Incidental Mutation 'IGL03197:Speer1k'
ID 412853
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Speer1k
Ensembl Gene ENSMUSG00000091933
Gene Name spermatogenesis associated glutamate (E)-rich protein 1K
Synonyms Gm8857
Accession Numbers
Essential gene? Not available question?
Stock # IGL03197
Quality Score
Status
Chromosome 5
Chromosomal Location 10997774-11002559 bp(+) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to A at 11000501 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000132192 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000168945]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000168945
SMART Domains Protein: ENSMUSP00000132192
Gene: ENSMUSG00000095710

DomainStartEndE-ValueType
Pfam:Takusan 2 90 2.5e-29 PFAM
Predicted Effect unknown
Transcript: ENSMUST00000170064
AA Change: I126K
SMART Domains Protein: ENSMUSP00000127481
Gene: ENSMUSG00000091933
AA Change: I126K

DomainStartEndE-ValueType
Pfam:Takusan 56 142 7.6e-25 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000199217
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700030J22Rik A G 8: 117,698,541 (GRCm39) W189R probably damaging Het
Abcb7 A T X: 103,327,797 (GRCm39) M704K possibly damaging Het
Anp32e A G 3: 95,844,364 (GRCm39) D71G probably damaging Het
Asphd1 T C 7: 126,545,298 (GRCm39) D353G probably damaging Het
Baz2b T C 2: 59,731,898 (GRCm39) K2047E possibly damaging Het
Cyp2c39 G T 19: 39,555,361 (GRCm39) V394F probably damaging Het
Ddx43 G A 9: 78,325,402 (GRCm39) M482I probably benign Het
Dnah2 A T 11: 69,350,089 (GRCm39) V2348E probably damaging Het
Fam135a A G 1: 24,083,263 (GRCm39) F304L probably damaging Het
Gabra3 A G X: 71,583,734 (GRCm39) I66T possibly damaging Het
Irf4 A T 13: 30,947,503 (GRCm39) probably benign Het
Kif11 A G 19: 37,395,475 (GRCm39) D578G probably benign Het
Lrig1 A G 6: 94,583,099 (GRCm39) S1006P probably benign Het
Mfsd14a A C 3: 116,430,012 (GRCm39) S307A probably benign Het
Mill1 A G 7: 17,998,590 (GRCm39) T267A probably benign Het
Nfyc C A 4: 120,630,958 (GRCm39) D62Y probably damaging Het
Nin T C 12: 70,073,584 (GRCm39) T1190A probably benign Het
Nup42 T C 5: 24,372,463 (GRCm39) S84P probably damaging Het
Ociad1 T C 5: 73,451,675 (GRCm39) S15P probably benign Het
Or4c104 A T 2: 88,586,545 (GRCm39) I158K probably damaging Het
Or6c69c A T 10: 129,910,548 (GRCm39) I90F probably damaging Het
Or7g25 A G 9: 19,160,098 (GRCm39) I199T probably benign Het
Pcdhb11 T A 18: 37,555,477 (GRCm39) L269* probably null Het
Pigo A C 4: 43,022,103 (GRCm39) M352R possibly damaging Het
Plch1 T C 3: 63,660,591 (GRCm39) M343V probably damaging Het
Podnl1 G A 8: 84,858,818 (GRCm39) V548I probably benign Het
Prkag1 A G 15: 98,713,058 (GRCm39) probably benign Het
Rasa4 A G 5: 136,130,866 (GRCm39) K379R probably damaging Het
Rraga G A 4: 86,494,513 (GRCm39) A120T probably damaging Het
Serpina3a C T 12: 104,082,500 (GRCm39) A91V probably damaging Het
Sik2 T C 9: 50,807,073 (GRCm39) E779G probably damaging Het
Slc15a3 T G 19: 10,832,443 (GRCm39) probably null Het
Smc1b C T 15: 84,955,064 (GRCm39) D1063N possibly damaging Het
Speer1e T G 5: 11,233,080 (GRCm39) N14K probably damaging Het
Srsf12 G A 4: 33,231,040 (GRCm39) G183E probably damaging Het
Taf8 A G 17: 47,809,127 (GRCm39) S112P probably benign Het
Trhde A G 10: 114,249,213 (GRCm39) L851P probably benign Het
Wapl G T 14: 34,467,588 (GRCm39) V1182F possibly damaging Het
Zfp326 A G 5: 106,039,059 (GRCm39) I231V probably benign Het
Other mutations in Speer1k
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00087:Speer1k APN 5 10,997,805 (GRCm39) utr 5 prime probably benign
IGL01555:Speer1k APN 5 10,999,051 (GRCm39) intron probably benign
R1844:Speer1k UTSW 5 10,998,994 (GRCm39) intron probably benign
R7033:Speer1k UTSW 5 11,000,518 (GRCm39) splice site probably null
R9304:Speer1k UTSW 5 10,998,949 (GRCm39) missense
R9753:Speer1k UTSW 5 10,999,020 (GRCm39) missense
Posted On 2016-08-02