Incidental Mutation 'IGL00796:Ssxb2'
ID 14245
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Ssxb2
Ensembl Gene ENSMUSG00000023165
Gene Name SSX member B2
Synonyms
Accession Numbers
Essential gene? Not available question?
Stock # IGL00796
Quality Score
Status
Chromosome X
Chromosomal Location 8320584-8327965 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 8324459 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000100065 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000023931] [ENSMUST00000103000]
AlphaFold Q8C5Z3
Predicted Effect probably benign
Transcript: ENSMUST00000023931
SMART Domains Protein: ENSMUSP00000023931
Gene: ENSMUSG00000023165

DomainStartEndE-ValueType
KRAB 60 119 1.19e-7 SMART
Pfam:SSXRD 130 163 3.6e-18 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000103000
SMART Domains Protein: ENSMUSP00000100065
Gene: ENSMUSG00000023165

DomainStartEndE-ValueType
KRAB 23 82 1.19e-7 SMART
Pfam:SSXRD 92 125 9.7e-25 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 22 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adh5 A G 3: 138,156,742 (GRCm39) T143A probably benign Het
Alk T A 17: 72,212,137 (GRCm39) N802I possibly damaging Het
Aspn A G 13: 49,710,893 (GRCm39) I179M probably damaging Het
Bptf A G 11: 106,945,376 (GRCm39) L2506P probably damaging Het
Cacna1f T A X: 7,497,270 (GRCm39) D1594E probably damaging Het
Chd7 T A 4: 8,847,271 (GRCm39) N1671K possibly damaging Het
Dnah7b T C 1: 46,250,497 (GRCm39) V1706A probably damaging Het
Elmo2 A T 2: 165,133,934 (GRCm39) probably benign Het
Ercc6 T C 14: 32,291,959 (GRCm39) S1108P probably benign Het
Fam53a A T 5: 33,758,171 (GRCm39) D317E probably benign Het
Gria2 T C 3: 80,618,097 (GRCm39) N313D probably benign Het
Itch A T 2: 155,051,002 (GRCm39) H563L probably damaging Het
Kdm1a G A 4: 136,281,558 (GRCm39) A651V probably damaging Het
Myb T G 10: 21,017,698 (GRCm39) Q631P probably benign Het
Myh9 A T 15: 77,681,195 (GRCm39) probably benign Het
Nars2 C A 7: 96,680,786 (GRCm39) L319I probably benign Het
Nars2 T A 7: 96,680,787 (GRCm39) L319Q probably benign Het
Pdcl2 G A 5: 76,467,022 (GRCm39) T57I probably damaging Het
Pde6g T A 11: 120,341,390 (GRCm39) I17L probably benign Het
Ppp1r9a T A 6: 5,157,014 (GRCm39) M964K probably benign Het
Tonsl T C 15: 76,509,349 (GRCm39) T8A probably benign Het
Zdbf2 T C 1: 63,346,364 (GRCm39) M1581T probably benign Het
Other mutations in Ssxb2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02034:Ssxb2 APN X 8,324,743 (GRCm39) splice site probably benign
Posted On 2012-12-06