Mutagenetix > Incidental Mutation

Incidental Mutation 'R3745:Myo3b'

271151

Institutional Source

Beutler Lab

Gene Symbol

Myo3b

Ensembl Gene

ENSMUSG00000042064

Gene Name

myosin IIIB

Synonyms

A430065P19Rik

MMRRC Submission

040731-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R3745 (G1)

Quality Score

197

Status

Validated

Chromosome

Chromosomal Location

70039126-70429198 bp(+) (GRCm38)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 70234485 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000107862 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000060208] [ENSMUST00000112243]

AlphaFold

Q1EG27

Predicted Effect

probably benign
Transcript: ENSMUST00000060208

SMART Domains

Protein: ENSMUSP00000055362
Gene: ENSMUSG00000042064

Domain	Start	End	E-Value	Type
S_TKc	43	309	2.24e-85	SMART
MYSc	353	1075	6.61e-260	SMART
IQ	1075	1097	9.51e1	SMART
IQ	1102	1124	1.73e-5	SMART
low complexity region	1319	1324	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000112243

SMART Domains

Protein: ENSMUSP00000107862
Gene: ENSMUSG00000042064

Domain	Start	End	E-Value	Type
S_TKc	15	281	2.24e-85	SMART
MYSc	325	1047	6.61e-260	SMART
IQ	1047	1069	9.51e1	SMART
IQ	1074	1096	1.73e-5	SMART
low complexity region	1291	1296	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 94.8%

Validation Efficiency

98% (44/45)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes one of the class III myosins. Myosins are ATPases, activated by actin, that move along actin filaments in the cell. This class of myosins are characterized by an amino-terminal kinase domain and shown to be present in photoreceptors. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2014]

Allele List at MGI

Other mutations in this stock

Total: 44 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700012B07Rik	G	T	11: 109,794,154 (GRCm38)	C172*	probably null	Het
Acot9	G	A	X: 155,271,945 (GRCm38)		probably benign	Het
Akap10	A	G	11: 61,915,305 (GRCm38)	V199A	probably benign	Het
Aox4	C	T	1: 58,245,870 (GRCm38)	H594Y	probably damaging	Het
Arhgap35	A	T	7: 16,563,722 (GRCm38)	Y473N	probably damaging	Het
Aspn	G	A	13: 49,566,560 (GRCm38)	E351K	probably damaging	Het
Astn1	G	T	1: 158,502,060 (GRCm38)	A162S	probably damaging	Het
Auts2	A	G	5: 131,476,587 (GRCm38)		probably benign	Het
Cog6	A	T	3: 52,992,819 (GRCm38)	M507K	probably benign	Het
Crct1	C	A	3: 93,014,707 (GRCm38)		probably benign	Het
Cyp2d11	A	C	15: 82,391,855 (GRCm38)	I175S	probably benign	Het
Dclk1	A	G	3: 55,247,442 (GRCm38)	N98D	possibly damaging	Het
Erich5	T	A	15: 34,470,732 (GRCm38)	C36S	probably damaging	Het
F5	A	G	1: 164,186,779 (GRCm38)	I540V	possibly damaging	Het
Fam20a	A	T	11: 109,677,790 (GRCm38)	S303R	probably benign	Het
Fam214a	T	C	9: 75,009,862 (GRCm38)	V581A	probably benign	Het
Fat3	G	A	9: 15,998,271 (GRCm38)	S2145F	probably damaging	Het
Gbp9	C	A	5: 105,105,858 (GRCm38)		probably benign	Het
Gm6408	G	T	5: 146,484,436 (GRCm38)	V292F	probably damaging	Het
Kmt2a	A	G	9: 44,831,340 (GRCm38)		probably benign	Het
Lrriq1	T	C	10: 103,170,856 (GRCm38)	D1136G	probably damaging	Het
Macrod2	C	A	2: 141,810,629 (GRCm38)	T204K	probably damaging	Het
Mlkl	A	G	8: 111,315,567 (GRCm38)		probably benign	Het
Msantd1	T	A	5: 34,923,467 (GRCm38)	V155E	possibly damaging	Het
Nbn	T	A	4: 15,976,163 (GRCm38)	C375S	possibly damaging	Het
Nell2	A	C	15: 95,432,673 (GRCm38)	C231W	probably damaging	Het
Nipbl	A	G	15: 8,358,874 (GRCm38)	S421P	probably benign	Het
Npr3	A	T	15: 11,905,491 (GRCm38)	V50E	probably damaging	Het
Olfr1425	A	G	19: 12,074,380 (GRCm38)	L84P	probably damaging	Het
Pclo	T	C	5: 14,678,421 (GRCm38)		probably benign	Het
Pkn3	A	G	2: 30,090,341 (GRCm38)	K785R	probably damaging	Het
Ppef2	T	A	5: 92,239,151 (GRCm38)		probably benign	Het
Prdm10	T	C	9: 31,340,407 (GRCm38)	I357T	possibly damaging	Het
Prrc2c	G	A	1: 162,698,185 (GRCm38)	T284I	unknown	Het
Psma3	T	C	12: 70,978,748 (GRCm38)	S13P	possibly damaging	Het
Ptch1	T	G	13: 63,524,959 (GRCm38)	E944A	probably benign	Het
Rpl6l	T	C	10: 111,126,365 (GRCm38)		noncoding transcript	Het
Tex11	A	G	X: 100,916,572 (GRCm38)	V522A	probably benign	Het
Thsd7b	A	G	1: 129,678,241 (GRCm38)	E573G	probably benign	Het
Tom1l1	A	G	11: 90,657,741 (GRCm38)	S259P	probably benign	Het
Trpm8	A	G	1: 88,348,327 (GRCm38)	E549G	probably benign	Het
Vmn1r66	C	T	7: 10,274,321 (GRCm38)	A262T	possibly damaging	Het
Zc3h13	T	A	14: 75,330,661 (GRCm38)	D1131E	probably benign	Het
Zfp445	A	C	9: 122,854,726 (GRCm38)	D289E	probably benign	Het

Other mutations in Myo3b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00736:Myo3b	APN	2	70,105,645 (GRCm38)	splice site	probably benign
IGL00959:Myo3b	APN	2	70,314,292 (GRCm38)	missense	probably damaging	1.00
IGL01069:Myo3b	APN	2	70,245,391 (GRCm38)	missense	probably benign	0.22
IGL01116:Myo3b	APN	2	70,289,386 (GRCm38)	missense	probably damaging	1.00
IGL02097:Myo3b	APN	2	70,238,829 (GRCm38)	missense	probably damaging	1.00
IGL02220:Myo3b	APN	2	70,289,579 (GRCm38)	splice site	probably benign
IGL02553:Myo3b	APN	2	70,095,224 (GRCm38)	missense	probably benign	0.00
IGL02557:Myo3b	APN	2	70,255,319 (GRCm38)	missense	probably benign	0.16
IGL02648:Myo3b	APN	2	70,105,372 (GRCm38)	splice site	probably benign
IGL02902:Myo3b	APN	2	70,289,401 (GRCm38)	missense	probably benign	0.36
IGL02981:Myo3b	APN	2	70,108,625 (GRCm38)	missense	probably damaging	1.00
IGL03030:Myo3b	APN	2	70,426,816 (GRCm38)	splice site	probably benign
IGL03031:Myo3b	APN	2	70,255,377 (GRCm38)	missense	possibly damaging	0.64
IGL03068:Myo3b	APN	2	70,426,816 (GRCm38)	splice site	probably benign
IGL03078:Myo3b	APN	2	70,286,991 (GRCm38)	missense	probably damaging	1.00
IGL03224:Myo3b	APN	2	70,349,939 (GRCm38)	missense	probably benign
IGL03329:Myo3b	APN	2	70,254,459 (GRCm38)	missense	probably damaging	1.00
R0079:Myo3b	UTSW	2	70,095,158 (GRCm38)	missense	possibly damaging	0.58
R0226:Myo3b	UTSW	2	70,217,166 (GRCm38)	missense	probably benign	0.00
R0238:Myo3b	UTSW	2	70,105,425 (GRCm38)	missense	probably benign	0.00
R0238:Myo3b	UTSW	2	70,105,425 (GRCm38)	missense	probably benign	0.00
R0239:Myo3b	UTSW	2	70,105,425 (GRCm38)	missense	probably benign	0.00
R0239:Myo3b	UTSW	2	70,105,425 (GRCm38)	missense	probably benign	0.00
R0313:Myo3b	UTSW	2	70,348,959 (GRCm38)	nonsense	probably null
R0331:Myo3b	UTSW	2	70,095,261 (GRCm38)	missense	probably damaging	1.00
R0371:Myo3b	UTSW	2	70,252,960 (GRCm38)	splice site	probably benign
R0442:Myo3b	UTSW	2	70,238,961 (GRCm38)	critical splice donor site	probably null
R0964:Myo3b	UTSW	2	70,426,849 (GRCm38)	missense	probably damaging	1.00
R1217:Myo3b	UTSW	2	70,330,880 (GRCm38)	missense	probably benign	0.02
R1429:Myo3b	UTSW	2	70,253,007 (GRCm38)	missense	probably damaging	0.97
R1460:Myo3b	UTSW	2	70,232,454 (GRCm38)	missense	probably benign	0.31
R1617:Myo3b	UTSW	2	70,281,218 (GRCm38)	missense	probably benign	0.00
R1628:Myo3b	UTSW	2	70,286,962 (GRCm38)	missense	probably benign	0.01
R1708:Myo3b	UTSW	2	70,245,385 (GRCm38)	nonsense	probably null
R1940:Myo3b	UTSW	2	70,258,075 (GRCm38)	missense	probably benign	0.01
R2407:Myo3b	UTSW	2	70,255,253 (GRCm38)	missense	probably damaging	1.00
R3081:Myo3b	UTSW	2	70,256,583 (GRCm38)	splice site	probably benign
R3687:Myo3b	UTSW	2	70,245,314 (GRCm38)	missense	probably benign
R4011:Myo3b	UTSW	2	70,096,376 (GRCm38)	missense	probably benign	0.15
R4074:Myo3b	UTSW	2	70,289,464 (GRCm38)	missense	probably damaging	1.00
R4419:Myo3b	UTSW	2	70,096,362 (GRCm38)	missense	probably damaging	1.00
R4496:Myo3b	UTSW	2	70,254,404 (GRCm38)	missense	probably benign
R4539:Myo3b	UTSW	2	70,039,147 (GRCm38)	start codon destroyed	probably null	0.00
R4643:Myo3b	UTSW	2	70,238,842 (GRCm38)	missense	possibly damaging	0.49
R4657:Myo3b	UTSW	2	70,238,899 (GRCm38)	missense	possibly damaging	0.95
R4807:Myo3b	UTSW	2	70,105,712 (GRCm38)	missense	probably damaging	1.00
R4849:Myo3b	UTSW	2	70,244,909 (GRCm38)	missense	probably damaging	0.98
R4997:Myo3b	UTSW	2	70,258,083 (GRCm38)	missense	possibly damaging	0.49
R5008:Myo3b	UTSW	2	70,258,068 (GRCm38)	missense	probably damaging	0.99
R5070:Myo3b	UTSW	2	70,253,112 (GRCm38)	missense	probably damaging	1.00
R5072:Myo3b	UTSW	2	70,095,249 (GRCm38)	missense	possibly damaging	0.96
R5082:Myo3b	UTSW	2	70,258,030 (GRCm38)	missense	probably benign	0.01
R5103:Myo3b	UTSW	2	70,096,403 (GRCm38)	missense	probably benign	0.08
R5109:Myo3b	UTSW	2	70,095,293 (GRCm38)	missense	possibly damaging	0.66
R5304:Myo3b	UTSW	2	70,426,888 (GRCm38)	missense	probably damaging	0.97
R5396:Myo3b	UTSW	2	70,126,985 (GRCm38)	missense	probably damaging	0.99
R5400:Myo3b	UTSW	2	70,105,380 (GRCm38)	missense	probably damaging	1.00
R5468:Myo3b	UTSW	2	70,234,441 (GRCm38)	missense	probably benign	0.00
R5620:Myo3b	UTSW	2	70,238,910 (GRCm38)	missense	probably benign	0.04
R5646:Myo3b	UTSW	2	70,314,430 (GRCm38)	missense	probably damaging	0.97
R5729:Myo3b	UTSW	2	70,105,739 (GRCm38)	missense	probably damaging	1.00
R5943:Myo3b	UTSW	2	70,286,941 (GRCm38)	missense	probably benign	0.03
R5971:Myo3b	UTSW	2	70,238,899 (GRCm38)	missense	possibly damaging	0.95
R6091:Myo3b	UTSW	2	70,238,769 (GRCm38)	missense	probably benign	0.00
R6138:Myo3b	UTSW	2	70,238,899 (GRCm38)	missense	possibly damaging	0.95
R6164:Myo3b	UTSW	2	70,245,410 (GRCm38)	critical splice donor site	probably null
R6177:Myo3b	UTSW	2	70,313,363 (GRCm38)	missense	probably benign	0.00
R6421:Myo3b	UTSW	2	70,313,356 (GRCm38)	missense	probably benign	0.02
R6478:Myo3b	UTSW	2	70,348,960 (GRCm38)	missense	probably benign
R6606:Myo3b	UTSW	2	70,232,485 (GRCm38)	missense	possibly damaging	0.94
R6752:Myo3b	UTSW	2	70,289,512 (GRCm38)	missense	probably damaging	1.00
R6982:Myo3b	UTSW	2	70,426,065 (GRCm38)	missense	probably benign	0.02
R6997:Myo3b	UTSW	2	70,126,985 (GRCm38)	missense	probably damaging	0.99
R7032:Myo3b	UTSW	2	70,095,264 (GRCm38)	missense	probably damaging	0.98
R7038:Myo3b	UTSW	2	70,095,208 (GRCm38)	missense	probably benign	0.00
R7062:Myo3b	UTSW	2	70,217,157 (GRCm38)	missense	probably benign	0.00
R7537:Myo3b	UTSW	2	70,217,169 (GRCm38)	missense	probably benign	0.01
R7861:Myo3b	UTSW	2	70,108,688 (GRCm38)	missense	probably damaging	1.00
R7955:Myo3b	UTSW	2	70,095,279 (GRCm38)	missense	probably benign	0.37
R7977:Myo3b	UTSW	2	70,330,933 (GRCm38)	missense	probably benign
R7978:Myo3b	UTSW	2	70,253,114 (GRCm38)	missense	probably damaging	1.00
R7987:Myo3b	UTSW	2	70,330,933 (GRCm38)	missense	probably benign
R8803:Myo3b	UTSW	2	70,252,994 (GRCm38)	missense	probably benign
R8843:Myo3b	UTSW	2	70,257,981 (GRCm38)	missense	probably damaging	1.00
R8896:Myo3b	UTSW	2	70,238,816 (GRCm38)	missense	probably damaging	1.00
R8904:Myo3b	UTSW	2	70,426,908 (GRCm38)	missense	probably benign	0.07
R8909:Myo3b	UTSW	2	70,253,096 (GRCm38)	missense	probably damaging	1.00
R9031:Myo3b	UTSW	2	70,251,750 (GRCm38)	missense	probably damaging	0.99
R9052:Myo3b	UTSW	2	70,232,403 (GRCm38)	missense	probably benign	0.00
R9251:Myo3b	UTSW	2	70,258,081 (GRCm38)	nonsense	probably null
R9268:Myo3b	UTSW	2	70,426,961 (GRCm38)	makesense	probably null
R9334:Myo3b	UTSW	2	70,217,016 (GRCm38)	missense	probably damaging	1.00
R9377:Myo3b	UTSW	2	70,238,898 (GRCm38)	missense	possibly damaging	0.78
R9457:Myo3b	UTSW	2	70,095,209 (GRCm38)	missense	probably benign	0.01
R9520:Myo3b	UTSW	2	70,232,409 (GRCm38)	missense	possibly damaging	0.67
R9593:Myo3b	UTSW	2	70,245,304 (GRCm38)	missense	probably benign	0.43
R9671:Myo3b	UTSW	2	70,256,564 (GRCm38)	missense	probably damaging	1.00
R9790:Myo3b	UTSW	2	70,349,943 (GRCm38)	missense	probably benign	0.35
R9791:Myo3b	UTSW	2	70,349,943 (GRCm38)	missense	probably benign	0.35
U15987:Myo3b	UTSW	2	70,238,899 (GRCm38)	missense	possibly damaging	0.95
X0025:Myo3b	UTSW	2	70,232,403 (GRCm38)	missense	probably benign	0.00
X0065:Myo3b	UTSW	2	70,257,969 (GRCm38)	missense	probably damaging	1.00
Z1177:Myo3b	UTSW	2	70,258,027 (GRCm38)	missense	probably benign	0.01
Z1177:Myo3b	UTSW	2	70,096,361 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GTCCCCTAAGGTGAAAAGCC -3'
(R):5'- GTGTTATGTCTCCCAAAAGGGTC -3'

Sequencing Primer
(F):5'- CCCTAAGGTGAAAAGCCTTGTTTTTC -3'
(R):5'- AAAAGGGTCTTCTCCTTCTCAGG -3'

Posted On

2015-03-18