Incidental Mutation 'R5082:Aspm'
ID 387165
Institutional Source Beutler Lab
Gene Symbol Aspm
Ensembl Gene ENSMUSG00000033952
Gene Name abnormal spindle microtubule assembly
Synonyms Sha1, D330028K02Rik, Calmbp1, MCPH5, Aspm
MMRRC Submission 042671-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5082 (G1)
Quality Score 225
Status Not validated
Chromosome 1
Chromosomal Location 139382510-139421829 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) T to A at 139406414 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Leucine to Stop codon at position 1767 (L1767*)
Ref Sequence ENSEMBL: ENSMUSP00000059159 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053364] [ENSMUST00000200083]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000053364
AA Change: L1767*
SMART Domains Protein: ENSMUSP00000059159
Gene: ENSMUSG00000033952
AA Change: L1767*

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 noncoding transcript
Transcript: ENSMUST00000199998
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: 99.2%
  • 3x: 98.6%
  • 10x: 96.9%
  • 20x: 94.3%
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: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca9 T A 11: 110,022,694 (GRCm39) M1015L probably benign Het
Aftph T C 11: 20,677,100 (GRCm39) S170G probably damaging Het
Aox4 C T 1: 58,270,642 (GRCm39) P274S possibly damaging Het
Ash1l G A 3: 88,873,541 (GRCm39) R108Q probably damaging Het
Baz2b T A 2: 59,731,835 (GRCm39) K2068* probably null Het
Bcl9 A T 3: 97,117,218 (GRCm39) V492D probably damaging Het
Bicc1 G T 10: 70,776,352 (GRCm39) H782Q probably benign Het
Cabin1 T A 10: 75,574,164 (GRCm39) I640F probably damaging Het
Ccng1 A G 11: 40,643,015 (GRCm39) V144A possibly damaging Het
Cdc23 C A 18: 34,784,742 (GRCm39) V7L unknown Het
Ddx1 G T 12: 13,270,436 (GRCm39) C668* probably null Het
Dhx58 G A 11: 100,587,802 (GRCm39) S585L probably benign Het
Dnttip2 A T 3: 122,069,590 (GRCm39) K268N probably damaging Het
Ecd C T 14: 20,374,436 (GRCm39) probably null Het
Entpd1 A G 19: 40,713,473 (GRCm39) probably null Het
Erlin2 T C 8: 27,523,435 (GRCm39) V224A probably damaging Het
Exoc3l4 A G 12: 111,394,424 (GRCm39) S515G probably benign Het
Fcho1 T C 8: 72,169,829 (GRCm39) D98G possibly damaging Het
Fhod1 T A 8: 106,057,145 (GRCm39) D943V probably damaging Het
Gm10322 A T 10: 59,452,090 (GRCm39) E69V possibly damaging Het
Gm14295 T A 2: 176,499,210 (GRCm39) L19* probably null Het
Gm7347 T A 5: 26,262,372 (GRCm39) R50* probably null Het
Hesx1 T C 14: 26,722,731 (GRCm39) C19R probably benign Het
Hgh1 T A 15: 76,253,752 (GRCm39) F199L probably benign Het
Irak2 T C 6: 113,649,805 (GRCm39) F147L probably damaging Het
Kif22 G A 7: 126,632,549 (GRCm39) R254C possibly damaging Het
Klhl9 A T 4: 88,639,622 (GRCm39) S206R probably damaging Het
Maip1 T C 1: 57,451,010 (GRCm39) probably null Het
Mcm9 T A 10: 53,414,156 (GRCm39) E308V possibly damaging Het
Mfsd13b A T 7: 120,598,201 (GRCm39) N369I possibly damaging Het
Mga T A 2: 119,733,825 (GRCm39) H224Q probably damaging Het
Mtss1 A T 15: 58,842,868 (GRCm39) W115R probably damaging Het
Myo3b T C 2: 70,088,374 (GRCm39) V851A probably benign Het
Nectin2 A T 7: 19,472,049 (GRCm39) D113E probably damaging Het
Notch2 G A 3: 98,007,690 (GRCm39) C480Y probably damaging Het
Or6b6 G A 7: 106,570,871 (GRCm39) R227C probably benign Het
Or8b55 T C 9: 38,727,441 (GRCm39) I214T possibly damaging Het
Pfdn1 G T 18: 36,537,466 (GRCm39) N111K probably damaging Het
Pfkl A T 10: 77,832,242 (GRCm39) V283E probably damaging Het
Plbd2 G T 5: 120,629,249 (GRCm39) S305* probably null Het
Prom1 T C 5: 44,158,174 (GRCm39) probably null Het
Ptbp2 T A 3: 119,546,613 (GRCm39) M90L probably benign Het
Rai1 G A 11: 60,076,745 (GRCm39) E270K possibly damaging Het
Rbbp6 G A 7: 122,599,925 (GRCm39) probably benign Het
Reln T C 5: 22,101,075 (GRCm39) M3399V probably benign Het
Ros1 T A 10: 52,040,037 (GRCm39) Y318F possibly damaging Het
Sh2d2a A G 3: 87,759,091 (GRCm39) D231G probably benign Het
Smn1 T C 13: 100,273,890 (GRCm39) probably benign Het
Snrnp200 C T 2: 127,068,290 (GRCm39) Q877* probably null Het
Taf2 G T 15: 54,923,441 (GRCm39) H279N probably benign Het
Tnfaip3 T C 10: 18,881,032 (GRCm39) Y345C probably damaging Het
Vmn2r68 C T 7: 84,883,076 (GRCm39) M225I probably benign Het
Vps13a A T 19: 16,722,257 (GRCm39) W352R 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
R1625:Aspm UTSW 1 139,408,777 (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
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'- TGCGTGAATCCTGTATCAAACTG -3'
(R):5'- TAAGCAACCTTCTGTGCCCTG -3'

Sequencing Primer
(F):5'- CAGTCACACTTTAGAGGATGCCTG -3'
(R):5'- GTACCATCTCTGAATCTTCACAGCAG -3'
Posted On 2016-06-06