Incidental Mutation 'IGL00470:Cysrt1'
ID 26791
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Cysrt1
Ensembl Gene ENSMUSG00000036731
Gene Name cysteine rich tail 1
Synonyms 2310002J15Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # IGL00470
Quality Score
Status
Chromosome 2
Chromosomal Location 25128831-25129876 bp(-) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) T to C at 25129513 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000145127 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000043379] [ENSMUST00000060818] [ENSMUST00000091318] [ENSMUST00000114355] [ENSMUST00000114356] [ENSMUST00000205192] [ENSMUST00000154498] [ENSMUST00000186719]
AlphaFold Q9D1E4
Predicted Effect probably benign
Transcript: ENSMUST00000043379
SMART Domains Protein: ENSMUSP00000045363
Gene: ENSMUSG00000036731

DomainStartEndE-ValueType
Pfam:DUF2477 1 141 2.2e-92 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000060818
SMART Domains Protein: ENSMUSP00000057742
Gene: ENSMUSG00000044628

DomainStartEndE-ValueType
low complexity region 45 63 N/A INTRINSIC
low complexity region 126 138 N/A INTRINSIC
RING 147 193 1.11e-2 SMART
low complexity region 227 238 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000091318
SMART Domains Protein: ENSMUSP00000088868
Gene: ENSMUSG00000089953

DomainStartEndE-ValueType
RING 23 69 8.23e-6 SMART
low complexity region 137 148 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000091318
SMART Domains Protein: ENSMUSP00000145470
Gene: ENSMUSG00000089953

DomainStartEndE-ValueType
RING 23 69 8.23e-6 SMART
low complexity region 137 148 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000114355
SMART Domains Protein: ENSMUSP00000109995
Gene: ENSMUSG00000044628

DomainStartEndE-ValueType
low complexity region 45 63 N/A INTRINSIC
low complexity region 126 138 N/A INTRINSIC
RING 147 193 1.11e-2 SMART
low complexity region 227 238 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000114356
SMART Domains Protein: ENSMUSP00000109996
Gene: ENSMUSG00000036731

DomainStartEndE-ValueType
Pfam:DUF2477 1 141 2.3e-85 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000205192
SMART Domains Protein: ENSMUSP00000145127
Gene: ENSMUSG00000089953

DomainStartEndE-ValueType
RING 23 69 8.23e-6 SMART
low complexity region 137 148 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000154498
Predicted Effect probably benign
Transcript: ENSMUST00000186719
SMART Domains Protein: ENSMUSP00000140416
Gene: ENSMUSG00000036731

DomainStartEndE-ValueType
Pfam:DUF2477 1 141 2.2e-92 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 35 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4732463B04Rik G T 12: 84,090,578 (GRCm39) probably benign Het
Abcd1 T C X: 72,761,154 (GRCm39) L173P probably damaging Het
Adam18 T A 8: 25,118,149 (GRCm39) D41V probably damaging Het
Armh4 A T 14: 50,010,460 (GRCm39) S416T probably damaging Het
Aspa T G 11: 73,204,447 (GRCm39) probably benign Het
Cacna2d1 T A 5: 16,451,654 (GRCm39) probably benign Het
Cracd G A 5: 77,013,903 (GRCm39) probably benign Het
Cubn T A 2: 13,283,229 (GRCm39) I3570L probably benign Het
Cyp2j13 G A 4: 95,950,275 (GRCm39) P242L probably damaging Het
Dchs1 A T 7: 105,407,414 (GRCm39) L2100H probably damaging Het
Ddb1 G A 19: 10,589,028 (GRCm39) A229T possibly damaging Het
Dst A T 1: 34,228,043 (GRCm39) I1554F probably damaging Het
Dvl3 C T 16: 20,349,689 (GRCm39) P554L probably damaging Het
Fcgbp C A 7: 27,774,511 (GRCm39) C28* probably null Het
Gm773 T C X: 55,247,373 (GRCm39) D53G probably benign Het
Hhat A G 1: 192,399,325 (GRCm39) Y272H probably damaging Het
Inpp5k T C 11: 75,536,351 (GRCm39) S310P probably benign Het
Kat2a G A 11: 100,596,210 (GRCm39) R782W probably damaging Het
Kcnh5 T C 12: 74,944,570 (GRCm39) D893G probably benign Het
Lama2 T C 10: 27,119,738 (GRCm39) T709A probably benign Het
Mcm8 G A 2: 132,669,457 (GRCm39) V281I probably benign Het
Men1 G A 19: 6,387,237 (GRCm39) probably null Het
Nup133 T G 8: 124,665,822 (GRCm39) D201A probably damaging Het
Oxct2a A G 4: 123,217,183 (GRCm39) L66P possibly damaging Het
Pcbp2 C T 15: 102,399,148 (GRCm39) A224V probably damaging Het
Phf8-ps T A 17: 33,284,837 (GRCm39) H655L probably benign Het
Pla2g4e G A 2: 120,015,719 (GRCm39) S275F probably benign Het
Pxk T C 14: 8,130,754 (GRCm38) F118L probably damaging Het
Sp2 C T 11: 96,845,387 (GRCm39) R578H probably damaging Het
Sphkap A G 1: 83,255,631 (GRCm39) M706T possibly damaging Het
Tars3 T C 7: 65,338,656 (GRCm39) M689T probably benign Het
Trrap T C 5: 144,754,848 (GRCm39) V2008A probably damaging Het
Txndc2 A T 17: 65,945,569 (GRCm39) S203T probably benign Het
Txnrd1 T G 10: 82,711,496 (GRCm39) D42E probably damaging Het
Zswim8 G A 14: 20,773,249 (GRCm39) D1746N probably damaging Het
Other mutations in Cysrt1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02420:Cysrt1 APN 2 25,129,360 (GRCm39) missense probably benign
R1637:Cysrt1 UTSW 2 25,129,297 (GRCm39) missense probably benign 0.01
R5113:Cysrt1 UTSW 2 25,129,363 (GRCm39) missense possibly damaging 0.71
R7455:Cysrt1 UTSW 2 25,129,422 (GRCm39) missense probably benign 0.00
R7684:Cysrt1 UTSW 2 25,129,094 (GRCm39) nonsense probably null
R7771:Cysrt1 UTSW 2 25,129,237 (GRCm39) missense probably benign 0.32
R8687:Cysrt1 UTSW 2 25,129,399 (GRCm39) missense possibly damaging 0.86
Posted On 2013-04-17