Mutagenetix > Incidental Mutation

Incidental Mutation 'R7422:Dnm1l'

575782

Institutional Source

Beutler Lab

Gene Symbol

Dnm1l

Ensembl Gene

ENSMUSG00000022789

Gene Name

dynamin 1-like

Synonyms

Drp1, python, 6330417M19Rik, Dnmlp1

MMRRC Submission

045500-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7422 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

16130094-16176823 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 16136338 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 411 (I411V)

Ref Sequence

ENSEMBL: ENSMUSP00000111415 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000023477] [ENSMUST00000096229] [ENSMUST00000115749] [ENSMUST00000230022] [ENSMUST00000230980]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000023477

SMART Domains

Protein: ENSMUSP00000023477
Gene: ENSMUSG00000022789

Domain	Start	End	E-Value	Type
DYNc	1	255	9.83e-124	SMART
low complexity region	556	571	N/A	INTRINSIC
GED	602	693	2.52e-45	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000096229

SMART Domains

Protein: ENSMUSP00000093945
Gene: ENSMUSG00000022789

Domain	Start	End	E-Value	Type
DYNc	1	268	1.75e-120	SMART
low complexity region	569	584	N/A	INTRINSIC
GED	615	706	2.52e-45	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000115749
AA Change: I411V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000111415
Gene: ENSMUSG00000022789
AA Change: I411V

Domain	Start	End	E-Value	Type
DYNc	1	261	2.08e-122	SMART
low complexity region	573	588	N/A	INTRINSIC
GED	619	710	2.52e-45	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000230022
AA Change: I436V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

Predicted Effect

probably benign
Transcript: ENSMUST00000230980
AA Change: I540V

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

Meta Mutation Damage Score

0.0716

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.1%
20x: 96.9%

Validation Efficiency

97% (98/101)

MGI Phenotype

FUNCTION: This gene encodes a member of the dynamin family. The encoded protein is localized to the cytoplasm and mitochondrial membrane, is involved in mitochondrial and peroxisomal division, and is essential for mitochondrial fission. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 2. [provided by RefSeq, Feb 2013]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit embryonic lethality at E11.5 with internal hemorrhage and small size. Mice heterozygous for an ENU induced allele have dilated cardiomyopathy and congestive heart failure, homozygous are embryonic lethal with posterior truncation at E11.5. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 99 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2810021J22Rik	T	A	11: 58,771,885 (GRCm39)	C456S	probably damaging	Het
4930524J08Rik	T	C	5: 100,127,068 (GRCm39)		probably benign	Het
Adam28	T	G	14: 68,864,326 (GRCm39)	R492S	probably damaging	Het
Adarb2	G	A	13: 8,807,313 (GRCm39)	A705T	possibly damaging	Het
Adprhl1	T	C	8: 13,272,873 (GRCm39)	D1295G	probably benign	Het
Aldh3b3	A	G	19: 4,016,476 (GRCm39)	I365V	probably benign	Het
Aldh8a1	T	C	10: 21,264,996 (GRCm39)	F208L	possibly damaging	Het
Ap3b1	G	A	13: 94,664,673 (GRCm39)	V871I	unknown	Het
Apol7e	A	T	15: 77,598,552 (GRCm39)	R6*	probably null	Het
Arfgap3	T	C	15: 83,191,150 (GRCm39)	E456G	probably damaging	Het
Arhgef1	T	C	7: 24,615,461 (GRCm39)	L285P	probably benign	Het
Arhgef7	T	A	8: 11,850,861 (GRCm39)	C315S	probably benign	Het
Atp9a	A	T	2: 168,490,513 (GRCm39)	L829Q	probably damaging	Het
Babam2	T	A	5: 31,888,393 (GRCm39)		probably null	Het
Bptf	C	T	11: 106,951,384 (GRCm39)	R2185H	probably damaging	Het
Brd9	A	C	13: 74,102,697 (GRCm39)	M473L	probably benign	Het
C7	T	C	15: 5,041,538 (GRCm39)	H456R	probably benign	Het
Cabp7	C	A	11: 4,688,856 (GRCm39)	A205S	probably damaging	Het
Catsperb	A	G	12: 101,554,293 (GRCm39)	I662M	probably damaging	Het
Ccl21a	T	C	4: 42,773,906 (GRCm39)	M5V	probably benign	Het
Cdyl	G	T	13: 36,042,177 (GRCm39)	R405L	possibly damaging	Het
Cep89	T	C	7: 35,127,672 (GRCm39)	L538P	probably damaging	Het
Cercam	A	G	2: 29,762,892 (GRCm39)	M209V	possibly damaging	Het
Chfr	T	A	5: 110,310,571 (GRCm39)		probably null	Het
Cntnap5c	T	A	17: 58,717,226 (GRCm39)	Y1269*	probably null	Het
Col6a2	G	T	10: 76,439,170 (GRCm39)	C833*	probably null	Het
Cpeb3	T	A	19: 37,151,900 (GRCm39)	I159F	probably benign	Het
Cplx2	G	A	13: 54,526,663 (GRCm39)	E24K	possibly damaging	Het
Ctsb	A	G	14: 63,379,752 (GRCm39)	T332A	probably benign	Het
Cyp2j12	T	A	4: 96,029,222 (GRCm39)	T20S	probably benign	Het
Dcst2	T	A	3: 89,273,993 (GRCm39)	H181Q	probably damaging	Het
Dock5	T	A	14: 68,046,479 (GRCm39)	I768F	probably benign	Het
Ecel1	A	G	1: 87,077,334 (GRCm39)	Y625H	probably damaging	Het
Efl1	T	G	7: 82,330,587 (GRCm39)	S253R	probably damaging	Het
Elmod1	T	A	9: 53,820,127 (GRCm39)	D287V	probably damaging	Het
Fam171a2	T	C	11: 102,329,491 (GRCm39)	S423G	probably benign	Het
Fbxo8	A	T	8: 57,022,317 (GRCm39)		probably null	Het
Flnc	G	T	6: 29,455,470 (GRCm39)	G2040W	probably damaging	Het
Fras1	C	T	5: 96,821,458 (GRCm39)	A1405V	probably benign	Het
Frem3	A	C	8: 81,342,392 (GRCm39)	I1562L	probably benign	Het
Fxr1	C	T	3: 34,103,369 (GRCm39)	A233V	probably damaging	Het
H1f9	A	G	11: 94,859,184 (GRCm39)	R160G	possibly damaging	Het
Helb	A	G	10: 119,944,799 (GRCm39)	F246L	probably damaging	Het
Hoxb6	G	T	11: 96,183,510 (GRCm39)		probably benign	Het
Hspa2	A	G	12: 76,452,884 (GRCm39)	E526G	probably damaging	Het
Hyal5	A	T	6: 24,875,983 (GRCm39)		probably benign	Het
Ints6	A	T	14: 62,942,224 (GRCm39)	V503E	probably benign	Het
Ints9	C	T	14: 65,269,747 (GRCm39)	T479I	possibly damaging	Het
Jag1	C	T	2: 136,926,975 (GRCm39)	R928H	probably benign	Het
Lman2	A	T	13: 55,499,338 (GRCm39)	I179N	probably damaging	Het
Lta	T	C	17: 35,422,805 (GRCm39)	S173G	probably benign	Het
Mki67	G	A	7: 135,300,099 (GRCm39)	P1645L	probably damaging	Het
Mrc2	A	T	11: 105,183,609 (GRCm39)		probably benign	Het
Muc4	T	A	16: 32,754,689 (GRCm38)	M1521K	probably benign	Het
Mucl3	T	A	17: 35,949,312 (GRCm39)	T96S	probably benign	Het
Mylk3	T	G	8: 86,081,873 (GRCm39)	D438A	probably benign	Het
Myo7a	T	A	7: 97,700,833 (GRCm39)		probably null	Het
Nsmce4a	G	T	7: 130,135,547 (GRCm39)	Q342K	probably benign	Het
Or10ac1	A	G	6: 42,515,053 (GRCm39)	I301T	possibly damaging	Het
Or4c124	T	A	2: 89,156,423 (GRCm39)	I34F	probably benign	Het
Or5p60	A	G	7: 107,724,068 (GRCm39)	L134P	probably damaging	Het
Or6c65	A	T	10: 129,604,136 (GRCm39)	Y257F	possibly damaging	Het
Osbpl6	T	A	2: 76,423,730 (GRCm39)	F864L	probably damaging	Het
Pla2g4a	A	G	1: 149,808,438 (GRCm39)	S2P	probably benign	Het
Plce1	T	C	19: 38,640,329 (GRCm39)	L525P	probably damaging	Het
Por	A	T	5: 135,763,773 (GRCm39)	M667L	probably benign	Het
Psma4	T	C	9: 54,862,166 (GRCm39)	Y97H	probably benign	Het
Qtrt1	A	T	9: 21,323,753 (GRCm39)	H126L	probably benign	Het
Rab3a	A	T	8: 71,209,170 (GRCm39)	Y102F	possibly damaging	Het
Rnf212	T	A	5: 108,879,555 (GRCm39)	H87L	probably benign	Het
Rnf216	A	G	5: 143,076,591 (GRCm39)	S98P	probably benign	Het
Ryr1	G	T	7: 28,785,295 (GRCm39)	R1806S	probably benign	Het
Scgb1b3	A	T	7: 31,075,262 (GRCm39)	L37F	probably benign	Het
Sds	T	C	5: 120,617,254 (GRCm39)	S37P	probably damaging	Het
Senp6	A	G	9: 80,021,159 (GRCm39)	R280G	probably damaging	Het
She	T	A	3: 89,761,864 (GRCm39)	I441K	possibly damaging	Het
Slc6a20b	A	G	9: 123,436,682 (GRCm39)	S244P	possibly damaging	Het
Slc9a3	A	T	13: 74,299,004 (GRCm39)	Y141F	probably damaging	Het
Slco6c1	A	T	1: 97,009,207 (GRCm39)	H426Q	probably benign	Het
Smc2	C	A	4: 52,440,301 (GRCm39)	Q16K	probably benign	Het
Sphkap	A	C	1: 83,241,547 (GRCm39)	V1535G	probably benign	Het
Stard9	C	A	2: 120,532,633 (GRCm39)	N2963K	probably benign	Het
Sycp2	C	T	2: 178,035,944 (GRCm39)	A248T	probably damaging	Het
Taar8a	T	C	10: 23,952,762 (GRCm39)	L122P	probably damaging	Het
Tab1	T	A	15: 80,044,445 (GRCm39)	V491E	probably benign	Het
Tanc1	T	C	2: 59,636,688 (GRCm39)	M857T	probably benign	Het
Tcirg1	C	A	19: 3,949,008 (GRCm39)	R427L	possibly damaging	Het
Tmem109	A	C	19: 10,849,124 (GRCm39)	*244G	probably null	Het
Tox2	A	G	2: 163,163,435 (GRCm39)	Y136C		Het
Tubb1	T	C	2: 174,298,825 (GRCm39)	V169A	possibly damaging	Het
Ubr3	T	C	2: 69,783,886 (GRCm39)		probably null	Het
Vmn1r225	T	A	17: 20,723,059 (GRCm39)	F167I	probably benign	Het
Vmn2r65	A	C	7: 84,595,569 (GRCm39)	W372G	probably damaging	Het
Vps13a	A	T	19: 16,727,537 (GRCm39)	D188E	probably damaging	Het
Vsnl1	G	T	12: 11,376,439 (GRCm39)	Q149K	probably benign	Het
Wdr35	A	G	12: 9,054,105 (GRCm39)	N466S	probably benign	Het
Ywhae	T	A	11: 75,650,169 (GRCm39)	S210R	probably damaging	Het
Zfp28	T	A	7: 6,397,748 (GRCm39)	S728T	probably damaging	Het
Zfpm1	A	G	8: 123,063,698 (GRCm39)	D919G	unknown	Het

Other mutations in Dnm1l

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00675:Dnm1l	APN	16	16,151,691 (GRCm39)	critical splice donor site	probably null
IGL00696:Dnm1l	APN	16	16,160,579 (GRCm39)	missense	probably benign
IGL01146:Dnm1l	APN	16	16,132,189 (GRCm39)	missense	probably benign	0.01
IGL01385:Dnm1l	APN	16	16,159,317 (GRCm39)	missense	probably damaging	1.00
IGL01694:Dnm1l	APN	16	16,134,515 (GRCm39)	missense	probably benign	0.08
IGL02250:Dnm1l	APN	16	16,139,550 (GRCm39)	splice site	probably benign
IGL02335:Dnm1l	APN	16	16,160,604 (GRCm39)	intron	probably benign
IGL02345:Dnm1l	APN	16	16,147,758 (GRCm39)	missense	possibly damaging	0.61
IGL02403:Dnm1l	APN	16	16,154,840 (GRCm39)	missense	possibly damaging	0.78
IGL02684:Dnm1l	APN	16	16,139,521 (GRCm39)	missense	possibly damaging	0.95
IGL02869:Dnm1l	APN	16	16,159,288 (GRCm39)	nonsense	probably null
IGL03388:Dnm1l	APN	16	16,131,916 (GRCm39)	splice site	probably benign
welter	UTSW	16	16,139,510 (GRCm39)	missense	probably damaging	1.00
R0068:Dnm1l	UTSW	16	16,141,883 (GRCm39)	missense	probably damaging	1.00
R0068:Dnm1l	UTSW	16	16,141,883 (GRCm39)	missense	probably damaging	1.00
R1259:Dnm1l	UTSW	16	16,141,870 (GRCm39)	missense	possibly damaging	0.67
R1554:Dnm1l	UTSW	16	16,159,290 (GRCm39)	missense	probably benign	0.13
R1756:Dnm1l	UTSW	16	16,160,559 (GRCm39)	critical splice donor site	probably null
R1913:Dnm1l	UTSW	16	16,147,830 (GRCm39)	missense	probably benign	0.45
R2906:Dnm1l	UTSW	16	16,132,175 (GRCm39)	missense	probably damaging	0.96
R2907:Dnm1l	UTSW	16	16,132,175 (GRCm39)	missense	probably damaging	0.96
R3756:Dnm1l	UTSW	16	16,139,476 (GRCm39)	missense	possibly damaging	0.86
R4226:Dnm1l	UTSW	16	16,132,251 (GRCm39)	missense	possibly damaging	0.80
R4414:Dnm1l	UTSW	16	16,160,559 (GRCm39)	critical splice donor site	probably null
R5287:Dnm1l	UTSW	16	16,151,732 (GRCm39)	missense	probably damaging	1.00
R5574:Dnm1l	UTSW	16	16,147,685 (GRCm39)	missense	probably damaging	1.00
R5653:Dnm1l	UTSW	16	16,137,353 (GRCm39)	missense	probably damaging	1.00
R6113:Dnm1l	UTSW	16	16,158,867 (GRCm39)	missense	probably benign	0.00
R6320:Dnm1l	UTSW	16	16,149,952 (GRCm39)	missense	probably damaging	1.00
R6644:Dnm1l	UTSW	16	16,147,737 (GRCm39)	missense	probably benign	0.14
R6995:Dnm1l	UTSW	16	16,147,671 (GRCm39)	nonsense	probably null
R7309:Dnm1l	UTSW	16	16,139,510 (GRCm39)	missense	probably damaging	1.00
R8399:Dnm1l	UTSW	16	16,139,536 (GRCm39)	missense	probably damaging	0.98
R8444:Dnm1l	UTSW	16	16,158,906 (GRCm39)	missense	probably damaging	1.00
R8536:Dnm1l	UTSW	16	16,176,639 (GRCm39)	missense	probably benign	0.00
R9151:Dnm1l	UTSW	16	16,176,668 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- GCTAGACTAATGCCACCTTACAAG -3'
(R):5'- CCTAGTGTGGAGACAGTACACTG -3'

Sequencing Primer
(F):5'- TAATGCCACCTTACAAGATAAAAGG -3'
(R):5'- GGGATACTGTGTTAGACTATTAGCC -3'

Posted On

2019-10-07