Mutagenetix > Incidental Mutation

Incidental Mutation 'R9563:Herc1'

721238

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

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R9563 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

66350450-66508775 bp(+) (GRCm38)

Type of Mutation

critical splice donor site (1 bp from exon)

DNA Base Change (assembly)

G to T at 66386911 bp (GRCm38)

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

Domain	Start	End	E-Value	Type
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

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.9%

Validation Efficiency

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: 127 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2410089E03Rik	T	G	15: 8,187,079 (GRCm38)	L594V	probably benign	Het
9130409I23Rik	G	T	1: 181,055,245 (GRCm38)	V191F	possibly damaging	Het
A2m	T	A	6: 121,668,050 (GRCm38)	D953E	probably damaging	Het
Acod1	A	C	14: 103,049,673 (GRCm38)	Y80S	probably damaging	Het
Actr5	A	G	2: 158,628,215 (GRCm38)	D255G	probably damaging	Het
Akna	A	G	4: 63,394,707 (GRCm38)	V393A	probably damaging	Het
Amotl1	T	C	9: 14,562,217 (GRCm38)	K562R	possibly damaging	Het
Amz1	T	A	5: 140,752,378 (GRCm38)	D464E	probably damaging	Het
Anapc1	G	A	2: 128,664,060 (GRCm38)	Q619*	probably null	Het
Arfgef3	C	T	10: 18,646,527 (GRCm38)	G584R	probably damaging	Het
Armt1	AC	A	10: 4,450,848 (GRCm38)		probably null	Het
Atr	G	C	9: 95,920,780 (GRCm38)	V1832L	probably damaging	Het
Bsn	T	C	9: 108,107,417 (GRCm38)	D374G		Het
Cap1	A	G	4: 122,864,712 (GRCm38)	V225A	probably benign	Het
Cc2d1a	A	G	8: 84,137,129 (GRCm38)	S562P	probably benign	Het
Ccdc30	T	C	4: 119,393,624 (GRCm38)	N141S	possibly damaging	Het
Cdc42bpb	A	G	12: 111,299,328 (GRCm38)	V1390A	possibly damaging	Het
Cdc42ep1	A	T	15: 78,849,582 (GRCm38)	H294L	probably benign	Het
Col6a6	C	A	9: 105,695,753 (GRCm38)	G2185C	probably benign	Het
Col7a1	T	C	9: 108,962,741 (GRCm38)	V1232A	unknown	Het
Copb1	A	G	7: 114,236,799 (GRCm38)	I449T	possibly damaging	Het
Ctdsp2	A	G	10: 126,996,171 (GRCm38)	D216G	probably damaging	Het
Cttnbp2	A	T	6: 18,427,468 (GRCm38)	L738*	probably null	Het
Cttnbp2	T	A	6: 18,367,383 (GRCm38)	K1645N	probably benign	Het
Cul9	T	A	17: 46,509,971 (GRCm38)	T1927S	probably benign	Het
Cyfip2	A	G	11: 46,260,880 (GRCm38)	C531R	probably benign	Het
Cyp2j6	A	G	4: 96,526,008 (GRCm38)	I340T	probably damaging	Het
Daam1	A	G	12: 71,945,477 (GRCm38)	E322G	unknown	Het
Dab2ip	T	A	2: 35,719,903 (GRCm38)	L710*	probably null	Het
Dph1	T	C	11: 75,185,999 (GRCm38)	T60A	possibly damaging	Het
Eme1	T	C	11: 94,650,513 (GRCm38)	D161G	probably benign	Het
Epha3	C	T	16: 63,546,147 (GRCm38)	G980D	possibly damaging	Het
Eri3	T	A	4: 117,564,816 (GRCm38)	V136E	probably benign	Het
Espl1	T	A	15: 102,319,798 (GRCm38)	I1669N	possibly damaging	Het
Exoc6	T	C	19: 37,599,623 (GRCm38)	I568T	probably damaging	Het
F3	T	A	3: 121,734,173 (GRCm38)	L85H		Het
Fam186b	G	A	15: 99,279,735 (GRCm38)	A570V	probably damaging	Het
Fam212a	T	A	9: 107,984,289 (GRCm38)	Y276F	probably benign	Het
Fbxw14	T	C	9: 109,277,267 (GRCm38)	Y234C	probably benign	Het
Fbxw25	T	A	9: 109,654,608 (GRCm38)	N179Y		Het
Foxr1	T	A	9: 44,440,902 (GRCm38)		probably benign	Het
Gas8	T	A	8: 123,536,440 (GRCm38)	V452E	possibly damaging	Het
Gdpd4	T	C	7: 98,000,162 (GRCm38)	V450A	probably damaging	Het
Gm17359	A	T	3: 79,449,309 (GRCm38)	M140L	probably benign	Het
Greb1	T	C	12: 16,724,823 (GRCm38)	Y191C	probably benign	Het
Haus3	G	A	5: 34,167,956 (GRCm38)	R120W	probably benign	Het
Hist1h3i	T	C	13: 21,783,051 (GRCm38)	D107G	probably damaging	Het
Hyal2	T	C	9: 107,570,645 (GRCm38)	W166R	probably damaging	Het
Itga7	C	T	10: 128,953,800 (GRCm38)	A1003V	probably damaging	Het
Itga8	T	A	2: 12,160,408 (GRCm38)	I797F	possibly damaging	Het
Kank2	T	C	9: 21,794,556 (GRCm38)	T389A	possibly damaging	Het
Kcnb2	T	A	1: 15,709,513 (GRCm38)	I203N	probably damaging	Het
Kif21b	T	A	1: 136,149,428 (GRCm38)	L396Q	probably damaging	Het
Kng1	T	G	16: 23,060,420 (GRCm38)	I78S	probably damaging	Het
Ldlrad4	T	C	18: 68,254,480 (GRCm38)	S288P	probably benign	Het
Lmntd2	A	G	7: 141,210,788 (GRCm38)	S516P		Het
Lrp1b	T	A	2: 41,295,699 (GRCm38)	I1449F		Het
Lrrk2	T	A	15: 91,749,840 (GRCm38)	I1380K	possibly damaging	Het
Lvrn	T	G	18: 46,884,439 (GRCm38)	I612S	probably damaging	Het
Lyst	T	C	13: 13,637,823 (GRCm38)	L940P	probably benign	Het
Man2a2	T	A	7: 80,356,353 (GRCm38)	M996L	probably benign	Het
Map3k3	T	A	11: 106,151,034 (GRCm38)	I413N	probably damaging	Het
Map4k5	A	G	12: 69,816,393 (GRCm38)	V629A	probably benign	Het
Mapre2	A	G	18: 23,890,924 (GRCm38)	E325G	unknown	Het
Mbnl1	A	G	3: 60,613,294 (GRCm38)	N101S	probably benign	Het
Meltf	T	A	16: 31,885,051 (GRCm38)	C199S	probably damaging	Het
Mmab	T	C	5: 114,436,789 (GRCm38)	E141G	probably benign	Het
Mtus2	T	C	5: 148,313,407 (GRCm38)	L1317P		Het
Muc6	T	A	7: 141,637,870 (GRCm38)	T2297S	possibly damaging	Het
Myom2	A	T	8: 15,108,399 (GRCm38)	K784*	probably null	Het
Nek1	A	G	8: 61,124,123 (GRCm38)	E1118G	probably benign	Het
Nrtn	A	G	17: 56,751,416 (GRCm38)	V195A	probably damaging	Het
Nsd3	G	A	8: 25,714,203 (GRCm38)	V420I		Het
Olfr1094	A	G	2: 86,828,754 (GRCm38)	M1V	probably null	Het
Olfr1451	T	A	19: 12,999,619 (GRCm38)	I211N	probably damaging	Het
Olfr205	T	C	16: 59,329,402 (GRCm38)	I36V	probably benign	Het
Olfr522	G	A	7: 140,162,320 (GRCm38)	T210I	probably damaging	Het
Olfr618	A	T	7: 103,598,018 (GRCm38)	Q234L	probably benign	Het
Olfr677	T	C	7: 105,057,074 (GRCm38)	L276P	possibly damaging	Het
Olfr820	T	C	10: 130,017,418 (GRCm38)	I19T	probably benign	Het
Olfr923	A	T	9: 38,827,718 (GRCm38)	H3L	probably benign	Het
Pde10a	G	T	17: 8,801,878 (GRCm38)	A216S	unknown	Het
Phldb2	T	C	16: 45,824,884 (GRCm38)	T400A	possibly damaging	Het
Pkd1l1	T	A	11: 8,865,502 (GRCm38)	T1920S		Het
Ptgs2	T	A	1: 150,105,668 (GRCm38)	N567K	probably benign	Het
Pwp1	T	A	10: 85,876,506 (GRCm38)	D141E	probably damaging	Het
Rab3ip	T	C	10: 116,918,763 (GRCm38)	E296G	probably null	Het
Rb1cc1	A	G	1: 6,244,115 (GRCm38)	K337R	probably benign	Het
Rbp3	A	G	14: 33,955,520 (GRCm38)	D475G	probably damaging	Het
Ric3	T	C	7: 109,038,790 (GRCm38)	E253G	possibly damaging	Het
Rictor	A	T	15: 6,768,081 (GRCm38)	N306I	possibly damaging	Het
Rnf214	A	T	9: 45,899,843 (GRCm38)	V174E	possibly damaging	Het
Robo3	A	G	9: 37,429,604 (GRCm38)	F124S	probably damaging	Het
Rrad	A	G	8: 104,628,692 (GRCm38)	F228S	probably damaging	Het
Scn3a	A	T	2: 65,461,251 (GRCm38)	M1717K	probably damaging	Het
Scn3b	A	G	9: 40,282,433 (GRCm38)	D152G	probably benign	Het
Scn5a	C	A	9: 119,486,737 (GRCm38)	R1635L	probably damaging	Het
Sec61b	A	G	4: 47,483,049 (GRCm38)	Y93C	probably damaging	Het
Shprh	T	A	10: 11,166,491 (GRCm38)	Y739*	probably null	Het
Skor2	C	T	18: 76,858,681 (GRCm38)	H33Y	unknown	Het
Slc26a7	T	C	4: 14,519,496 (GRCm38)	N508S	probably benign	Het
Slc7a12	A	G	3: 14,499,300 (GRCm38)	I349V	possibly damaging	Het
Slit1	T	C	19: 41,608,435 (GRCm38)	Y1075C	probably damaging	Het
Sltm	C	T	9: 70,573,559 (GRCm38)	A231V	unknown	Het
Smg1	A	G	7: 118,212,985 (GRCm38)	S52P	unknown	Het
Soga1	G	A	2: 157,060,262 (GRCm38)	R278C	probably damaging	Het
Sorl1	A	G	9: 42,046,597 (GRCm38)	Y584H	probably damaging	Het
Ssbp1	T	A	6: 40,478,034 (GRCm38)	S142R	probably benign	Het
Stard3	A	G	11: 98,379,971 (GRCm38)		probably null	Het
Strn3	G	T	12: 51,627,517 (GRCm38)	H531N	possibly damaging	Het
Stx17	A	G	4: 48,180,739 (GRCm38)	T195A	probably damaging	Het
Tekt2	C	T	4: 126,323,651 (GRCm38)	R207H	probably damaging	Het
Tmed5	A	C	5: 108,132,234 (GRCm38)		probably null	Het
Tmem132a	C	T	19: 10,861,596 (GRCm38)	R494H	probably benign	Het
Tom1	A	G	8: 75,060,549 (GRCm38)	K406E	probably benign	Het
Trav5d-4	A	T	14: 53,002,016 (GRCm38)	N43Y	probably damaging	Het
Trbv19	G	T	6: 41,179,011 (GRCm38)	K105N	possibly damaging	Het
Trim34a	C	T	7: 104,261,121 (GRCm38)	Q377*	probably null	Het
Trp53bp2	T	A	1: 182,448,813 (GRCm38)	N786K	probably benign	Het
Trpc3	A	G	3: 36,651,534 (GRCm38)	M504T	probably benign	Het
Ttc28	A	T	5: 111,223,226 (GRCm38)	M545L	probably benign	Het
Uggt1	A	C	1: 36,165,546 (GRCm38)	V996G	possibly damaging	Het
Vmn2r65	G	A	7: 84,940,672 (GRCm38)	Q679*	probably null	Het
Wdfy4	T	C	14: 32,970,876 (GRCm38)	I2958V		Het
Zbtb37	C	T	1: 161,020,270 (GRCm38)	S389N	possibly damaging	Het
Zfp235	T	C	7: 24,142,244 (GRCm38)	V696A	possibly damaging	Het
Zzef1	T	A	11: 72,874,906 (GRCm38)	C1420S	probably damaging	Het

Other mutations in Herc1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00092:Herc1	APN	9	66,483,966 (GRCm38)	missense	probably benign	0.02
IGL00159:Herc1	APN	9	66,437,682 (GRCm38)	missense	possibly damaging	0.94
IGL00486:Herc1	APN	9	66,476,120 (GRCm38)	missense	probably benign
IGL00717:Herc1	APN	9	66,485,002 (GRCm38)	missense	probably damaging	1.00
IGL00766:Herc1	APN	9	66,450,741 (GRCm38)	missense	probably damaging	1.00
IGL00776:Herc1	APN	9	66,421,038 (GRCm38)	missense	probably benign
IGL00987:Herc1	APN	9	66,408,052 (GRCm38)	missense	probably benign	0.07
IGL01090:Herc1	APN	9	66,469,175 (GRCm38)	nonsense	probably null
IGL01098:Herc1	APN	9	66,461,922 (GRCm38)	critical splice donor site	probably null
IGL01106:Herc1	APN	9	66,476,438 (GRCm38)	splice site	probably benign
IGL01120:Herc1	APN	9	66,428,880 (GRCm38)	missense	probably benign
IGL01359:Herc1	APN	9	66,439,268 (GRCm38)	missense	probably benign	0.01
IGL01360:Herc1	APN	9	66,483,699 (GRCm38)	missense	probably benign
IGL01364:Herc1	APN	9	66,399,361 (GRCm38)	missense	probably benign	0.00
IGL01470:Herc1	APN	9	66,497,636 (GRCm38)	missense	possibly damaging	0.94
IGL01670:Herc1	APN	9	66,487,060 (GRCm38)	missense	probably damaging	1.00
IGL01825:Herc1	APN	9	66,399,807 (GRCm38)	missense	probably benign	0.00
IGL01903:Herc1	APN	9	66,386,872 (GRCm38)	nonsense	probably null
IGL01988:Herc1	APN	9	66,488,075 (GRCm38)	splice site	probably benign
IGL02074:Herc1	APN	9	66,450,983 (GRCm38)	missense	probably benign
IGL02089:Herc1	APN	9	66,480,869 (GRCm38)	missense	probably damaging	1.00
IGL02177:Herc1	APN	9	66,434,511 (GRCm38)	missense	probably benign
IGL02300:Herc1	APN	9	66,476,363 (GRCm38)	missense	probably benign	0.01
IGL02304:Herc1	APN	9	66,476,414 (GRCm38)	missense	probably benign	0.06
IGL02369:Herc1	APN	9	66,492,011 (GRCm38)	nonsense	probably null
IGL02445:Herc1	APN	9	66,433,482 (GRCm38)	missense	possibly damaging	0.95
IGL02447:Herc1	APN	9	66,497,328 (GRCm38)	missense	possibly damaging	0.59
IGL02549:Herc1	APN	9	66,399,901 (GRCm38)	missense	probably damaging	0.98
IGL02571:Herc1	APN	9	66,434,605 (GRCm38)	splice site	probably benign
IGL02709:Herc1	APN	9	66,497,680 (GRCm38)	missense	probably damaging	0.97
IGL02717:Herc1	APN	9	66,371,921 (GRCm38)	nonsense	probably null
IGL02726:Herc1	APN	9	66,441,988 (GRCm38)	missense	probably benign	0.37
IGL02733:Herc1	APN	9	66,450,992 (GRCm38)	missense	probably benign
IGL02963:Herc1	APN	9	66,388,823 (GRCm38)	missense	probably damaging	0.99
IGL03101:Herc1	APN	9	66,487,997 (GRCm38)	missense	probably benign
IGL03193:Herc1	APN	9	66,402,680 (GRCm38)	missense	probably benign
IGL03203:Herc1	APN	9	66,388,900 (GRCm38)	critical splice donor site	probably null
IGL03216:Herc1	APN	9	66,478,946 (GRCm38)	missense	probably benign	0.06
IGL03282:Herc1	APN	9	66,451,459 (GRCm38)	missense	probably benign	0.05
IGL03295:Herc1	APN	9	66,396,703 (GRCm38)	missense	possibly damaging	0.56
cradle	UTSW	9	66,483,866 (GRCm38)	splice site	probably null
miracles	UTSW	9	66,462,837 (GRCm38)	nonsense	probably null
newton	UTSW	9	66,467,803 (GRCm38)	missense	probably damaging	1.00
R0907_Herc1_362	UTSW	9	66,433,428 (GRCm38)	missense	possibly damaging	0.94
R4427_Herc1_231	UTSW	9	66,496,005 (GRCm38)	missense	probably damaging	1.00
R5026_Herc1_363	UTSW	9	66,486,126 (GRCm38)	missense	probably benign	0.03
stables	UTSW	9	66,479,453 (GRCm38)	missense	probably benign	0.13
strangle	UTSW	9	66,501,188 (GRCm38)	frame shift	probably null
IGL03134:Herc1	UTSW	9	66,434,063 (GRCm38)	critical splice acceptor site	probably benign
PIT4243001:Herc1	UTSW	9	66,372,207 (GRCm38)	missense	probably benign	0.00
PIT4486001:Herc1	UTSW	9	66,372,389 (GRCm38)	missense	probably damaging	1.00
PIT4696001:Herc1	UTSW	9	66,479,009 (GRCm38)	missense	probably damaging	1.00
R0044:Herc1	UTSW	9	66,448,175 (GRCm38)	missense	probably benign	0.04
R0044:Herc1	UTSW	9	66,448,175 (GRCm38)	missense	probably benign	0.04
R0052:Herc1	UTSW	9	66,400,156 (GRCm38)	missense	probably damaging	0.99
R0114:Herc1	UTSW	9	66,461,846 (GRCm38)	missense	probably damaging	0.99
R0129:Herc1	UTSW	9	66,448,075 (GRCm38)	missense	probably damaging	1.00
R0131:Herc1	UTSW	9	66,480,910 (GRCm38)	missense	probably benign	0.00
R0131:Herc1	UTSW	9	66,480,910 (GRCm38)	missense	probably benign	0.00
R0132:Herc1	UTSW	9	66,480,910 (GRCm38)	missense	probably benign	0.00
R0158:Herc1	UTSW	9	66,495,921 (GRCm38)	nonsense	probably null
R0333:Herc1	UTSW	9	66,464,699 (GRCm38)	splice site	probably null
R0384:Herc1	UTSW	9	66,481,050 (GRCm38)	splice site	probably benign
R0419:Herc1	UTSW	9	66,446,074 (GRCm38)	splice site	probably benign
R0453:Herc1	UTSW	9	66,399,772 (GRCm38)	missense	probably benign	0.20
R0458:Herc1	UTSW	9	66,476,381 (GRCm38)	missense	probably benign	0.12
R0490:Herc1	UTSW	9	66,484,999 (GRCm38)	missense	probably damaging	1.00
R0506:Herc1	UTSW	9	66,448,159 (GRCm38)	missense	probably damaging	0.99
R0513:Herc1	UTSW	9	66,445,645 (GRCm38)	missense	possibly damaging	0.96
R0628:Herc1	UTSW	9	66,450,881 (GRCm38)	missense	probably benign	0.35
R0666:Herc1	UTSW	9	66,484,888 (GRCm38)	splice site	probably benign
R0674:Herc1	UTSW	9	66,501,192 (GRCm38)	missense	probably damaging	0.99
R0682:Herc1	UTSW	9	66,481,981 (GRCm38)	missense	possibly damaging	0.95
R0690:Herc1	UTSW	9	66,386,838 (GRCm38)	nonsense	probably null
R0701:Herc1	UTSW	9	66,487,950 (GRCm38)	missense	probably damaging	1.00
R0766:Herc1	UTSW	9	66,504,840 (GRCm38)	missense	probably damaging	1.00
R0850:Herc1	UTSW	9	66,466,670 (GRCm38)	missense	probably damaging	1.00
R0907:Herc1	UTSW	9	66,433,428 (GRCm38)	missense	possibly damaging	0.94
R0972:Herc1	UTSW	9	66,372,145 (GRCm38)	missense	probably damaging	1.00
R0976:Herc1	UTSW	9	66,439,878 (GRCm38)	missense	possibly damaging	0.74
R1027:Herc1	UTSW	9	66,455,968 (GRCm38)	missense	probably benign
R1200:Herc1	UTSW	9	66,486,124 (GRCm38)	missense	probably damaging	1.00
R1226:Herc1	UTSW	9	66,416,263 (GRCm38)	missense	probably benign	0.00
R1364:Herc1	UTSW	9	66,400,093 (GRCm38)	missense	probably damaging	1.00
R1395:Herc1	UTSW	9	66,439,181 (GRCm38)	missense	probably benign	0.13
R1432:Herc1	UTSW	9	66,465,469 (GRCm38)	missense	probably benign	0.13
R1440:Herc1	UTSW	9	66,467,803 (GRCm38)	missense	probably damaging	1.00
R1476:Herc1	UTSW	9	66,508,266 (GRCm38)	missense	probably damaging	1.00
R1590:Herc1	UTSW	9	66,491,953 (GRCm38)	splice site	probably benign
R1634:Herc1	UTSW	9	66,473,538 (GRCm38)	missense	possibly damaging	0.51
R1700:Herc1	UTSW	9	66,450,678 (GRCm38)	splice site	probably null
R1753:Herc1	UTSW	9	66,502,084 (GRCm38)	critical splice donor site	probably null
R1753:Herc1	UTSW	9	66,469,010 (GRCm38)	missense	probably damaging	1.00
R1796:Herc1	UTSW	9	66,388,856 (GRCm38)	nonsense	probably null
R1830:Herc1	UTSW	9	66,497,599 (GRCm38)	missense	possibly damaging	0.95
R1855:Herc1	UTSW	9	66,391,426 (GRCm38)	missense	possibly damaging	0.95
R1866:Herc1	UTSW	9	66,450,791 (GRCm38)	missense	probably damaging	1.00
R1894:Herc1	UTSW	9	66,479,461 (GRCm38)	missense	probably damaging	1.00
R1918:Herc1	UTSW	9	66,476,126 (GRCm38)	splice site	probably null
R1999:Herc1	UTSW	9	66,486,078 (GRCm38)	missense	probably benign	0.07
R2034:Herc1	UTSW	9	66,441,972 (GRCm38)	missense	probably benign	0.01
R2138:Herc1	UTSW	9	66,470,307 (GRCm38)	missense	possibly damaging	0.94
R2186:Herc1	UTSW	9	66,439,901 (GRCm38)	missense	probably benign	0.45
R2192:Herc1	UTSW	9	66,465,406 (GRCm38)	missense	probably damaging	0.99
R2312:Herc1	UTSW	9	66,508,281 (GRCm38)	nonsense	probably null
R2338:Herc1	UTSW	9	66,428,969 (GRCm38)	missense	possibly damaging	0.69
R3035:Herc1	UTSW	9	66,483,935 (GRCm38)	missense	possibly damaging	0.89
R3732:Herc1	UTSW	9	66,445,640 (GRCm38)	missense	probably damaging	1.00
R3732:Herc1	UTSW	9	66,445,640 (GRCm38)	missense	probably damaging	1.00
R3733:Herc1	UTSW	9	66,445,640 (GRCm38)	missense	probably damaging	1.00
R3917:Herc1	UTSW	9	66,434,466 (GRCm38)	missense	possibly damaging	0.94
R3953:Herc1	UTSW	9	66,433,793 (GRCm38)	nonsense	probably null
R4073:Herc1	UTSW	9	66,418,492 (GRCm38)	missense	probably benign	0.12
R4075:Herc1	UTSW	9	66,418,492 (GRCm38)	missense	probably benign	0.12
R4241:Herc1	UTSW	9	66,448,348 (GRCm38)	frame shift	probably null
R4260:Herc1	UTSW	9	66,448,348 (GRCm38)	frame shift	probably null
R4261:Herc1	UTSW	9	66,448,348 (GRCm38)	frame shift	probably null
R4300:Herc1	UTSW	9	66,489,406 (GRCm38)	missense	probably damaging	1.00
R4398:Herc1	UTSW	9	66,479,453 (GRCm38)	missense	probably benign	0.13
R4426:Herc1	UTSW	9	66,496,005 (GRCm38)	missense	probably damaging	1.00
R4427:Herc1	UTSW	9	66,496,005 (GRCm38)	missense	probably damaging	1.00
R4590:Herc1	UTSW	9	66,437,664 (GRCm38)	missense	probably damaging	0.97
R4630:Herc1	UTSW	9	66,433,714 (GRCm38)	splice site	probably null
R4656:Herc1	UTSW	9	66,394,711 (GRCm38)	missense	probably damaging	0.97
R4658:Herc1	UTSW	9	66,479,491 (GRCm38)	missense	possibly damaging	0.50
R4663:Herc1	UTSW	9	66,433,378 (GRCm38)	missense	probably damaging	0.98
R4675:Herc1	UTSW	9	66,391,458 (GRCm38)	missense	probably damaging	1.00
R4678:Herc1	UTSW	9	66,416,269 (GRCm38)	missense	probably benign	0.00
R4754:Herc1	UTSW	9	66,501,206 (GRCm38)	missense	probably benign	0.00
R4766:Herc1	UTSW	9	66,441,929 (GRCm38)	missense	probably benign	0.00
R4792:Herc1	UTSW	9	66,495,984 (GRCm38)	missense	possibly damaging	0.67
R4828:Herc1	UTSW	9	66,497,343 (GRCm38)	splice site	probably null
R4832:Herc1	UTSW	9	66,495,971 (GRCm38)	missense	probably benign	0.11
R4879:Herc1	UTSW	9	66,462,837 (GRCm38)	nonsense	probably null
R4948:Herc1	UTSW	9	66,484,902 (GRCm38)	missense	probably benign
R5021:Herc1	UTSW	9	66,470,326 (GRCm38)	missense	possibly damaging	0.48
R5022:Herc1	UTSW	9	66,470,326 (GRCm38)	missense	possibly damaging	0.48
R5023:Herc1	UTSW	9	66,470,326 (GRCm38)	missense	possibly damaging	0.48
R5024:Herc1	UTSW	9	66,470,326 (GRCm38)	missense	possibly damaging	0.48
R5025:Herc1	UTSW	9	66,470,326 (GRCm38)	missense	possibly damaging	0.48
R5026:Herc1	UTSW	9	66,486,126 (GRCm38)	missense	probably benign	0.03
R5027:Herc1	UTSW	9	66,473,529 (GRCm38)	missense	probably benign	0.01
R5027:Herc1	UTSW	9	66,504,618 (GRCm38)	missense	probably damaging	0.98
R5038:Herc1	UTSW	9	66,476,460 (GRCm38)	intron	probably benign
R5041:Herc1	UTSW	9	66,429,045 (GRCm38)	missense	possibly damaging	0.86
R5053:Herc1	UTSW	9	66,470,326 (GRCm38)	missense	possibly damaging	0.48
R5137:Herc1	UTSW	9	66,448,223 (GRCm38)	missense	probably benign
R5197:Herc1	UTSW	9	66,448,504 (GRCm38)	missense	probably damaging	0.99
R5207:Herc1	UTSW	9	66,399,869 (GRCm38)	nonsense	probably null
R5247:Herc1	UTSW	9	66,434,551 (GRCm38)	missense	probably benign	0.01
R5267:Herc1	UTSW	9	66,461,809 (GRCm38)	missense	probably damaging	1.00
R5274:Herc1	UTSW	9	66,399,409 (GRCm38)	missense	probably benign
R5375:Herc1	UTSW	9	66,467,887 (GRCm38)	missense	probably damaging	0.99
R5401:Herc1	UTSW	9	66,502,056 (GRCm38)	missense	probably damaging	1.00
R5560:Herc1	UTSW	9	66,451,119 (GRCm38)	missense	probably benign	0.02
R5566:Herc1	UTSW	9	66,465,537 (GRCm38)	missense	possibly damaging	0.95
R5577:Herc1	UTSW	9	66,481,981 (GRCm38)	missense	probably damaging	0.99
R5596:Herc1	UTSW	9	66,434,063 (GRCm38)	critical splice acceptor site	probably benign
R5665:Herc1	UTSW	9	66,465,435 (GRCm38)	missense	probably damaging	1.00
R5744:Herc1	UTSW	9	66,508,193 (GRCm38)	missense	probably damaging	1.00
R5802:Herc1	UTSW	9	66,462,878 (GRCm38)	missense	probably damaging	1.00
R5822:Herc1	UTSW	9	66,445,612 (GRCm38)	missense	probably benign	0.00
R5954:Herc1	UTSW	9	66,451,492 (GRCm38)	splice site	probably benign
R5977:Herc1	UTSW	9	66,433,322 (GRCm38)	missense	possibly damaging	0.77
R6022:Herc1	UTSW	9	66,483,685 (GRCm38)	missense	probably damaging	1.00
R6043:Herc1	UTSW	9	66,408,154 (GRCm38)	missense	probably benign
R6046:Herc1	UTSW	9	66,445,549 (GRCm38)	missense	probably damaging	0.99
R6089:Herc1	UTSW	9	66,445,532 (GRCm38)	missense	probably damaging	1.00
R6123:Herc1	UTSW	9	66,497,250 (GRCm38)	missense	probably damaging	0.97
R6155:Herc1	UTSW	9	66,433,423 (GRCm38)	missense	possibly damaging	0.95
R6190:Herc1	UTSW	9	66,376,381 (GRCm38)	missense	possibly damaging	0.56
R6220:Herc1	UTSW	9	66,433,788 (GRCm38)	missense	probably damaging	1.00
R6265:Herc1	UTSW	9	66,372,016 (GRCm38)	missense	probably benign	0.05
R6348:Herc1	UTSW	9	66,487,976 (GRCm38)	missense	possibly damaging	0.77
R6362:Herc1	UTSW	9	66,471,908 (GRCm38)	missense	probably damaging	1.00
R6394:Herc1	UTSW	9	66,395,059 (GRCm38)	missense	probably damaging	0.99
R6434:Herc1	UTSW	9	66,486,182 (GRCm38)	missense	probably damaging	0.99
R6483:Herc1	UTSW	9	66,448,529 (GRCm38)	missense	possibly damaging	0.64
R6607:Herc1	UTSW	9	66,418,567 (GRCm38)	missense	probably benign	0.02
R6633:Herc1	UTSW	9	66,439,252 (GRCm38)	nonsense	probably null
R6634:Herc1	UTSW	9	66,437,744 (GRCm38)	missense	probably benign
R6693:Herc1	UTSW	9	66,478,976 (GRCm38)	missense	probably damaging	0.99
R6695:Herc1	UTSW	9	66,483,866 (GRCm38)	splice site	probably null
R6748:Herc1	UTSW	9	66,501,188 (GRCm38)	frame shift	probably null
R6750:Herc1	UTSW	9	66,501,188 (GRCm38)	frame shift	probably null
R6751:Herc1	UTSW	9	66,501,188 (GRCm38)	frame shift	probably null
R6774:Herc1	UTSW	9	66,501,188 (GRCm38)	frame shift	probably null
R6785:Herc1	UTSW	9	66,501,188 (GRCm38)	frame shift	probably null
R6786:Herc1	UTSW	9	66,501,188 (GRCm38)	frame shift	probably null
R6856:Herc1	UTSW	9	66,397,898 (GRCm38)	missense	probably benign	0.05
R6966:Herc1	UTSW	9	66,411,065 (GRCm38)	missense	probably benign	0.07
R7020:Herc1	UTSW	9	66,486,078 (GRCm38)	missense	probably benign	0.07
R7109:Herc1	UTSW	9	66,481,889 (GRCm38)	missense	probably benign	0.03
R7122:Herc1	UTSW	9	66,399,774 (GRCm38)	missense	possibly damaging	0.69
R7209:Herc1	UTSW	9	66,385,032 (GRCm38)	missense	possibly damaging	0.95
R7222:Herc1	UTSW	9	66,467,499 (GRCm38)	missense	probably damaging	0.98
R7303:Herc1	UTSW	9	66,450,816 (GRCm38)	missense	possibly damaging	0.93
R7305:Herc1	UTSW	9	66,461,868 (GRCm38)	missense
R7438:Herc1	UTSW	9	66,394,756 (GRCm38)	missense	probably benign	0.00
R7535:Herc1	UTSW	9	66,474,853 (GRCm38)	missense	probably damaging	1.00
R7585:Herc1	UTSW	9	66,445,547 (GRCm38)	missense	probably damaging	1.00
R7603:Herc1	UTSW	9	66,451,383 (GRCm38)	nonsense	probably null
R7670:Herc1	UTSW	9	66,416,347 (GRCm38)	missense	probably damaging	0.99
R7705:Herc1	UTSW	9	66,439,834 (GRCm38)	missense	possibly damaging	0.86
R7723:Herc1	UTSW	9	66,371,876 (GRCm38)	missense	probably benign	0.24
R7730:Herc1	UTSW	9	66,493,190 (GRCm38)	small deletion	probably benign
R7880:Herc1	UTSW	9	66,508,224 (GRCm38)	missense	probably damaging	0.99
R7958:Herc1	UTSW	9	66,486,193 (GRCm38)	missense	probably damaging	1.00
R7976:Herc1	UTSW	9	66,434,270 (GRCm38)	missense	possibly damaging	0.94
R8006:Herc1	UTSW	9	66,445,560 (GRCm38)	nonsense	probably null
R8084:Herc1	UTSW	9	66,475,935 (GRCm38)	missense	probably benign	0.45
R8094:Herc1	UTSW	9	66,493,180 (GRCm38)	missense	probably damaging	0.98
R8099:Herc1	UTSW	9	66,372,140 (GRCm38)	missense	probably damaging	1.00
R8151:Herc1	UTSW	9	66,433,791 (GRCm38)	missense	probably damaging	0.98
R8159:Herc1	UTSW	9	66,461,721 (GRCm38)	missense	probably null
R8190:Herc1	UTSW	9	66,418,451 (GRCm38)	missense	probably benign	0.00
R8213:Herc1	UTSW	9	66,450,888 (GRCm38)	missense	probably damaging	0.99
R8230:Herc1	UTSW	9	66,470,316 (GRCm38)	missense	probably damaging	0.99
R8265:Herc1	UTSW	9	66,386,704 (GRCm38)	nonsense	probably null
R8270:Herc1	UTSW	9	66,487,950 (GRCm38)	missense	probably damaging	1.00
R8353:Herc1	UTSW	9	66,508,289 (GRCm38)	missense	possibly damaging	0.88
R8423:Herc1	UTSW	9	66,508,160 (GRCm38)	missense	probably damaging	0.99
R8506:Herc1	UTSW	9	66,473,581 (GRCm38)	missense	possibly damaging	0.52
R8523:Herc1	UTSW	9	66,450,942 (GRCm38)	missense	probably benign
R8530:Herc1	UTSW	9	66,418,628 (GRCm38)	missense	probably benign
R8545:Herc1	UTSW	9	66,371,975 (GRCm38)	nonsense	probably null
R8682:Herc1	UTSW	9	66,462,848 (GRCm38)	missense
R8720:Herc1	UTSW	9	66,481,823 (GRCm38)	missense	probably benign	0.38
R8792:Herc1	UTSW	9	66,465,486 (GRCm38)	missense	probably damaging	1.00
R8915:Herc1	UTSW	9	66,411,174 (GRCm38)	missense	probably damaging	1.00
R8964:Herc1	UTSW	9	66,445,590 (GRCm38)	missense	probably damaging	1.00
R9056:Herc1	UTSW	9	66,473,500 (GRCm38)	missense	probably benign	0.10
R9158:Herc1	UTSW	9	66,469,118 (GRCm38)	missense	probably benign	0.00
R9167:Herc1	UTSW	9	66,504,618 (GRCm38)	missense	possibly damaging	0.75
R9192:Herc1	UTSW	9	66,414,131 (GRCm38)	missense	probably benign	0.35
R9252:Herc1	UTSW	9	66,402,552 (GRCm38)	missense	probably damaging	1.00
R9260:Herc1	UTSW	9	66,418,409 (GRCm38)	nonsense	probably null
R9261:Herc1	UTSW	9	66,504,847 (GRCm38)	missense	probably damaging	0.98
R9430:Herc1	UTSW	9	66,418,503 (GRCm38)	nonsense	probably null
R9519:Herc1	UTSW	9	66,400,074 (GRCm38)	missense	probably damaging	0.97
R9589:Herc1	UTSW	9	66,465,558 (GRCm38)	missense	possibly damaging	0.95
R9600:Herc1	UTSW	9	66,397,312 (GRCm38)	missense	possibly damaging	0.95
R9659:Herc1	UTSW	9	66,399,903 (GRCm38)	missense	probably benign	0.03
R9740:Herc1	UTSW	9	66,448,514 (GRCm38)	missense	probably damaging	1.00
R9774:Herc1	UTSW	9	66,464,750 (GRCm38)	missense	probably null
R9781:Herc1	UTSW	9	66,372,722 (GRCm38)	missense	probably benign
R9788:Herc1	UTSW	9	66,399,903 (GRCm38)	missense	probably benign	0.03
RF023:Herc1	UTSW	9	66,458,334 (GRCm38)	missense
X0011:Herc1	UTSW	9	66,400,159 (GRCm38)	missense	probably benign	0.28
X0067:Herc1	UTSW	9	66,448,524 (GRCm38)	missense	probably benign	0.03
Z1176:Herc1	UTSW	9	66,434,576 (GRCm38)	missense	probably benign
Z1177:Herc1	UTSW	9	66,471,911 (GRCm38)	missense	probably damaging	0.99
Z1177:Herc1	UTSW	9	66,458,425 (GRCm38)	missense	probably null

Predicted Primers

PCR Primer
(F):5'- GAGCCTCACCGGTCTATTAAG -3'
(R):5'- GACTAACCTCACATGTCCCC -3'

Sequencing Primer
(F):5'- CCTCACCGGTCTATTAAGAAAGTTTC -3'
(R):5'- TAACCTCACATGTCCCCACACAC -3'

Posted On

2022-08-09