign Het
Tbc1d4 A G 14: 101,845,548 (GRCm39) F117L probably damaging Het
Tcf20 A G 15: 82,739,096 (GRCm39) V785A probably damaging Het
Ticrr A G 7: 79,327,031 (GRCm39) K580E probably damaging Het
Ubr4 A T 4: 139,192,633 (GRCm39) E4225D possibly damaging Het
Uck1 A T 2: 32,149,681 (GRCm39) V66D probably damaging Het
Vmn2r25 A G 6: 123,830,130 (GRCm39) F7S probably benign Het
Zan C T 5: 137,386,082 (GRCm39) probably null Het
Zfp819 T A 7: 43,261,403 (GRCm39) probably benign Het
Other mutations in Spaca7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02385:Spaca7 APN 8 12,636,498 (GRCm39) missense possibly damaging 0.88
R1211:Spaca7 UTSW 8 12,623,139 (GRCm39) missense probably damaging 0.99
R1597:Spaca7 UTSW 8 12,630,991 (GRCm39) nonsense probably null
R1653:Spaca7 UTSW 8 12,636,501 (GRCm39) missense possibly damaging 0.92
R2148:Spaca7 UTSW 8 12,636,447 (GRCm39) missense probably damaging 0.98
R2308:Spaca7 UTSW 8 12,648,959 (GRCm39) missense probably benign 0.01
R4179:Spaca7 UTSW 8 12,636,435 (GRCm39) missense probably damaging 1.00
R5208:Spaca7 UTSW 8 12,636,456 (GRCm39) missense probably damaging 0.98
R5720:Spaca7 UTSW 8 12,649,004 (GRCm39) missense possibly damaging 0.92
R7352:Spaca7 UTSW 8 12,635,742 (GRCm39) missense probably benign
R7838:Spaca7 UTSW 8 12,635,696 (GRCm39) missense probably damaging 0.97
R8375:Spaca7 UTSW 8 12,648,998 (GRCm39) missense probably benign 0.25
R8717:Spaca7 UTSW 8 12,636,480 (GRCm39) missense probably damaging 1.00
Z1176:Spaca7 UTSW 8 12,630,949 (GRCm39) missense probably benign 0.14
Posted On 2011-07-12