Mutagenetix > Incidental Mutation

Incidental Mutation 'R1928:Hectd2'

215122

Institutional Source

Beutler Lab

Gene Symbol

Hectd2

Ensembl Gene

ENSMUSG00000041180

Gene Name

HECT domain E3 ubiquitin protein ligase 2

Synonyms

A630025O09Rik

MMRRC Submission

039946-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1928 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

36532039-36598535 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 36589719 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Histidine at position 615 (Y615H)

Ref Sequence

ENSEMBL: ENSMUSP00000128387 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000047247] [ENSMUST00000139215] [ENSMUST00000169036] [ENSMUST00000177381]

AlphaFold

Q8CDU6

Predicted Effect

probably damaging
Transcript: ENSMUST00000047247
AA Change: Y614H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000042646
Gene: ENSMUSG00000041180
AA Change: Y614H

Domain	Start	End	E-Value	Type
low complexity region	10	36	N/A	INTRINSIC
low complexity region	55	65	N/A	INTRINSIC
low complexity region	109	128	N/A	INTRINSIC
low complexity region	270	281	N/A	INTRINSIC
low complexity region	314	327	N/A	INTRINSIC
HECTc	433	774	1.33e-115	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000139215

SMART Domains

Protein: ENSMUSP00000117273
Gene: ENSMUSG00000041180

Domain	Start	End	E-Value	Type
low complexity region	10	36	N/A	INTRINSIC
low complexity region	55	65	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000142404

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000149601

Predicted Effect

probably benign
Transcript: ENSMUST00000155594

SMART Domains

Protein: ENSMUSP00000120791
Gene: ENSMUSG00000041180

Domain	Start	End	E-Value	Type
low complexity region	28	38	N/A	INTRINSIC
low complexity region	82	101	N/A	INTRINSIC
low complexity region	243	254	N/A	INTRINSIC
low complexity region	287	300	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000169036
AA Change: Y615H

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000128387
Gene: ENSMUSG00000041180
AA Change: Y615H

Domain	Start	End	E-Value	Type
low complexity region	10	36	N/A	INTRINSIC
low complexity region	55	65	N/A	INTRINSIC
low complexity region	109	128	N/A	INTRINSIC
low complexity region	270	281	N/A	INTRINSIC
low complexity region	314	327	N/A	INTRINSIC
HECTc	434	775	1.33e-115	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000177381

SMART Domains

Protein: ENSMUSP00000134964
Gene: ENSMUSG00000041180

Domain	Start	End	E-Value	Type
low complexity region	87	98	N/A	INTRINSIC
low complexity region	131	144	N/A	INTRINSIC

Meta Mutation Damage Score

0.9271

Coding Region Coverage

1x: 97.5%
3x: 96.9%
10x: 95.4%
20x: 92.6%

Validation Efficiency

98% (120/123)

Allele List at MGI

Other mutations in this stock

Total: 117 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A630073D07Rik	T	G	6: 132,603,564 (GRCm39)	Q64P	unknown	Het
Adgrv1	A	T	13: 81,668,905 (GRCm39)	F1830L	probably benign	Het
Anks3	C	T	16: 4,763,918 (GRCm39)		probably null	Het
Aqp12	G	A	1: 92,934,332 (GRCm39)	D70N	probably damaging	Het
B4galnt4	C	T	7: 140,648,061 (GRCm39)	R526*	probably null	Het
Best2	A	G	8: 85,737,882 (GRCm39)	F171S	probably benign	Het
C2cd5	A	T	6: 142,958,956 (GRCm39)	V965D	probably damaging	Het
Cd33	T	C	7: 43,179,303 (GRCm39)	E282G	probably benign	Het
Cep95	C	T	11: 106,681,554 (GRCm39)		probably benign	Het
Chd6	A	T	2: 160,809,920 (GRCm39)		probably benign	Het
Clec4d	A	T	6: 123,244,120 (GRCm39)		probably null	Het
Cntd1	C	T	11: 101,174,678 (GRCm39)	S128L	probably damaging	Het
Col19a1	T	C	1: 24,490,835 (GRCm39)		probably benign	Het
Ctrb1	C	A	8: 112,415,324 (GRCm39)	V117L	probably benign	Het
Dclk1	T	C	3: 55,154,942 (GRCm39)	V124A	possibly damaging	Het
Dcp2	T	C	18: 44,538,638 (GRCm39)		probably null	Het
Dctn1	C	A	6: 83,176,166 (GRCm39)		probably benign	Het
Dennd11	A	G	6: 40,388,648 (GRCm39)	F238L	probably benign	Het
Ephb3	T	A	16: 21,041,045 (GRCm39)	M701K	possibly damaging	Het
Ero1b	A	G	13: 12,616,648 (GRCm39)	E359G	probably damaging	Het
Exosc8	G	T	3: 54,636,266 (GRCm39)	A255E	probably damaging	Het
Fhip1a	G	A	3: 85,595,838 (GRCm39)	P349L	probably damaging	Het
Fndc3c1	C	T	X: 105,477,128 (GRCm39)	A824T	probably benign	Het
Gja10	G	A	4: 32,601,812 (GRCm39)	Q191*	probably null	Het
Gm1587	C	T	14: 78,036,288 (GRCm39)	R6Q	unknown	Het
Gm3409	A	G	5: 146,476,418 (GRCm39)	I190V	probably benign	Het
Gm4952	G	T	19: 12,600,973 (GRCm39)	M64I	probably damaging	Het
Gramd1b	C	T	9: 40,217,765 (GRCm39)	M595I	possibly damaging	Het
Grik1	C	T	16: 87,848,241 (GRCm39)	V176M	probably damaging	Het
Grin2b	A	G	6: 136,021,044 (GRCm39)	C86R	probably damaging	Het
Gtse1	C	T	15: 85,746,264 (GRCm39)		probably benign	Het
Hydin	T	C	8: 111,229,579 (GRCm39)	F1552S	possibly damaging	Het
Ifi207	A	G	1: 173,557,211 (GRCm39)	V516A	possibly damaging	Het
Igfbp5	G	T	1: 72,913,184 (GRCm39)	P39T	probably damaging	Het
Il23r	T	A	6: 67,400,719 (GRCm39)	D537V	possibly damaging	Het
Invs	A	G	4: 48,390,095 (GRCm39)	Y251C	probably damaging	Het
Isl1	G	T	13: 116,444,953 (GRCm39)	H25Q	probably damaging	Het
Kif13a	A	G	13: 46,966,221 (GRCm39)	L399P	probably damaging	Het
Klhl1	A	G	14: 96,584,225 (GRCm39)	V335A	probably benign	Het
Klhl14	C	A	18: 21,784,843 (GRCm39)	A195S	probably damaging	Het
Lepr	A	G	4: 101,639,927 (GRCm39)		probably benign	Het
Map1b	A	C	13: 99,567,454 (GRCm39)	S1756A	unknown	Het
Med23	C	T	10: 24,785,710 (GRCm39)	A877V	probably benign	Het
Mfsd4b2	T	C	10: 39,797,458 (GRCm39)	Y299C	probably damaging	Het
Mipol1	T	A	12: 57,379,205 (GRCm39)	M221K	probably damaging	Het
Muc4	A	T	16: 32,569,350 (GRCm39)	S137C	probably damaging	Het
Mutyh	T	C	4: 116,673,855 (GRCm39)	Y189H	probably damaging	Het
Nabp2	T	C	10: 128,245,182 (GRCm39)	T21A	possibly damaging	Het
Nalf1	T	C	8: 9,820,217 (GRCm39)	T268A	probably benign	Het
Nell1	T	A	7: 50,350,943 (GRCm39)	V530E	possibly damaging	Het
Npc1	G	C	18: 12,346,435 (GRCm39)	P254A	possibly damaging	Het
Nup153	A	G	13: 46,854,502 (GRCm39)	V530A	probably damaging	Het
Nxpe2	T	C	9: 48,237,914 (GRCm39)	T114A	probably damaging	Het
Or10j5	T	C	1: 172,784,881 (GRCm39)	V173A	probably damaging	Het
Or11h4b	A	G	14: 50,918,872 (GRCm39)	V73A	probably benign	Het
Or7e177	T	C	9: 20,212,354 (GRCm39)	V287A	probably benign	Het
Pabpc1l	T	A	2: 163,874,174 (GRCm39)	I193N	possibly damaging	Het
Pabpc4l	A	G	3: 46,401,066 (GRCm39)	Y193H	probably damaging	Het
Pank1	T	C	19: 34,856,281 (GRCm39)	S66G	probably benign	Het
Pcdhb1	A	T	18: 37,399,233 (GRCm39)	K395*	probably null	Het
Pcna	A	G	2: 132,093,817 (GRCm39)		probably benign	Het
Pgr	T	A	9: 8,903,630 (GRCm39)	Y550*	probably null	Het
Phf11a	A	G	14: 59,519,316 (GRCm39)		probably benign	Het
Pkhd1	A	T	1: 20,151,524 (GRCm39)		probably benign	Het
Pofut2	T	A	10: 77,096,642 (GRCm39)	Y122*	probably null	Het
Pole	A	G	5: 110,475,644 (GRCm39)	M1818V	probably benign	Het
Rapgef3	A	G	15: 97,647,914 (GRCm39)	L696P	probably damaging	Het
Rasal3	T	C	17: 32,616,327 (GRCm39)	D310G	probably damaging	Het
Rhoq	A	G	17: 87,302,486 (GRCm39)	K141E	probably benign	Het
Rilpl1	A	G	5: 124,652,813 (GRCm39)		probably benign	Het
Rnaseh1	T	C	12: 28,703,088 (GRCm39)	S91P	probably benign	Het
Rsf1	G	GACGGCGGCT	7: 97,229,116 (GRCm39)		probably benign	Het
Saa1	C	A	7: 46,391,856 (GRCm39)	G31W	probably null	Het
Saxo5	T	A	8: 3,536,947 (GRCm39)	I431K	possibly damaging	Het
Scaf8	A	G	17: 3,218,352 (GRCm39)	T241A	unknown	Het
Scarb2	C	T	5: 92,592,125 (GRCm39)	A473T	possibly damaging	Het
Scnn1b	T	C	7: 121,509,670 (GRCm39)	F273S	probably damaging	Het
Sdccag8	T	C	1: 176,656,536 (GRCm39)	V136A	probably damaging	Het
Sdr16c6	A	T	4: 4,069,926 (GRCm39)	V138E	probably damaging	Het
Sf3a3	G	A	4: 124,615,886 (GRCm39)	A180T	possibly damaging	Het
Slc16a5	T	A	11: 115,360,842 (GRCm39)	S342T	probably damaging	Het
Slc18a1	A	G	8: 69,526,464 (GRCm39)	S75P	probably benign	Het
Slc7a6	T	A	8: 106,920,120 (GRCm39)		probably benign	Het
Smco3	G	A	6: 136,808,845 (GRCm39)	Q10*	probably null	Het
Spem2	T	C	11: 69,708,290 (GRCm39)	Q225R	probably benign	Het
Ssb	G	T	2: 69,697,901 (GRCm39)		probably null	Het
Stx8	T	C	11: 68,000,106 (GRCm39)	I182T	probably damaging	Het
Synj2	T	A	17: 6,040,542 (GRCm39)	I121N	probably damaging	Het
Tbc1d1	T	C	5: 64,502,643 (GRCm39)	Y1055H	probably damaging	Het
Thbs3	G	T	3: 89,125,067 (GRCm39)	R52L	probably damaging	Het
Tmem101	C	T	11: 102,044,222 (GRCm39)	V222I	probably benign	Het
Tnks2	C	T	19: 36,823,068 (GRCm39)	Q112*	probably null	Het
Tnrc6b	T	A	15: 80,764,924 (GRCm39)	W809R	probably damaging	Het
Trib2	T	A	12: 15,865,454 (GRCm39)	R16S	probably damaging	Het
Trim12a	T	C	7: 103,956,331 (GRCm39)	N70D	probably damaging	Het
Trim55	T	A	3: 19,716,046 (GRCm39)		probably null	Het
Tspyl5	T	A	15: 33,687,153 (GRCm39)	D264V	probably damaging	Het
Ttn	A	G	2: 76,555,388 (GRCm39)	V30539A	probably damaging	Het
Tubgcp3	A	G	8: 12,713,988 (GRCm39)	F43S	possibly damaging	Het
Tut7	A	G	13: 59,964,548 (GRCm39)	L209P	probably damaging	Het
Ube3d	A	G	9: 86,305,056 (GRCm39)	L262P	probably damaging	Het
Ugt1a7c	T	C	1: 88,023,651 (GRCm39)	V270A	probably benign	Het
Vav3	T	A	3: 109,413,738 (GRCm39)	F225L	possibly damaging	Het
Vmn1r21	G	T	6: 57,821,077 (GRCm39)	Y122*	probably null	Het
Vmn1r225	C	A	17: 20,723,071 (GRCm39)	Q171K	probably benign	Het
Vmn2r103	T	C	17: 20,032,029 (GRCm39)	V601A	possibly damaging	Het
Vmn2r19	T	A	6: 123,308,589 (GRCm39)	N555K	probably damaging	Het
Vps33a	G	A	5: 123,696,684 (GRCm39)	A323V	probably benign	Het
Wdr77	C	T	3: 105,874,618 (GRCm39)	P337S	probably benign	Het
Wnk1	A	T	6: 119,929,884 (GRCm39)	I93N	probably damaging	Het
Zbtb9	T	A	17: 27,193,612 (GRCm39)	I339N	probably damaging	Het
Zfp202	T	A	9: 40,121,083 (GRCm39)	D241E	probably damaging	Het
Zfp235	T	A	7: 23,840,563 (GRCm39)	Y327*	probably null	Het
Zfp820	A	C	17: 22,038,316 (GRCm39)	D337E	probably benign	Het
Zfp944	T	C	17: 22,560,065 (GRCm39)	T14A	probably damaging	Het
Zfy1	A	G	Y: 729,733 (GRCm39)	V303A	unknown	Het
Zfyve26	C	T	12: 79,286,744 (GRCm39)	W2281*	probably null	Het

Other mutations in Hectd2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00515:Hectd2	APN	19	36,562,336 (GRCm39)	missense	probably benign
IGL01024:Hectd2	APN	19	36,583,793 (GRCm39)	missense	probably damaging	1.00
IGL01111:Hectd2	APN	19	36,574,520 (GRCm39)	missense	probably damaging	1.00
IGL01301:Hectd2	APN	19	36,546,770 (GRCm39)	splice site	probably benign
IGL02019:Hectd2	APN	19	36,592,916 (GRCm39)	missense	possibly damaging	0.94
IGL02410:Hectd2	APN	19	36,572,613 (GRCm39)	nonsense	probably null
IGL02793:Hectd2	APN	19	36,564,821 (GRCm39)	missense	probably damaging	0.99
IGL03010:Hectd2	APN	19	36,593,002 (GRCm39)	missense	probably benign	0.01
IGL03115:Hectd2	APN	19	36,577,121 (GRCm39)	critical splice donor site	probably null
IGL03251:Hectd2	APN	19	36,562,926 (GRCm39)	missense	probably damaging	1.00
chopstix1	UTSW	19	36,586,816 (GRCm39)	missense	possibly damaging	0.75
Chopstix3	UTSW	19	36,592,908 (GRCm39)	nonsense	probably null
R0402:Hectd2	UTSW	19	36,578,929 (GRCm39)	critical splice donor site	probably null
R0415:Hectd2	UTSW	19	36,562,284 (GRCm39)	unclassified	probably benign
R0576:Hectd2	UTSW	19	36,562,897 (GRCm39)	missense	probably benign
R0685:Hectd2	UTSW	19	36,546,831 (GRCm39)	missense	probably damaging	0.99
R1460:Hectd2	UTSW	19	36,592,908 (GRCm39)	nonsense	probably null
R1791:Hectd2	UTSW	19	36,586,816 (GRCm39)	missense	possibly damaging	0.75
R1895:Hectd2	UTSW	19	36,591,860 (GRCm39)	missense	probably damaging	1.00
R2116:Hectd2	UTSW	19	36,591,824 (GRCm39)	missense	probably damaging	0.99
R2520:Hectd2	UTSW	19	36,589,633 (GRCm39)	critical splice donor site	probably null
R4693:Hectd2	UTSW	19	36,591,738 (GRCm39)	splice site	probably benign
R4858:Hectd2	UTSW	19	36,582,682 (GRCm39)	missense	probably damaging	0.98
R4943:Hectd2	UTSW	19	36,581,647 (GRCm39)	splice site	probably null
R5031:Hectd2	UTSW	19	36,577,004 (GRCm39)	missense	probably damaging	1.00
R5408:Hectd2	UTSW	19	36,532,296 (GRCm39)	missense	possibly damaging	0.46
R5621:Hectd2	UTSW	19	36,596,151 (GRCm39)	missense	probably damaging	1.00
R5652:Hectd2	UTSW	19	36,581,720 (GRCm39)	missense	probably damaging	1.00
R5704:Hectd2	UTSW	19	36,576,291 (GRCm39)	missense	possibly damaging	0.93
R5950:Hectd2	UTSW	19	36,574,639 (GRCm39)	intron	probably benign
R6414:Hectd2	UTSW	19	36,596,186 (GRCm39)	missense	probably benign	0.21
R6438:Hectd2	UTSW	19	36,596,242 (GRCm39)	makesense	probably null
R6544:Hectd2	UTSW	19	36,589,728 (GRCm39)	missense	probably damaging	1.00
R6545:Hectd2	UTSW	19	36,564,778 (GRCm39)	missense	probably benign	0.35
R6629:Hectd2	UTSW	19	36,592,938 (GRCm39)	missense	probably damaging	1.00
R6672:Hectd2	UTSW	19	36,564,780 (GRCm39)	missense	probably damaging	1.00
R6741:Hectd2	UTSW	19	36,589,759 (GRCm39)	missense	probably damaging	1.00
R7117:Hectd2	UTSW	19	36,577,055 (GRCm39)	missense	probably benign	0.29
R7238:Hectd2	UTSW	19	36,574,478 (GRCm39)	missense	probably damaging	0.98
R7555:Hectd2	UTSW	19	36,589,803 (GRCm39)	missense	probably damaging	1.00
R8184:Hectd2	UTSW	19	36,581,754 (GRCm39)	missense	possibly damaging	0.83
R9069:Hectd2	UTSW	19	36,562,862 (GRCm39)	missense	probably benign	0.00
R9149:Hectd2	UTSW	19	36,576,402 (GRCm39)	missense	probably damaging	0.99
R9418:Hectd2	UTSW	19	36,589,574 (GRCm39)	missense	probably benign	0.01
R9514:Hectd2	UTSW	19	36,582,689 (GRCm39)	missense	possibly damaging	0.67

Predicted Primers

PCR Primer
(F):5'- AACATATGGTATCGCCCACC -3'
(R):5'- AGCGCTAAAGTCACATTTCTCTC -3'

Sequencing Primer
(F):5'- GCCCACCAGGTTTTTCAAGAAG -3'
(R):5'- GTGAGGTTCCCATCATGCAC -3'

Posted On

2014-07-14