Incidental Mutation 'IGL00966:Hmcn2'
ID 306615
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Hmcn2
Ensembl Gene ENSMUSG00000055632
Gene Name hemicentin 2
Synonyms
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL00966
Quality Score
Status
Chromosome 2
Chromosomal Location 31204427-31350750 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to G at 31319006 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Glycine at position 3902 (V3902G)
Ref Sequence ENSEMBL: ENSMUSP00000109160 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000113532] [ENSMUST00000226996]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000113532
AA Change: V3902G

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000109160
Gene: ENSMUSG00000055632
AA Change: V3902G

DomainStartEndE-ValueType
signal peptide 1 19 N/A INTRINSIC
VWA 37 211 1.21e-1 SMART
Blast:IG_like 263 340 2e-38 BLAST
IG 434 515 7.36e-2 SMART
IGc2 530 595 1.91e-9 SMART
IGc2 621 685 4.81e-15 SMART
IGc2 711 773 1.09e-13 SMART
IGc2 799 866 2.72e-14 SMART
IGc2 894 959 1.95e-15 SMART
IGc2 985 1049 5e-13 SMART
IGc2 1082 1147 1.09e-13 SMART
low complexity region 1151 1169 N/A INTRINSIC
IGc2 1173 1232 7.07e-13 SMART
IGc2 1260 1326 4.31e-17 SMART
IGc2 1354 1428 3e-16 SMART
IGc2 1456 1522 1.82e-15 SMART
IGc2 1550 1615 2.7e-18 SMART
IGc2 1644 1708 1.3e-11 SMART
IGc2 1736 1801 6.69e-14 SMART
IG 1826 1917 2.31e0 SMART
IGc2 1932 1997 4.62e-17 SMART
IGc2 2024 2091 3.25e-12 SMART
IGc2 2117 2182 1.28e-10 SMART
IGc2 2209 2276 3.76e-8 SMART
IGc2 2305 2370 2.6e-11 SMART
IGc2 2399 2464 1.32e-12 SMART
IGc2 2492 2557 2.06e-14 SMART
IGc2 2588 2653 3.9e-15 SMART
IGc2 2686 2751 2.64e-12 SMART
IGc2 2797 2862 9.05e-11 SMART
IGc2 2892 2957 4.7e-9 SMART
IGc2 2984 3049 1.44e-13 SMART
IGc2 3079 3144 9.33e-13 SMART
IGc2 3171 3236 3.79e-13 SMART
IGc2 3264 3331 1.85e-16 SMART
IGc2 3360 3425 9.61e-15 SMART
low complexity region 3433 3445 N/A INTRINSIC
IGc2 3453 3514 5.83e-14 SMART
IGc2 3542 3600 1.76e-8 SMART
low complexity region 3613 3627 N/A INTRINSIC
IGc2 3628 3693 5.2e-11 SMART
IGc2 3719 3784 2.64e-12 SMART
IGc2 3810 3877 3.35e-5 SMART
IGc2 3903 3968 3.73e-12 SMART
IGc2 3994 4058 4.39e-9 SMART
IGc2 4084 4149 1.79e-14 SMART
low complexity region 4157 4169 N/A INTRINSIC
IGc2 4175 4238 9.33e-13 SMART
IGc2 4265 4329 7.22e-19 SMART
IGc2 4355 4419 1.59e-15 SMART
Pfam:G2F 4431 4613 1.7e-56 PFAM
EGF_CA 4668 4708 5.78e-11 SMART
EGF_CA 4709 4753 9.39e-11 SMART
EGF_CA 4754 4796 7.69e-7 SMART
EGF_CA 4797 4837 2.19e-11 SMART
EGF_CA 4904 4943 6.74e-12 SMART
EGF_like 4944 4989 1.87e-5 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000226996
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acad11 A G 9: 104,003,855 (GRCm39) E649G probably damaging Het
Adgre1 C A 17: 57,726,335 (GRCm39) T402K probably benign Het
Agap3 A G 5: 24,706,000 (GRCm39) probably benign Het
Amy1 T C 3: 113,349,689 (GRCm39) I494V probably benign Het
Arhgef40 G A 14: 52,229,155 (GRCm39) probably null Het
Atp2c2 T C 8: 120,472,329 (GRCm39) V461A probably benign Het
Bub1 A G 2: 127,652,583 (GRCm39) S595P probably damaging Het
Cdcp3 T A 7: 130,844,836 (GRCm39) Y692* probably null Het
Cmya5 C T 13: 93,234,414 (GRCm39) V225I probably benign Het
Cnbd1 T C 4: 18,906,988 (GRCm39) probably benign Het
Cux1 A T 5: 136,340,345 (GRCm39) probably benign Het
Dsg3 T A 18: 20,656,664 (GRCm39) I178N probably benign Het
Dus2 T A 8: 106,752,533 (GRCm39) probably null Het
Enpp1 G A 10: 24,529,929 (GRCm39) H570Y probably damaging Het
Ephb3 A C 16: 21,036,044 (GRCm39) T57P probably benign Het
Fat3 C A 9: 15,910,390 (GRCm39) V1871F possibly damaging Het
Fbll1 T C 11: 35,688,874 (GRCm39) T130A probably benign Het
Fbxl20 C T 11: 98,001,800 (GRCm39) S99N probably damaging Het
Folr2 T C 7: 101,489,593 (GRCm39) E182G probably damaging Het
Fras1 A G 5: 96,703,080 (GRCm39) D281G probably benign Het
Gm17175 G T 14: 51,810,526 (GRCm39) Q34K possibly damaging Het
Gm5592 T A 7: 40,938,519 (GRCm39) D600E probably damaging Het
Gtf2e1 T C 16: 37,336,092 (GRCm39) E294G probably benign Het
Gtf3c2 A G 5: 31,327,517 (GRCm39) probably benign Het
Heg1 T C 16: 33,530,977 (GRCm39) L151P probably damaging Het
Ift140 A G 17: 25,237,776 (GRCm39) Y4C probably damaging Het
Ighv1-19 A C 12: 114,672,569 (GRCm39) V17G possibly damaging Het
Iqca1 T A 1: 89,973,379 (GRCm39) I770F probably benign Het
Jak3 T A 8: 72,131,656 (GRCm39) C115S probably benign Het
Kif18b A T 11: 102,805,501 (GRCm39) M252K probably damaging Het
Klhdc7a A T 4: 139,694,236 (GRCm39) V237D probably benign Het
Klhl11 C T 11: 100,354,031 (GRCm39) V597I possibly damaging Het
Krt72 T A 15: 101,689,396 (GRCm39) Y312F probably damaging Het
Lonp2 T A 8: 87,360,600 (GRCm39) I191N probably damaging Het
Npc2 A T 12: 84,819,619 (GRCm39) I8N possibly damaging Het
Nr4a1 T C 15: 101,170,669 (GRCm39) L413P probably damaging Het
Nup133 T C 8: 124,638,645 (GRCm39) N895S probably damaging Het
Or7e175 T C 9: 20,048,531 (GRCm39) F40L probably benign Het
Ppef1 A G X: 159,468,290 (GRCm39) I94T probably benign Het
Prrt4 G A 6: 29,176,455 (GRCm39) T290I probably benign Het
Ptpru A T 4: 131,499,927 (GRCm39) V1239E probably damaging Het
Rab8b T G 9: 66,760,274 (GRCm39) M117L probably benign Het
S1pr5 T A 9: 21,155,512 (GRCm39) I305F possibly damaging Het
Sdr39u1 A G 14: 56,135,463 (GRCm39) V160A probably damaging Het
Slc6a21 C T 7: 44,937,668 (GRCm39) T653M probably benign Het
Stk39 T A 2: 68,042,302 (GRCm39) E544D probably benign Het
Tgfbr3 T C 5: 107,290,367 (GRCm39) T313A probably benign Het
Tle6 A T 10: 81,430,292 (GRCm39) L287M probably damaging Het
Tmc2 A G 2: 130,105,932 (GRCm39) H821R probably benign Het
Tmem230 G T 2: 132,087,897 (GRCm39) D26E probably benign Het
Tnfaip3 A G 10: 18,880,885 (GRCm39) F394S probably damaging Het
Ttn T A 2: 76,641,721 (GRCm39) L13458F probably damaging Het
Vwa5a A T 9: 38,634,675 (GRCm39) N161I probably benign Het
Wdr87-ps C A 7: 29,236,888 (GRCm39) noncoding transcript Het
Other mutations in Hmcn2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00965:Hmcn2 APN 2 31,233,108 (GRCm39) missense probably damaging 1.00
IGL00973:Hmcn2 APN 2 31,273,833 (GRCm39) intron probably benign
IGL01364:Hmcn2 APN 2 31,251,826 (GRCm39) nonsense probably null
IGL01486:Hmcn2 APN 2 31,226,633 (GRCm39) missense probably damaging 1.00
IGL01530:Hmcn2 APN 2 31,244,276 (GRCm39) missense possibly damaging 0.85
IGL01550:Hmcn2 APN 2 31,314,264 (GRCm39) missense possibly damaging 0.84
IGL01710:Hmcn2 APN 2 31,233,114 (GRCm39) missense probably damaging 1.00
IGL01764:Hmcn2 APN 2 31,295,642 (GRCm39) missense possibly damaging 0.93
IGL01924:Hmcn2 APN 2 31,288,929 (GRCm39) missense probably benign 0.00
IGL02003:Hmcn2 APN 2 31,318,994 (GRCm39) missense possibly damaging 0.90
IGL02117:Hmcn2 APN 2 31,347,185 (GRCm39) missense possibly damaging 0.75
IGL02205:Hmcn2 APN 2 31,290,139 (GRCm39) missense probably damaging 1.00
IGL02273:Hmcn2 APN 2 31,314,389 (GRCm39) missense probably benign 0.06
IGL02313:Hmcn2 APN 2 31,343,617 (GRCm39) missense possibly damaging 0.68
IGL02326:Hmcn2 APN 2 31,340,964 (GRCm39) missense probably damaging 0.97
IGL02486:Hmcn2 APN 2 31,310,107 (GRCm39) missense probably damaging 0.98
IGL02551:Hmcn2 APN 2 31,344,823 (GRCm39) missense possibly damaging 0.83
IGL02695:Hmcn2 APN 2 31,298,985 (GRCm39) missense possibly damaging 0.87
IGL02725:Hmcn2 APN 2 31,295,540 (GRCm39) missense probably damaging 1.00
IGL02792:Hmcn2 APN 2 31,236,602 (GRCm39) missense probably damaging 1.00
IGL02882:Hmcn2 APN 2 31,303,379 (GRCm39) nonsense probably null
IGL03003:Hmcn2 APN 2 31,323,498 (GRCm39) missense probably damaging 0.98
IGL03067:Hmcn2 APN 2 31,236,642 (GRCm39) missense probably damaging 1.00
IGL03137:Hmcn2 APN 2 31,252,242 (GRCm39) missense probably damaging 0.98
IGL03220:Hmcn2 APN 2 31,236,633 (GRCm39) missense possibly damaging 0.94
IGL03411:Hmcn2 APN 2 31,236,649 (GRCm39) missense possibly damaging 0.83
PIT4544001:Hmcn2 UTSW 2 31,318,262 (GRCm39) missense probably damaging 0.98
R0044:Hmcn2 UTSW 2 31,302,520 (GRCm39) missense probably damaging 0.98
R0044:Hmcn2 UTSW 2 31,302,520 (GRCm39) missense probably damaging 0.98
R0048:Hmcn2 UTSW 2 31,318,249 (GRCm39) missense possibly damaging 0.92
R0048:Hmcn2 UTSW 2 31,318,249 (GRCm39) missense possibly damaging 0.92
R0078:Hmcn2 UTSW 2 31,278,356 (GRCm39) missense probably damaging 1.00
R0090:Hmcn2 UTSW 2 31,316,210 (GRCm39) missense probably damaging 1.00
R0173:Hmcn2 UTSW 2 31,328,343 (GRCm39) critical splice donor site probably null
R0257:Hmcn2 UTSW 2 31,259,176 (GRCm39) splice site probably benign
R0266:Hmcn2 UTSW 2 31,335,365 (GRCm39) splice site probably benign
R0266:Hmcn2 UTSW 2 31,284,839 (GRCm39) missense probably benign 0.03
R0326:Hmcn2 UTSW 2 31,313,237 (GRCm39) nonsense probably null
R0366:Hmcn2 UTSW 2 31,314,218 (GRCm39) missense possibly damaging 0.88
R0400:Hmcn2 UTSW 2 31,290,141 (GRCm39) missense probably damaging 0.98
R0412:Hmcn2 UTSW 2 31,278,259 (GRCm39) missense probably damaging 0.98
R0436:Hmcn2 UTSW 2 31,295,624 (GRCm39) missense probably damaging 1.00
R0457:Hmcn2 UTSW 2 31,305,296 (GRCm39) critical splice donor site probably null
R0487:Hmcn2 UTSW 2 31,276,689 (GRCm39) missense possibly damaging 0.60
R0568:Hmcn2 UTSW 2 31,305,248 (GRCm39) missense probably benign 0.02
R0755:Hmcn2 UTSW 2 31,343,172 (GRCm39) missense probably damaging 0.99
R0811:Hmcn2 UTSW 2 31,310,383 (GRCm39) missense probably damaging 0.99
R0812:Hmcn2 UTSW 2 31,310,383 (GRCm39) missense probably damaging 0.99
R0964:Hmcn2 UTSW 2 31,281,523 (GRCm39) missense probably benign 0.23
R0988:Hmcn2 UTSW 2 31,225,463 (GRCm39) missense probably damaging 1.00
R1484:Hmcn2 UTSW 2 31,236,507 (GRCm39) missense probably damaging 1.00
R1509:Hmcn2 UTSW 2 31,204,491 (GRCm39) missense possibly damaging 0.86
R1535:Hmcn2 UTSW 2 31,310,419 (GRCm39) missense possibly damaging 0.91
R1574:Hmcn2 UTSW 2 31,294,899 (GRCm39) missense probably damaging 0.97
R1574:Hmcn2 UTSW 2 31,294,899 (GRCm39) missense probably damaging 0.97
R1600:Hmcn2 UTSW 2 31,320,799 (GRCm39) missense probably damaging 0.98
R1623:Hmcn2 UTSW 2 31,348,051 (GRCm39) missense possibly damaging 0.84
R1692:Hmcn2 UTSW 2 31,340,856 (GRCm39) missense possibly damaging 0.47
R1719:Hmcn2 UTSW 2 31,244,733 (GRCm39) missense probably damaging 1.00
R1747:Hmcn2 UTSW 2 31,347,997 (GRCm39) missense probably benign 0.00
R1756:Hmcn2 UTSW 2 31,286,132 (GRCm39) missense probably damaging 0.99
R1763:Hmcn2 UTSW 2 31,204,602 (GRCm39) missense probably damaging 1.00
R1815:Hmcn2 UTSW 2 31,283,055 (GRCm39) missense probably damaging 0.97
R1822:Hmcn2 UTSW 2 31,273,704 (GRCm39) missense probably damaging 0.99
R1858:Hmcn2 UTSW 2 31,305,295 (GRCm39) critical splice donor site probably null
R1895:Hmcn2 UTSW 2 31,295,647 (GRCm39) missense probably damaging 0.99
R1908:Hmcn2 UTSW 2 31,301,922 (GRCm39) critical splice donor site probably null
R1946:Hmcn2 UTSW 2 31,295,647 (GRCm39) missense probably damaging 0.99
R1966:Hmcn2 UTSW 2 31,279,341 (GRCm39) missense probably damaging 0.99
R2007:Hmcn2 UTSW 2 31,328,267 (GRCm39) missense possibly damaging 0.91
R2050:Hmcn2 UTSW 2 31,225,448 (GRCm39) missense probably damaging 1.00
R2055:Hmcn2 UTSW 2 31,268,294 (GRCm39) missense probably benign 0.33
R2097:Hmcn2 UTSW 2 31,270,431 (GRCm39) missense probably damaging 1.00
R2145:Hmcn2 UTSW 2 31,223,943 (GRCm39) splice site probably benign
R2155:Hmcn2 UTSW 2 31,350,361 (GRCm39) missense possibly damaging 0.68
R2170:Hmcn2 UTSW 2 31,270,293 (GRCm39) missense probably benign 0.08
R2188:Hmcn2 UTSW 2 31,309,947 (GRCm39) missense probably benign 0.14
R2208:Hmcn2 UTSW 2 31,270,309 (GRCm39) missense probably damaging 1.00
R2217:Hmcn2 UTSW 2 31,240,586 (GRCm39) missense probably benign 0.02
R2407:Hmcn2 UTSW 2 31,225,424 (GRCm39) critical splice acceptor site probably null
R2764:Hmcn2 UTSW 2 31,278,310 (GRCm39) missense probably damaging 0.98
R2913:Hmcn2 UTSW 2 31,350,222 (GRCm39) missense possibly damaging 0.68
R2986:Hmcn2 UTSW 2 31,251,010 (GRCm39) missense probably damaging 1.00
R3157:Hmcn2 UTSW 2 31,290,267 (GRCm39) missense probably damaging 0.99
R3406:Hmcn2 UTSW 2 31,323,284 (GRCm39) splice site probably benign
R3429:Hmcn2 UTSW 2 31,299,156 (GRCm39) missense possibly damaging 0.87
R3737:Hmcn2 UTSW 2 31,226,624 (GRCm39) nonsense probably null
R3739:Hmcn2 UTSW 2 31,226,624 (GRCm39) nonsense probably null
R3771:Hmcn2 UTSW 2 31,250,908 (GRCm39) missense probably damaging 0.99
R3772:Hmcn2 UTSW 2 31,250,908 (GRCm39) missense probably damaging 0.99
R3773:Hmcn2 UTSW 2 31,250,908 (GRCm39) missense probably damaging 0.99
R3804:Hmcn2 UTSW 2 31,242,897 (GRCm39) splice site probably null
R3837:Hmcn2 UTSW 2 31,303,419 (GRCm39) missense probably damaging 0.99
R3838:Hmcn2 UTSW 2 31,303,419 (GRCm39) missense probably damaging 0.99
R3846:Hmcn2 UTSW 2 31,320,362 (GRCm39) missense possibly damaging 0.51
R3925:Hmcn2 UTSW 2 31,343,169 (GRCm39) missense probably benign 0.00
R3934:Hmcn2 UTSW 2 31,270,496 (GRCm39) critical splice donor site probably null
R3946:Hmcn2 UTSW 2 31,272,406 (GRCm39) missense possibly damaging 0.91
R4035:Hmcn2 UTSW 2 31,226,624 (GRCm39) nonsense probably null
R4057:Hmcn2 UTSW 2 31,290,250 (GRCm39) missense probably damaging 1.00
R4583:Hmcn2 UTSW 2 31,303,277 (GRCm39) missense possibly damaging 0.84
R4623:Hmcn2 UTSW 2 31,286,722 (GRCm39) missense probably damaging 1.00
R4647:Hmcn2 UTSW 2 31,289,031 (GRCm39) missense possibly damaging 0.82
R4668:Hmcn2 UTSW 2 31,325,804 (GRCm39) missense probably benign 0.40
R4669:Hmcn2 UTSW 2 31,325,804 (GRCm39) missense probably benign 0.40
R4687:Hmcn2 UTSW 2 31,328,297 (GRCm39) missense probably benign 0.14
R4735:Hmcn2 UTSW 2 31,273,787 (GRCm39) missense probably benign 0.06
R4772:Hmcn2 UTSW 2 31,335,326 (GRCm39) missense probably benign 0.02
R4866:Hmcn2 UTSW 2 31,279,403 (GRCm39) missense possibly damaging 0.88
R4916:Hmcn2 UTSW 2 31,250,992 (GRCm39) missense probably damaging 0.98
R4943:Hmcn2 UTSW 2 31,225,504 (GRCm39) missense probably damaging 1.00
R4967:Hmcn2 UTSW 2 31,244,176 (GRCm39) critical splice acceptor site probably null
R4973:Hmcn2 UTSW 2 31,234,108 (GRCm39) missense probably benign 0.15
R4975:Hmcn2 UTSW 2 31,283,037 (GRCm39) missense possibly damaging 0.88
R4994:Hmcn2 UTSW 2 31,348,067 (GRCm39) critical splice donor site probably null
R4997:Hmcn2 UTSW 2 31,291,720 (GRCm39) missense probably damaging 1.00
R5045:Hmcn2 UTSW 2 31,299,093 (GRCm39) missense probably damaging 1.00
R5117:Hmcn2 UTSW 2 31,348,061 (GRCm39) missense possibly damaging 0.95
R5151:Hmcn2 UTSW 2 31,279,455 (GRCm39) missense probably null
R5232:Hmcn2 UTSW 2 31,347,760 (GRCm39) missense probably damaging 0.99
R5237:Hmcn2 UTSW 2 31,304,728 (GRCm39) missense probably benign 0.01
R5288:Hmcn2 UTSW 2 31,350,333 (GRCm39) missense probably benign 0.11
R5375:Hmcn2 UTSW 2 31,320,453 (GRCm39) missense possibly damaging 0.92
R5379:Hmcn2 UTSW 2 31,299,023 (GRCm39) missense probably damaging 0.99
R5385:Hmcn2 UTSW 2 31,350,333 (GRCm39) missense probably benign 0.11
R5412:Hmcn2 UTSW 2 31,236,629 (GRCm39) missense possibly damaging 0.77
R5426:Hmcn2 UTSW 2 31,226,556 (GRCm39) missense possibly damaging 0.95
R5434:Hmcn2 UTSW 2 31,310,375 (GRCm39) missense probably damaging 1.00
R5441:Hmcn2 UTSW 2 31,296,428 (GRCm39) missense possibly damaging 0.82
R5484:Hmcn2 UTSW 2 31,283,066 (GRCm39) nonsense probably null
R5492:Hmcn2 UTSW 2 31,310,318 (GRCm39) missense probably benign 0.03
R5572:Hmcn2 UTSW 2 31,304,538 (GRCm39) critical splice acceptor site probably null
R5572:Hmcn2 UTSW 2 31,304,537 (GRCm39) critical splice acceptor site probably null
R5591:Hmcn2 UTSW 2 31,234,059 (GRCm39) missense probably damaging 1.00
R5614:Hmcn2 UTSW 2 31,318,315 (GRCm39) missense probably damaging 0.99
R5634:Hmcn2 UTSW 2 31,223,893 (GRCm39) missense probably damaging 1.00
R5645:Hmcn2 UTSW 2 31,310,824 (GRCm39) missense possibly damaging 0.92
R5716:Hmcn2 UTSW 2 31,348,750 (GRCm39) missense possibly damaging 0.68
R5716:Hmcn2 UTSW 2 31,226,579 (GRCm39) missense probably damaging 1.00
R5725:Hmcn2 UTSW 2 31,273,827 (GRCm39) critical splice donor site probably null
R5760:Hmcn2 UTSW 2 31,304,580 (GRCm39) missense possibly damaging 0.91
R5774:Hmcn2 UTSW 2 31,299,147 (GRCm39) missense possibly damaging 0.94
R5838:Hmcn2 UTSW 2 31,347,819 (GRCm39) missense probably damaging 0.99
R5899:Hmcn2 UTSW 2 31,244,685 (GRCm39) missense possibly damaging 0.93
R5916:Hmcn2 UTSW 2 31,286,151 (GRCm39) missense probably damaging 1.00
R5973:Hmcn2 UTSW 2 31,310,335 (GRCm39) missense probably damaging 0.99
R6002:Hmcn2 UTSW 2 31,310,321 (GRCm39) missense probably damaging 0.99
R6018:Hmcn2 UTSW 2 31,260,804 (GRCm39) missense probably benign 0.13
R6063:Hmcn2 UTSW 2 31,324,725 (GRCm39) missense probably benign 0.06
R6161:Hmcn2 UTSW 2 31,246,266 (GRCm39) missense probably benign
R6166:Hmcn2 UTSW 2 31,259,274 (GRCm39) missense probably damaging 1.00
R6177:Hmcn2 UTSW 2 31,310,118 (GRCm39) nonsense probably null
R6191:Hmcn2 UTSW 2 31,348,758 (GRCm39) missense probably damaging 0.99
R6195:Hmcn2 UTSW 2 31,274,127 (GRCm39) missense probably damaging 0.96
R6273:Hmcn2 UTSW 2 31,301,846 (GRCm39) missense probably damaging 0.99
R6293:Hmcn2 UTSW 2 31,225,463 (GRCm39) missense probably damaging 1.00
R6349:Hmcn2 UTSW 2 31,278,385 (GRCm39) missense probably damaging 1.00
R6395:Hmcn2 UTSW 2 31,259,269 (GRCm39) missense probably damaging 1.00
R6448:Hmcn2 UTSW 2 31,310,832 (GRCm39) missense probably benign 0.02
R6450:Hmcn2 UTSW 2 31,251,812 (GRCm39) missense probably benign 0.11
R6479:Hmcn2 UTSW 2 31,315,480 (GRCm39) missense probably damaging 0.99
R6502:Hmcn2 UTSW 2 31,272,490 (GRCm39) missense probably damaging 0.99
R6511:Hmcn2 UTSW 2 31,246,354 (GRCm39) missense possibly damaging 0.79
R6537:Hmcn2 UTSW 2 31,305,280 (GRCm39) missense probably benign 0.00
R6880:Hmcn2 UTSW 2 31,233,068 (GRCm39) missense probably damaging 1.00
R6924:Hmcn2 UTSW 2 31,240,517 (GRCm39) splice site probably null
R6971:Hmcn2 UTSW 2 31,322,333 (GRCm39) missense probably benign 0.02
R7057:Hmcn2 UTSW 2 31,312,661 (GRCm39) missense probably damaging 0.99
R7141:Hmcn2 UTSW 2 31,250,908 (GRCm39) missense probably benign 0.17
R7268:Hmcn2 UTSW 2 31,347,978 (GRCm39) missense possibly damaging 0.48
R7307:Hmcn2 UTSW 2 31,233,093 (GRCm39) missense probably damaging 0.96
R7322:Hmcn2 UTSW 2 31,349,093 (GRCm39) missense probably damaging 0.99
R7334:Hmcn2 UTSW 2 31,343,147 (GRCm39) missense possibly damaging 0.82
R7334:Hmcn2 UTSW 2 31,325,806 (GRCm39) missense probably damaging 0.98
R7335:Hmcn2 UTSW 2 31,282,169 (GRCm39) missense possibly damaging 0.88
R7358:Hmcn2 UTSW 2 31,306,824 (GRCm39) missense probably damaging 1.00
R7359:Hmcn2 UTSW 2 31,278,395 (GRCm39) missense probably benign 0.13
R7488:Hmcn2 UTSW 2 31,310,842 (GRCm39) missense probably damaging 1.00
R7498:Hmcn2 UTSW 2 31,273,487 (GRCm39) splice site probably null
R7560:Hmcn2 UTSW 2 31,347,185 (GRCm39) missense probably benign
R7566:Hmcn2 UTSW 2 31,344,869 (GRCm39) missense probably damaging 0.96
R7570:Hmcn2 UTSW 2 31,313,923 (GRCm39) missense probably benign
R7574:Hmcn2 UTSW 2 31,345,531 (GRCm39) missense possibly damaging 0.68
R7599:Hmcn2 UTSW 2 31,246,298 (GRCm39) missense possibly damaging 0.93
R7654:Hmcn2 UTSW 2 31,236,581 (GRCm39) missense probably benign 0.00
R7662:Hmcn2 UTSW 2 31,272,357 (GRCm39) missense probably benign 0.01
R7666:Hmcn2 UTSW 2 31,270,245 (GRCm39) missense probably damaging 1.00
R7698:Hmcn2 UTSW 2 31,313,165 (GRCm39) missense probably damaging 0.98
R7722:Hmcn2 UTSW 2 31,272,512 (GRCm39) nonsense probably null
R7739:Hmcn2 UTSW 2 31,348,038 (GRCm39) missense possibly damaging 0.48
R7749:Hmcn2 UTSW 2 31,343,045 (GRCm39) splice site probably null
R7828:Hmcn2 UTSW 2 31,295,887 (GRCm39) missense possibly damaging 0.95
R7912:Hmcn2 UTSW 2 31,310,311 (GRCm39) missense probably benign 0.00
R7978:Hmcn2 UTSW 2 31,279,359 (GRCm39) missense probably benign 0.40
R8075:Hmcn2 UTSW 2 31,279,403 (GRCm39) missense possibly damaging 0.88
R8088:Hmcn2 UTSW 2 31,316,915 (GRCm39) nonsense probably null
R8101:Hmcn2 UTSW 2 31,240,082 (GRCm39) missense probably benign 0.08
R8124:Hmcn2 UTSW 2 31,290,136 (GRCm39) missense probably benign 0.01
R8145:Hmcn2 UTSW 2 31,313,117 (GRCm39) missense probably damaging 1.00
R8230:Hmcn2 UTSW 2 31,234,485 (GRCm39) missense possibly damaging 0.91
R8267:Hmcn2 UTSW 2 31,349,191 (GRCm39) missense probably benign
R8277:Hmcn2 UTSW 2 31,259,189 (GRCm39) missense probably benign 0.16
R8307:Hmcn2 UTSW 2 31,286,127 (GRCm39) missense probably damaging 0.99
R8353:Hmcn2 UTSW 2 31,275,353 (GRCm39) splice site probably null
R8415:Hmcn2 UTSW 2 31,281,088 (GRCm39) missense probably benign 0.15
R8416:Hmcn2 UTSW 2 31,281,088 (GRCm39) missense probably benign 0.15
R8437:Hmcn2 UTSW 2 31,281,088 (GRCm39) missense probably benign 0.15
R8438:Hmcn2 UTSW 2 31,281,088 (GRCm39) missense probably benign 0.15
R8440:Hmcn2 UTSW 2 31,281,088 (GRCm39) missense probably benign 0.15
R8442:Hmcn2 UTSW 2 31,281,088 (GRCm39) missense probably benign 0.15
R8497:Hmcn2 UTSW 2 31,313,357 (GRCm39) missense possibly damaging 0.92
R8520:Hmcn2 UTSW 2 31,244,726 (GRCm39) missense probably damaging 1.00
R8530:Hmcn2 UTSW 2 31,281,088 (GRCm39) missense probably benign 0.15
R8537:Hmcn2 UTSW 2 31,281,088 (GRCm39) missense probably benign 0.15
R8550:Hmcn2 UTSW 2 31,240,654 (GRCm39) critical splice donor site probably null
R8721:Hmcn2 UTSW 2 31,315,189 (GRCm39) missense probably damaging 1.00
R8795:Hmcn2 UTSW 2 31,315,393 (GRCm39) missense probably benign 0.01
R8802:Hmcn2 UTSW 2 31,301,288 (GRCm39) missense probably damaging 0.97
R8804:Hmcn2 UTSW 2 31,315,393 (GRCm39) missense probably benign 0.01
R8805:Hmcn2 UTSW 2 31,315,393 (GRCm39) missense probably benign 0.01
R8904:Hmcn2 UTSW 2 31,323,404 (GRCm39) missense possibly damaging 0.92
R8937:Hmcn2 UTSW 2 31,204,427 (GRCm39) start codon destroyed probably benign 0.01
R8947:Hmcn2 UTSW 2 31,278,220 (GRCm39) missense probably damaging 0.99
R8948:Hmcn2 UTSW 2 31,244,741 (GRCm39) missense probably damaging 1.00
R8950:Hmcn2 UTSW 2 31,244,741 (GRCm39) missense probably damaging 1.00
R8959:Hmcn2 UTSW 2 31,282,159 (GRCm39) missense probably damaging 1.00
R9025:Hmcn2 UTSW 2 31,347,967 (GRCm39) missense possibly damaging 0.56
R9039:Hmcn2 UTSW 2 31,244,646 (GRCm39) missense probably damaging 0.97
R9068:Hmcn2 UTSW 2 31,303,685 (GRCm39) missense probably benign 0.01
R9161:Hmcn2 UTSW 2 31,242,758 (GRCm39) missense probably benign 0.02
R9178:Hmcn2 UTSW 2 31,281,521 (GRCm39) missense possibly damaging 0.77
R9204:Hmcn2 UTSW 2 31,278,377 (GRCm39) missense probably damaging 0.98
R9317:Hmcn2 UTSW 2 31,350,328 (GRCm39) missense possibly damaging 0.91
R9341:Hmcn2 UTSW 2 31,279,359 (GRCm39) missense probably benign 0.40
R9343:Hmcn2 UTSW 2 31,279,359 (GRCm39) missense probably benign 0.40
R9355:Hmcn2 UTSW 2 31,328,302 (GRCm39) missense probably benign 0.18
R9371:Hmcn2 UTSW 2 31,301,917 (GRCm39) missense probably damaging 1.00
R9450:Hmcn2 UTSW 2 31,316,845 (GRCm39) missense probably damaging 1.00
R9477:Hmcn2 UTSW 2 31,286,031 (GRCm39) critical splice acceptor site probably null
R9483:Hmcn2 UTSW 2 31,320,375 (GRCm39) missense
R9536:Hmcn2 UTSW 2 31,335,130 (GRCm39) missense possibly damaging 0.86
R9580:Hmcn2 UTSW 2 31,294,875 (GRCm39) missense probably benign 0.16
R9593:Hmcn2 UTSW 2 31,244,742 (GRCm39) missense probably damaging 0.99
R9649:Hmcn2 UTSW 2 31,292,450 (GRCm39) missense possibly damaging 0.95
R9706:Hmcn2 UTSW 2 31,305,279 (GRCm39) missense probably benign 0.00
X0066:Hmcn2 UTSW 2 31,344,823 (GRCm39) missense possibly damaging 0.83
X0067:Hmcn2 UTSW 2 31,295,879 (GRCm39) missense possibly damaging 0.82
Z1088:Hmcn2 UTSW 2 31,349,076 (GRCm39) splice site probably null
Z1088:Hmcn2 UTSW 2 31,271,079 (GRCm39) missense probably benign 0.01
Z1176:Hmcn2 UTSW 2 31,319,103 (GRCm39) missense probably damaging 0.97
Z1176:Hmcn2 UTSW 2 31,315,428 (GRCm39) missense probably damaging 1.00
Z1176:Hmcn2 UTSW 2 31,234,041 (GRCm39) missense possibly damaging 0.95
Z1177:Hmcn2 UTSW 2 31,316,836 (GRCm39) missense probably damaging 0.99
Z1177:Hmcn2 UTSW 2 31,234,518 (GRCm39) missense probably damaging 1.00
Posted On 2015-04-16