Incidental Mutation 'IGL02351:Susd1'
ID 289449
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Susd1
Ensembl Gene ENSMUSG00000038578
Gene Name sushi domain containing 1
Synonyms Gm12528
Accession Numbers
Essential gene? Probably non essential (E-score: 0.083) question?
Stock # IGL02351
Quality Score
Status
Chromosome 4
Chromosomal Location 59314683-59438633 bp(-) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) A to T at 59427985 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Stop codon at position 66 (Y66*)
Ref Sequence ENSEMBL: ENSMUSP00000048201 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000040166] [ENSMUST00000107544]
AlphaFold E9Q3H4
Predicted Effect probably null
Transcript: ENSMUST00000040166
AA Change: Y66*
SMART Domains Protein: ENSMUSP00000048201
Gene: ENSMUSG00000038578
AA Change: Y66*

DomainStartEndE-ValueType
low complexity region 2 15 N/A INTRINSIC
low complexity region 16 30 N/A INTRINSIC
EGF 43 77 1.36e1 SMART
EGF_CA 78 129 2.92e-7 SMART
EGF_CA 130 180 2.22e-12 SMART
CCP 184 239 7.87e-9 SMART
CCP 244 299 5.48e-8 SMART
Blast:FN3 306 379 2e-6 BLAST
Blast:FN3 459 580 8e-50 BLAST
transmembrane domain 729 751 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000107544
AA Change: W15R
SMART Domains Protein: ENSMUSP00000103168
Gene: ENSMUSG00000038578
AA Change: W15R

DomainStartEndE-ValueType
EGF 28 76 2.02e-1 SMART
EGF_CA 77 127 2.22e-12 SMART
CCP 131 186 7.87e-9 SMART
CCP 191 246 5.48e-8 SMART
Blast:FN3 253 326 2e-6 BLAST
Blast:FN3 406 527 4e-50 BLAST
transmembrane domain 676 698 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abi3bp A G 16: 56,474,418 (GRCm39) T448A possibly damaging Het
Adamtsl1 T A 4: 86,075,110 (GRCm39) probably null Het
Adgra3 A G 5: 50,215,900 (GRCm39) V73A probably benign Het
Aggf1 T C 13: 95,489,358 (GRCm39) probably benign Het
Aktip C T 8: 91,853,520 (GRCm39) V96I possibly damaging Het
Atm A G 9: 53,433,476 (GRCm39) I258T probably benign Het
Baz1b C T 5: 135,273,160 (GRCm39) T1428I probably damaging Het
C3ar1 A T 6: 122,826,934 (GRCm39) Y428N probably damaging Het
Cadps A G 14: 12,597,380 (GRCm38) S437P probably damaging Het
Car4 C T 11: 84,856,593 (GRCm39) P294S probably damaging Het
Cenpq A G 17: 41,235,223 (GRCm39) L213P probably damaging Het
Cept1 A G 3: 106,446,504 (GRCm39) probably null Het
Cln6 A G 9: 62,754,407 (GRCm39) I150V probably benign Het
Cyb5r3 T C 15: 83,045,136 (GRCm39) T94A probably benign Het
Cyp2c67 A G 19: 39,605,861 (GRCm39) M345T probably damaging Het
Dapk2 T A 9: 66,153,805 (GRCm39) I187N probably damaging Het
Dkk2 A G 3: 131,883,673 (GRCm39) D191G probably benign Het
Dnah8 T A 17: 30,986,785 (GRCm39) F3145I probably damaging Het
Dock1 A C 7: 134,710,548 (GRCm39) D1190A possibly damaging Het
Ehhadh T A 16: 21,581,620 (GRCm39) L457F probably damaging Het
Ercc6l2 T C 13: 64,001,497 (GRCm39) L552P probably damaging Het
Ghrhr T G 6: 55,361,138 (GRCm39) I284S probably damaging Het
Gm10288 A T 3: 146,544,954 (GRCm39) noncoding transcript Het
Gp6 T G 7: 4,397,507 (GRCm39) I19L probably benign Het
Gria4 G A 9: 4,456,206 (GRCm39) S698L possibly damaging Het
Ifng A T 10: 118,278,410 (GRCm39) I53F possibly damaging Het
Kazn A C 4: 141,874,327 (GRCm39) probably null Het
Khk A T 5: 31,085,848 (GRCm39) I136F probably damaging Het
Lnx1 T A 5: 74,788,027 (GRCm39) N98Y probably damaging Het
Lsp1 T C 7: 142,042,679 (GRCm39) probably null Het
Lta4h A T 10: 93,314,329 (GRCm39) N467I probably benign Het
Mcmbp C A 7: 128,311,505 (GRCm39) probably null Het
Me2 A T 18: 73,931,038 (GRCm39) I85K probably benign Het
Muc4 C T 16: 32,569,804 (GRCm39) T288I possibly damaging Het
Nadsyn1 A T 7: 143,353,649 (GRCm39) Y525N probably damaging Het
Nt5e G A 9: 88,209,946 (GRCm39) V70M probably damaging Het
Or52e4 G A 7: 104,706,182 (GRCm39) G243D probably damaging Het
Or8b36 A T 9: 37,937,332 (GRCm39) I77L possibly damaging Het
Or9k7 T G 10: 130,046,603 (GRCm39) Y132S probably damaging Het
Pkd1l3 A G 8: 110,373,129 (GRCm39) probably benign Het
Ppm1d A T 11: 85,236,541 (GRCm39) E440V probably damaging Het
Pramel32 A T 4: 88,546,127 (GRCm39) I405N probably damaging Het
Ripor2 A T 13: 24,915,572 (GRCm39) E1047D probably damaging Het
Rwdd2b G A 16: 87,234,336 (GRCm39) A18V probably benign Het
Serpina5 G T 12: 104,068,384 (GRCm39) K148N probably damaging Het
Setx A G 2: 29,036,976 (GRCm39) K1154E probably benign Het
Skap1 T A 11: 96,599,382 (GRCm39) probably null Het
Spcs2 T C 7: 99,498,241 (GRCm39) K81R probably damaging Het
Stt3b T A 9: 115,079,975 (GRCm39) M646L possibly damaging Het
Suco T C 1: 161,646,195 (GRCm39) T1169A probably benign Het
Trim34a T A 7: 103,910,441 (GRCm39) C414* probably null Het
Trim58 G A 11: 58,542,176 (GRCm39) G379S probably damaging Het
Vmn2r50 T A 7: 9,787,002 (GRCm39) Q35L probably benign Het
Zfp418 T C 7: 7,177,690 (GRCm39) probably benign Het
Zfp57 G A 17: 37,320,919 (GRCm39) V258I probably benign Het
Zng1 A T 19: 24,909,026 (GRCm39) probably null Het
Other mutations in Susd1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01630:Susd1 APN 4 59,365,817 (GRCm39) missense possibly damaging 0.85
IGL01705:Susd1 APN 4 59,332,931 (GRCm39) splice site probably benign
IGL01727:Susd1 APN 4 59,412,329 (GRCm39) splice site probably benign
IGL02015:Susd1 APN 4 59,315,745 (GRCm39) missense possibly damaging 0.86
IGL02102:Susd1 APN 4 59,369,636 (GRCm39) missense possibly damaging 0.70
IGL02358:Susd1 APN 4 59,427,985 (GRCm39) nonsense probably null
IGL03210:Susd1 APN 4 59,333,035 (GRCm39) critical splice acceptor site probably null
IGL03258:Susd1 APN 4 59,379,655 (GRCm39) missense possibly damaging 0.73
R0612:Susd1 UTSW 4 59,390,561 (GRCm39) splice site probably benign
R0719:Susd1 UTSW 4 59,329,506 (GRCm39) missense possibly damaging 0.56
R0722:Susd1 UTSW 4 59,379,749 (GRCm39) missense possibly damaging 0.73
R1355:Susd1 UTSW 4 59,424,114 (GRCm39) missense possibly damaging 0.86
R1672:Susd1 UTSW 4 59,411,395 (GRCm39) missense probably damaging 0.98
R1677:Susd1 UTSW 4 59,424,089 (GRCm39) missense possibly damaging 0.85
R1921:Susd1 UTSW 4 59,412,191 (GRCm39) missense probably benign 0.03
R1933:Susd1 UTSW 4 59,351,695 (GRCm39) missense possibly damaging 0.72
R1998:Susd1 UTSW 4 59,349,925 (GRCm39) missense probably benign 0.03
R2202:Susd1 UTSW 4 59,349,843 (GRCm39) missense possibly damaging 0.96
R2203:Susd1 UTSW 4 59,349,843 (GRCm39) missense possibly damaging 0.96
R2204:Susd1 UTSW 4 59,349,843 (GRCm39) missense possibly damaging 0.96
R2329:Susd1 UTSW 4 59,379,715 (GRCm39) missense possibly damaging 0.85
R2510:Susd1 UTSW 4 59,349,855 (GRCm39) missense possibly damaging 0.86
R4512:Susd1 UTSW 4 59,329,491 (GRCm39) missense possibly damaging 0.96
R4732:Susd1 UTSW 4 59,428,029 (GRCm39) missense possibly damaging 0.53
R4733:Susd1 UTSW 4 59,428,029 (GRCm39) missense possibly damaging 0.53
R4969:Susd1 UTSW 4 59,351,679 (GRCm39) missense probably benign 0.04
R5121:Susd1 UTSW 4 59,379,657 (GRCm39) missense possibly damaging 0.73
R5548:Susd1 UTSW 4 59,369,577 (GRCm39) missense probably benign 0.05
R5747:Susd1 UTSW 4 59,424,108 (GRCm39) missense probably damaging 0.98
R5776:Susd1 UTSW 4 59,315,363 (GRCm39) utr 3 prime probably benign
R5875:Susd1 UTSW 4 59,412,203 (GRCm39) missense possibly damaging 0.71
R6056:Susd1 UTSW 4 59,379,687 (GRCm39) missense possibly damaging 0.53
R6081:Susd1 UTSW 4 59,411,359 (GRCm39) missense possibly damaging 0.86
R7018:Susd1 UTSW 4 59,390,627 (GRCm39) missense probably benign 0.44
R7122:Susd1 UTSW 4 59,411,318 (GRCm39) nonsense probably null
R7161:Susd1 UTSW 4 59,329,581 (GRCm39) missense possibly damaging 0.85
R7172:Susd1 UTSW 4 59,315,420 (GRCm39) splice site probably null
R7891:Susd1 UTSW 4 59,349,915 (GRCm39) missense possibly damaging 0.85
R8103:Susd1 UTSW 4 59,365,916 (GRCm39) critical splice acceptor site probably null
R8299:Susd1 UTSW 4 59,315,773 (GRCm39) missense probably benign 0.33
R8472:Susd1 UTSW 4 59,332,985 (GRCm39) missense possibly damaging 0.96
R8831:Susd1 UTSW 4 59,379,594 (GRCm39) splice site probably benign
R8903:Susd1 UTSW 4 59,390,576 (GRCm39) missense probably benign 0.02
R8981:Susd1 UTSW 4 59,380,883 (GRCm39) missense probably benign 0.07
R9002:Susd1 UTSW 4 59,324,882 (GRCm39) missense probably benign 0.00
R9091:Susd1 UTSW 4 59,412,226 (GRCm39) missense probably benign 0.44
R9270:Susd1 UTSW 4 59,412,226 (GRCm39) missense probably benign 0.44
R9296:Susd1 UTSW 4 59,427,865 (GRCm39) intron probably benign
Posted On 2015-04-16