Incidental Mutation 'IGL01792:Speer4c2'
ID 278925
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 # IGL01792
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: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9830107B12Rik G T 17: 48,452,680 (GRCm39) F86L probably damaging Het
A2ml1 T C 6: 128,537,642 (GRCm39) T690A probably benign Het
Adam3 T C 8: 25,187,219 (GRCm39) N424S probably benign Het
Adarb2 T C 13: 8,620,185 (GRCm39) F224L probably damaging Het
Clcn3 T C 8: 61,382,356 (GRCm39) T438A probably damaging Het
Cyp2c55 A G 19: 39,030,631 (GRCm39) I488V probably benign Het
Dennd1a A G 2: 38,016,592 (GRCm39) F84S probably damaging Het
Dennd4b A G 3: 90,187,152 (GRCm39) R1475G probably damaging Het
Ift172 G A 5: 31,434,215 (GRCm39) R508W probably damaging Het
Khdrbs2 C T 1: 32,696,548 (GRCm39) R326C probably damaging Het
Krt78 T G 15: 101,855,085 (GRCm39) M909L probably benign Het
Ncapg2 T A 12: 116,389,438 (GRCm39) F353I probably damaging Het
Or10d4c A T 9: 39,558,955 (GRCm39) N311I probably benign Het
Pigb A T 9: 72,925,268 (GRCm39) H396Q probably damaging Het
Rev3l C T 10: 39,699,336 (GRCm39) P1278S probably benign Het
Setd1b T A 5: 123,295,209 (GRCm39) V955D unknown Het
Slc22a16 T A 10: 40,449,928 (GRCm39) H121Q possibly damaging Het
Slc22a29 A T 19: 8,195,893 (GRCm39) C49S probably damaging Het
Smad1 T C 8: 80,098,752 (GRCm39) K21E probably damaging Het
Spic A G 10: 88,515,807 (GRCm39) I5T possibly damaging Het
Srpk1 G A 17: 28,818,441 (GRCm39) probably benign Het
Tubgcp6 T C 15: 88,985,484 (GRCm39) D1559G probably damaging Het
Unc13b T C 4: 43,250,218 (GRCm39) F992L probably damaging 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
IGL01795: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