Incidental Mutation 'IGL01789:Speer4c2'
ID 278921
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 # IGL01789
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: 18 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Afm C T 5: 90,673,443 (GRCm39) P232S probably benign Het
Atp11b A T 3: 35,843,741 (GRCm39) Q81L possibly damaging Het
Cgn G A 3: 94,683,528 (GRCm39) P413S possibly damaging Het
Eps8 C T 6: 137,516,364 (GRCm39) M5I probably benign Het
Fam83h A T 15: 75,877,969 (GRCm39) M143K probably damaging Het
Gzf1 G A 2: 148,525,981 (GRCm39) A151T probably benign Het
Hmcn1 C T 1: 150,566,352 (GRCm39) C2217Y probably damaging Het
Leo1 T C 9: 75,361,896 (GRCm39) probably benign Het
Lipm A G 19: 34,096,147 (GRCm39) D321G probably damaging Het
Nos2 C T 11: 78,835,483 (GRCm39) probably benign Het
Phtf2 T C 5: 20,999,372 (GRCm39) Y257C probably benign Het
Rnpep T C 1: 135,195,833 (GRCm39) K359E possibly damaging Het
Tas2r130 T A 6: 131,607,118 (GRCm39) S226C probably damaging Het
Tpbg A T 9: 85,726,954 (GRCm39) M308L probably benign Het
Trip11 G A 12: 101,838,090 (GRCm39) S1715L probably benign Het
Unc13b T A 4: 43,239,462 (GRCm39) N3508K probably damaging Het
Utp20 A T 10: 88,634,141 (GRCm39) probably null Het
Wdhd1 A T 14: 47,512,274 (GRCm39) M39K 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
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
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