Mutagenetix > Incidental Mutation

Incidental Mutation 'R8887:Hectd4'

677395

Institutional Source

Beutler Lab

Gene Symbol

Hectd4

Ensembl Gene

ENSMUSG00000042744

Gene Name

HECT domain E3 ubiquitin protein ligase 4

Synonyms

Gm15800

MMRRC Submission

068752-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.934) question?

Stock #

R8887 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

121220219-121368577 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 121295478 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 952 (D952G)

Ref Sequence

ENSEMBL: ENSMUSP00000048345 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000042614]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000042614
AA Change: D952G

PolyPhen 2 Score 0.439 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000048345
Gene: ENSMUSG00000042744
AA Change: D952G

Domain	Start	End	E-Value	Type
low complexity region	224	234	N/A	INTRINSIC
low complexity region	266	282	N/A	INTRINSIC
low complexity region	553	564	N/A	INTRINSIC
low complexity region	725	735	N/A	INTRINSIC
low complexity region	1252	1265	N/A	INTRINSIC
coiled coil region	1372	1398	N/A	INTRINSIC
low complexity region	1551	1562	N/A	INTRINSIC
low complexity region	1725	1741	N/A	INTRINSIC
low complexity region	1892	1904	N/A	INTRINSIC
low complexity region	2656	2666	N/A	INTRINSIC
low complexity region	2857	2872	N/A	INTRINSIC
low complexity region	2901	2917	N/A	INTRINSIC
low complexity region	2921	2933	N/A	INTRINSIC
low complexity region	3232	3246	N/A	INTRINSIC
low complexity region	3275	3335	N/A	INTRINSIC
low complexity region	3441	3448	N/A	INTRINSIC
low complexity region	3473	3506	N/A	INTRINSIC
low complexity region	3512	3533	N/A	INTRINSIC
low complexity region	3540	3554	N/A	INTRINSIC
low complexity region	3794	3822	N/A	INTRINSIC
HECTc	4048	4412	4.78e-11	SMART

Predicted Effect

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.5%

Validation Efficiency

98% (93/95)

Allele List at MGI

Other mutations in this stock

Total: 97 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4932438A13Rik	G	T	3: 37,033,354 (GRCm38)	A615S	possibly damaging	Het
Acsbg2	T	C	17: 56,868,285 (GRCm38)	T76A	probably benign	Het
Actn1	A	G	12: 80,168,423 (GRCm38)	C860R	probably damaging	Het
Adam23	T	A	1: 63,515,585 (GRCm38)	L170Q	probably damaging	Het
Afdn	C	T	17: 13,896,139 (GRCm38)	R1620*	probably null	Het
Agfg1	A	G	1: 82,870,804 (GRCm38)		probably benign	Het
Aire	A	G	10: 78,034,464 (GRCm38)	S476P	probably damaging	Het
Arhgef26	A	G	3: 62,339,980 (GRCm38)	T162A	probably benign	Het
Atp1a2	T	C	1: 172,285,655 (GRCm38)	Q487R	probably null	Het
BC048507	T	A	13: 67,863,509 (GRCm38)	C2S	probably benign	Het
Bnc2	A	C	4: 84,291,470 (GRCm38)		probably benign	Het
Bop1	C	T	15: 76,454,324 (GRCm38)	G473R	probably damaging	Het
C1galt1	A	G	6: 7,866,379 (GRCm38)	E75G	probably benign	Het
Cacna1i	T	C	15: 80,374,693 (GRCm38)	V1201A	possibly damaging	Het
Cecr2	C	A	6: 120,738,201 (GRCm38)	T249K	probably damaging	Het
Clca2	C	A	3: 145,085,049 (GRCm38)	G421*	probably null	Het
Clec1b	A	T	6: 129,401,740 (GRCm38)		probably null	Het
Cnksr3	C	T	10: 7,154,467 (GRCm38)	D79N	probably damaging	Het
Col15a1	A	G	4: 47,287,091 (GRCm38)	Q843R	probably damaging	Het
Col6a3	T	C	1: 90,828,226 (GRCm38)	S114G	probably benign	Het
Corin	A	T	5: 72,329,610 (GRCm38)		probably null	Het
Cyp2u1	A	G	3: 131,302,854 (GRCm38)	Y92H	probably damaging	Het
Dcbld2	T	C	16: 58,408,907 (GRCm38)	L51P	probably damaging	Het
Dip2c	T	A	13: 9,623,953 (GRCm38)		probably benign	Het
Dlc1	A	T	8: 36,584,327 (GRCm38)	V299E	probably benign	Het
Dlgap2	G	A	8: 14,179,682 (GRCm38)		probably null	Het
Dnah1	A	G	14: 31,311,040 (GRCm38)	L346P	probably damaging	Het
Dnah9	T	C	11: 65,855,384 (GRCm38)	T3968A	probably benign	Het
Duox2	A	C	2: 122,289,563 (GRCm38)	M822R	probably null	Het
E2f7	A	T	10: 110,774,813 (GRCm38)	Q433L	probably benign	Het
Eif3k	A	C	7: 28,980,476 (GRCm38)	Y42*	probably null	Het
Elmod3	A	G	6: 72,586,511 (GRCm38)	S45P	probably damaging	Het
Emilin3	C	A	2: 160,909,188 (GRCm38)	V214F	possibly damaging	Het
Fbxo10	A	T	4: 45,058,887 (GRCm38)	F283L	probably benign	Het
Fbxw7	T	C	3: 84,969,242 (GRCm38)	Y358H		Het
G430095P16Rik	A	G	8: 84,726,414 (GRCm38)	N10S	unknown	Het
Gldc	A	G	19: 30,133,756 (GRCm38)	V540A	possibly damaging	Het
Gm13084	A	G	4: 143,812,687 (GRCm38)	F79L	probably damaging	Het
Gm3667	T	A	14: 6,874,222 (GRCm38)	E67D	probably benign	Het
Golga3	T	A	5: 110,205,760 (GRCm38)		probably benign	Het
H60c	T	C	10: 3,267,255 (GRCm38)	E38G	probably benign	Het
Hoxb8	T	A	11: 96,284,397 (GRCm38)	L220Q	probably damaging	Het
Ice1	A	T	13: 70,602,931 (GRCm38)	L1679M	probably damaging	Het
Ifi202b	T	A	1: 173,974,914 (GRCm38)	Y118F	probably damaging	Het
Ift122	A	T	6: 115,891,919 (GRCm38)	T456S	probably benign	Het
Ighg3	G	A	12: 113,360,225 (GRCm38)	T181I		Het
Ighv1-66	C	A	12: 115,593,412 (GRCm38)	V17F	probably damaging	Het
Ighv5-12-4	A	G	12: 113,762,510 (GRCm38)	V31A	possibly damaging	Het
Ints12	T	A	3: 133,109,242 (GRCm38)	N403K	probably damaging	Het
Itpr3	G	A	17: 27,118,677 (GRCm38)		probably benign	Het
Kalrn	A	C	16: 34,227,126 (GRCm38)	N908K	probably benign	Het
Kctd9	G	A	14: 67,724,567 (GRCm38)	V20I	unknown	Het
Krt78	G	T	15: 101,953,311 (GRCm38)	L167M	probably damaging	Het
Ldb1	T	C	19: 46,034,855 (GRCm38)	E206G	probably damaging	Het
Lig1	A	G	7: 13,296,787 (GRCm38)	Y455C	probably damaging	Het
Ltbp1	T	G	17: 75,179,082 (GRCm38)	I34S	probably damaging	Het
Map2	T	C	1: 66,415,599 (GRCm38)	I1216T	possibly damaging	Het
Mex3c	T	C	18: 73,573,729 (GRCm38)	V229A	probably damaging	Het
Mfsd11	T	C	11: 116,854,700 (GRCm38)		probably null	Het
Mroh1	A	G	15: 76,447,274 (GRCm38)	T1233A	probably benign	Het
Myct1	C	T	10: 5,604,208 (GRCm38)	T25I	probably damaging	Het
Nipbl	A	T	15: 8,361,787 (GRCm38)	H234Q	probably damaging	Het
Npc1l1	G	A	11: 6,225,665 (GRCm38)	P549S	probably damaging	Het
Olfr102	A	T	17: 37,313,751 (GRCm38)	L211Q	probably damaging	Het
Olfr1264	A	G	2: 90,021,925 (GRCm38)	V47A	probably benign	Het
Olfr153	A	G	2: 87,532,843 (GRCm38)	D270G	possibly damaging	Het
Olfr190	A	T	16: 59,074,483 (GRCm38)	V199D	possibly damaging	Het
Olfr803	A	T	10: 129,691,503 (GRCm38)	Y179*	probably null	Het
Padi3	A	T	4: 140,796,484 (GRCm38)	C228*	probably null	Het
Palld	T	A	8: 61,533,478 (GRCm38)	D1015V	unknown	Het
Pcna-ps2	A	T	19: 9,284,124 (GRCm38)	Y249F	probably benign	Het
Pelo	C	T	13: 115,088,915 (GRCm38)	C258Y	probably benign	Het
Ppp1r13b	A	T	12: 111,836,996 (GRCm38)		probably benign	Het
Prdm2	A	G	4: 143,134,201 (GRCm38)	W840R	probably damaging	Het
Prkcg	A	G	7: 3,322,341 (GRCm38)	D428G	possibly damaging	Het
Pus7	G	A	5: 23,743,478 (GRCm38)	R571*	probably null	Het
Rab11fip3	A	G	17: 26,067,953 (GRCm38)	C409R	possibly damaging	Het
Rdh13	T	C	7: 4,431,523 (GRCm38)	D186G	probably damaging	Het
Rslcan18	T	A	13: 67,098,729 (GRCm38)	H273L	probably damaging	Het
Rxfp1	T	A	3: 79,651,982 (GRCm38)		probably benign	Het
Sh3bp1	T	A	15: 78,904,340 (GRCm38)		probably null	Het
Siglecg	T	A	7: 43,408,584 (GRCm38)	S9T	probably benign	Het
Slc9a1	T	C	4: 133,411,947 (GRCm38)	F159L	probably benign	Het
Slc9a2	A	G	1: 40,718,849 (GRCm38)	I183V	probably benign	Het
St6galnac4	A	G	2: 32,594,098 (GRCm38)	M103V	probably damaging	Het
Tbc1d30	T	C	10: 121,351,154 (GRCm38)	D42G	possibly damaging	Het
Tlr5	C	A	1: 182,973,767 (GRCm38)	T212K	probably benign	Het
Trim43b	T	G	9: 89,087,589 (GRCm38)	I269L	probably benign	Het
Ttll6	T	C	11: 96,156,666 (GRCm38)	L697P	possibly damaging	Het
Ttn	T	G	2: 76,718,895 (GRCm38)	T31813P	probably damaging	Het
Ttn	A	T	2: 76,741,588 (GRCm38)	D26320E	probably damaging	Het
Uba6	A	G	5: 86,159,202 (GRCm38)		probably null	Het
Usp1	C	G	4: 98,930,948 (GRCm38)	Q216E	probably benign	Het
Vcan	T	C	13: 89,704,907 (GRCm38)	T645A	probably benign	Het
Wdr64	C	A	1: 175,772,284 (GRCm38)	P559H	probably benign	Het
Zfat	T	C	15: 68,184,466 (GRCm38)	Y247C	probably damaging	Het
Zfp979	A	T	4: 147,613,762 (GRCm38)	N163K	probably damaging	Het

Other mutations in Hectd4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00156:Hectd4	APN	5	121,363,870 (GRCm38)	missense	possibly damaging	0.51
IGL00976:Hectd4	APN	5	121,349,106 (GRCm38)	missense	probably benign	0.18
IGL01085:Hectd4	APN	5	121,331,701 (GRCm38)	missense	probably damaging	1.00
IGL01112:Hectd4	APN	5	121,306,950 (GRCm38)	missense	probably benign	0.01
IGL01402:Hectd4	APN	5	121,339,417 (GRCm38)	splice site	probably benign
IGL01474:Hectd4	APN	5	121,336,649 (GRCm38)	missense	possibly damaging	0.53
IGL01503:Hectd4	APN	5	121,318,651 (GRCm38)	missense	probably benign	0.28
IGL01548:Hectd4	APN	5	121,364,660 (GRCm38)	missense	possibly damaging	0.71
IGL01656:Hectd4	APN	5	121,322,700 (GRCm38)	missense	probably damaging	0.99
IGL01756:Hectd4	APN	5	121,344,824 (GRCm38)	missense	probably benign	0.28
IGL01819:Hectd4	APN	5	121,328,418 (GRCm38)	missense	possibly damaging	0.85
IGL02080:Hectd4	APN	5	121,366,606 (GRCm38)	utr 3 prime	probably benign
IGL02488:Hectd4	APN	5	121,292,087 (GRCm38)	missense	probably benign	0.33
IGL02490:Hectd4	APN	5	121,318,613 (GRCm38)	missense	possibly damaging	0.82
IGL02558:Hectd4	APN	5	121,344,785 (GRCm38)	missense	probably benign	0.28
IGL02626:Hectd4	APN	5	121,353,881 (GRCm38)	missense	possibly damaging	0.86
IGL02649:Hectd4	APN	5	121,349,402 (GRCm38)	missense	possibly damaging	0.73
IGL02736:Hectd4	APN	5	121,342,719 (GRCm38)	missense	possibly damaging	0.73
IGL02861:Hectd4	APN	5	121,307,004 (GRCm38)	missense	possibly damaging	0.81
IGL02880:Hectd4	APN	5	121,365,053 (GRCm38)	missense	possibly damaging	0.93
IGL02889:Hectd4	APN	5	121,365,053 (GRCm38)	missense	possibly damaging	0.93
IGL02953:Hectd4	APN	5	121,365,053 (GRCm38)	missense	possibly damaging	0.93
IGL02969:Hectd4	APN	5	121,365,053 (GRCm38)	missense	possibly damaging	0.93
IGL03031:Hectd4	APN	5	121,348,794 (GRCm38)	missense	possibly damaging	0.96
IGL03066:Hectd4	APN	5	121,365,053 (GRCm38)	missense	possibly damaging	0.93
IGL03160:Hectd4	APN	5	121,259,879 (GRCm38)	missense	probably benign
IGL03181:Hectd4	APN	5	121,353,958 (GRCm38)	missense	possibly damaging	0.91
IGL03265:Hectd4	APN	5	121,259,939 (GRCm38)	splice site	probably benign
IGL03375:Hectd4	APN	5	121,328,382 (GRCm38)	missense	possibly damaging	0.72
Achilles	UTSW	5	121,307,381 (GRCm38)	nonsense	probably null
agamemnon	UTSW	5	121,253,858 (GRCm38)	splice site	probably benign
clymnestra	UTSW	5	121,334,375 (GRCm38)	missense	possibly damaging	0.86
hector	UTSW	5	121,315,437 (GRCm38)	missense	probably damaging	1.00
helen	UTSW	5	121,310,663 (GRCm38)	missense	probably damaging	0.97
Merriwether	UTSW	5	121,353,551 (GRCm38)	missense	possibly damaging	0.53
PIT4466001:Hectd4	UTSW	5	121,333,060 (GRCm38)	critical splice donor site	probably null
R0018:Hectd4	UTSW	5	121,254,179 (GRCm38)	missense	possibly damaging	0.53
R0024:Hectd4	UTSW	5	121,308,576 (GRCm38)	missense	possibly damaging	0.92
R0030:Hectd4	UTSW	5	121,262,588 (GRCm38)	nonsense	probably null
R0080:Hectd4	UTSW	5	121,349,372 (GRCm38)	missense	probably benign	0.18
R0110:Hectd4	UTSW	5	121,305,673 (GRCm38)	missense	possibly damaging	0.53
R0110:Hectd4	UTSW	5	121,281,896 (GRCm38)	missense	possibly damaging	0.90
R0115:Hectd4	UTSW	5	121,295,506 (GRCm38)	splice site	probably benign
R0128:Hectd4	UTSW	5	121,349,243 (GRCm38)	missense	possibly damaging	0.86
R0131:Hectd4	UTSW	5	121,333,024 (GRCm38)	missense	probably benign	0.44
R0131:Hectd4	UTSW	5	121,333,024 (GRCm38)	missense	probably benign	0.44
R0132:Hectd4	UTSW	5	121,333,024 (GRCm38)	missense	probably benign	0.44
R0244:Hectd4	UTSW	5	121,329,605 (GRCm38)	missense	probably benign	0.33
R0281:Hectd4	UTSW	5	121,254,251 (GRCm38)	missense	possibly damaging	0.85
R0329:Hectd4	UTSW	5	121,259,864 (GRCm38)	missense	probably benign
R0410:Hectd4	UTSW	5	121,286,266 (GRCm38)	missense	possibly damaging	0.86
R0422:Hectd4	UTSW	5	121,343,082 (GRCm38)	splice site	probably null
R0442:Hectd4	UTSW	5	121,323,982 (GRCm38)	missense	possibly damaging	0.66
R0449:Hectd4	UTSW	5	121,364,590 (GRCm38)	splice site	probably null
R0469:Hectd4	UTSW	5	121,305,673 (GRCm38)	missense	possibly damaging	0.53
R0469:Hectd4	UTSW	5	121,281,896 (GRCm38)	missense	possibly damaging	0.90
R0481:Hectd4	UTSW	5	121,295,506 (GRCm38)	splice site	probably benign
R0510:Hectd4	UTSW	5	121,305,673 (GRCm38)	missense	possibly damaging	0.53
R0510:Hectd4	UTSW	5	121,281,896 (GRCm38)	missense	possibly damaging	0.90
R0520:Hectd4	UTSW	5	121,331,707 (GRCm38)	missense	possibly damaging	0.53
R0534:Hectd4	UTSW	5	121,348,476 (GRCm38)	missense	possibly damaging	0.96
R0603:Hectd4	UTSW	5	121,304,337 (GRCm38)	missense	possibly damaging	0.46
R0617:Hectd4	UTSW	5	121,343,232 (GRCm38)	splice site	probably benign
R0622:Hectd4	UTSW	5	121,348,625 (GRCm38)	missense	possibly damaging	0.53
R0626:Hectd4	UTSW	5	121,277,824 (GRCm38)	missense	probably benign	0.18
R0708:Hectd4	UTSW	5	121,286,463 (GRCm38)	critical splice donor site	probably null
R0710:Hectd4	UTSW	5	121,336,628 (GRCm38)	missense	probably benign	0.08
R0763:Hectd4	UTSW	5	121,307,033 (GRCm38)	unclassified	probably benign
R0764:Hectd4	UTSW	5	121,286,769 (GRCm38)	missense	possibly damaging	0.46
R1123:Hectd4	UTSW	5	121,286,736 (GRCm38)	missense	probably damaging	0.96
R1129:Hectd4	UTSW	5	121,310,599 (GRCm38)	missense	possibly damaging	0.66
R1204:Hectd4	UTSW	5	121,350,485 (GRCm38)	missense	possibly damaging	0.85
R1237:Hectd4	UTSW	5	121,321,507 (GRCm38)	missense	possibly damaging	0.90
R1257:Hectd4	UTSW	5	121,318,624 (GRCm38)	nonsense	probably null
R1391:Hectd4	UTSW	5	121,353,695 (GRCm38)	missense	possibly damaging	0.96
R1395:Hectd4	UTSW	5	121,328,513 (GRCm38)	critical splice donor site	probably null
R1468:Hectd4	UTSW	5	121,349,172 (GRCm38)	missense	possibly damaging	0.65
R1468:Hectd4	UTSW	5	121,349,172 (GRCm38)	missense	possibly damaging	0.65
R1545:Hectd4	UTSW	5	121,323,956 (GRCm38)	missense	possibly damaging	0.87
R1553:Hectd4	UTSW	5	121,349,259 (GRCm38)	missense	probably benign	0.00
R1572:Hectd4	UTSW	5	121,301,878 (GRCm38)	missense	possibly damaging	0.85
R1662:Hectd4	UTSW	5	121,317,245 (GRCm38)	missense	probably benign	0.01
R1705:Hectd4	UTSW	5	121,298,104 (GRCm38)	missense	probably benign
R1715:Hectd4	UTSW	5	121,344,818 (GRCm38)	missense	possibly damaging	0.85
R1728:Hectd4	UTSW	5	121,301,839 (GRCm38)	missense	possibly damaging	0.51
R1736:Hectd4	UTSW	5	121,349,530 (GRCm38)	missense	possibly damaging	0.53
R1768:Hectd4	UTSW	5	121,358,303 (GRCm38)	missense	possibly damaging	0.70
R1775:Hectd4	UTSW	5	121,291,191 (GRCm38)	splice site	probably benign
R1784:Hectd4	UTSW	5	121,301,839 (GRCm38)	missense	possibly damaging	0.51
R1843:Hectd4	UTSW	5	121,297,180 (GRCm38)	missense	possibly damaging	0.53
R1914:Hectd4	UTSW	5	121,322,294 (GRCm38)	missense	probably benign	0.08
R1915:Hectd4	UTSW	5	121,322,294 (GRCm38)	missense	probably benign	0.08
R2024:Hectd4	UTSW	5	121,281,918 (GRCm38)	missense	possibly damaging	0.86
R2103:Hectd4	UTSW	5	121,355,629 (GRCm38)	missense	probably benign	0.04
R2108:Hectd4	UTSW	5	121,333,424 (GRCm38)	missense	possibly damaging	0.72
R2124:Hectd4	UTSW	5	121,318,639 (GRCm38)	missense	probably damaging	0.97
R2150:Hectd4	UTSW	5	121,253,858 (GRCm38)	splice site	probably benign
R2192:Hectd4	UTSW	5	121,315,143 (GRCm38)	missense	possibly damaging	0.46
R2301:Hectd4	UTSW	5	121,353,537 (GRCm38)	missense	probably benign	0.18
R2324:Hectd4	UTSW	5	121,315,437 (GRCm38)	missense	probably damaging	1.00
R2331:Hectd4	UTSW	5	121,320,026 (GRCm38)	missense	probably benign	0.05
R2504:Hectd4	UTSW	5	121,263,967 (GRCm38)	missense	possibly damaging	0.73
R2504:Hectd4	UTSW	5	121,220,620 (GRCm38)	missense	unknown
R2904:Hectd4	UTSW	5	121,292,724 (GRCm38)	splice site	probably benign
R3843:Hectd4	UTSW	5	121,259,873 (GRCm38)	missense	possibly damaging	0.72
R3934:Hectd4	UTSW	5	121,320,101 (GRCm38)	critical splice donor site	probably null
R3944:Hectd4	UTSW	5	121,303,525 (GRCm38)	splice site	probably benign
R4133:Hectd4	UTSW	5	121,277,834 (GRCm38)	critical splice donor site	probably null
R4271:Hectd4	UTSW	5	121,220,504 (GRCm38)	small deletion	probably benign
R4413:Hectd4	UTSW	5	121,350,481 (GRCm38)	missense	possibly damaging	0.53
R4456:Hectd4	UTSW	5	121,308,271 (GRCm38)	missense	possibly damaging	0.65
R4489:Hectd4	UTSW	5	121,286,257 (GRCm38)	missense	possibly damaging	0.73
R4539:Hectd4	UTSW	5	121,314,907 (GRCm38)	nonsense	probably null
R4564:Hectd4	UTSW	5	121,350,431 (GRCm38)	missense	probably benign	0.33
R4582:Hectd4	UTSW	5	121,286,419 (GRCm38)	missense	possibly damaging	0.53
R4629:Hectd4	UTSW	5	121,297,203 (GRCm38)	missense	probably benign	0.01
R4633:Hectd4	UTSW	5	121,349,216 (GRCm38)	missense	probably benign	0.33
R4643:Hectd4	UTSW	5	121,349,055 (GRCm38)	missense	possibly damaging	0.53
R4679:Hectd4	UTSW	5	121,325,251 (GRCm38)	missense	possibly damaging	0.72
R4681:Hectd4	UTSW	5	121,303,615 (GRCm38)	missense	possibly damaging	0.86
R4734:Hectd4	UTSW	5	121,341,977 (GRCm38)	missense	possibly damaging	0.53
R4739:Hectd4	UTSW	5	121,348,442 (GRCm38)	missense	probably benign
R4781:Hectd4	UTSW	5	121,306,107 (GRCm38)	critical splice donor site	probably null
R4860:Hectd4	UTSW	5	121,305,818 (GRCm38)	missense	probably benign	0.04
R4860:Hectd4	UTSW	5	121,305,818 (GRCm38)	missense	probably benign	0.04
R4869:Hectd4	UTSW	5	121,322,672 (GRCm38)	missense	possibly damaging	0.46
R4909:Hectd4	UTSW	5	121,263,891 (GRCm38)	missense	probably benign	0.18
R4922:Hectd4	UTSW	5	121,359,315 (GRCm38)	missense	possibly damaging	0.86
R4925:Hectd4	UTSW	5	121,322,690 (GRCm38)	missense	possibly damaging	0.83
R5004:Hectd4	UTSW	5	121,329,565 (GRCm38)	missense	possibly damaging	0.93
R5004:Hectd4	UTSW	5	121,328,199 (GRCm38)	splice site	probably null
R5129:Hectd4	UTSW	5	121,343,510 (GRCm38)	missense	possibly damaging	0.87
R5217:Hectd4	UTSW	5	121,353,551 (GRCm38)	missense	possibly damaging	0.53
R5267:Hectd4	UTSW	5	121,344,824 (GRCm38)	missense	probably benign	0.28
R5344:Hectd4	UTSW	5	121,343,676 (GRCm38)	missense	probably benign	0.28
R5345:Hectd4	UTSW	5	121,263,974 (GRCm38)	missense	possibly damaging	0.85
R5347:Hectd4	UTSW	5	121,304,448 (GRCm38)	missense	probably benign	0.33
R5360:Hectd4	UTSW	5	121,315,401 (GRCm38)	missense	possibly damaging	0.90
R5363:Hectd4	UTSW	5	121,310,603 (GRCm38)	missense	probably benign	0.04
R5445:Hectd4	UTSW	5	121,266,274 (GRCm38)	missense	probably benign	0.00
R5479:Hectd4	UTSW	5	121,306,948 (GRCm38)	missense	probably benign
R5507:Hectd4	UTSW	5	121,281,101 (GRCm38)	missense	unknown
R5552:Hectd4	UTSW	5	121,342,851 (GRCm38)	missense	possibly damaging	0.96
R5691:Hectd4	UTSW	5	121,348,815 (GRCm38)	missense	possibly damaging	0.85
R5745:Hectd4	UTSW	5	121,353,502 (GRCm38)	missense	possibly damaging	0.96
R5757:Hectd4	UTSW	5	121,348,619 (GRCm38)	missense	possibly damaging	0.72
R5845:Hectd4	UTSW	5	121,307,524 (GRCm38)	critical splice donor site	probably null
R5869:Hectd4	UTSW	5	121,343,225 (GRCm38)	critical splice donor site	probably null
R5913:Hectd4	UTSW	5	121,323,974 (GRCm38)	missense	possibly damaging	0.83
R5920:Hectd4	UTSW	5	121,308,271 (GRCm38)	missense	possibly damaging	0.65
R5943:Hectd4	UTSW	5	121,322,294 (GRCm38)	missense	probably benign	0.01
R6219:Hectd4	UTSW	5	121,308,878 (GRCm38)	missense	possibly damaging	0.92
R6250:Hectd4	UTSW	5	121,339,498 (GRCm38)	missense	possibly damaging	0.85
R6301:Hectd4	UTSW	5	121,254,220 (GRCm38)	missense	possibly damaging	0.91
R6428:Hectd4	UTSW	5	121,350,445 (GRCm38)	missense	possibly damaging	0.53
R6446:Hectd4	UTSW	5	121,334,375 (GRCm38)	missense	possibly damaging	0.86
R6453:Hectd4	UTSW	5	121,350,592 (GRCm38)	missense	probably damaging	1.00
R6513:Hectd4	UTSW	5	121,356,196 (GRCm38)	splice site	probably null
R6540:Hectd4	UTSW	5	121,303,571 (GRCm38)	missense	probably benign	0.33
R6706:Hectd4	UTSW	5	121,320,084 (GRCm38)	missense	possibly damaging	0.92
R6720:Hectd4	UTSW	5	121,307,381 (GRCm38)	nonsense	probably null
R6736:Hectd4	UTSW	5	121,277,725 (GRCm38)	missense	possibly damaging	0.86
R6776:Hectd4	UTSW	5	121,353,511 (GRCm38)	missense	possibly damaging	0.85
R7033:Hectd4	UTSW	5	121,364,568 (GRCm38)	missense	possibly damaging	0.86
R7038:Hectd4	UTSW	5	121,299,597 (GRCm38)	missense	possibly damaging	0.90
R7175:Hectd4	UTSW	5	121,273,629 (GRCm38)	missense	possibly damaging	0.85
R7180:Hectd4	UTSW	5	121,308,342 (GRCm38)	missense	probably benign	0.01
R7234:Hectd4	UTSW	5	121,329,073 (GRCm38)	missense	possibly damaging	0.53
R7253:Hectd4	UTSW	5	121,314,881 (GRCm38)	missense	possibly damaging	0.66
R7349:Hectd4	UTSW	5	121,310,663 (GRCm38)	missense	probably damaging	0.97
R7450:Hectd4	UTSW	5	121,281,932 (GRCm38)	missense	probably benign	0.00
R7467:Hectd4	UTSW	5	121,323,961 (GRCm38)	missense	possibly damaging	0.66
R7475:Hectd4	UTSW	5	121,358,133 (GRCm38)	splice site	probably null
R7482:Hectd4	UTSW	5	121,363,878 (GRCm38)	missense	possibly damaging	0.71
R7512:Hectd4	UTSW	5	121,297,109 (GRCm38)	missense	possibly damaging	0.72
R7525:Hectd4	UTSW	5	121,343,665 (GRCm38)	missense	possibly damaging	0.70
R7559:Hectd4	UTSW	5	121,315,510 (GRCm38)	splice site	probably null
R7560:Hectd4	UTSW	5	121,254,342 (GRCm38)	missense	possibly damaging	0.53
R7561:Hectd4	UTSW	5	121,291,225 (GRCm38)	missense	possibly damaging	0.91
R7576:Hectd4	UTSW	5	121,349,459 (GRCm38)	missense	possibly damaging	0.91
R7584:Hectd4	UTSW	5	121,318,735 (GRCm38)	missense	possibly damaging	0.83
R7648:Hectd4	UTSW	5	121,254,371 (GRCm38)	missense	possibly damaging	0.73
R7663:Hectd4	UTSW	5	121,324,031 (GRCm38)	missense	probably benign	0.06
R7692:Hectd4	UTSW	5	121,321,564 (GRCm38)	missense	possibly damaging	0.46
R7725:Hectd4	UTSW	5	121,220,617 (GRCm38)	missense	unknown
R7731:Hectd4	UTSW	5	121,307,014 (GRCm38)	missense	probably benign	0.00
R7732:Hectd4	UTSW	5	121,336,629 (GRCm38)	missense	probably benign	0.14
R7782:Hectd4	UTSW	5	121,305,721 (GRCm38)	missense	possibly damaging	0.53
R7854:Hectd4	UTSW	5	121,329,568 (GRCm38)	missense	probably benign	0.27
R7898:Hectd4	UTSW	5	121,331,817 (GRCm38)	missense	probably benign	0.18
R7910:Hectd4	UTSW	5	121,254,228 (GRCm38)	missense	possibly damaging	0.86
R7962:Hectd4	UTSW	5	121,310,629 (GRCm38)	missense	probably damaging	0.98
R8003:Hectd4	UTSW	5	121,339,518 (GRCm38)	missense	possibly damaging	0.85
R8098:Hectd4	UTSW	5	121,321,398 (GRCm38)	missense	possibly damaging	0.46
R8110:Hectd4	UTSW	5	121,332,949 (GRCm38)	missense	possibly damaging	0.96
R8118:Hectd4	UTSW	5	121,286,376 (GRCm38)	missense	probably benign	0.33
R8171:Hectd4	UTSW	5	121,318,756 (GRCm38)	missense	possibly damaging	0.82
R8234:Hectd4	UTSW	5	121,339,544 (GRCm38)	missense	possibly damaging	0.72
R8289:Hectd4	UTSW	5	121,266,361 (GRCm38)	missense	possibly damaging	0.53
R8292:Hectd4	UTSW	5	121,317,225 (GRCm38)	missense	possibly damaging	0.66
R8348:Hectd4	UTSW	5	121,220,256 (GRCm38)	start gained	probably benign
R8397:Hectd4	UTSW	5	121,259,894 (GRCm38)	missense	probably damaging	0.98
R8436:Hectd4	UTSW	5	121,343,147 (GRCm38)	missense	probably benign	0.00
R8436:Hectd4	UTSW	5	121,308,358 (GRCm38)	missense	possibly damaging	0.90
R8443:Hectd4	UTSW	5	121,329,109 (GRCm38)	missense	possibly damaging	0.72
R8448:Hectd4	UTSW	5	121,220,256 (GRCm38)	start gained	probably benign
R8516:Hectd4	UTSW	5	121,349,010 (GRCm38)	missense	possibly damaging	0.53
R8519:Hectd4	UTSW	5	121,304,426 (GRCm38)	nonsense	probably null
R8553:Hectd4	UTSW	5	121,353,598 (GRCm38)	missense	possibly damaging	0.73
R8557:Hectd4	UTSW	5	121,310,651 (GRCm38)	missense	possibly damaging	0.66
R8725:Hectd4	UTSW	5	121,350,494 (GRCm38)	missense	probably damaging	1.00
R8751:Hectd4	UTSW	5	121,363,775 (GRCm38)	nonsense	probably null
R8769:Hectd4	UTSW	5	121,281,873 (GRCm38)	missense	possibly damaging	0.53
R8803:Hectd4	UTSW	5	121,323,931 (GRCm38)	missense	probably benign	0.01
R8982:Hectd4	UTSW	5	121,328,242 (GRCm38)	missense	probably benign	0.02
R8988:Hectd4	UTSW	5	121,277,756 (GRCm38)	missense	possibly damaging	0.86
R8991:Hectd4	UTSW	5	121,358,284 (GRCm38)	missense	probably benign	0.33
R8994:Hectd4	UTSW	5	121,303,566 (GRCm38)	missense	probably benign	0.33
R8995:Hectd4	UTSW	5	121,254,359 (GRCm38)	missense	possibly damaging	0.96
R9049:Hectd4	UTSW	5	121,313,892 (GRCm38)	missense	possibly damaging	0.92
R9093:Hectd4	UTSW	5	121,273,614 (GRCm38)	missense	probably benign	0.14
R9106:Hectd4	UTSW	5	121,329,556 (GRCm38)	missense	possibly damaging	0.53
R9137:Hectd4	UTSW	5	121,358,175 (GRCm38)	missense	possibly damaging	0.53
R9146:Hectd4	UTSW	5	121,349,034 (GRCm38)	missense	probably benign	0.33
R9154:Hectd4	UTSW	5	121,253,904 (GRCm38)	missense
R9162:Hectd4	UTSW	5	121,306,979 (GRCm38)	missense	possibly damaging	0.66
R9166:Hectd4	UTSW	5	121,308,627 (GRCm38)	missense	probably damaging	0.96
R9183:Hectd4	UTSW	5	121,299,488 (GRCm38)	missense	possibly damaging	0.51
R9207:Hectd4	UTSW	5	121,295,433 (GRCm38)	missense	possibly damaging	0.86
R9291:Hectd4	UTSW	5	121,348,965 (GRCm38)	missense	probably benign	0.14
R9300:Hectd4	UTSW	5	121,348,889 (GRCm38)	missense	probably benign	0.33
R9314:Hectd4	UTSW	5	121,299,645 (GRCm38)	critical splice donor site	probably null
R9381:Hectd4	UTSW	5	121,334,429 (GRCm38)	missense	possibly damaging	0.53
R9432:Hectd4	UTSW	5	121,322,801 (GRCm38)	missense	probably benign	0.01
R9491:Hectd4	UTSW	5	121,314,918 (GRCm38)	missense	probably damaging	0.97
R9532:Hectd4	UTSW	5	121,364,553 (GRCm38)	missense	probably benign	0.00
R9557:Hectd4	UTSW	5	121,321,554 (GRCm38)	missense	possibly damaging	0.66
R9561:Hectd4	UTSW	5	121,334,469 (GRCm38)	missense	possibly damaging	0.53
R9593:Hectd4	UTSW	5	121,286,781 (GRCm38)	nonsense	probably null
R9704:Hectd4	UTSW	5	121,310,681 (GRCm38)	missense	probably benign	0.00
R9705:Hectd4	UTSW	5	121,310,681 (GRCm38)	missense	probably benign	0.00
R9712:Hectd4	UTSW	5	121,310,681 (GRCm38)	missense	probably benign	0.00
R9713:Hectd4	UTSW	5	121,310,681 (GRCm38)	missense	probably benign	0.00
R9726:Hectd4	UTSW	5	121,310,681 (GRCm38)	missense	probably benign	0.00
R9732:Hectd4	UTSW	5	121,254,191 (GRCm38)	nonsense	probably null
R9750:Hectd4	UTSW	5	121,310,681 (GRCm38)	missense	probably benign	0.00
R9752:Hectd4	UTSW	5	121,334,352 (GRCm38)	missense	possibly damaging	0.85
R9752:Hectd4	UTSW	5	121,310,681 (GRCm38)	missense	probably benign	0.00
R9772:Hectd4	UTSW	5	121,310,681 (GRCm38)	missense	probably benign	0.00
X0026:Hectd4	UTSW	5	121,349,637 (GRCm38)	missense	probably benign	0.04
X0027:Hectd4	UTSW	5	121,321,404 (GRCm38)	missense	probably benign	0.27
Z1088:Hectd4	UTSW	5	121,295,503 (GRCm38)	splice site	probably null
Z1177:Hectd4	UTSW	5	121,358,320 (GRCm38)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- TGGCCACATCATTTCATCTGG -3'
(R):5'- TTTGAAGCGCTGACCACAC -3'

Sequencing Primer
(F):5'- ATGTCCCATCATGTTGTCTTTATGAG -3'
(R):5'- AAGCGCTGACCACACTGGAG -3'

Posted On

2021-08-02