Mutagenetix > Incidental Mutation

Incidental Mutation 'R7537:Myl10'

583641

Institutional Source

Beutler Lab

Gene Symbol

Myl10

Ensembl Gene

ENSMUSG00000005474

Gene Name

myosin, light chain 10, regulatory

Synonyms

PLRLC-C, 1700027I08Rik, PLRLC, PLRLC-A, Mylc2pl, PLRLC-B

MMRRC Submission

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7537 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

136693146-136701094 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to C at 136697971 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Leucine at position 70 (V70L)

Ref Sequence

ENSEMBL: ENSMUSP00000143165 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000005611] [ENSMUST00000196068] [ENSMUST00000196436] [ENSMUST00000197186]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000005611
AA Change: V86L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000005611
Gene: ENSMUSG00000005474
AA Change: V86L

Domain	Start	End	E-Value	Type
EFh	9	37	1.5e-5	SMART
EFh	79	107	3.16e1	SMART
Blast:EFh	115	143	6e-14	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000196068
AA Change: K115N

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

SMART Domains

Protein: ENSMUSP00000142570
Gene: ENSMUSG00000005474
AA Change: K115N

Domain	Start	End	E-Value	Type
Pfam:EF-hand_1	9	37	9.4e-7	PFAM
Pfam:EF-hand_6	9	40	9.1e-7	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000196436
AA Change: V70L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000142495
Gene: ENSMUSG00000005474
AA Change: V70L

Domain	Start	End	E-Value	Type
Pfam:EF-hand_6	1	24	5.4e-3	PFAM
Pfam:EF-hand_8	5	39	1.3e-3	PFAM
Blast:EFh	63	91	1e-11	BLAST
Blast:EFh	99	127	4e-14	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000197186
AA Change: V70L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000143165
Gene: ENSMUSG00000005474
AA Change: V70L

Domain	Start	End	E-Value	Type
Pfam:EF-hand_6	1	24	5.4e-3	PFAM
Pfam:EF-hand_8	5	39	1.3e-3	PFAM
Blast:EFh	63	91	1e-11	BLAST
Blast:EFh	99	127	4e-14	BLAST

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197849

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000199074

Meta Mutation Damage Score

0.0667

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.4%
20x: 97.9%

Validation Efficiency

100% (63/63)

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca4	T	C	3: 122,173,988	L2229P	possibly damaging	Het
Acaca	T	A	11: 84,260,634	M786K	probably damaging	Het
Acta2	G	A	19: 34,252,531	T8I	probably benign	Het
Adap1	T	G	5: 139,293,173	E117D	possibly damaging	Het
Ap5z1	T	C	5: 142,477,298	S746P	probably benign	Het
Appl2	A	G	10: 83,617,428	I208T	possibly damaging	Het
Astn1	G	A	1: 158,667,638		probably null	Het
Astn1	A	G	1: 158,505,386	E346G	possibly damaging	Het
Atp23	T	A	10: 126,868,725	I180L	unknown	Het
Bean1	CT	C	8: 104,182,032		probably null	Het
Cdh23	A	T	10: 60,384,945	I1340N	probably benign	Het
Cdh8	G	A	8: 99,098,885	Q493*	probably null	Het
Ces1g	T	C	8: 93,319,827	I357V	probably benign	Het
Ddx46	A	G	13: 55,650,478	D226G	probably damaging	Het
Eea1	C	T	10: 95,994,905	Q143*	probably null	Het
Erlin2	G	T	8: 27,031,772		probably null	Het
Fat3	T	A	9: 15,938,319	D3929V	probably damaging	Het
Flt3	T	C	5: 147,334,437	D898G	probably damaging	Het
Gm16519	A	G	17: 70,929,356	N100S	probably benign	Het
Gnl1	A	G	17: 35,988,536	H533R	probably damaging	Het
Gphn	A	G	12: 78,504,680	T301A	possibly damaging	Het
Herc2	C	T	7: 56,219,779	R4295*	probably null	Het
Insm2	T	C	12: 55,599,518	S16P	possibly damaging	Het
Jak2	C	T	19: 29,298,637	T778I	probably benign	Het
Lrriq3	A	G	3: 155,101,097	T128A	probably damaging	Het
Lst1	A	G	17: 35,186,944		probably null	Het
Magi1	G	T	6: 93,708,110	Y762*	probably null	Het
Man2b1	T	A	8: 85,090,965	C358*	probably null	Het
Mga	T	C	2: 119,935,551	V1432A	probably damaging	Het
Mmp1a	TG	TGG	9: 7,465,083		probably null	Het
Morc2a	C	T	11: 3,683,566	Q587*	probably null	Het
Mrc2	T	C	11: 105,292,797	I4T	probably benign	Het
Muc16	C	A	9: 18,638,135	V5621F	probably benign	Het
Myo3b	A	G	2: 70,217,169	R340G	probably benign	Het
Nipal3	T	C	4: 135,490,937	Y34C	probably damaging	Het
Nktr	T	A	9: 121,749,279	D804E	unknown	Het
Nlrp4b	A	G	7: 10,714,889	M340V	probably benign	Het
Olfr1039	A	G	2: 86,131,264	V133A	probably benign	Het
Olfr385	T	A	11: 73,589,268	T157S	probably benign	Het
Olfr680-ps1	A	T	7: 105,092,771	M16K	probably benign	Het
Olfr701	G	A	7: 106,818,374	C97Y	probably damaging	Het
Pard3	T	A	8: 127,610,582	N1271K	probably damaging	Het
Pcdhb11	A	T	18: 37,421,619	M1L	possibly damaging	Het
Pclo	T	C	5: 14,682,104	V3540A	unknown	Het
Pemt	A	G	11: 59,976,844	F154S	probably damaging	Het
Ptpn18	G	A	1: 34,473,364	D417N	possibly damaging	Het
Rnpc3	G	T	3: 113,613,832	T376K	probably benign	Het
Rpe65	A	G	3: 159,604,609	Y143C	probably damaging	Het
Sbk2	T	C	7: 4,963,149	E12G	probably benign	Het
Slc2a5	T	C	4: 150,129,069	I106T	possibly damaging	Het
Snx13	A	G	12: 35,085,982	D92G	probably damaging	Het
Sorl1	C	T	9: 41,980,688	V1889I	probably benign	Het
Spag17	A	T	3: 99,939,247	N29I	possibly damaging	Het
Speg	T	C	1: 75,401,464	V878A	probably damaging	Het
Timp4	A	G	6: 115,250,460	S53P	probably damaging	Het
Tssk1	G	T	16: 17,895,084	E244D	probably benign	Het
Usp29	A	C	7: 6,961,220	T21P	possibly damaging	Het
Vmn2r85	A	T	10: 130,422,866	V440E	probably benign	Het
Wdr59	T	C	8: 111,490,369	D270G		Het
Zbbx	G	A	3: 75,085,519	P223S	probably damaging	Het
Zfp936	T	A	7: 43,189,815	C235*	probably null	Het
Zranb3	A	T	1: 128,032,847		probably null	Het

Other mutations in Myl10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03206:Myl10	APN	5	136697942	nonsense	probably null
G1Funyon:Myl10	UTSW	5	136697971	missense	probably benign	0.00
PIT4243001:Myl10	UTSW	5	136694293	missense	probably benign	0.05
R4066:Myl10	UTSW	5	136695450	missense	probably damaging	1.00
R5712:Myl10	UTSW	5	136694238	missense	probably damaging	1.00
R6321:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R6322:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R6566:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R6756:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R6757:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R6894:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R7033:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R7152:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R7242:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R7411:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R7484:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R7535:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R7630:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R7631:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R7635:Myl10	UTSW	5	136700864	missense	probably benign	0.00
R7764:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R7829:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R7969:Myl10	UTSW	5	136700853	critical splice acceptor site	probably null
R8065:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8066:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8067:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8202:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8203:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8204:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8206:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8217:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8248:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8300:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8301:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8343:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8731:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8732:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R8831:Myl10	UTSW	5	136697971	missense	probably benign	0.00
R9324:Myl10	UTSW	5	136700933	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GATGCAGCTGGAGTAGTTCC -3'
(R):5'- TATACCAGGAGGAACGGCTG -3'

Sequencing Primer
(F):5'- CTGCCTAGAATCTTCCAGTGAGG -3'
(R):5'- CAGGAGGAACGGCTGGTTTG -3'

Posted On

2019-10-17