Incidental Mutation 'R1918:Herc1'
ID 212733
Institutional Source Beutler Lab
Gene Symbol Herc1
Ensembl Gene ENSMUSG00000038664
Gene Name HECT and RLD domain containing E3 ubiquitin protein ligase family member 1
Synonyms tbl, D130015N03Rik, 2810449H11Rik
MMRRC Submission 039936-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1918 (G1)
Quality Score 225
Status Validated
Chromosome 9
Chromosomal Location 66257732-66416057 bp(+) (GRCm39)
Type of Mutation splice site (6 bp from exon)
DNA Base Change (assembly) T to C at 66383408 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000044801 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000042824]
AlphaFold no structure available at present
Predicted Effect probably null
Transcript: ENSMUST00000042824
SMART Domains Protein: ENSMUSP00000044801
Gene: ENSMUSG00000038664

DomainStartEndE-ValueType
low complexity region 79 90 N/A INTRINSIC
low complexity region 136 147 N/A INTRINSIC
Pfam:RCC1 476 526 5.4e-15 PFAM
Pfam:RCC1_2 513 542 1.3e-9 PFAM
Pfam:RCC1 529 576 5.5e-16 PFAM
Pfam:RCC1 579 629 1.5e-10 PFAM
Pfam:RCC1 632 680 3.6e-9 PFAM
Pfam:RCC1_2 667 696 2.2e-11 PFAM
Pfam:RCC1 683 733 1.2e-14 PFAM
low complexity region 787 807 N/A INTRINSIC
low complexity region 852 864 N/A INTRINSIC
low complexity region 1014 1025 N/A INTRINSIC
low complexity region 1080 1100 N/A INTRINSIC
low complexity region 1348 1378 N/A INTRINSIC
low complexity region 1659 1676 N/A INTRINSIC
low complexity region 1865 1874 N/A INTRINSIC
low complexity region 2002 2030 N/A INTRINSIC
SPRY 2067 2188 1.8e-30 SMART
coiled coil region 2251 2280 N/A INTRINSIC
low complexity region 2410 2423 N/A INTRINSIC
low complexity region 2613 2629 N/A INTRINSIC
low complexity region 2633 2648 N/A INTRINSIC
low complexity region 2650 2667 N/A INTRINSIC
low complexity region 2736 2749 N/A INTRINSIC
low complexity region 2882 2896 N/A INTRINSIC
low complexity region 2924 2935 N/A INTRINSIC
low complexity region 2971 2987 N/A INTRINSIC
low complexity region 3045 3051 N/A INTRINSIC
low complexity region 3168 3186 N/A INTRINSIC
low complexity region 3191 3213 N/A INTRINSIC
low complexity region 3364 3379 N/A INTRINSIC
WD40 3415 3454 1.68e-6 SMART
WD40 3570 3608 3.68e1 SMART
WD40 3613 3652 4.3e-1 SMART
WD40 3657 3702 3.17e-2 SMART
WD40 3734 3773 8.29e-6 SMART
low complexity region 3950 3964 N/A INTRINSIC
Pfam:RCC1_2 4079 4111 7.3e-9 PFAM
Pfam:RCC1 4098 4147 3.4e-16 PFAM
Pfam:RCC1_2 4134 4163 1.8e-7 PFAM
Pfam:RCC1 4150 4199 7.2e-16 PFAM
Pfam:RCC1 4204 4252 6.1e-12 PFAM
Pfam:RCC1 4255 4304 2.4e-7 PFAM
Pfam:RCC1_2 4291 4320 5.8e-12 PFAM
Pfam:RCC1 4307 4356 8.9e-16 PFAM
Blast:HECTc 4389 4423 2e-11 BLAST
HECTc 4497 4846 8.2e-148 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000124969
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 97.5%
  • 3x: 97.0%
  • 10x: 95.7%
  • 20x: 93.5%
Validation Efficiency 97% (113/116)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gen encodes a member of the HERC protein family. This protein stimulates guanine nucleotide exchange on ARF1 and Rab proteins. This protein may be involved in membrane transport processes. [provided by RefSeq, Mar 2012]
PHENOTYPE: Homozygotes for this spontaneous mutation exhibit an abnormal cerebellar Purkinje cell layer and Purkinje cell degeneration. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 116 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930432E11Rik T G 7: 29,273,514 (GRCm39) noncoding transcript Het
A2m T C 6: 121,621,895 (GRCm39) S314P probably benign Het
Abcc9 T A 6: 142,643,408 (GRCm39) I47F probably damaging Het
Abcd2 C T 15: 91,075,684 (GRCm39) R43H probably benign Het
Adgre5 A G 8: 84,455,738 (GRCm39) V190A probably damaging Het
Aen C T 7: 78,555,777 (GRCm39) H242Y possibly damaging Het
Arfgef1 C T 1: 10,270,103 (GRCm39) A349T probably benign Het
Arhgap10 T C 8: 77,985,708 (GRCm39) I698V probably benign Het
Arpp21 C T 9: 111,948,246 (GRCm39) probably benign Het
Atp10a T C 7: 58,477,683 (GRCm39) I1294T possibly damaging Het
Atp13a2 T C 4: 140,723,682 (GRCm39) Y337H possibly damaging Het
Bsn C T 9: 107,984,772 (GRCm39) G3094D unknown Het
Cadm2 G A 16: 66,544,270 (GRCm39) probably benign Het
Cadps T C 14: 12,546,372 (GRCm38) M495V probably damaging Het
Cass4 A G 2: 172,269,259 (GRCm39) H447R possibly damaging Het
Ccdc124 C A 8: 71,321,588 (GRCm39) R108L probably benign Het
Ccdc141 C T 2: 76,845,047 (GRCm39) R1340Q probably benign Het
Ccdc148 T G 2: 58,872,911 (GRCm39) R299S probably damaging Het
Cd300lg A G 11: 101,944,936 (GRCm39) E382G probably damaging Het
Cd36 A T 5: 18,002,034 (GRCm39) C322* probably null Het
Celsr2 C T 3: 108,305,966 (GRCm39) G2046D probably benign Het
Clasrp C T 7: 19,319,188 (GRCm39) W492* probably null Het
Cmtr1 T C 17: 29,897,983 (GRCm39) V154A possibly damaging Het
Ctnnb1 C T 9: 120,780,100 (GRCm39) P128S possibly damaging Het
Cyp11a1 A G 9: 57,934,040 (GRCm39) I496V probably damaging Het
Disp2 G A 2: 118,622,408 (GRCm39) V1047I probably benign Het
Dync2i1 A C 12: 116,196,221 (GRCm39) S509A probably damaging Het
Eps8l2 T C 7: 140,941,637 (GRCm39) V636A probably damaging Het
Fars2 T C 13: 36,388,529 (GRCm39) L6P probably damaging Het
Fem1al A G 11: 29,774,039 (GRCm39) S473P probably benign Het
Fnip1 C T 11: 54,371,510 (GRCm39) T177I probably damaging Het
Fut8 G T 12: 77,378,992 (GRCm39) R31L probably benign Het
G6pd2 T C 5: 61,967,664 (GRCm39) F480L probably benign Het
Glipr1l2 T A 10: 111,928,550 (GRCm39) C148* probably null Het
Gm10142 G A 10: 77,551,821 (GRCm39) V61M probably benign Het
Gm5134 T A 10: 75,812,180 (GRCm39) M145K possibly damaging Het
Gnpda1 T C 18: 38,466,243 (GRCm39) probably null Het
Gpc2 T C 5: 138,276,641 (GRCm39) T162A probably benign Het
Gtf2h4 G A 17: 35,981,090 (GRCm39) L246F possibly damaging Het
Hal C T 10: 93,332,469 (GRCm39) P294S probably damaging Het
Hectd3 C T 4: 116,857,540 (GRCm39) A573V possibly damaging Het
Hephl1 T A 9: 14,988,114 (GRCm39) I665F probably benign Het
Hif1an A G 19: 44,559,551 (GRCm39) probably null Het
Iho1 T A 9: 108,290,184 (GRCm39) H140L probably benign Het
Il12rb1 T A 8: 71,266,324 (GRCm39) M223K probably benign Het
Ilf3 C T 9: 21,305,010 (GRCm39) T201M probably damaging Het
Inpp5f T C 7: 128,265,693 (GRCm39) probably benign Het
Jcad T C 18: 4,674,292 (GRCm39) Y685H probably damaging Het
Kcnj1 C A 9: 32,308,034 (GRCm39) Q153K probably benign Het
Kctd18 A C 1: 57,998,379 (GRCm39) H73Q probably damaging Het
Klhl36 T A 8: 120,603,463 (GRCm39) W573R probably damaging Het
Ldc1 A T 4: 130,105,186 (GRCm39) V328D probably benign Het
Lepr A G 4: 101,630,033 (GRCm39) T583A probably benign Het
Ltbp4 G A 7: 27,036,994 (GRCm39) probably benign Het
Mapt A T 11: 104,189,325 (GRCm39) E114D probably benign Het
Mib1 T A 18: 10,740,972 (GRCm39) probably null Het
Mthfd1 G T 12: 76,361,750 (GRCm39) A119S probably damaging Het
Mylk4 A T 13: 32,908,836 (GRCm39) D90E probably benign Het
Nceh1 T G 3: 27,237,324 (GRCm39) L33R probably damaging Het
Nfat5 T C 8: 108,092,868 (GRCm39) I91T probably damaging Het
Nxn A G 11: 76,152,498 (GRCm39) probably benign Het
Oasl1 G A 5: 115,061,528 (GRCm39) A20T possibly damaging Het
Or2m12 A T 16: 19,105,052 (GRCm39) M147K probably benign Het
Or4c127 T C 2: 89,832,918 (GRCm39) F56S probably benign Het
Or4d6 A G 19: 12,086,871 (GRCm39) V13A probably benign Het
Or5b97 A G 19: 12,878,215 (GRCm39) *310Q probably null Het
Or5t18 C T 2: 86,637,171 (GRCm39) M57I probably damaging Het
Or6c2 T A 10: 129,362,918 (GRCm39) V274D probably damaging Het
Pepd T C 7: 34,671,101 (GRCm39) V215A probably benign Het
Pfkl A T 10: 77,837,260 (GRCm39) N104K probably damaging Het
Phf24 T C 4: 42,938,165 (GRCm39) probably benign Het
Pink1 T C 4: 138,041,331 (GRCm39) N530S probably benign Het
Pou3f2 T C 4: 22,487,119 (GRCm39) D338G probably damaging Het
Ppp1r13b A G 12: 111,801,244 (GRCm39) V480A probably damaging Het
Ptgfrn A T 3: 100,963,623 (GRCm39) I663N probably benign Het
Rad54b A C 4: 11,601,693 (GRCm39) N416T probably damaging Het
Rasef A G 4: 73,662,351 (GRCm39) S200P possibly damaging Het
Rbm33 T A 5: 28,592,915 (GRCm39) I605N probably damaging Het
Rps19bp1 T C 15: 80,148,280 (GRCm39) T31A probably benign Het
Ryr2 T A 13: 11,571,584 (GRCm39) T4885S possibly damaging Het
Serpinb6b A G 13: 33,162,223 (GRCm39) I222V probably benign Het
Sik3 C G 9: 46,132,387 (GRCm39) H1276Q probably benign Het
Skor2 T C 18: 76,947,051 (GRCm39) S258P unknown Het
Slc22a29 C T 19: 8,195,123 (GRCm39) probably null Het
Slc8a3 A T 12: 81,361,618 (GRCm39) F400L probably damaging Het
Slc9a8 T C 2: 167,266,134 (GRCm39) I37T possibly damaging Het
Smchd1 A G 17: 71,714,232 (GRCm39) I877T possibly damaging Het
Spag5 A G 11: 78,195,002 (GRCm39) N103S probably benign Het
Sptbn1 A T 11: 30,092,414 (GRCm39) F450L probably damaging Het
Strn4 T A 7: 16,567,846 (GRCm39) Y507N probably damaging Het
Stxbp5 C A 10: 9,688,042 (GRCm39) V420F possibly damaging Het
Syt17 G T 7: 118,033,208 (GRCm39) L267I possibly damaging Het
Tcstv4 T C 13: 120,769,758 (GRCm39) L26P probably damaging Het
Tdo2 T A 3: 81,866,247 (GRCm39) R339W probably damaging Het
Tex55 A G 16: 38,648,450 (GRCm39) Y220H possibly damaging Het
Timd5 A G 11: 46,419,358 (GRCm39) D58G possibly damaging Het
Ttn A G 2: 76,571,745 (GRCm39) S26383P probably damaging Het
Ttn G T 2: 76,638,868 (GRCm39) T13938K probably damaging Het
Tulp2 A G 7: 45,167,365 (GRCm39) N188D possibly damaging Het
Ube3c C T 5: 29,792,315 (GRCm39) R37C probably damaging Het
Uggt2 G T 14: 119,245,467 (GRCm39) probably benign Het
Umodl1 G A 17: 31,203,017 (GRCm39) V457M probably damaging Het
Usp17la C T 7: 104,509,953 (GRCm39) T186I probably benign Het
Vmn1r226 T C 17: 20,907,842 (GRCm39) S25P probably damaging Het
Vmn1r235 T A 17: 21,482,659 (GRCm39) I328K possibly damaging Het
Vmn2r50 A T 7: 9,781,610 (GRCm39) S378R probably benign Het
Vwa2 C T 19: 56,897,366 (GRCm39) T557I probably benign Het
Vxn T C 1: 9,671,852 (GRCm39) F15S probably damaging Het
Yes1 G T 5: 32,842,079 (GRCm39) Q534H probably benign Het
Zbtb25 A T 12: 76,396,075 (GRCm39) Y382* probably null Het
Zc3h3 G A 15: 75,648,967 (GRCm39) P722S probably damaging Het
Zfp36l2 T C 17: 84,494,164 (GRCm39) T158A probably damaging Het
Zfp536 T C 7: 37,179,624 (GRCm39) T994A probably damaging Het
Zfp592 C T 7: 80,687,168 (GRCm39) Q824* probably null Het
Zfp629 C A 7: 127,211,172 (GRCm39) K212N probably damaging Het
Zfp930 C A 8: 69,681,357 (GRCm39) Q350K probably benign Het
Other mutations in Herc1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00092:Herc1 APN 9 66,391,248 (GRCm39) missense probably benign 0.02
IGL00159:Herc1 APN 9 66,344,964 (GRCm39) missense possibly damaging 0.94
IGL00486:Herc1 APN 9 66,383,402 (GRCm39) missense probably benign
IGL00717:Herc1 APN 9 66,392,284 (GRCm39) missense probably damaging 1.00
IGL00766:Herc1 APN 9 66,358,023 (GRCm39) missense probably damaging 1.00
IGL00776:Herc1 APN 9 66,328,320 (GRCm39) missense probably benign
IGL00987:Herc1 APN 9 66,315,334 (GRCm39) missense probably benign 0.07
IGL01090:Herc1 APN 9 66,376,457 (GRCm39) nonsense probably null
IGL01098:Herc1 APN 9 66,369,204 (GRCm39) critical splice donor site probably null
IGL01106:Herc1 APN 9 66,383,720 (GRCm39) splice site probably benign
IGL01120:Herc1 APN 9 66,336,162 (GRCm39) missense probably benign
IGL01359:Herc1 APN 9 66,346,550 (GRCm39) missense probably benign 0.01
IGL01360:Herc1 APN 9 66,390,981 (GRCm39) missense probably benign
IGL01364:Herc1 APN 9 66,306,643 (GRCm39) missense probably benign 0.00
IGL01470:Herc1 APN 9 66,404,918 (GRCm39) missense possibly damaging 0.94
IGL01670:Herc1 APN 9 66,394,342 (GRCm39) missense probably damaging 1.00
IGL01825:Herc1 APN 9 66,307,089 (GRCm39) missense probably benign 0.00
IGL01903:Herc1 APN 9 66,294,154 (GRCm39) nonsense probably null
IGL01988:Herc1 APN 9 66,395,357 (GRCm39) splice site probably benign
IGL02074:Herc1 APN 9 66,358,265 (GRCm39) missense probably benign
IGL02089:Herc1 APN 9 66,388,151 (GRCm39) missense probably damaging 1.00
IGL02177:Herc1 APN 9 66,341,793 (GRCm39) missense probably benign
IGL02300:Herc1 APN 9 66,383,645 (GRCm39) missense probably benign 0.01
IGL02304:Herc1 APN 9 66,383,696 (GRCm39) missense probably benign 0.06
IGL02369:Herc1 APN 9 66,399,293 (GRCm39) nonsense probably null
IGL02445:Herc1 APN 9 66,340,764 (GRCm39) missense possibly damaging 0.95
IGL02447:Herc1 APN 9 66,404,610 (GRCm39) missense possibly damaging 0.59
IGL02549:Herc1 APN 9 66,307,183 (GRCm39) missense probably damaging 0.98
IGL02571:Herc1 APN 9 66,341,887 (GRCm39) splice site probably benign
IGL02709:Herc1 APN 9 66,404,962 (GRCm39) missense probably damaging 0.97
IGL02717:Herc1 APN 9 66,279,203 (GRCm39) nonsense probably null
IGL02726:Herc1 APN 9 66,349,270 (GRCm39) missense probably benign 0.37
IGL02733:Herc1 APN 9 66,358,274 (GRCm39) missense probably benign
IGL02963:Herc1 APN 9 66,296,105 (GRCm39) missense probably damaging 0.99
IGL03101:Herc1 APN 9 66,395,279 (GRCm39) missense probably benign
IGL03193:Herc1 APN 9 66,309,962 (GRCm39) missense probably benign
IGL03203:Herc1 APN 9 66,296,182 (GRCm39) critical splice donor site probably null
IGL03216:Herc1 APN 9 66,386,228 (GRCm39) missense probably benign 0.06
IGL03282:Herc1 APN 9 66,358,741 (GRCm39) missense probably benign 0.05
IGL03295:Herc1 APN 9 66,303,985 (GRCm39) missense possibly damaging 0.56
cradle UTSW 9 66,391,148 (GRCm39) splice site probably null
miracles UTSW 9 66,370,119 (GRCm39) nonsense probably null
newton UTSW 9 66,375,085 (GRCm39) missense probably damaging 1.00
R0907_Herc1_362 UTSW 9 66,340,710 (GRCm39) missense possibly damaging 0.94
R4427_Herc1_231 UTSW 9 66,403,287 (GRCm39) missense probably damaging 1.00
R5026_Herc1_363 UTSW 9 66,393,408 (GRCm39) missense probably benign 0.03
stables UTSW 9 66,386,735 (GRCm39) missense probably benign 0.13
strangle UTSW 9 66,408,470 (GRCm39) frame shift probably null
IGL03134:Herc1 UTSW 9 66,341,345 (GRCm39) critical splice acceptor site probably benign
PIT4243001:Herc1 UTSW 9 66,279,489 (GRCm39) missense probably benign 0.00
PIT4486001:Herc1 UTSW 9 66,279,671 (GRCm39) missense probably damaging 1.00
PIT4696001:Herc1 UTSW 9 66,386,291 (GRCm39) missense probably damaging 1.00
R0044:Herc1 UTSW 9 66,355,457 (GRCm39) missense probably benign 0.04
R0044:Herc1 UTSW 9 66,355,457 (GRCm39) missense probably benign 0.04
R0052:Herc1 UTSW 9 66,307,438 (GRCm39) missense probably damaging 0.99
R0114:Herc1 UTSW 9 66,369,128 (GRCm39) missense probably damaging 0.99
R0129:Herc1 UTSW 9 66,355,357 (GRCm39) missense probably damaging 1.00
R0131:Herc1 UTSW 9 66,388,192 (GRCm39) missense probably benign 0.00
R0131:Herc1 UTSW 9 66,388,192 (GRCm39) missense probably benign 0.00
R0132:Herc1 UTSW 9 66,388,192 (GRCm39) missense probably benign 0.00
R0158:Herc1 UTSW 9 66,403,203 (GRCm39) nonsense probably null
R0333:Herc1 UTSW 9 66,371,981 (GRCm39) splice site probably null
R0384:Herc1 UTSW 9 66,388,332 (GRCm39) splice site probably benign
R0419:Herc1 UTSW 9 66,353,356 (GRCm39) splice site probably benign
R0453:Herc1 UTSW 9 66,307,054 (GRCm39) missense probably benign 0.20
R0458:Herc1 UTSW 9 66,383,663 (GRCm39) missense probably benign 0.12
R0490:Herc1 UTSW 9 66,392,281 (GRCm39) missense probably damaging 1.00
R0506:Herc1 UTSW 9 66,355,441 (GRCm39) missense probably damaging 0.99
R0513:Herc1 UTSW 9 66,352,927 (GRCm39) missense possibly damaging 0.96
R0628:Herc1 UTSW 9 66,358,163 (GRCm39) missense probably benign 0.35
R0666:Herc1 UTSW 9 66,392,170 (GRCm39) splice site probably benign
R0674:Herc1 UTSW 9 66,408,474 (GRCm39) missense probably damaging 0.99
R0682:Herc1 UTSW 9 66,389,263 (GRCm39) missense possibly damaging 0.95
R0690:Herc1 UTSW 9 66,294,120 (GRCm39) nonsense probably null
R0701:Herc1 UTSW 9 66,395,232 (GRCm39) missense probably damaging 1.00
R0766:Herc1 UTSW 9 66,412,122 (GRCm39) missense probably damaging 1.00
R0850:Herc1 UTSW 9 66,373,952 (GRCm39) missense probably damaging 1.00
R0907:Herc1 UTSW 9 66,340,710 (GRCm39) missense possibly damaging 0.94
R0972:Herc1 UTSW 9 66,279,427 (GRCm39) missense probably damaging 1.00
R0976:Herc1 UTSW 9 66,347,160 (GRCm39) missense possibly damaging 0.74
R1027:Herc1 UTSW 9 66,363,250 (GRCm39) missense probably benign
R1200:Herc1 UTSW 9 66,393,406 (GRCm39) missense probably damaging 1.00
R1226:Herc1 UTSW 9 66,323,545 (GRCm39) missense probably benign 0.00
R1364:Herc1 UTSW 9 66,307,375 (GRCm39) missense probably damaging 1.00
R1395:Herc1 UTSW 9 66,346,463 (GRCm39) missense probably benign 0.13
R1432:Herc1 UTSW 9 66,372,751 (GRCm39) missense probably benign 0.13
R1440:Herc1 UTSW 9 66,375,085 (GRCm39) missense probably damaging 1.00
R1476:Herc1 UTSW 9 66,415,548 (GRCm39) missense probably damaging 1.00
R1590:Herc1 UTSW 9 66,399,235 (GRCm39) splice site probably benign
R1634:Herc1 UTSW 9 66,380,820 (GRCm39) missense possibly damaging 0.51
R1700:Herc1 UTSW 9 66,357,960 (GRCm39) splice site probably null
R1753:Herc1 UTSW 9 66,409,366 (GRCm39) critical splice donor site probably null
R1753:Herc1 UTSW 9 66,376,292 (GRCm39) missense probably damaging 1.00
R1796:Herc1 UTSW 9 66,296,138 (GRCm39) nonsense probably null
R1830:Herc1 UTSW 9 66,404,881 (GRCm39) missense possibly damaging 0.95
R1855:Herc1 UTSW 9 66,298,708 (GRCm39) missense possibly damaging 0.95
R1866:Herc1 UTSW 9 66,358,073 (GRCm39) missense probably damaging 1.00
R1894:Herc1 UTSW 9 66,386,743 (GRCm39) missense probably damaging 1.00
R1999:Herc1 UTSW 9 66,393,360 (GRCm39) missense probably benign 0.07
R2034:Herc1 UTSW 9 66,349,254 (GRCm39) missense probably benign 0.01
R2138:Herc1 UTSW 9 66,377,589 (GRCm39) missense possibly damaging 0.94
R2186:Herc1 UTSW 9 66,347,183 (GRCm39) missense probably benign 0.45
R2192:Herc1 UTSW 9 66,372,688 (GRCm39) missense probably damaging 0.99
R2312:Herc1 UTSW 9 66,415,563 (GRCm39) nonsense probably null
R2338:Herc1 UTSW 9 66,336,251 (GRCm39) missense possibly damaging 0.69
R3035:Herc1 UTSW 9 66,391,217 (GRCm39) missense possibly damaging 0.89
R3732:Herc1 UTSW 9 66,352,922 (GRCm39) missense probably damaging 1.00
R3732:Herc1 UTSW 9 66,352,922 (GRCm39) missense probably damaging 1.00
R3733:Herc1 UTSW 9 66,352,922 (GRCm39) missense probably damaging 1.00
R3917:Herc1 UTSW 9 66,341,748 (GRCm39) missense possibly damaging 0.94
R3953:Herc1 UTSW 9 66,341,075 (GRCm39) nonsense probably null
R4073:Herc1 UTSW 9 66,325,774 (GRCm39) missense probably benign 0.12
R4075:Herc1 UTSW 9 66,325,774 (GRCm39) missense probably benign 0.12
R4241:Herc1 UTSW 9 66,355,630 (GRCm39) frame shift probably null
R4260:Herc1 UTSW 9 66,355,630 (GRCm39) frame shift probably null
R4261:Herc1 UTSW 9 66,355,630 (GRCm39) frame shift probably null
R4300:Herc1 UTSW 9 66,396,688 (GRCm39) missense probably damaging 1.00
R4398:Herc1 UTSW 9 66,386,735 (GRCm39) missense probably benign 0.13
R4426:Herc1 UTSW 9 66,403,287 (GRCm39) missense probably damaging 1.00
R4427:Herc1 UTSW 9 66,403,287 (GRCm39) missense probably damaging 1.00
R4590:Herc1 UTSW 9 66,344,946 (GRCm39) missense probably damaging 0.97
R4630:Herc1 UTSW 9 66,340,996 (GRCm39) splice site probably null
R4656:Herc1 UTSW 9 66,301,993 (GRCm39) missense probably damaging 0.97
R4658:Herc1 UTSW 9 66,386,773 (GRCm39) missense possibly damaging 0.50
R4663:Herc1 UTSW 9 66,340,660 (GRCm39) missense probably damaging 0.98
R4675:Herc1 UTSW 9 66,298,740 (GRCm39) missense probably damaging 1.00
R4678:Herc1 UTSW 9 66,323,551 (GRCm39) missense probably benign 0.00
R4754:Herc1 UTSW 9 66,408,488 (GRCm39) missense probably benign 0.00
R4766:Herc1 UTSW 9 66,349,211 (GRCm39) missense probably benign 0.00
R4792:Herc1 UTSW 9 66,403,266 (GRCm39) missense possibly damaging 0.67
R4828:Herc1 UTSW 9 66,404,625 (GRCm39) splice site probably null
R4832:Herc1 UTSW 9 66,403,253 (GRCm39) missense probably benign 0.11
R4879:Herc1 UTSW 9 66,370,119 (GRCm39) nonsense probably null
R4948:Herc1 UTSW 9 66,392,184 (GRCm39) missense probably benign
R5021:Herc1 UTSW 9 66,377,608 (GRCm39) missense possibly damaging 0.48
R5022:Herc1 UTSW 9 66,377,608 (GRCm39) missense possibly damaging 0.48
R5023:Herc1 UTSW 9 66,377,608 (GRCm39) missense possibly damaging 0.48
R5024:Herc1 UTSW 9 66,377,608 (GRCm39) missense possibly damaging 0.48
R5025:Herc1 UTSW 9 66,377,608 (GRCm39) missense possibly damaging 0.48
R5026:Herc1 UTSW 9 66,393,408 (GRCm39) missense probably benign 0.03
R5027:Herc1 UTSW 9 66,380,811 (GRCm39) missense probably benign 0.01
R5027:Herc1 UTSW 9 66,411,900 (GRCm39) missense probably damaging 0.98
R5038:Herc1 UTSW 9 66,383,742 (GRCm39) intron probably benign
R5041:Herc1 UTSW 9 66,336,327 (GRCm39) missense possibly damaging 0.86
R5053:Herc1 UTSW 9 66,377,608 (GRCm39) missense possibly damaging 0.48
R5137:Herc1 UTSW 9 66,355,505 (GRCm39) missense probably benign
R5197:Herc1 UTSW 9 66,355,786 (GRCm39) missense probably damaging 0.99
R5207:Herc1 UTSW 9 66,307,151 (GRCm39) nonsense probably null
R5247:Herc1 UTSW 9 66,341,833 (GRCm39) missense probably benign 0.01
R5267:Herc1 UTSW 9 66,369,091 (GRCm39) missense probably damaging 1.00
R5274:Herc1 UTSW 9 66,306,691 (GRCm39) missense probably benign
R5375:Herc1 UTSW 9 66,375,169 (GRCm39) missense probably damaging 0.99
R5401:Herc1 UTSW 9 66,409,338 (GRCm39) missense probably damaging 1.00
R5560:Herc1 UTSW 9 66,358,401 (GRCm39) missense probably benign 0.02
R5566:Herc1 UTSW 9 66,372,819 (GRCm39) missense possibly damaging 0.95
R5577:Herc1 UTSW 9 66,389,263 (GRCm39) missense probably damaging 0.99
R5596:Herc1 UTSW 9 66,341,345 (GRCm39) critical splice acceptor site probably benign
R5665:Herc1 UTSW 9 66,372,717 (GRCm39) missense probably damaging 1.00
R5744:Herc1 UTSW 9 66,415,475 (GRCm39) missense probably damaging 1.00
R5802:Herc1 UTSW 9 66,370,160 (GRCm39) missense probably damaging 1.00
R5822:Herc1 UTSW 9 66,352,894 (GRCm39) missense probably benign 0.00
R5954:Herc1 UTSW 9 66,358,774 (GRCm39) splice site probably benign
R5977:Herc1 UTSW 9 66,340,604 (GRCm39) missense possibly damaging 0.77
R6022:Herc1 UTSW 9 66,390,967 (GRCm39) missense probably damaging 1.00
R6043:Herc1 UTSW 9 66,315,436 (GRCm39) missense probably benign
R6046:Herc1 UTSW 9 66,352,831 (GRCm39) missense probably damaging 0.99
R6089:Herc1 UTSW 9 66,352,814 (GRCm39) missense probably damaging 1.00
R6123:Herc1 UTSW 9 66,404,532 (GRCm39) missense probably damaging 0.97
R6155:Herc1 UTSW 9 66,340,705 (GRCm39) missense possibly damaging 0.95
R6190:Herc1 UTSW 9 66,283,663 (GRCm39) missense possibly damaging 0.56
R6220:Herc1 UTSW 9 66,341,070 (GRCm39) missense probably damaging 1.00
R6265:Herc1 UTSW 9 66,279,298 (GRCm39) missense probably benign 0.05
R6348:Herc1 UTSW 9 66,395,258 (GRCm39) missense possibly damaging 0.77
R6362:Herc1 UTSW 9 66,379,190 (GRCm39) missense probably damaging 1.00
R6394:Herc1 UTSW 9 66,302,341 (GRCm39) missense probably damaging 0.99
R6434:Herc1 UTSW 9 66,393,464 (GRCm39) missense probably damaging 0.99
R6483:Herc1 UTSW 9 66,355,811 (GRCm39) missense possibly damaging 0.64
R6607:Herc1 UTSW 9 66,325,849 (GRCm39) missense probably benign 0.02
R6633:Herc1 UTSW 9 66,346,534 (GRCm39) nonsense probably null
R6634:Herc1 UTSW 9 66,345,026 (GRCm39) missense probably benign
R6693:Herc1 UTSW 9 66,386,258 (GRCm39) missense probably damaging 0.99
R6695:Herc1 UTSW 9 66,391,148 (GRCm39) splice site probably null
R6748:Herc1 UTSW 9 66,408,470 (GRCm39) frame shift probably null
R6750:Herc1 UTSW 9 66,408,470 (GRCm39) frame shift probably null
R6751:Herc1 UTSW 9 66,408,470 (GRCm39) frame shift probably null
R6774:Herc1 UTSW 9 66,408,470 (GRCm39) frame shift probably null
R6785:Herc1 UTSW 9 66,408,470 (GRCm39) frame shift probably null
R6786:Herc1 UTSW 9 66,408,470 (GRCm39) frame shift probably null
R6856:Herc1 UTSW 9 66,305,180 (GRCm39) missense probably benign 0.05
R6966:Herc1 UTSW 9 66,318,347 (GRCm39) missense probably benign 0.07
R7020:Herc1 UTSW 9 66,393,360 (GRCm39) missense probably benign 0.07
R7109:Herc1 UTSW 9 66,389,171 (GRCm39) missense probably benign 0.03
R7122:Herc1 UTSW 9 66,307,056 (GRCm39) missense possibly damaging 0.69
R7209:Herc1 UTSW 9 66,292,314 (GRCm39) missense possibly damaging 0.95
R7222:Herc1 UTSW 9 66,374,781 (GRCm39) missense probably damaging 0.98
R7303:Herc1 UTSW 9 66,358,098 (GRCm39) missense possibly damaging 0.93
R7305:Herc1 UTSW 9 66,369,150 (GRCm39) missense
R7438:Herc1 UTSW 9 66,302,038 (GRCm39) missense probably benign 0.00
R7535:Herc1 UTSW 9 66,382,135 (GRCm39) missense probably damaging 1.00
R7585:Herc1 UTSW 9 66,352,829 (GRCm39) missense probably damaging 1.00
R7603:Herc1 UTSW 9 66,358,665 (GRCm39) nonsense probably null
R7670:Herc1 UTSW 9 66,323,629 (GRCm39) missense probably damaging 0.99
R7705:Herc1 UTSW 9 66,347,116 (GRCm39) missense possibly damaging 0.86
R7723:Herc1 UTSW 9 66,279,158 (GRCm39) missense probably benign 0.24
R7730:Herc1 UTSW 9 66,400,472 (GRCm39) small deletion probably benign
R7880:Herc1 UTSW 9 66,415,506 (GRCm39) missense probably damaging 0.99
R7958:Herc1 UTSW 9 66,393,475 (GRCm39) missense probably damaging 1.00
R7976:Herc1 UTSW 9 66,341,552 (GRCm39) missense possibly damaging 0.94
R8006:Herc1 UTSW 9 66,352,842 (GRCm39) nonsense probably null
R8084:Herc1 UTSW 9 66,383,217 (GRCm39) missense probably benign 0.45
R8094:Herc1 UTSW 9 66,400,462 (GRCm39) missense probably damaging 0.98
R8099:Herc1 UTSW 9 66,279,422 (GRCm39) missense probably damaging 1.00
R8151:Herc1 UTSW 9 66,341,073 (GRCm39) missense probably damaging 0.98
R8159:Herc1 UTSW 9 66,369,003 (GRCm39) missense probably null
R8190:Herc1 UTSW 9 66,325,733 (GRCm39) missense probably benign 0.00
R8213:Herc1 UTSW 9 66,358,170 (GRCm39) missense probably damaging 0.99
R8230:Herc1 UTSW 9 66,377,598 (GRCm39) missense probably damaging 0.99
R8265:Herc1 UTSW 9 66,293,986 (GRCm39) nonsense probably null
R8270:Herc1 UTSW 9 66,395,232 (GRCm39) missense probably damaging 1.00
R8353:Herc1 UTSW 9 66,415,571 (GRCm39) missense possibly damaging 0.88
R8423:Herc1 UTSW 9 66,415,442 (GRCm39) missense probably damaging 0.99
R8506:Herc1 UTSW 9 66,380,863 (GRCm39) missense possibly damaging 0.52
R8523:Herc1 UTSW 9 66,358,224 (GRCm39) missense probably benign
R8530:Herc1 UTSW 9 66,325,910 (GRCm39) missense probably benign
R8545:Herc1 UTSW 9 66,279,257 (GRCm39) nonsense probably null
R8682:Herc1 UTSW 9 66,370,130 (GRCm39) missense
R8720:Herc1 UTSW 9 66,389,105 (GRCm39) missense probably benign 0.38
R8792:Herc1 UTSW 9 66,372,768 (GRCm39) missense probably damaging 1.00
R8915:Herc1 UTSW 9 66,318,456 (GRCm39) missense probably damaging 1.00
R8964:Herc1 UTSW 9 66,352,872 (GRCm39) missense probably damaging 1.00
R9056:Herc1 UTSW 9 66,380,782 (GRCm39) missense probably benign 0.10
R9158:Herc1 UTSW 9 66,376,400 (GRCm39) missense probably benign 0.00
R9167:Herc1 UTSW 9 66,411,900 (GRCm39) missense possibly damaging 0.75
R9192:Herc1 UTSW 9 66,321,413 (GRCm39) missense probably benign 0.35
R9252:Herc1 UTSW 9 66,309,834 (GRCm39) missense probably damaging 1.00
R9260:Herc1 UTSW 9 66,325,691 (GRCm39) nonsense probably null
R9261:Herc1 UTSW 9 66,412,129 (GRCm39) missense probably damaging 0.98
R9430:Herc1 UTSW 9 66,325,785 (GRCm39) nonsense probably null
R9519:Herc1 UTSW 9 66,307,356 (GRCm39) missense probably damaging 0.97
R9563:Herc1 UTSW 9 66,294,193 (GRCm39) critical splice donor site probably null
R9589:Herc1 UTSW 9 66,372,840 (GRCm39) missense possibly damaging 0.95
R9600:Herc1 UTSW 9 66,304,594 (GRCm39) missense possibly damaging 0.95
R9659:Herc1 UTSW 9 66,307,185 (GRCm39) missense probably benign 0.03
R9740:Herc1 UTSW 9 66,355,796 (GRCm39) missense probably damaging 1.00
R9774:Herc1 UTSW 9 66,372,032 (GRCm39) missense probably null
R9781:Herc1 UTSW 9 66,280,004 (GRCm39) missense probably benign
R9788:Herc1 UTSW 9 66,307,185 (GRCm39) missense probably benign 0.03
RF023:Herc1 UTSW 9 66,365,616 (GRCm39) missense
X0011:Herc1 UTSW 9 66,307,441 (GRCm39) missense probably benign 0.28
X0067:Herc1 UTSW 9 66,355,806 (GRCm39) missense probably benign 0.03
Z1176:Herc1 UTSW 9 66,341,858 (GRCm39) missense probably benign
Z1177:Herc1 UTSW 9 66,379,193 (GRCm39) missense probably damaging 0.99
Z1177:Herc1 UTSW 9 66,365,707 (GRCm39) missense probably null
Predicted Primers PCR Primer
(F):5'- GGACCCAACAGGCCATATTC -3'
(R):5'- GCCATTTTGACAGCCACTTAAGAG -3'

Sequencing Primer
(F):5'- CAGGCCATATTCTCATGACATGTG -3'
(R):5'- TTGACAGCCACTTAAGAGAAAAATC -3'
Posted On 2014-07-14