Incidental Mutation 'R5911:Clasp1'
ID 460968
Institutional Source Beutler Lab
Gene Symbol Clasp1
Ensembl Gene ENSMUSG00000064302
Gene Name CLIP associating protein 1
Synonyms CLASP1alpha, 1700030C23Rik, 5730583A19Rik, CLASP1, B130045P17Rik, mCLASP1
MMRRC Submission 044108-MU
Accession Numbers
Essential gene? Probably essential (E-score: 0.948) question?
Stock # R5911 (G1)
Quality Score 225
Status Validated
Chromosome 1
Chromosomal Location 118314976-118537192 bp(+) (GRCm39)
Type of Mutation unclassified
DNA Base Change (assembly) C to A at 118434638 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000049404] [ENSMUST00000070989] [ENSMUST00000165223] [ENSMUST00000178710] [ENSMUST00000185405] [ENSMUST00000186349] [ENSMUST00000187713] [ENSMUST00000189262] [ENSMUST00000189738] [ENSMUST00000189570] [ENSMUST00000188710] [ENSMUST00000191445] [ENSMUST00000191823] [ENSMUST00000190571] [ENSMUST00000190733]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000049404
SMART Domains Protein: ENSMUSP00000042266
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
TOG 1 232 7.31e-51 SMART
low complexity region 252 266 N/A INTRINSIC
low complexity region 280 296 N/A INTRINSIC
TOG 319 551 1.14e-11 SMART
low complexity region 579 594 N/A INTRINSIC
low complexity region 606 633 N/A INTRINSIC
low complexity region 674 707 N/A INTRINSIC
low complexity region 751 763 N/A INTRINSIC
low complexity region 821 831 N/A INTRINSIC
TOG 847 1085 3.23e-1 SMART
low complexity region 1096 1113 N/A INTRINSIC
low complexity region 1134 1147 N/A INTRINSIC
low complexity region 1225 1236 N/A INTRINSIC
TOG 1287 1525 4.96e-30 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000070989
SMART Domains Protein: ENSMUSP00000067858
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
TOG 1 232 7.31e-51 SMART
low complexity region 252 266 N/A INTRINSIC
low complexity region 280 296 N/A INTRINSIC
TOG 319 551 1.14e-11 SMART
low complexity region 579 594 N/A INTRINSIC
low complexity region 606 633 N/A INTRINSIC
low complexity region 674 707 N/A INTRINSIC
low complexity region 751 763 N/A INTRINSIC
low complexity region 850 860 N/A INTRINSIC
TOG 876 1114 3.23e-1 SMART
low complexity region 1125 1142 N/A INTRINSIC
low complexity region 1215 1226 N/A INTRINSIC
TOG 1277 1515 4.96e-30 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000165223
SMART Domains Protein: ENSMUSP00000128089
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
TOG 1 232 7.31e-51 SMART
low complexity region 252 266 N/A INTRINSIC
low complexity region 280 296 N/A INTRINSIC
TOG 319 551 1.14e-11 SMART
low complexity region 579 594 N/A INTRINSIC
low complexity region 606 633 N/A INTRINSIC
low complexity region 684 714 N/A INTRINSIC
low complexity region 792 802 N/A INTRINSIC
TOG 818 1056 3.23e-1 SMART
low complexity region 1067 1084 N/A INTRINSIC
low complexity region 1157 1168 N/A INTRINSIC
TOG 1219 1457 4.96e-30 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000178710
SMART Domains Protein: ENSMUSP00000137137
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
TOG 1 232 7.31e-51 SMART
low complexity region 252 266 N/A INTRINSIC
low complexity region 280 296 N/A INTRINSIC
TOG 319 551 1.14e-11 SMART
low complexity region 579 594 N/A INTRINSIC
low complexity region 606 633 N/A INTRINSIC
low complexity region 668 698 N/A INTRINSIC
low complexity region 752 766 N/A INTRINSIC
low complexity region 784 794 N/A INTRINSIC
TOG 810 1047 6.55e-2 SMART
low complexity region 1058 1075 N/A INTRINSIC
low complexity region 1148 1159 N/A INTRINSIC
TOG 1210 1448 4.96e-30 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000185405
SMART Domains Protein: ENSMUSP00000139619
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
TOG 1 232 3.4e-55 SMART
low complexity region 252 266 N/A INTRINSIC
low complexity region 280 296 N/A INTRINSIC
TOG 319 551 5.5e-16 SMART
low complexity region 579 594 N/A INTRINSIC
low complexity region 606 633 N/A INTRINSIC
low complexity region 682 715 N/A INTRINSIC
low complexity region 769 783 N/A INTRINSIC
low complexity region 801 811 N/A INTRINSIC
TOG 827 1065 1.6e-5 SMART
low complexity region 1076 1093 N/A INTRINSIC
low complexity region 1166 1177 N/A INTRINSIC
TOG 1228 1466 2.3e-34 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000186349
SMART Domains Protein: ENSMUSP00000141105
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
TOG 1 232 7.31e-51 SMART
low complexity region 252 266 N/A INTRINSIC
low complexity region 280 296 N/A INTRINSIC
TOG 319 551 1.14e-11 SMART
low complexity region 579 594 N/A INTRINSIC
low complexity region 606 633 N/A INTRINSIC
low complexity region 674 707 N/A INTRINSIC
low complexity region 751 763 N/A INTRINSIC
low complexity region 821 831 N/A INTRINSIC
TOG 847 1085 3.23e-1 SMART
low complexity region 1096 1113 N/A INTRINSIC
low complexity region 1134 1147 N/A INTRINSIC
low complexity region 1225 1236 N/A INTRINSIC
TOG 1287 1525 4.96e-30 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000187713
SMART Domains Protein: ENSMUSP00000139526
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
TOG 1 232 3.4e-55 SMART
low complexity region 252 266 N/A INTRINSIC
low complexity region 280 296 N/A INTRINSIC
TOG 319 551 5.5e-16 SMART
low complexity region 579 594 N/A INTRINSIC
low complexity region 606 633 N/A INTRINSIC
low complexity region 684 714 N/A INTRINSIC
low complexity region 768 782 N/A INTRINSIC
low complexity region 800 810 N/A INTRINSIC
TOG 826 1064 1.6e-5 SMART
low complexity region 1075 1092 N/A INTRINSIC
low complexity region 1165 1176 N/A INTRINSIC
TOG 1227 1465 2.3e-34 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000190135
Predicted Effect noncoding transcript
Transcript: ENSMUST00000189676
Predicted Effect probably benign
Transcript: ENSMUST00000204904
Predicted Effect noncoding transcript
Transcript: ENSMUST00000204886
Predicted Effect noncoding transcript
Transcript: ENSMUST00000189216
Predicted Effect noncoding transcript
Transcript: ENSMUST00000203646
Predicted Effect probably benign
Transcript: ENSMUST00000189262
SMART Domains Protein: ENSMUSP00000140860
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
TOG 1 232 3.4e-55 SMART
low complexity region 252 266 N/A INTRINSIC
low complexity region 280 296 N/A INTRINSIC
TOG 319 551 5.5e-16 SMART
low complexity region 579 594 N/A INTRINSIC
low complexity region 606 633 N/A INTRINSIC
low complexity region 668 698 N/A INTRINSIC
low complexity region 776 786 N/A INTRINSIC
TOG 802 1040 1.6e-5 SMART
low complexity region 1051 1068 N/A INTRINSIC
low complexity region 1141 1152 N/A INTRINSIC
TOG 1203 1441 2.3e-34 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000189738
SMART Domains Protein: ENSMUSP00000140665
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
TOG 1 232 7.31e-51 SMART
low complexity region 252 266 N/A INTRINSIC
low complexity region 280 296 N/A INTRINSIC
TOG 319 551 1.14e-11 SMART
low complexity region 579 594 N/A INTRINSIC
low complexity region 606 633 N/A INTRINSIC
low complexity region 668 698 N/A INTRINSIC
low complexity region 752 766 N/A INTRINSIC
low complexity region 784 794 N/A INTRINSIC
TOG 810 1048 3.23e-1 SMART
low complexity region 1059 1076 N/A INTRINSIC
low complexity region 1149 1160 N/A INTRINSIC
TOG 1211 1449 4.96e-30 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000189570
SMART Domains Protein: ENSMUSP00000140167
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
TOG 1 232 3.4e-55 SMART
low complexity region 252 266 N/A INTRINSIC
low complexity region 280 296 N/A INTRINSIC
TOG 319 551 5.5e-16 SMART
low complexity region 579 594 N/A INTRINSIC
low complexity region 606 633 N/A INTRINSIC
low complexity region 684 714 N/A INTRINSIC
low complexity region 792 802 N/A INTRINSIC
TOG 818 1055 3.2e-6 SMART
low complexity region 1066 1083 N/A INTRINSIC
low complexity region 1156 1167 N/A INTRINSIC
TOG 1218 1456 2.3e-34 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000188710
SMART Domains Protein: ENSMUSP00000140593
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
TOG 1 232 3.4e-55 SMART
low complexity region 252 266 N/A INTRINSIC
low complexity region 280 296 N/A INTRINSIC
TOG 319 551 5.5e-16 SMART
low complexity region 579 594 N/A INTRINSIC
low complexity region 606 633 N/A INTRINSIC
low complexity region 674 707 N/A INTRINSIC
low complexity region 751 763 N/A INTRINSIC
low complexity region 818 832 N/A INTRINSIC
low complexity region 850 860 N/A INTRINSIC
TOG 876 1114 1.6e-5 SMART
low complexity region 1125 1142 N/A INTRINSIC
low complexity region 1215 1226 N/A INTRINSIC
TOG 1277 1515 2.3e-34 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000191445
SMART Domains Protein: ENSMUSP00000140095
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
TOG 1 232 3.4e-55 SMART
low complexity region 252 266 N/A INTRINSIC
low complexity region 280 296 N/A INTRINSIC
TOG 319 551 5.5e-16 SMART
low complexity region 579 594 N/A INTRINSIC
low complexity region 606 633 N/A INTRINSIC
low complexity region 674 707 N/A INTRINSIC
low complexity region 761 775 N/A INTRINSIC
low complexity region 793 803 N/A INTRINSIC
TOG 819 1056 3.2e-6 SMART
low complexity region 1067 1084 N/A INTRINSIC
low complexity region 1157 1168 N/A INTRINSIC
TOG 1219 1457 2.3e-34 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000191823
SMART Domains Protein: ENSMUSP00000142203
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
low complexity region 20 34 N/A INTRINSIC
low complexity region 48 64 N/A INTRINSIC
TOG 87 319 5.6e-16 SMART
low complexity region 347 362 N/A INTRINSIC
low complexity region 374 401 N/A INTRINSIC
low complexity region 450 483 N/A INTRINSIC
low complexity region 537 551 N/A INTRINSIC
low complexity region 568 578 N/A INTRINSIC
TOG 594 832 1.6e-5 SMART
low complexity region 843 860 N/A INTRINSIC
low complexity region 933 944 N/A INTRINSIC
TOG 995 1233 2.4e-34 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000190571
SMART Domains Protein: ENSMUSP00000140019
Gene: ENSMUSG00000064302

DomainStartEndE-ValueType
TOG 1 232 3.4e-55 SMART
low complexity region 252 266 N/A INTRINSIC
low complexity region 280 296 N/A INTRINSIC
TOG 319 551 5.5e-16 SMART
low complexity region 579 594 N/A INTRINSIC
low complexity region 606 633 N/A INTRINSIC
low complexity region 682 715 N/A INTRINSIC
low complexity region 759 771 N/A INTRINSIC
low complexity region 805 819 N/A INTRINSIC
low complexity region 837 847 N/A INTRINSIC
TOG 863 1101 1.6e-5 SMART
low complexity region 1112 1129 N/A INTRINSIC
low complexity region 1150 1163 N/A INTRINSIC
low complexity region 1241 1252 N/A INTRINSIC
TOG 1303 1541 2.3e-34 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000190733
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.1%
  • 20x: 94.4%
Validation Efficiency 92% (77/84)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] CLASPs, such as CLASP1, are nonmotor microtubule-associated proteins that interact with CLIPs (e.g., CLIP170; MIM 179838). CLASP1 is involved in the regulation of microtubule dynamics at the kinetochore and throughout the spindle (Maiato et al., 2003 [PubMed 12837247]).[supplied by OMIM, Mar 2008]
Allele List at MGI
Other mutations in this stock
Total: 66 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700003H04Rik C T 3: 124,350,380 (GRCm39) probably benign Het
Acacb A T 5: 114,370,951 (GRCm39) D1731V probably damaging Het
Afg3l1 G A 8: 124,226,778 (GRCm39) V563I possibly damaging Het
Ak7 A G 12: 105,692,471 (GRCm39) E175G probably damaging Het
Arhgap5 C T 12: 52,565,525 (GRCm39) T832I possibly damaging Het
Arid4a A T 12: 71,116,747 (GRCm39) T602S probably damaging Het
Caps2 C T 10: 112,001,591 (GRCm39) probably benign Het
Ccdc170 G T 10: 4,508,551 (GRCm39) E592* probably null Het
Crhbp T A 13: 95,568,564 (GRCm39) M291L probably benign Het
Cyp3a41b T A 5: 145,519,349 (GRCm39) L47F probably benign Het
Dgcr6 A G 16: 17,884,598 (GRCm39) D82G probably damaging Het
Drc7 A G 8: 95,800,754 (GRCm39) E592G probably damaging Het
Dtl G A 1: 191,300,519 (GRCm39) T115I probably damaging Het
Ece2 A G 16: 20,457,510 (GRCm39) Y338C probably damaging Het
Egr3 A G 14: 70,316,897 (GRCm39) D198G probably damaging Het
Ereg A C 5: 91,222,552 (GRCm39) probably benign Het
Esp31 G C 17: 38,951,933 (GRCm39) probably null Het
Faap100 T C 11: 120,267,958 (GRCm39) I272V possibly damaging Het
Fam3c T C 6: 22,328,560 (GRCm39) D109G probably damaging Het
Fam3c T A 6: 22,339,299 (GRCm39) M51L probably benign Het
Fcnb A T 2: 27,966,701 (GRCm39) N277K probably damaging Het
Fgfr1 A G 8: 26,009,325 (GRCm39) probably benign Het
Gpr158 T C 2: 21,373,932 (GRCm39) F289S possibly damaging Het
Grik4 C A 9: 42,502,720 (GRCm39) V468F probably damaging Het
Gtdc1 T A 2: 44,642,076 (GRCm39) R168S probably benign Het
Gucy2c C T 6: 136,699,440 (GRCm39) G610R probably damaging Het
Gulp1 A T 1: 44,793,534 (GRCm39) Q65L possibly damaging Het
Hectd1 A T 12: 51,849,035 (GRCm39) D356E probably damaging Het
Hnrnpu T C 1: 178,157,737 (GRCm39) probably benign Het
Igkv13-57-2 T C 6: 69,500,971 (GRCm39) noncoding transcript Het
Itih4 A G 14: 30,612,612 (GRCm39) I213V possibly damaging Het
Itpr2 T C 6: 146,214,441 (GRCm39) K1469E probably benign Het
Jkampl T C 6: 73,445,674 (GRCm39) T292A probably damaging Het
Jrk T C 15: 74,577,617 (GRCm39) D556G possibly damaging Het
Kctd16 A T 18: 40,663,905 (GRCm39) I345F probably benign Het
Klhdc1 A G 12: 69,303,025 (GRCm39) E187G possibly damaging Het
Lrch3 T C 16: 32,779,833 (GRCm39) Y111H probably damaging Het
Mlh3 A T 12: 85,315,229 (GRCm39) V319D probably damaging Het
Nsd3 T C 8: 26,156,092 (GRCm39) L553P probably damaging Het
Or1e23 T A 11: 73,407,351 (GRCm39) I225F probably damaging Het
Or51q1 A T 7: 103,628,915 (GRCm39) H172L probably benign Het
Or5d38 C T 2: 87,955,027 (GRCm39) V101I probably benign Het
Or5e1 T A 7: 108,354,882 (GRCm39) I273N probably benign Het
Or5p66 T A 7: 107,885,605 (GRCm39) T243S probably damaging Het
Or7g26 T C 9: 19,230,445 (GRCm39) I205T probably benign Het
Pelp1 C T 11: 70,287,740 (GRCm39) R394H probably damaging Het
Ppp1r13l G T 7: 19,109,817 (GRCm39) probably null Het
Prr5 C A 15: 84,585,635 (GRCm39) S201* probably null Het
Rad23b T A 4: 55,370,474 (GRCm39) probably null Het
Rasgef1a T A 6: 118,061,335 (GRCm39) probably null Het
Ryr3 A T 2: 112,738,832 (GRCm39) I565N probably damaging Het
Slc30a5 T C 13: 100,945,600 (GRCm39) N527S probably damaging Het
Slc39a5 T A 10: 128,235,812 (GRCm39) N49Y probably damaging Het
Spast T A 17: 74,694,058 (GRCm39) S571T probably benign Het
Spdye4c C T 2: 128,437,994 (GRCm39) R245* probably null Het
Tbc1d2 C T 4: 46,629,912 (GRCm39) G252R probably benign Het
Tgm7 T A 2: 120,926,454 (GRCm39) D480V probably benign Het
Thpo T A 16: 20,547,546 (GRCm39) S22C probably null Het
Top2a T A 11: 98,907,291 (GRCm39) T180S possibly damaging Het
Trim37 T A 11: 87,087,663 (GRCm39) Y34* probably null Het
Tsc2 T C 17: 24,819,361 (GRCm39) E1254G possibly damaging Het
Ttc39a C T 4: 109,280,168 (GRCm39) P150L possibly damaging Het
Ttc4 T C 4: 106,525,240 (GRCm39) D298G probably damaging Het
Ttll1 A G 15: 83,386,482 (GRCm39) V41A probably benign Het
Vmn1r20 C A 6: 57,408,774 (GRCm39) H33Q probably benign Het
Zan A T 5: 137,456,174 (GRCm39) Y1329N unknown Het
Other mutations in Clasp1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01785:Clasp1 APN 1 118,425,466 (GRCm39) missense possibly damaging 0.74
IGL01786:Clasp1 APN 1 118,425,466 (GRCm39) missense possibly damaging 0.74
IGL01871:Clasp1 APN 1 118,498,619 (GRCm39) missense probably damaging 1.00
IGL02066:Clasp1 APN 1 118,492,990 (GRCm39) critical splice donor site probably null
IGL02602:Clasp1 APN 1 118,399,515 (GRCm39) missense probably damaging 0.99
IGL02683:Clasp1 APN 1 118,466,996 (GRCm39) missense probably benign 0.33
IGL02728:Clasp1 APN 1 118,530,107 (GRCm39) missense probably damaging 1.00
IGL02820:Clasp1 APN 1 118,478,834 (GRCm39) missense possibly damaging 0.77
IGL02874:Clasp1 APN 1 118,479,773 (GRCm39) missense possibly damaging 0.86
IGL02975:Clasp1 APN 1 118,390,277 (GRCm39) missense probably damaging 1.00
IGL03100:Clasp1 APN 1 118,395,626 (GRCm39) missense possibly damaging 0.79
IGL03115:Clasp1 APN 1 118,429,053 (GRCm39) nonsense probably null
IGL03122:Clasp1 APN 1 118,438,007 (GRCm39) missense probably damaging 1.00
IGL03180:Clasp1 APN 1 118,433,255 (GRCm39) missense probably benign 0.33
IGL03248:Clasp1 APN 1 118,530,206 (GRCm39) missense probably benign 0.01
IGL03388:Clasp1 APN 1 118,433,233 (GRCm39) missense possibly damaging 0.95
F5770:Clasp1 UTSW 1 118,509,078 (GRCm39) missense probably damaging 1.00
I2288:Clasp1 UTSW 1 118,492,959 (GRCm39) missense probably benign 0.09
PIT4585001:Clasp1 UTSW 1 118,390,285 (GRCm39) missense probably damaging 0.99
R0079:Clasp1 UTSW 1 118,471,034 (GRCm39) missense probably damaging 1.00
R0395:Clasp1 UTSW 1 118,467,061 (GRCm39) missense possibly damaging 0.48
R0960:Clasp1 UTSW 1 118,479,756 (GRCm39) missense probably benign 0.39
R1448:Clasp1 UTSW 1 118,436,646 (GRCm39) missense probably benign 0.01
R1497:Clasp1 UTSW 1 118,479,788 (GRCm39) missense probably benign 0.42
R1607:Clasp1 UTSW 1 118,432,689 (GRCm39) missense probably damaging 0.98
R1722:Clasp1 UTSW 1 118,518,194 (GRCm39) missense probably damaging 1.00
R1758:Clasp1 UTSW 1 118,475,755 (GRCm39) missense probably damaging 1.00
R1765:Clasp1 UTSW 1 118,433,261 (GRCm39) missense probably damaging 0.99
R1855:Clasp1 UTSW 1 118,436,624 (GRCm39) missense probably damaging 1.00
R1861:Clasp1 UTSW 1 118,498,661 (GRCm39) missense possibly damaging 0.93
R1874:Clasp1 UTSW 1 118,528,315 (GRCm39) critical splice donor site probably null
R1942:Clasp1 UTSW 1 118,429,078 (GRCm39) missense possibly damaging 0.94
R2025:Clasp1 UTSW 1 118,432,629 (GRCm39) missense probably damaging 1.00
R2174:Clasp1 UTSW 1 118,487,825 (GRCm39) missense probably damaging 1.00
R2280:Clasp1 UTSW 1 118,492,913 (GRCm39) missense probably benign 0.05
R2288:Clasp1 UTSW 1 118,506,608 (GRCm39) missense probably benign
R2895:Clasp1 UTSW 1 118,387,568 (GRCm39) missense probably damaging 1.00
R3958:Clasp1 UTSW 1 118,395,611 (GRCm39) missense probably damaging 0.99
R4073:Clasp1 UTSW 1 118,431,578 (GRCm39) missense probably damaging 1.00
R4206:Clasp1 UTSW 1 118,506,636 (GRCm39) missense probably damaging 1.00
R4465:Clasp1 UTSW 1 118,488,808 (GRCm39) missense probably damaging 1.00
R4609:Clasp1 UTSW 1 118,430,765 (GRCm39) intron probably benign
R4679:Clasp1 UTSW 1 118,471,001 (GRCm39) missense probably damaging 0.99
R4707:Clasp1 UTSW 1 118,470,927 (GRCm39) nonsense probably null
R4809:Clasp1 UTSW 1 118,388,980 (GRCm39) missense probably benign 0.00
R4906:Clasp1 UTSW 1 118,436,640 (GRCm39) nonsense probably null
R5048:Clasp1 UTSW 1 118,475,340 (GRCm39) intron probably benign
R5298:Clasp1 UTSW 1 118,475,650 (GRCm39) missense possibly damaging 0.71
R5485:Clasp1 UTSW 1 118,395,643 (GRCm39) missense possibly damaging 0.95
R5516:Clasp1 UTSW 1 118,425,451 (GRCm39) missense probably damaging 1.00
R5821:Clasp1 UTSW 1 118,518,214 (GRCm39) missense probably damaging 1.00
R6092:Clasp1 UTSW 1 118,438,028 (GRCm39) missense probably damaging 0.97
R6181:Clasp1 UTSW 1 118,347,547 (GRCm39) missense probably benign 0.18
R6478:Clasp1 UTSW 1 118,439,910 (GRCm39) nonsense probably null
R7090:Clasp1 UTSW 1 118,409,816 (GRCm39) missense probably benign 0.45
R7216:Clasp1 UTSW 1 118,475,648 (GRCm39) missense probably benign 0.00
R7508:Clasp1 UTSW 1 118,473,164 (GRCm39) missense probably benign 0.30
R7541:Clasp1 UTSW 1 118,470,727 (GRCm39) splice site probably null
R7644:Clasp1 UTSW 1 118,440,480 (GRCm39) splice site probably null
R7825:Clasp1 UTSW 1 118,473,123 (GRCm39) missense probably benign 0.00
R7910:Clasp1 UTSW 1 118,530,144 (GRCm39) nonsense probably null
R7971:Clasp1 UTSW 1 118,449,559 (GRCm39) missense probably damaging 0.99
R8074:Clasp1 UTSW 1 118,390,213 (GRCm39) missense probably benign
R8344:Clasp1 UTSW 1 118,431,629 (GRCm39) missense probably damaging 1.00
R8847:Clasp1 UTSW 1 118,506,705 (GRCm39) missense probably damaging 1.00
R9035:Clasp1 UTSW 1 118,431,583 (GRCm39) missense probably damaging 1.00
R9073:Clasp1 UTSW 1 118,390,193 (GRCm39) splice site probably null
R9161:Clasp1 UTSW 1 118,474,651 (GRCm39) missense probably damaging 0.98
R9184:Clasp1 UTSW 1 118,470,908 (GRCm39) missense probably benign 0.17
R9379:Clasp1 UTSW 1 118,509,168 (GRCm39) utr 3 prime probably benign
R9379:Clasp1 UTSW 1 118,509,157 (GRCm39) utr 3 prime probably benign
R9422:Clasp1 UTSW 1 118,390,257 (GRCm39) missense possibly damaging 0.46
R9516:Clasp1 UTSW 1 118,431,560 (GRCm39) missense possibly damaging 0.88
R9566:Clasp1 UTSW 1 118,479,801 (GRCm39) missense probably benign 0.01
R9776:Clasp1 UTSW 1 118,509,108 (GRCm39) missense possibly damaging 0.89
V7581:Clasp1 UTSW 1 118,509,078 (GRCm39) missense probably damaging 1.00
X0028:Clasp1 UTSW 1 118,478,855 (GRCm39) missense possibly damaging 0.93
Predicted Primers PCR Primer
(F):5'- AAATCCTTCTGTGAGAGTGAGG -3'
(R):5'- CAGTTGCACTTAGGCAACCAC -3'

Sequencing Primer
(F):5'- CTGTGAGAGTGAGGTGGGGAC -3'
(R):5'- TGGAACAACAGGACTGCC -3'
Posted On 2017-02-28