Incidental Mutation 'IGL01795:Speer4c2'
ID 278929
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Speer4c2
Ensembl Gene ENSMUSG00000069720
Gene Name spermatogenesis associated glutamate (E)-rich protein 4C2
Synonyms 4930572O03Rik
Accession Numbers
Essential gene? Not available question?
Stock # IGL01795
Quality Score
Status
Chromosome 5
Chromosomal Location 15857286-15862057 bp(-) (GRCm39)
Type of Mutation utr 5 prime
DNA Base Change (assembly) C to A at 15861884 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000090370 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000092696]
AlphaFold Q8C5Y0
Predicted Effect probably benign
Transcript: ENSMUST00000092696
SMART Domains Protein: ENSMUSP00000090370
Gene: ENSMUSG00000069720

DomainStartEndE-ValueType
Pfam:Takusan 6 90 5.2e-29 PFAM
low complexity region 203 210 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000178227
SMART Domains Protein: ENSMUSP00000136079
Gene: ENSMUSG00000094230

DomainStartEndE-ValueType
low complexity region 43 54 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930590J08Rik C T 6: 91,895,093 (GRCm39) R263* probably null Het
Arfgef1 A T 1: 10,217,753 (GRCm39) I1562K probably benign Het
B4galt1 T A 4: 40,807,760 (GRCm39) D347V probably damaging Het
Ccdc178 T A 18: 22,152,175 (GRCm39) R646S probably benign Het
Ccr1 A T 9: 123,764,149 (GRCm39) L127* probably null Het
Cd109 A G 9: 78,569,047 (GRCm39) probably benign Het
Chd6 A G 2: 160,803,294 (GRCm39) V2128A probably benign Het
Chil6 T A 3: 106,296,108 (GRCm39) I376F probably damaging Het
Chit1 T C 1: 134,076,167 (GRCm39) S275P probably damaging Het
Dnaaf8 T G 16: 4,791,935 (GRCm39) noncoding transcript Het
Erap1 T A 13: 74,814,209 (GRCm39) probably null Het
F5 T C 1: 164,021,959 (GRCm39) V1478A probably benign Het
Fras1 G T 5: 96,925,904 (GRCm39) V3703F probably damaging Het
Hmmr C T 11: 40,612,561 (GRCm39) M185I probably benign Het
Kcnu1 A G 8: 26,403,733 (GRCm39) Y8C probably damaging Het
Krt16 A G 11: 100,138,550 (GRCm39) probably benign Het
Mcf2l A G 8: 13,050,749 (GRCm39) probably null Het
Mgat5 C T 1: 127,396,968 (GRCm39) R572W probably damaging Het
Neil2 T C 14: 63,426,199 (GRCm39) D57G probably benign Het
Nom1 A G 5: 29,651,869 (GRCm39) T736A probably benign Het
Or4k51 A T 2: 111,584,731 (GRCm39) M46L probably benign Het
Or5m5 T A 2: 85,814,478 (GRCm39) I98N probably damaging Het
Or6p1 A T 1: 174,258,215 (GRCm39) I74F possibly damaging Het
Prr14l A T 5: 32,989,189 (GRCm39) probably benign Het
Sall1 A G 8: 89,755,308 (GRCm39) S1224P probably benign Het
Slc44a2 A C 9: 21,256,645 (GRCm39) K336Q probably damaging Het
Sptan1 C T 2: 29,908,501 (GRCm39) T1754I probably benign Het
Zdhhc5 T C 2: 84,520,390 (GRCm39) S596G probably benign Het
Other mutations in Speer4c2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00087:Speer4c2 APN 5 15,861,884 (GRCm39) utr 5 prime probably benign
IGL00088:Speer4c2 APN 5 15,861,884 (GRCm39) utr 5 prime probably benign
IGL01443:Speer4c2 APN 5 15,857,642 (GRCm39) makesense probably null
IGL01789:Speer4c2 APN 5 15,861,884 (GRCm39) utr 5 prime probably benign
IGL01790:Speer4c2 APN 5 15,861,884 (GRCm39) utr 5 prime probably benign
IGL01791:Speer4c2 APN 5 15,861,884 (GRCm39) utr 5 prime probably benign
IGL01792:Speer4c2 APN 5 15,861,884 (GRCm39) utr 5 prime probably benign
IGL02344:Speer4c2 APN 5 15,861,884 (GRCm39) utr 5 prime probably benign
R8385:Speer4c2 UTSW 5 15,857,669 (GRCm39) missense unknown
R8990:Speer4c2 UTSW 5 15,858,598 (GRCm39) missense probably benign
Posted On 2015-04-16