Mutagenetix > Incidental Mutation

Incidental Mutation 'R0138:Myo7b'

22142

Institutional Source

Beutler Lab

Gene Symbol

Myo7b

Ensembl Gene

ENSMUSG00000024388

Gene Name

myosin VIIB

Synonyms

MMRRC Submission

038423-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0138 (G1)

Quality Score

225

Status

Validated (trace)

Chromosome

Chromosomal Location

31959234-32036961 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 32010151 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Serine at position 165 (T165S)

Ref Sequence

ENSEMBL: ENSMUSP00000118046 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000134663]

AlphaFold

Q99MZ6

Predicted Effect

probably damaging
Transcript: ENSMUST00000134663
AA Change: T165S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000118046
Gene: ENSMUSG00000024388
AA Change: T165S

Domain	Start	End	E-Value	Type
MYSc	59	761	N/A	SMART
IQ	762	784	1.07e-1	SMART
IQ	785	807	7.01e-6	SMART
IQ	831	853	4.93e-1	SMART
IQ	854	876	1.63e-1	SMART
MyTH4	989	1189	1.14e-71	SMART
B41	1190	1409	3.66e-16	SMART
SH3	1501	1563	3.25e-7	SMART
MyTH4	1641	1790	7.66e-55	SMART
B41	1792	2009	8.19e-28	SMART

Meta Mutation Damage Score

0.4096

Coding Region Coverage

1x: 99.0%
3x: 98.3%
10x: 96.4%
20x: 92.8%

Validation Efficiency

97% (76/78)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is found in brush border microvilli of epithelial cells in the intestines and kidneys. The encoded protein is involved in linking protocadherins to the actin cytoskeleton and is essential for proper microvilli function. This protein aids in the accumulation of intermicrovillar adhesion components such as harmonin and ANKS4B, and this accumulation is necessary for normal brush border action. [provided by RefSeq, Jan 2017]

Allele List at MGI

Other mutations in this stock

Total: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca4	T	A	3: 122,105,449 (GRCm38)	N693K	probably damaging	Het
Adgrl3	T	A	5: 81,693,607 (GRCm38)	V845D	probably damaging	Het
Anxa8	T	A	14: 34,097,939 (GRCm38)	F269Y	probably benign	Het
Anxa8	T	A	14: 34,097,940 (GRCm38)	F295L	possibly damaging	Het
Aox4	C	G	1: 58,228,866 (GRCm38)	L202V	probably damaging	Het
Ap3s2	A	G	7: 79,909,869 (GRCm38)	V104A	probably benign	Het
Aqp3	G	A	4: 41,094,843 (GRCm38)		probably benign	Het
Arhgef26	C	T	3: 62,448,259 (GRCm38)	H751Y	probably benign	Het
Asic4	A	T	1: 75,469,687 (GRCm38)	Q291L	possibly damaging	Het
Bap1	T	C	14: 31,256,724 (GRCm38)	Y31H	probably damaging	Het
Brf1	A	T	12: 112,961,139 (GRCm38)	V655D	probably damaging	Het
Cebpz	A	G	17: 78,931,391 (GRCm38)	S663P	probably benign	Het
Ces2h	A	G	8: 105,018,061 (GRCm38)	D357G	probably benign	Het
Cfap36	T	C	11: 29,244,073 (GRCm38)	T90A	probably benign	Het
Ciita	A	T	16: 10,512,270 (GRCm38)	D803V	probably damaging	Het
Clnk	C	A	5: 38,774,608 (GRCm38)		probably benign	Het
Cyp46a1	A	G	12: 108,351,211 (GRCm38)	N158S	probably damaging	Het
Cyp4f13	A	G	17: 32,941,106 (GRCm38)	I98T	possibly damaging	Het
Def8	G	A	8: 123,456,495 (GRCm38)	A278T	probably damaging	Het
Dll3	T	A	7: 28,301,321 (GRCm38)	D103V	possibly damaging	Het
Dnaic1	T	A	4: 41,629,814 (GRCm38)	M446K	possibly damaging	Het
Dppa4	A	T	16: 48,291,062 (GRCm38)	T85S	probably benign	Het
Eif4g1	A	T	16: 20,675,345 (GRCm38)	H57L	probably damaging	Het
Fmnl3	G	C	15: 99,322,738 (GRCm38)		probably benign	Het
Fn1	T	A	1: 71,624,110 (GRCm38)	Q1073L	possibly damaging	Het
Foxp4	T	C	17: 47,869,179 (GRCm38)	D599G	unknown	Het
Frrs1	T	C	3: 116,881,807 (GRCm38)	V128A	possibly damaging	Het
Gcfc2	G	A	6: 81,949,954 (GRCm38)	D608N	probably damaging	Het
Gm1043	T	C	5: 37,192,973 (GRCm38)		probably benign	Het
Gm5148	T	C	3: 37,714,777 (GRCm38)	E98G	probably benign	Het
Gpr141	T	C	13: 19,752,258 (GRCm38)	I116V	probably benign	Het
Hic1	T	C	11: 75,167,343 (GRCm38)	N240S	probably damaging	Het
Hpx	G	A	7: 105,592,238 (GRCm38)	T322I	probably damaging	Het
Hs3st4	A	T	7: 124,397,193 (GRCm38)	M361L	probably benign	Het
Ifrd1	A	G	12: 40,207,130 (GRCm38)		probably benign	Het
Ino80	G	A	2: 119,382,960 (GRCm38)	R1249C	probably damaging	Het
Klk1b21	T	A	7: 44,105,895 (GRCm38)	C173S	probably damaging	Het
Krt25	A	T	11: 99,322,698 (GRCm38)	V65E	probably benign	Het
Lrrc15	A	T	16: 30,273,449 (GRCm38)	D357E	possibly damaging	Het
Lrrd1	T	A	5: 3,851,345 (GRCm38)	V550E	probably benign	Het
Macf1	A	G	4: 123,440,747 (GRCm38)	Y1490H	probably damaging	Het
Macrod1	A	G	19: 7,196,916 (GRCm38)		probably benign	Het
Mcm5	T	A	8: 75,120,880 (GRCm38)	V435D	probably damaging	Het
Mctp1	C	T	13: 76,827,712 (GRCm38)	R478C	probably damaging	Het
Med10	T	C	13: 69,811,698 (GRCm38)		probably benign	Het
Mrpl4	T	C	9: 21,008,592 (GRCm38)	Y280H	probably benign	Het
Msrb3	T	C	10: 120,851,987 (GRCm38)	E61G	probably damaging	Het
Myo1c	T	C	11: 75,661,001 (GRCm38)	Y337H	possibly damaging	Het
Myrfl	T	A	10: 116,849,233 (GRCm38)	R81W	probably damaging	Het
Neil1	T	C	9: 57,143,746 (GRCm38)		probably benign	Het
Neto2	A	G	8: 85,641,044 (GRCm38)	I357T	possibly damaging	Het
Nfat5	C	T	8: 107,339,075 (GRCm38)	R156W	probably damaging	Het
Nkx6-3	T	C	8: 23,153,591 (GRCm38)	S3P	probably benign	Het
Olfr652	A	T	7: 104,565,003 (GRCm38)	I261L	probably benign	Het
Plce1	T	C	19: 38,524,419 (GRCm38)	I54T	possibly damaging	Het
Prex2	A	T	1: 11,285,043 (GRCm38)		probably benign	Het
Psapl1	T	A	5: 36,204,631 (GRCm38)	V189E	probably damaging	Het
Ptdss2	T	G	7: 141,155,319 (GRCm38)		probably benign	Het
Rnf213	T	C	11: 119,416,496 (GRCm38)	C661R	probably benign	Het
Rpap1	T	C	2: 119,764,899 (GRCm38)		probably null	Het
Rrp1b	A	G	17: 32,060,452 (GRCm38)	T696A	probably benign	Het
Sacm1l	T	A	9: 123,548,917 (GRCm38)	H87Q	probably benign	Het
Serpinb11	T	A	1: 107,377,530 (GRCm38)	M212K	probably damaging	Het
Tbc1d22a	C	A	15: 86,299,684 (GRCm38)	T248K	probably damaging	Het
Tcerg1	C	T	18: 42,568,614 (GRCm38)		probably benign	Het
Tpst1	T	A	5: 130,101,786 (GRCm38)	H32Q	probably damaging	Het
Tsc2	A	T	17: 24,599,626 (GRCm38)	V1412E	possibly damaging	Het
Usp19	C	A	9: 108,501,315 (GRCm38)	P1326Q	possibly damaging	Het
Vmn1r235	T	A	17: 21,262,334 (GRCm38)	M307K	probably damaging	Het
Vmn2r58	T	A	7: 41,837,624 (GRCm38)	T616S	probably damaging	Het
Vps13a	G	A	19: 16,660,499 (GRCm38)	T2406I	possibly damaging	Het
Zbtb26	T	A	2: 37,436,041 (GRCm38)	M328L	probably benign	Het
Zp2	A	G	7: 120,137,200 (GRCm38)	F340S	probably damaging	Het

Other mutations in Myo7b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00391:Myo7b	APN	18	32,021,556 (GRCm38)	utr 5 prime	probably benign
IGL01799:Myo7b	APN	18	31,962,770 (GRCm38)	missense	probably damaging	1.00
IGL01881:Myo7b	APN	18	32,000,267 (GRCm38)	splice site	probably benign
IGL01883:Myo7b	APN	18	31,998,151 (GRCm38)	missense	probably damaging	1.00
IGL01934:Myo7b	APN	18	32,001,341 (GRCm38)	critical splice donor site	probably null
IGL01980:Myo7b	APN	18	31,961,900 (GRCm38)	missense	possibly damaging	0.86
IGL02506:Myo7b	APN	18	31,967,154 (GRCm38)	missense	probably damaging	1.00
IGL02704:Myo7b	APN	18	31,966,961 (GRCm38)	missense	probably benign	0.13
IGL02929:Myo7b	APN	18	31,994,925 (GRCm38)	missense	probably benign	0.19
IGL03149:Myo7b	APN	18	32,014,302 (GRCm38)	missense	probably damaging	1.00
IGL03335:Myo7b	APN	18	31,985,020 (GRCm38)	missense	possibly damaging	0.81
IGL03372:Myo7b	APN	18	31,998,601 (GRCm38)	missense	probably damaging	1.00
IGL03385:Myo7b	APN	18	31,989,577 (GRCm38)	missense	probably benign	0.00
PIT4131001:Myo7b	UTSW	18	31,961,206 (GRCm38)	missense	probably benign	0.17
PIT4445001:Myo7b	UTSW	18	31,962,352 (GRCm38)	missense	probably damaging	0.96
PIT4445001:Myo7b	UTSW	18	31,959,466 (GRCm38)	missense	possibly damaging	0.80
R0034:Myo7b	UTSW	18	31,960,860 (GRCm38)	missense	probably damaging	1.00
R0149:Myo7b	UTSW	18	32,014,209 (GRCm38)	missense	probably damaging	1.00
R0226:Myo7b	UTSW	18	31,972,896 (GRCm38)	missense	probably benign	0.00
R0312:Myo7b	UTSW	18	32,014,337 (GRCm38)	missense	possibly damaging	0.68
R0361:Myo7b	UTSW	18	32,014,209 (GRCm38)	missense	probably damaging	1.00
R0506:Myo7b	UTSW	18	31,964,386 (GRCm38)	critical splice donor site	probably null
R0524:Myo7b	UTSW	18	32,013,424 (GRCm38)	missense	possibly damaging	0.91
R0645:Myo7b	UTSW	18	31,994,909 (GRCm38)	missense	probably benign	0.10
R0724:Myo7b	UTSW	18	32,005,549 (GRCm38)	splice site	probably benign
R0731:Myo7b	UTSW	18	31,961,825 (GRCm38)	splice site	probably null
R0762:Myo7b	UTSW	18	31,983,944 (GRCm38)	missense	probably benign	0.01
R0843:Myo7b	UTSW	18	31,974,084 (GRCm38)	missense	possibly damaging	0.83
R0894:Myo7b	UTSW	18	32,000,070 (GRCm38)	missense	probably damaging	1.00
R0966:Myo7b	UTSW	18	31,998,763 (GRCm38)	missense	probably damaging	1.00
R1205:Myo7b	UTSW	18	31,994,342 (GRCm38)	missense	probably damaging	1.00
R1387:Myo7b	UTSW	18	31,983,752 (GRCm38)	splice site	probably benign
R1523:Myo7b	UTSW	18	31,966,876 (GRCm38)	missense	probably damaging	1.00
R1544:Myo7b	UTSW	18	31,994,909 (GRCm38)	missense	probably benign	0.10
R1623:Myo7b	UTSW	18	32,000,051 (GRCm38)	missense	probably damaging	1.00
R1780:Myo7b	UTSW	18	31,961,185 (GRCm38)	missense	probably damaging	1.00
R1785:Myo7b	UTSW	18	31,994,897 (GRCm38)	missense	probably benign
R1786:Myo7b	UTSW	18	31,994,897 (GRCm38)	missense	probably benign
R1796:Myo7b	UTSW	18	31,986,675 (GRCm38)	missense	possibly damaging	0.93
R1907:Myo7b	UTSW	18	31,976,999 (GRCm38)	missense	possibly damaging	0.89
R2027:Myo7b	UTSW	18	31,984,960 (GRCm38)	missense	probably benign
R2102:Myo7b	UTSW	18	31,999,978 (GRCm38)	missense	probably damaging	1.00
R2174:Myo7b	UTSW	18	31,983,557 (GRCm38)	missense	probably damaging	1.00
R2272:Myo7b	UTSW	18	31,977,043 (GRCm38)	missense	probably benign	0.41
R2323:Myo7b	UTSW	18	31,971,345 (GRCm38)	missense	probably damaging	1.00
R2365:Myo7b	UTSW	18	32,014,331 (GRCm38)	missense	probably damaging	0.98
R3078:Myo7b	UTSW	18	31,967,184 (GRCm38)	missense	probably benign	0.04
R3522:Myo7b	UTSW	18	32,010,079 (GRCm38)	missense	probably damaging	1.00
R3788:Myo7b	UTSW	18	31,974,112 (GRCm38)	missense	possibly damaging	0.95
R3880:Myo7b	UTSW	18	31,969,514 (GRCm38)	missense	probably damaging	0.96
R4334:Myo7b	UTSW	18	31,976,987 (GRCm38)	missense	probably damaging	1.00
R4343:Myo7b	UTSW	18	31,983,627 (GRCm38)	missense	probably damaging	1.00
R4497:Myo7b	UTSW	18	32,014,229 (GRCm38)	missense	probably benign	0.06
R4498:Myo7b	UTSW	18	32,014,229 (GRCm38)	missense	probably benign	0.06
R4551:Myo7b	UTSW	18	31,985,108 (GRCm38)	missense	probably benign	0.01
R4593:Myo7b	UTSW	18	32,013,375 (GRCm38)	missense	possibly damaging	0.77
R4616:Myo7b	UTSW	18	32,003,487 (GRCm38)	splice site	probably null
R4646:Myo7b	UTSW	18	31,994,369 (GRCm38)	missense	probably benign	0.25
R4648:Myo7b	UTSW	18	31,967,125 (GRCm38)	splice site	probably null
R4737:Myo7b	UTSW	18	31,998,602 (GRCm38)	missense	probably damaging	1.00
R4765:Myo7b	UTSW	18	31,961,900 (GRCm38)	missense	probably benign	0.00
R4790:Myo7b	UTSW	18	32,000,105 (GRCm38)	splice site	probably null
R4909:Myo7b	UTSW	18	31,964,436 (GRCm38)	missense	probably benign	0.01
R5027:Myo7b	UTSW	18	31,975,212 (GRCm38)	missense	probably benign	0.22
R5034:Myo7b	UTSW	18	31,971,387 (GRCm38)	missense	probably damaging	1.00
R5112:Myo7b	UTSW	18	31,983,587 (GRCm38)	missense	probably damaging	1.00
R5266:Myo7b	UTSW	18	31,998,734 (GRCm38)	missense	probably damaging	1.00
R5267:Myo7b	UTSW	18	31,998,734 (GRCm38)	missense	probably damaging	1.00
R5348:Myo7b	UTSW	18	31,983,919 (GRCm38)	missense	probably damaging	0.96
R5457:Myo7b	UTSW	18	31,971,450 (GRCm38)	splice site	probably null
R5540:Myo7b	UTSW	18	32,007,090 (GRCm38)	missense	probably damaging	1.00
R5628:Myo7b	UTSW	18	31,974,187 (GRCm38)	missense	probably benign
R5815:Myo7b	UTSW	18	31,966,288 (GRCm38)	missense	probably damaging	1.00
R6062:Myo7b	UTSW	18	31,967,990 (GRCm38)	missense	possibly damaging	0.94
R6137:Myo7b	UTSW	18	31,999,974 (GRCm38)	missense	probably damaging	1.00
R6158:Myo7b	UTSW	18	31,988,549 (GRCm38)	missense	probably benign	0.00
R6218:Myo7b	UTSW	18	31,959,454 (GRCm38)	missense	probably benign	0.10
R6256:Myo7b	UTSW	18	31,983,695 (GRCm38)	missense	probably damaging	1.00
R6257:Myo7b	UTSW	18	32,013,415 (GRCm38)	missense	probably damaging	1.00
R6265:Myo7b	UTSW	18	31,998,150 (GRCm38)	missense	probably damaging	1.00
R6302:Myo7b	UTSW	18	31,994,386 (GRCm38)	missense	probably damaging	0.98
R6438:Myo7b	UTSW	18	31,966,329 (GRCm38)	missense	probably damaging	1.00
R6654:Myo7b	UTSW	18	31,990,269 (GRCm38)	missense	possibly damaging	0.46
R7030:Myo7b	UTSW	18	31,971,573 (GRCm38)	missense	probably damaging	1.00
R7090:Myo7b	UTSW	18	31,998,712 (GRCm38)	missense	probably damaging	1.00
R7210:Myo7b	UTSW	18	32,007,102 (GRCm38)	missense	probably damaging	1.00
R7218:Myo7b	UTSW	18	31,981,001 (GRCm38)	missense	probably benign	0.05
R7378:Myo7b	UTSW	18	31,966,239 (GRCm38)	missense	probably damaging	1.00
R7458:Myo7b	UTSW	18	31,988,551 (GRCm38)	missense	possibly damaging	0.89
R7517:Myo7b	UTSW	18	32,013,267 (GRCm38)	missense	probably damaging	0.99
R7559:Myo7b	UTSW	18	31,983,360 (GRCm38)	missense	probably benign	0.01
R7667:Myo7b	UTSW	18	31,961,905 (GRCm38)	missense	probably benign
R7737:Myo7b	UTSW	18	32,014,204 (GRCm38)	nonsense	probably null
R7942:Myo7b	UTSW	18	32,013,369 (GRCm38)	missense	probably damaging	0.98
R8030:Myo7b	UTSW	18	31,998,082 (GRCm38)	missense	probably damaging	0.96
R8114:Myo7b	UTSW	18	31,965,624 (GRCm38)	missense	probably damaging	1.00
R8338:Myo7b	UTSW	18	31,971,355 (GRCm38)	missense	probably damaging	0.96
R8341:Myo7b	UTSW	18	31,983,926 (GRCm38)	missense	probably benign	0.39
R8406:Myo7b	UTSW	18	31,959,813 (GRCm38)	missense	probably damaging	1.00
R8464:Myo7b	UTSW	18	31,962,704 (GRCm38)	missense	probably benign	0.00
R8517:Myo7b	UTSW	18	31,967,191 (GRCm38)	missense	possibly damaging	0.87
R8537:Myo7b	UTSW	18	31,977,089 (GRCm38)	missense	probably benign	0.08
R8546:Myo7b	UTSW	18	31,990,148 (GRCm38)	missense	probably benign	0.19
R8721:Myo7b	UTSW	18	32,007,011 (GRCm38)	missense	probably damaging	1.00
R8770:Myo7b	UTSW	18	31,981,071 (GRCm38)	missense	probably benign	0.03
R8841:Myo7b	UTSW	18	31,964,437 (GRCm38)	missense	probably benign	0.06
R8853:Myo7b	UTSW	18	31,986,691 (GRCm38)	missense	possibly damaging	0.67
R8960:Myo7b	UTSW	18	31,994,246 (GRCm38)	splice site	probably benign
R8984:Myo7b	UTSW	18	31,966,349 (GRCm38)	missense	probably null	0.68
R9356:Myo7b	UTSW	18	31,977,043 (GRCm38)	missense	probably damaging	1.00
R9357:Myo7b	UTSW	18	31,960,076 (GRCm38)	missense	probably damaging	1.00
R9364:Myo7b	UTSW	18	32,000,360 (GRCm38)	missense	probably benign	0.12
R9405:Myo7b	UTSW	18	31,976,303 (GRCm38)	missense	probably benign	0.00
R9533:Myo7b	UTSW	18	31,975,244 (GRCm38)	missense	probably benign	0.27
R9776:Myo7b	UTSW	18	32,000,015 (GRCm38)	missense	probably benign	0.45
X0027:Myo7b	UTSW	18	31,965,636 (GRCm38)	missense	probably damaging	1.00
Z1176:Myo7b	UTSW	18	31,980,998 (GRCm38)	missense	possibly damaging	0.82
Z1177:Myo7b	UTSW	18	31,985,056 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCCCAGCCTTGTGTGAAGGTTATG -3'
(R):5'- GGGACTTCAGAGCAAAGGCATTGTG -3'

Sequencing Primer
(F):5'- ATGACTTGTGCCACGGCTAC -3'
(R):5'- ATTCATGTTAGCATGGCCCAGG -3'

Posted On

2013-04-12