Incidental Mutation 'R1625:Aspm'
ID 174938
Institutional Source Beutler Lab
Gene Symbol Aspm
Ensembl Gene ENSMUSG00000033952
Gene Name abnormal spindle microtubule assembly
Synonyms Sha1, D330028K02Rik, Calmbp1, MCPH5, Aspm
MMRRC Submission 039662-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1625 (G1)
Quality Score 225
Status Not validated
Chromosome 1
Chromosomal Location 139382510-139421829 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 139408777 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Alanine to Threonine at position 2555 (A2555T)
Ref Sequence ENSEMBL: ENSMUSP00000059159 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053364] [ENSMUST00000200083]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000053364
AA Change: A2555T

PolyPhen 2 Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)
SMART Domains Protein: ENSMUSP00000059159
Gene: ENSMUSG00000033952
AA Change: A2555T

DomainStartEndE-ValueType
Pfam:ASH 29 126 8.9e-35 PFAM
low complexity region 855 861 N/A INTRINSIC
CH 890 1022 2.04e0 SMART
CH 1080 1224 5.56e-9 SMART
IQ 1233 1255 7.57e0 SMART
IQ 1259 1281 1.12e1 SMART
IQ 1282 1304 3.73e-1 SMART
IQ 1314 1336 2.41e-4 SMART
IQ 1360 1382 2.12e1 SMART
IQ 1387 1408 7.61e1 SMART
IQ 1409 1431 6.97e0 SMART
IQ 1432 1452 1.44e1 SMART
IQ 1453 1475 1.15e-1 SMART
IQ 1476 1495 1.66e2 SMART
IQ 1503 1525 1.65e-2 SMART
IQ 1526 1548 1.32e1 SMART
IQ 1549 1571 1.48e1 SMART
IQ 1572 1594 2.5e1 SMART
IQ 1599 1621 2.58e-4 SMART
IQ 1622 1644 6.7e-3 SMART
IQ 1645 1667 4.25e1 SMART
IQ 1668 1694 1.03e2 SMART
IQ 1695 1717 2.33e-2 SMART
IQ 1718 1740 7.79e0 SMART
IQ 1741 1763 1.57e2 SMART
IQ 1768 1790 2.68e-2 SMART
IQ 1791 1813 5.83e-3 SMART
IQ 1814 1836 5.93e1 SMART
IQ 1841 1863 1.92e-3 SMART
IQ 1864 1886 3.79e-2 SMART
IQ 1914 1936 4.11e0 SMART
IQ 1937 1959 1.87e-1 SMART
IQ 1960 1982 6.27e1 SMART
IQ 1987 2009 8.25e-3 SMART
IQ 2010 2032 5.73e0 SMART
IQ 2060 2082 1.39e0 SMART
IQ 2083 2105 4.62e1 SMART
IQ 2133 2155 5.58e0 SMART
IQ 2156 2178 7.07e-2 SMART
IQ 2206 2228 1.18e-3 SMART
IQ 2229 2251 4.59e0 SMART
IQ 2278 2300 1.85e-5 SMART
IQ 2301 2323 8.13e-2 SMART
IQ 2342 2364 9.62e-4 SMART
IQ 2365 2387 4.12e-3 SMART
IQ 2415 2437 7.58e-2 SMART
IQ 2438 2460 2.6e0 SMART
IQ 2490 2512 1.68e-3 SMART
IQ 2513 2535 8.51e1 SMART
IQ 2560 2582 2.14e-1 SMART
IQ 2601 2623 8.46e0 SMART
IQ 2647 2669 1.15e1 SMART
IQ 2673 2695 1.95e-4 SMART
IQ 2696 2718 4.13e1 SMART
IQ 2723 2745 1.02e-2 SMART
IQ 2761 2783 3.14e2 SMART
IQ 2784 2806 1e1 SMART
IQ 2825 2847 2.43e0 SMART
IQ 2848 2870 4.6e-1 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000196272
Predicted Effect probably benign
Transcript: ENSMUST00000200083
SMART Domains Protein: ENSMUSP00000142880
Gene: ENSMUSG00000033952

DomainStartEndE-ValueType
low complexity region 855 861 N/A INTRINSIC
CH 890 1022 2.04e0 SMART
CH 1080 1224 5.56e-9 SMART
IQ 1233 1255 7.57e0 SMART
IQ 1259 1281 1.12e1 SMART
IQ 1282 1304 3.73e-1 SMART
IQ 1314 1336 1.25e1 SMART
IQ 1337 1358 2.96e1 SMART
IQ 1382 1404 1.15e1 SMART
IQ 1408 1430 1.95e-4 SMART
IQ 1431 1453 4.13e1 SMART
IQ 1458 1480 1.02e-2 SMART
IQ 1496 1518 3.14e2 SMART
IQ 1519 1541 1e1 SMART
IQ 1560 1582 2.43e0 SMART
IQ 1583 1605 4.6e-1 SMART
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.1%
  • 10x: 95.3%
  • 20x: 89.1%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is the human ortholog of the Drosophila melanogaster 'abnormal spindle' gene (asp), which is essential for normal mitotic spindle function in embryonic neuroblasts. Studies in mouse also suggest a role of this gene in mitotic spindle regulation, with a preferential role in regulating neurogenesis. Mutations in this gene are associated with microcephaly primary type 5. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011]
PHENOTYPE: Mice homozygous for protein-truncating gene trap mutations of this gene exhibit decreased body weight, microcephaly, a severe reduction in brain, testis and ovary weight, oligozoospermia and asthenospermia, and reduced fertility in both sexes. [provided by MGI curators]
Allele List at MGI

All alleles(9) : Targeted, other(2) Gene trapped(7)

Other mutations in this stock
Total: 70 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca8b T A 11: 109,857,947 (GRCm39) M605L probably benign Het
Abcc5 A T 16: 20,184,567 (GRCm39) S1031T probably damaging Het
Acot7 T A 4: 152,270,748 (GRCm39) C31S probably benign Het
Acss3 A T 10: 106,773,263 (GRCm39) probably null Het
Adipor1 T C 1: 134,351,802 (GRCm39) F83S possibly damaging Het
Agrn G A 4: 156,257,317 (GRCm39) S1171L probably damaging Het
Aoc1l1 T A 6: 48,952,105 (GRCm39) L10Q probably damaging Het
Arhgap5 T A 12: 52,564,159 (GRCm39) C377S probably benign Het
Arid4b T A 13: 14,361,699 (GRCm39) V721D probably damaging Het
Atp6v0a1 T A 11: 100,946,380 (GRCm39) L791Q probably damaging Het
Car11 A G 7: 45,350,731 (GRCm39) K76E probably benign Het
Casp8ap2 T A 4: 32,648,068 (GRCm39) M1925K probably benign Het
Cc2d1a A T 8: 84,866,001 (GRCm39) L418Q probably damaging Het
Ccl9 G A 11: 83,466,736 (GRCm39) R64W probably damaging Het
Cfap20dc A G 14: 8,431,668 (GRCm38) Y655H probably damaging Het
Cfap43 T A 19: 47,739,527 (GRCm39) K1325N probably damaging Het
Dars2 G A 1: 160,881,614 (GRCm39) P305L possibly damaging Het
Ddx11 C T 17: 66,457,692 (GRCm39) T859I probably benign Het
Dock7 C T 4: 98,850,433 (GRCm39) probably null Het
Efcab6 A G 15: 83,831,839 (GRCm39) V570A probably benign Het
Fermt1 T A 2: 132,764,751 (GRCm39) I369F probably damaging Het
Fras1 A G 5: 96,861,849 (GRCm39) Y2161C probably damaging Het
Fras1 C A 5: 96,857,837 (GRCm39) P2044T possibly damaging Het
Gucy1a1 T C 3: 82,009,362 (GRCm39) I549V probably benign Het
Hspg2 G A 4: 137,246,282 (GRCm39) S1020N probably benign Het
Kif21a A G 15: 90,826,378 (GRCm39) S1360P probably damaging Het
Lrp3 T C 7: 34,903,350 (GRCm39) Y332C probably damaging Het
Ltc4s C A 11: 50,128,215 (GRCm39) A32S possibly damaging Het
Mgrn1 T C 16: 4,728,627 (GRCm39) L84P probably damaging Het
Muc2 C G 7: 141,283,405 (GRCm39) C672W probably damaging Het
Mvp A T 7: 126,600,845 (GRCm39) V52E probably damaging Het
Ndrg2 T C 14: 52,144,420 (GRCm39) T269A probably damaging Het
Notch2 T A 3: 98,018,891 (GRCm39) D684E probably damaging Het
Nup205 A G 6: 35,168,878 (GRCm39) D316G probably benign Het
Or12e7 T A 2: 87,288,016 (GRCm39) I169K probably damaging Het
Or2v2 T C 11: 49,004,071 (GRCm39) M161V probably benign Het
Or7d11 A G 9: 19,966,678 (GRCm39) L27P probably damaging Het
Pcsk1 A T 13: 75,274,971 (GRCm39) D520V probably benign Het
Pik3cg A T 12: 32,244,741 (GRCm39) D904E probably damaging Het
Pitpnm2 T A 5: 124,271,496 (GRCm39) D359V probably benign Het
Ppih T C 4: 119,175,779 (GRCm39) I69V probably damaging Het
Rab11fip3 T C 17: 26,287,865 (GRCm39) E96G possibly damaging Het
Retreg3 C A 11: 100,992,875 (GRCm39) M1I probably null Het
Rfpl4 C T 7: 5,118,409 (GRCm39) V54I possibly damaging Het
Rif1 T C 2: 51,993,652 (GRCm39) I855T probably benign Het
Rrm1 T A 7: 102,117,554 (GRCm39) I748N probably damaging Het
Sap130 T A 18: 31,807,517 (GRCm39) N441K probably damaging Het
Sf3b1 T A 1: 55,058,536 (GRCm39) I18F probably damaging Het
Skor2 A G 18: 76,946,499 (GRCm39) N74D unknown Het
Slc17a6 C A 7: 51,311,208 (GRCm39) F307L probably benign Het
Slc25a13 G A 6: 6,096,675 (GRCm39) L410F probably damaging Het
Slc47a1 A T 11: 61,262,625 (GRCm39) V38E probably damaging Het
Slc8a1 T A 17: 81,956,670 (GRCm39) T123S probably damaging Het
Slc9a5 C A 8: 106,094,755 (GRCm39) T782K possibly damaging Het
Spmip7 C A 11: 11,438,644 (GRCm39) probably benign Het
Sppl2c C A 11: 104,077,995 (GRCm39) T265K probably damaging Het
Srfbp1 A G 18: 52,621,788 (GRCm39) K283R probably benign Het
Ssr1 C T 13: 38,173,479 (GRCm39) probably null Het
Stard3nl T C 13: 19,556,754 (GRCm39) probably null Het
Timeless G T 10: 128,076,493 (GRCm39) S134I probably damaging Het
Tll1 A G 8: 64,494,476 (GRCm39) F760L probably damaging Het
Tspear A G 10: 77,706,333 (GRCm39) I368V probably benign Het
Txnrd2 G T 16: 18,257,116 (GRCm39) W144L probably damaging Het
Unc5d T C 8: 29,173,234 (GRCm39) E668G probably damaging Het
Urb1 C T 16: 90,570,936 (GRCm39) probably null Het
Uts2r A G 11: 121,052,033 (GRCm39) Y299C probably damaging Het
Vmn1r66 G T 7: 10,008,316 (GRCm39) T239K probably benign Het
Vps39 C T 2: 120,154,106 (GRCm39) V630M probably damaging Het
Wrn T C 8: 33,819,158 (GRCm39) T22A probably benign Het
Zfp7 T A 15: 76,765,374 (GRCm39) D22E probably damaging Het
Other mutations in Aspm
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00489:Aspm APN 1 139,406,429 (GRCm39) missense probably damaging 1.00
IGL00594:Aspm APN 1 139,415,160 (GRCm39) splice site probably benign
IGL00808:Aspm APN 1 139,389,214 (GRCm39) missense probably benign 0.03
IGL00897:Aspm APN 1 139,405,145 (GRCm39) missense probably damaging 0.98
IGL01024:Aspm APN 1 139,405,862 (GRCm39) missense possibly damaging 0.66
IGL01410:Aspm APN 1 139,410,182 (GRCm39) missense probably benign 0.25
IGL01588:Aspm APN 1 139,405,900 (GRCm39) missense probably benign 0.11
IGL01610:Aspm APN 1 139,417,408 (GRCm39) nonsense probably null
IGL01633:Aspm APN 1 139,408,574 (GRCm39) missense possibly damaging 0.93
IGL01982:Aspm APN 1 139,419,326 (GRCm39) missense probably benign 0.12
IGL02429:Aspm APN 1 139,407,548 (GRCm39) missense probably benign 0.27
IGL02468:Aspm APN 1 139,408,688 (GRCm39) missense probably damaging 1.00
IGL02519:Aspm APN 1 139,389,665 (GRCm39) splice site probably benign
IGL02526:Aspm APN 1 139,417,457 (GRCm39) missense probably benign 0.03
IGL02716:Aspm APN 1 139,407,425 (GRCm39) missense probably damaging 1.00
IGL02876:Aspm APN 1 139,401,391 (GRCm39) missense probably damaging 1.00
IGL02953:Aspm APN 1 139,385,157 (GRCm39) missense probably benign 0.01
IGL03275:Aspm APN 1 139,415,033 (GRCm39) missense probably damaging 1.00
Stemware UTSW 1 139,405,197 (GRCm39) nonsense probably null
3-1:Aspm UTSW 1 139,385,279 (GRCm39) missense probably benign
R0016:Aspm UTSW 1 139,407,282 (GRCm39) missense probably benign 0.01
R0016:Aspm UTSW 1 139,407,282 (GRCm39) missense probably benign 0.01
R0106:Aspm UTSW 1 139,404,614 (GRCm39) missense probably benign 0.02
R0106:Aspm UTSW 1 139,404,614 (GRCm39) missense probably benign 0.02
R0140:Aspm UTSW 1 139,408,379 (GRCm39) missense probably benign 0.00
R0195:Aspm UTSW 1 139,406,873 (GRCm39) missense probably damaging 1.00
R0217:Aspm UTSW 1 139,385,618 (GRCm39) missense possibly damaging 0.46
R0276:Aspm UTSW 1 139,406,209 (GRCm39) missense possibly damaging 0.95
R0309:Aspm UTSW 1 139,410,249 (GRCm39) splice site probably benign
R0466:Aspm UTSW 1 139,405,639 (GRCm39) missense probably damaging 1.00
R0520:Aspm UTSW 1 139,406,558 (GRCm39) missense possibly damaging 0.51
R0615:Aspm UTSW 1 139,415,027 (GRCm39) missense probably damaging 1.00
R0626:Aspm UTSW 1 139,419,339 (GRCm39) missense probably damaging 1.00
R0660:Aspm UTSW 1 139,385,502 (GRCm39) missense probably benign 0.03
R0751:Aspm UTSW 1 139,384,636 (GRCm39) splice site probably benign
R0830:Aspm UTSW 1 139,401,992 (GRCm39) missense probably damaging 0.99
R1109:Aspm UTSW 1 139,384,496 (GRCm39) missense probably damaging 0.99
R1114:Aspm UTSW 1 139,389,662 (GRCm39) splice site probably benign
R1130:Aspm UTSW 1 139,405,572 (GRCm39) missense possibly damaging 0.90
R1298:Aspm UTSW 1 139,385,157 (GRCm39) missense probably benign 0.01
R1386:Aspm UTSW 1 139,385,361 (GRCm39) missense probably benign 0.03
R1386:Aspm UTSW 1 139,406,710 (GRCm39) missense possibly damaging 0.80
R1557:Aspm UTSW 1 139,396,406 (GRCm39) missense probably benign 0.01
R1728:Aspm UTSW 1 139,401,312 (GRCm39) missense probably benign
R1729:Aspm UTSW 1 139,401,312 (GRCm39) missense probably benign
R1730:Aspm UTSW 1 139,401,312 (GRCm39) missense probably benign
R1733:Aspm UTSW 1 139,384,855 (GRCm39) missense probably benign 0.27
R1739:Aspm UTSW 1 139,401,312 (GRCm39) missense probably benign
R1762:Aspm UTSW 1 139,401,312 (GRCm39) missense probably benign
R1783:Aspm UTSW 1 139,401,312 (GRCm39) missense probably benign
R1784:Aspm UTSW 1 139,401,312 (GRCm39) missense probably benign
R1785:Aspm UTSW 1 139,401,312 (GRCm39) missense probably benign
R1793:Aspm UTSW 1 139,385,079 (GRCm39) missense probably benign 0.00
R1893:Aspm UTSW 1 139,407,605 (GRCm39) missense probably damaging 1.00
R1911:Aspm UTSW 1 139,405,832 (GRCm39) missense probably benign 0.06
R2103:Aspm UTSW 1 139,419,403 (GRCm39) missense probably damaging 0.99
R2128:Aspm UTSW 1 139,385,373 (GRCm39) missense probably benign 0.14
R2129:Aspm UTSW 1 139,385,373 (GRCm39) missense probably benign 0.14
R2239:Aspm UTSW 1 139,384,584 (GRCm39) missense possibly damaging 0.67
R2352:Aspm UTSW 1 139,385,300 (GRCm39) missense probably benign 0.02
R2353:Aspm UTSW 1 139,405,435 (GRCm39) missense probably damaging 1.00
R2380:Aspm UTSW 1 139,407,086 (GRCm39) missense probably damaging 1.00
R2413:Aspm UTSW 1 139,405,495 (GRCm39) missense probably damaging 1.00
R2421:Aspm UTSW 1 139,416,225 (GRCm39) missense possibly damaging 0.49
R3607:Aspm UTSW 1 139,408,406 (GRCm39) missense probably benign 0.13
R3711:Aspm UTSW 1 139,385,838 (GRCm39) missense probably benign 0.17
R3718:Aspm UTSW 1 139,418,165 (GRCm39) missense probably benign 0.31
R3718:Aspm UTSW 1 139,408,627 (GRCm39) missense probably benign 0.09
R3741:Aspm UTSW 1 139,406,357 (GRCm39) missense possibly damaging 0.47
R3788:Aspm UTSW 1 139,390,941 (GRCm39) missense probably damaging 1.00
R3838:Aspm UTSW 1 139,405,792 (GRCm39) missense probably benign 0.24
R3839:Aspm UTSW 1 139,405,792 (GRCm39) missense probably benign 0.24
R3849:Aspm UTSW 1 139,386,024 (GRCm39) missense probably benign 0.21
R4075:Aspm UTSW 1 139,402,023 (GRCm39) missense probably damaging 1.00
R4080:Aspm UTSW 1 139,398,493 (GRCm39) missense probably damaging 1.00
R4463:Aspm UTSW 1 139,382,748 (GRCm39) missense possibly damaging 0.95
R4537:Aspm UTSW 1 139,402,041 (GRCm39) missense probably benign 0.01
R4547:Aspm UTSW 1 139,405,925 (GRCm39) missense possibly damaging 0.75
R4573:Aspm UTSW 1 139,407,245 (GRCm39) missense probably damaging 0.98
R4680:Aspm UTSW 1 139,408,409 (GRCm39) missense probably benign 0.05
R4807:Aspm UTSW 1 139,405,657 (GRCm39) missense probably damaging 1.00
R4840:Aspm UTSW 1 139,398,269 (GRCm39) missense possibly damaging 0.83
R4854:Aspm UTSW 1 139,405,810 (GRCm39) nonsense probably null
R4859:Aspm UTSW 1 139,397,131 (GRCm39) missense probably damaging 1.00
R4893:Aspm UTSW 1 139,417,577 (GRCm39) critical splice donor site probably null
R4910:Aspm UTSW 1 139,419,281 (GRCm39) missense probably damaging 1.00
R4953:Aspm UTSW 1 139,399,472 (GRCm39) missense probably benign 0.00
R4974:Aspm UTSW 1 139,405,748 (GRCm39) missense probably benign 0.03
R4981:Aspm UTSW 1 139,398,498 (GRCm39) splice site probably null
R5082:Aspm UTSW 1 139,406,414 (GRCm39) nonsense probably null
R5223:Aspm UTSW 1 139,406,072 (GRCm39) missense probably damaging 1.00
R5268:Aspm UTSW 1 139,392,033 (GRCm39) missense probably damaging 1.00
R5371:Aspm UTSW 1 139,398,279 (GRCm39) nonsense probably null
R5377:Aspm UTSW 1 139,398,133 (GRCm39) splice site probably null
R5377:Aspm UTSW 1 139,385,221 (GRCm39) missense probably damaging 0.96
R5481:Aspm UTSW 1 139,384,799 (GRCm39) missense possibly damaging 0.85
R5513:Aspm UTSW 1 139,410,136 (GRCm39) missense probably damaging 1.00
R5578:Aspm UTSW 1 139,398,455 (GRCm39) missense probably damaging 1.00
R5649:Aspm UTSW 1 139,407,407 (GRCm39) missense probably benign
R5685:Aspm UTSW 1 139,415,026 (GRCm39) missense probably benign 0.10
R5695:Aspm UTSW 1 139,407,407 (GRCm39) missense probably benign
R5766:Aspm UTSW 1 139,406,740 (GRCm39) missense probably damaging 0.99
R5964:Aspm UTSW 1 139,382,965 (GRCm39) intron probably benign
R5993:Aspm UTSW 1 139,407,269 (GRCm39) missense probably benign 0.28
R6027:Aspm UTSW 1 139,390,794 (GRCm39) missense probably damaging 1.00
R6029:Aspm UTSW 1 139,408,728 (GRCm39) missense possibly damaging 0.83
R6102:Aspm UTSW 1 139,405,197 (GRCm39) nonsense probably null
R6188:Aspm UTSW 1 139,406,977 (GRCm39) missense possibly damaging 0.79
R6257:Aspm UTSW 1 139,409,791 (GRCm39) splice site probably null
R6433:Aspm UTSW 1 139,401,421 (GRCm39) missense probably damaging 1.00
R6682:Aspm UTSW 1 139,385,460 (GRCm39) missense possibly damaging 0.67
R6763:Aspm UTSW 1 139,398,255 (GRCm39) missense possibly damaging 0.64
R6798:Aspm UTSW 1 139,396,423 (GRCm39) missense possibly damaging 0.66
R6815:Aspm UTSW 1 139,407,880 (GRCm39) missense probably benign 0.04
R6854:Aspm UTSW 1 139,390,920 (GRCm39) missense possibly damaging 0.90
R6928:Aspm UTSW 1 139,407,944 (GRCm39) nonsense probably null
R6943:Aspm UTSW 1 139,408,280 (GRCm39) missense probably damaging 1.00
R6979:Aspm UTSW 1 139,408,223 (GRCm39) missense probably damaging 1.00
R6998:Aspm UTSW 1 139,397,210 (GRCm39) missense probably damaging 1.00
R7126:Aspm UTSW 1 139,408,541 (GRCm39) missense probably benign 0.27
R7237:Aspm UTSW 1 139,405,667 (GRCm39) missense possibly damaging 0.81
R7240:Aspm UTSW 1 139,406,389 (GRCm39) nonsense probably null
R7272:Aspm UTSW 1 139,386,066 (GRCm39) missense probably benign 0.14
R7427:Aspm UTSW 1 139,385,354 (GRCm39) missense probably benign 0.01
R7519:Aspm UTSW 1 139,418,074 (GRCm39) missense possibly damaging 0.53
R7776:Aspm UTSW 1 139,407,584 (GRCm39) missense possibly damaging 0.85
R7875:Aspm UTSW 1 139,382,872 (GRCm39) missense probably benign 0.02
R7883:Aspm UTSW 1 139,406,405 (GRCm39) missense possibly damaging 0.47
R7964:Aspm UTSW 1 139,408,424 (GRCm39) missense probably damaging 1.00
R8012:Aspm UTSW 1 139,385,202 (GRCm39) missense probably benign 0.03
R8029:Aspm UTSW 1 139,399,370 (GRCm39) missense probably benign 0.00
R8233:Aspm UTSW 1 139,385,042 (GRCm39) missense probably benign 0.28
R8277:Aspm UTSW 1 139,382,748 (GRCm39) missense probably damaging 1.00
R8345:Aspm UTSW 1 139,392,011 (GRCm39) nonsense probably null
R8491:Aspm UTSW 1 139,385,433 (GRCm39) missense probably damaging 0.98
R8511:Aspm UTSW 1 139,385,046 (GRCm39) missense probably damaging 1.00
R8557:Aspm UTSW 1 139,384,494 (GRCm39) missense probably benign 0.01
R8927:Aspm UTSW 1 139,418,125 (GRCm39) nonsense probably null
R8928:Aspm UTSW 1 139,418,125 (GRCm39) nonsense probably null
R8950:Aspm UTSW 1 139,406,690 (GRCm39) missense probably damaging 1.00
R9033:Aspm UTSW 1 139,405,865 (GRCm39) missense probably damaging 1.00
R9083:Aspm UTSW 1 139,421,436 (GRCm39) missense possibly damaging 0.70
R9133:Aspm UTSW 1 139,419,266 (GRCm39) missense probably damaging 1.00
R9160:Aspm UTSW 1 139,417,862 (GRCm39) missense probably damaging 1.00
R9179:Aspm UTSW 1 139,404,453 (GRCm39) missense probably damaging 1.00
R9265:Aspm UTSW 1 139,389,182 (GRCm39) missense probably benign 0.24
R9400:Aspm UTSW 1 139,407,641 (GRCm39) missense probably damaging 1.00
R9419:Aspm UTSW 1 139,384,923 (GRCm39) missense probably benign 0.29
R9454:Aspm UTSW 1 139,408,732 (GRCm39) missense probably benign 0.00
R9517:Aspm UTSW 1 139,407,167 (GRCm39) missense probably damaging 1.00
R9524:Aspm UTSW 1 139,408,607 (GRCm39) missense probably damaging 1.00
R9544:Aspm UTSW 1 139,385,523 (GRCm39) missense probably benign 0.01
R9640:Aspm UTSW 1 139,408,010 (GRCm39) missense possibly damaging 0.88
R9698:Aspm UTSW 1 139,389,646 (GRCm39) missense probably benign 0.28
R9790:Aspm UTSW 1 139,408,375 (GRCm39) missense probably damaging 0.98
R9791:Aspm UTSW 1 139,408,375 (GRCm39) missense probably damaging 0.98
R9794:Aspm UTSW 1 139,406,480 (GRCm39) missense probably damaging 0.99
X0063:Aspm UTSW 1 139,385,828 (GRCm39) missense probably benign 0.01
Predicted Primers PCR Primer
(F):5'- GGCAGCCATTACCATACAGTCCTC -3'
(R):5'- ACTTGGCAGTGACTAGTGTGGCAG -3'

Sequencing Primer
(F):5'- GTGCCTCGATTAGAATTCAGCAG -3'
(R):5'- ACTAGTGTGGCAGCCAGG -3'
Posted On 2014-04-24