Mutagenetix > Incidental Mutation

Incidental Mutation 'R7445:Lmntd1'

577226

Institutional Source

Beutler Lab

Gene Symbol

Lmntd1

Ensembl Gene

ENSMUSG00000054966

Gene Name

lamin tail domain containing 1

Synonyms

Ifltd1, 4933403M22Rik, Lmna-rs1

MMRRC Submission

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.053) question?

Stock #

R7445 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

145365134-145614319 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 145429967 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Cysteine at position 82 (S82C)

Ref Sequence

ENSEMBL: ENSMUSP00000107337 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000111706] [ENSMUST00000111708] [ENSMUST00000148739] [ENSMUST00000149666]

AlphaFold

Q9D4C1

Predicted Effect

probably damaging
Transcript: ENSMUST00000111706
AA Change: S32C

PolyPhen 2 Score 0.960 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000107335
Gene: ENSMUSG00000054966
AA Change: S32C

Domain	Start	End	E-Value	Type
Pfam:LTD	121	240	1.1e-18	PFAM
low complexity region	324	340	N/A	INTRINSIC
low complexity region	344	362	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000111708
AA Change: S82C

PolyPhen 2 Score 0.960 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000107337
Gene: ENSMUSG00000054966
AA Change: S82C

Domain	Start	End	E-Value	Type
Pfam:LTD	174	287	1.6e-12	PFAM
low complexity region	374	390	N/A	INTRINSIC
low complexity region	394	412	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000148739

SMART Domains

Protein: ENSMUSP00000120740
Gene: ENSMUSG00000054966

Domain	Start	End	E-Value	Type
Pfam:LTD	24	144	1.2e-18	PFAM
low complexity region	228	244	N/A	INTRINSIC
low complexity region	248	266	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000149666

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

100% (67/67)

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
0610040J01Rik	T	A	5: 63,898,619	S233T	probably damaging	Het
1700034E13Rik	T	A	18: 52,660,481	C29S	probably damaging	Het
1700061G19Rik	G	A	17: 56,882,973	R333Q	possibly damaging	Het
9130409I23Rik	A	G	1: 181,055,012	N113S	possibly damaging	Het
Ank3	A	G	10: 69,992,124	T2208A		Het
Ap4s1	T	C	12: 51,738,641	L132P	probably damaging	Het
Ascl4	C	T	10: 85,928,500	R4C	probably benign	Het
Brd7	A	T	8: 88,361,708	Y18N	probably damaging	Het
Cacna2d3	A	G	14: 29,058,618	S648P	possibly damaging	Het
Camta1	C	T	4: 151,144,291	E695K	possibly damaging	Het
Ccdc28b	A	G	4: 129,622,607	F53L	probably benign	Het
Chaf1a	A	G	17: 56,062,170	D467G	possibly damaging	Het
Cnnm1	G	A	19: 43,440,821	R126H	possibly damaging	Het
Cog5	T	G	12: 31,919,672	S730R	possibly damaging	Het
Col11a1	A	T	3: 114,193,929	E1374D	unknown	Het
Csmd1	A	G	8: 16,158,254	I1229T	possibly damaging	Het
Dnajc30	T	C	5: 135,064,378	L43P	probably damaging	Het
Eif3f	C	T	7: 108,934,658	T76M	unknown	Het
Ermap	G	A	4: 119,188,710	T42I	unknown	Het
Gpd1l	C	T	9: 114,920,674	G25S	probably damaging	Het
Heatr1	G	T	13: 12,431,038	W1632L	possibly damaging	Het
Ice1	T	C	13: 70,596,167	D29G		Het
Ipo8	T	C	6: 148,789,817	D685G	probably benign	Het
Klra10	T	C	6: 130,275,856	T152A	probably benign	Het
Maip1	T	C	1: 57,407,031	S87P	possibly damaging	Het
Mapkapk2	A	G	1: 131,097,519	S3P	unknown	Het
Mei4	A	G	9: 81,890,239	Y35C	possibly damaging	Het
Ms4a14	T	G	19: 11,302,972	K741Q	probably benign	Het
Naip2	A	C	13: 100,161,782	I582S	probably benign	Het
Ncapg2	A	G	12: 116,419,268	I240V	possibly damaging	Het
Ncbp1	T	A	4: 46,149,914	M145K	probably damaging	Het
Nmur2	A	G	11: 56,032,940	F263L	probably damaging	Het
Ntrk2	A	G	13: 58,846,762	E164G	probably benign	Het
Olfr48	T	A	2: 89,844,272	T234S	probably damaging	Het
Olfr705	A	G	7: 106,873,342	L301S	possibly damaging	Het
Olfr785	A	T	10: 129,409,885	D173V	probably benign	Het
P3h2	T	A	16: 25,985,065	Y317F	probably damaging	Het
Pcmtd1	C	T	1: 7,120,420	R38C	probably damaging	Het
Pcyox1	T	C	6: 86,391,679	T286A	possibly damaging	Het
Pdxk	T	C	10: 78,447,967	D131G	probably benign	Het
Ppl	T	C	16: 5,089,068	D1121G	probably damaging	Het
Prkra	T	C	2: 76,633,598	D240G	probably benign	Het
Ptgs1	C	A	2: 36,245,210	N395K	probably benign	Het
Ptprq	A	T	10: 107,590,959	Y1572N	probably damaging	Het
Pyroxd1	A	T	6: 142,358,501	H326L	probably benign	Het
Rapgef5	A	G	12: 117,755,969	D778G	probably benign	Het
Rbm46	T	A	3: 82,864,210	E366V	probably damaging	Het
Rnd1	G	T	15: 98,670,669	H209Q	probably benign	Het
Rnf122	A	T	8: 31,118,500	D32V	possibly damaging	Het
Samd4b	G	A	7: 28,406,456	P446S	probably benign	Het
Slco1a5	C	A	6: 142,259,008	A187S	possibly damaging	Het
Smarca4	G	A	9: 21,686,247	V1436M	probably damaging	Het
Smok2a	G	A	17: 13,226,639	G368R	possibly damaging	Het
Smok3c	T	A	5: 138,064,495	H81Q	probably damaging	Het
Soga3	T	C	10: 29,197,003	S764P	possibly damaging	Het
Stk16	T	C	1: 75,213,652	V245A	probably damaging	Het
Svep1	A	T	4: 58,094,122	N1505K	possibly damaging	Het
Tigd4	G	A	3: 84,595,164	A463T	probably benign	Het
Tmem117	T	C	15: 94,714,918	F112L	probably benign	Het
Tmem72	A	G	6: 116,698,330	I67T	probably benign	Het
Tnik	A	G	3: 28,663,909		probably null	Het
Trav14-2	A	G	14: 53,641,058	Q66R	probably damaging	Het
Trpv6	T	A	6: 41,621,342	D677V	probably damaging	Het
Vgll4	C	T	6: 114,862,196	S278N	unknown	Het
Wdfy4	C	T	14: 33,070,618	W2157*	probably null	Het

Other mutations in Lmntd1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01761:Lmntd1	APN	6	145433722	missense	possibly damaging	0.92
IGL01986:Lmntd1	APN	6	145419807	missense	probably damaging	1.00
IGL02064:Lmntd1	APN	6	145427276	splice site	probably null
IGL02430:Lmntd1	APN	6	145413414	missense	probably benign	0.34
IGL03296:Lmntd1	APN	6	145413477	missense	probably benign	0.23
PIT4514001:Lmntd1	UTSW	6	145427253	frame shift	probably null
R0022:Lmntd1	UTSW	6	145429990	missense	probably benign	0.06
R0050:Lmntd1	UTSW	6	145417476	missense	probably damaging	1.00
R0084:Lmntd1	UTSW	6	145404528	missense	unknown
R0631:Lmntd1	UTSW	6	145430000	missense	probably benign	0.00
R1716:Lmntd1	UTSW	6	145419874	missense	probably damaging	1.00
R1850:Lmntd1	UTSW	6	145413480	missense	probably benign	0.06
R3898:Lmntd1	UTSW	6	145413426	missense	probably benign	0.16
R4411:Lmntd1	UTSW	6	145427277	critical splice donor site	probably null
R5596:Lmntd1	UTSW	6	145413414	missense	probably benign	0.34
R5944:Lmntd1	UTSW	6	145427316	missense	probably damaging	0.99
R6711:Lmntd1	UTSW	6	145543502	missense	probably benign	0.04
R7369:Lmntd1	UTSW	6	145413575	missense	probably damaging	1.00
R7725:Lmntd1	UTSW	6	145543470	missense	probably benign	0.10
R8237:Lmntd1	UTSW	6	145427420	missense	probably damaging	0.99
R8886:Lmntd1	UTSW	6	145417426	missense	probably damaging	1.00
R8935:Lmntd1	UTSW	6	145543503	missense	probably benign	0.10
R9046:Lmntd1	UTSW	6	145419839	missense	probably damaging	0.98
R9258:Lmntd1	UTSW	6	145413530	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GGCCAACCTACTCTATGTGTG -3'
(R):5'- ATTCTGAGTAACACCTCGTGCC -3'

Sequencing Primer
(F):5'- GCCAACCTACTCTATGTGTGATACTG -3'
(R):5'- GAGTAACACCTCGTGCCTCCTG -3'

Posted On

2019-10-07