Mutagenetix > Incidental Mutation

Incidental Mutation 'R8221:Myl6b'

636706

Institutional Source

Beutler Lab

Gene Symbol

Myl6b

Ensembl Gene

ENSMUSG00000039824

Gene Name

myosin, light polypeptide 6B

Synonyms

5730437E04Rik

MMRRC Submission

067639-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.148) question?

Stock #

R8221 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

128330026-128334554 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 128333209 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Lysine to Arginine at position 11 (K11R)

Ref Sequence

ENSEMBL: ENSMUSP00000026428 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000026428] [ENSMUST00000164181]

AlphaFold

Q8CI43

Predicted Effect

unknown
Transcript: ENSMUST00000026428
AA Change: K11R

SMART Domains

Protein: ENSMUSP00000026428
Gene: ENSMUSG00000039824
AA Change: K11R

Domain	Start	End	E-Value	Type
low complexity region	2	15	N/A	INTRINSIC
low complexity region	31	50	N/A	INTRINSIC
EFh	67	95	5.08e-3	SMART
EFh	144	172	6.38e0	SMART
Blast:EFh	179	207	9e-7	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000164181

SMART Domains

Protein: ENSMUSP00000128803
Gene: ENSMUSG00000090841

Domain	Start	End	E-Value	Type
EFh	11	39	8.98e-4	SMART
EFh	88	116	3.64e1	SMART
EFh	123	151	6.63e1	SMART

Coding Region Coverage

1x: 99.9%
3x: 99.9%
10x: 99.6%
20x: 98.8%

Validation Efficiency

100% (74/74)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Myosin is a hexameric ATPase cellular motor protein. It is composed of two heavy chains, two nonphosphorylatable alkali light chains, and two phosphorylatable regulatory light chains. This gene encodes a myosin alkali light chain expressed in both slow-twitch skeletal muscle and in nonmuscle tissue. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acly	A	G	11: 100,410,576 (GRCm39)	F134S	probably damaging	Het
Acsl5	T	C	19: 55,257,262 (GRCm39)		probably null	Het
Adam29	G	T	8: 56,325,463 (GRCm39)	N330K	probably benign	Het
Adgrv1	A	G	13: 81,677,033 (GRCm39)	S1933P	probably benign	Het
Afap1l2	T	C	19: 56,902,824 (GRCm39)	H785R	probably damaging	Het
Ahnak	T	A	19: 8,987,800 (GRCm39)	L3028*	probably null	Het
Ajuba	T	C	14: 54,807,847 (GRCm39)	T462A	possibly damaging	Het
Ankrd36	A	G	11: 5,534,016 (GRCm39)	N289S	possibly damaging	Het
Ankrd46	A	T	15: 36,486,001 (GRCm39)	L84Q	probably damaging	Het
Ankrd54	T	G	15: 78,940,270 (GRCm39)	D163A	probably damaging	Het
Arhgef28	A	G	13: 98,282,064 (GRCm39)	L10P	probably benign	Het
Atm	A	T	9: 53,367,288 (GRCm39)		probably null	Het
Azin1	G	C	15: 38,492,572 (GRCm39)	F312L	probably damaging	Het
C2cd4c	A	G	10: 79,448,482 (GRCm39)	S222P	probably damaging	Het
Cdyl	A	G	13: 36,000,147 (GRCm39)	T143A	probably benign	Het
Clhc1	G	A	11: 29,503,751 (GRCm39)	V56I	possibly damaging	Het
Cntn4	T	C	6: 106,486,471 (GRCm39)	S300P	probably benign	Het
Col12a1	A	G	9: 79,551,224 (GRCm39)	Y2131H	probably damaging	Het
Cyp3a41b	A	G	5: 145,506,190 (GRCm39)	S287P	probably benign	Het
Dctn4	A	G	18: 60,689,401 (GRCm39)	D424G	probably benign	Het
Dnajb8	C	T	6: 88,199,940 (GRCm39)	R159C	possibly damaging	Het
Dop1b	A	G	16: 93,546,847 (GRCm39)	T284A	probably benign	Het
E330034G19Rik	A	C	14: 24,346,135 (GRCm39)		probably null	Het
Ehhadh	G	A	16: 21,581,373 (GRCm39)	P540S	possibly damaging	Het
Emsy	T	C	7: 98,297,111 (GRCm39)	E24G	probably damaging	Het
F930015N05Rik	A	C	11: 64,326,418 (GRCm39)	L74W	unknown	Het
Fat1	A	G	8: 45,406,390 (GRCm39)	D1047G		Het
Galnt7	A	G	8: 58,005,600 (GRCm39)	V211A	possibly damaging	Het
Gdap2	T	C	3: 100,109,611 (GRCm39)	C543R	unknown	Het
Ghr	A	C	15: 3,362,901 (GRCm39)	D190E	probably benign	Het
Glrx	A	G	13: 75,995,346 (GRCm39)	M89V	probably benign	Het
Gm10323	A	C	13: 67,000,859 (GRCm39)	Y91*	noncoding transcript	Het
Gnb4	A	T	3: 32,644,184 (GRCm39)	D153E	possibly damaging	Het
Gnptab	G	T	10: 88,276,254 (GRCm39)		probably null	Het
Grip2	T	C	6: 91,762,665 (GRCm39)	D193G	possibly damaging	Het
Igsf3	T	C	3: 101,347,038 (GRCm39)	W658R	probably damaging	Het
Ip6k1	T	A	9: 107,923,115 (GRCm39)	F416I	probably benign	Het
Klhl1	T	G	14: 96,517,546 (GRCm39)	T377P	possibly damaging	Het
Lrrc38	G	A	4: 143,077,303 (GRCm39)	G189R	probably damaging	Het
Lrrfip1	T	C	1: 91,042,878 (GRCm39)	S428P	probably benign	Het
Megf10	A	G	18: 57,416,893 (GRCm39)	D754G	probably benign	Het
Mrgprx2	T	A	7: 48,132,527 (GRCm39)	Y97F	probably benign	Het
Msantd2	T	G	9: 37,400,684 (GRCm39)	V22G	probably damaging	Het
Nab2	C	A	10: 127,498,645 (GRCm39)	V475L	probably benign	Het
Npas1	T	C	7: 16,189,890 (GRCm39)	E552G	probably damaging	Het
Pknox2	T	C	9: 36,821,040 (GRCm39)	N274S	possibly damaging	Het
Pmepa1	A	T	2: 173,069,700 (GRCm39)	L247Q	probably damaging	Het
Poll	T	C	19: 45,542,047 (GRCm39)	K420E	probably damaging	Het
Polr2a	A	G	11: 69,628,344 (GRCm39)	V1283A	probably benign	Het
Ppil4	A	T	10: 7,671,444 (GRCm39)	Y36F	probably benign	Het
Pramel20	T	G	4: 143,298,530 (GRCm39)	Y158D	probably benign	Het
Psd2	C	T	18: 36,113,478 (GRCm39)	R317W	probably damaging	Het
Pspc1	T	A	14: 57,015,616 (GRCm39)	M1L	probably benign	Het
Qrsl1	A	T	10: 43,758,080 (GRCm39)	F338I	possibly damaging	Het
Rcor3	A	G	1: 191,814,749 (GRCm39)	Y77H	unknown	Het
Sbno2	G	A	10: 79,905,845 (GRCm39)	P157L	probably benign	Het
Scn10a	C	T	9: 119,446,829 (GRCm39)	V1400I	probably damaging	Het
Setd3	C	G	12: 108,073,612 (GRCm39)	G555A	possibly damaging	Het
Slc12a4	A	T	8: 106,678,601 (GRCm39)	M245K	probably benign	Het
Slc1a5	T	A	7: 16,515,902 (GRCm39)	L26Q	probably benign	Het
Slc38a3	T	G	9: 107,534,908 (GRCm39)	M156L	probably damaging	Het
Slc45a2	A	T	15: 11,001,233 (GRCm39)	I111F	probably benign	Het
Slc4a3	T	A	1: 75,528,810 (GRCm39)	M491K	probably benign	Het
Son	A	G	16: 91,453,734 (GRCm39)	D827G	probably damaging	Het
Sppl2c	A	T	11: 104,077,710 (GRCm39)	H170L	probably damaging	Het
St6gal2	T	A	17: 55,797,935 (GRCm39)		probably null	Het
Taf4b	T	A	18: 15,031,106 (GRCm39)	L830H	probably damaging	Het
Tex22	A	G	12: 113,038,696 (GRCm39)		probably null	Het
Tiam2	C	T	17: 3,568,860 (GRCm39)	R1669C	probably damaging	Het
Tmprss15	T	A	16: 78,821,223 (GRCm39)	N506I	probably damaging	Het
Topors	A	T	4: 40,260,686 (GRCm39)	I866K	unknown	Het
Trip12	G	T	1: 84,743,771 (GRCm39)	T512K	possibly damaging	Het
Ubr1	T	A	2: 120,791,585 (GRCm39)	H133L	probably damaging	Het
Wwtr1	T	C	3: 57,366,441 (GRCm39)	D422G	probably damaging	Het
Zfp689	A	C	7: 127,043,758 (GRCm39)	C291G	probably damaging	Het
Zfyve9	A	G	4: 108,576,877 (GRCm39)	L68P	possibly damaging	Het
Zswim5	G	T	4: 116,735,219 (GRCm39)	R188L	probably benign	Het

Other mutations in Myl6b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01730:Myl6b	APN	10	128,332,211 (GRCm39)	missense	possibly damaging	0.54
IGL02257:Myl6b	APN	10	128,333,210 (GRCm39)	unclassified	probably benign
PIT4260001:Myl6b	UTSW	10	128,332,175 (GRCm39)	missense	possibly damaging	0.48
R1971:Myl6b	UTSW	10	128,330,512 (GRCm39)	missense	probably damaging	0.98
R5476:Myl6b	UTSW	10	128,333,216 (GRCm39)	unclassified	probably benign
R6361:Myl6b	UTSW	10	128,333,078 (GRCm39)	nonsense	probably null
R7149:Myl6b	UTSW	10	128,333,068 (GRCm39)	critical splice donor site	probably null
R7540:Myl6b	UTSW	10	128,332,149 (GRCm39)	nonsense	probably null
R9435:Myl6b	UTSW	10	128,331,066 (GRCm39)	missense	possibly damaging	0.87

Predicted Primers

PCR Primer
(F):5'- GCACCGCATCTCTGAACTATCC -3'
(R):5'- AGTCCTGAACCATAGGAGGC -3'

Sequencing Primer
(F):5'- TGAACTATCCCTTCCAGATTCACAC -3'
(R):5'- GGCAGACAGGCATAAGTCTCTTC -3'

Posted On

2020-07-13