Mutagenetix > Incidental Mutation

Incidental Mutation 'R1523:Myo7b'

167678

Institutional Source

Beutler Lab

Gene Symbol

Myo7b

Ensembl Gene

ENSMUSG00000024388

Gene Name

myosin VIIB

Synonyms

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R1523 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

31959234-32036961 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 31966876 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 1651 (L1651P)

Ref Sequence

ENSEMBL: ENSMUSP00000118046 (fasta)

Gene Model

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

AlphaFold

Q99MZ6

Predicted Effect

probably damaging
Transcript: ENSMUST00000134663
AA Change: L1651P

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

SMART Domains

Protein: ENSMUSP00000118046
Gene: ENSMUSG00000024388
AA Change: L1651P

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

Coding Region Coverage

1x: 99.2%
3x: 98.3%
10x: 96.3%
20x: 92.9%

Validation Efficiency

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: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700020L24Rik	G	T	11: 83,440,406 (GRCm38)	E48*	probably null	Het
4930503B20Rik	A	G	3: 146,651,109 (GRCm38)	S15P	probably damaging	Het
4933402E13Rik	T	A	X: 62,290,906 (GRCm38)	D177E	probably benign	Het
5530400C23Rik	A	G	6: 133,294,293 (GRCm38)	E100G	possibly damaging	Het
Abcg2	T	C	6: 58,685,694 (GRCm38)	F507S	possibly damaging	Het
Adgrf5	A	T	17: 43,450,153 (GRCm38)	Q913L	probably benign	Het
Ak7	A	T	12: 105,766,608 (GRCm38)	N537I	probably benign	Het
Anks1	T	A	17: 28,051,655 (GRCm38)		probably null	Het
Arhgap32	T	A	9: 32,256,752 (GRCm38)	V677D	probably damaging	Het
Arnt	C	T	3: 95,489,654 (GRCm38)	P466L	possibly damaging	Het
Arrb1	T	G	7: 99,594,665 (GRCm38)	L274R	probably damaging	Het
Atf2	A	T	2: 73,863,208 (GRCm38)	D3E	probably damaging	Het
Baz2b	C	T	2: 59,968,637 (GRCm38)	R381Q	possibly damaging	Het
Cacna1g	C	T	11: 94,442,729 (GRCm38)		probably null	Het
Ccr10	C	T	11: 101,173,675 (GRCm38)	R343Q	probably damaging	Het
Clca2	G	T	3: 145,071,644 (GRCm38)	S822*	probably null	Het
Col12a1	A	T	9: 79,660,996 (GRCm38)	Y1649N	probably benign	Het
Col23a1	G	A	11: 51,561,916 (GRCm38)		probably null	Het
Cp	T	C	3: 19,989,065 (GRCm38)	Y1006H	probably benign	Het
Ctbs	A	G	3: 146,454,980 (GRCm38)	T101A	probably benign	Het
Cyp4a31	T	C	4: 115,569,754 (GRCm38)	F170L	probably benign	Het
Dock1	A	C	7: 134,744,247 (GRCm38)	I173L	possibly damaging	Het
Dock4	A	G	12: 40,693,025 (GRCm38)	D393G	possibly damaging	Het
Dsg1a	T	A	18: 20,322,317 (GRCm38)	S113T	probably damaging	Het
Epha3	T	C	16: 63,610,948 (GRCm38)	D530G	probably damaging	Het
Erbb4	T	A	1: 68,396,252 (GRCm38)	H162L	possibly damaging	Het
Fam131c	C	T	4: 141,382,831 (GRCm38)	T180I	probably benign	Het
Fndc1	A	G	17: 7,773,209 (GRCm38)	S552P	unknown	Het
Foxf1	A	G	8: 121,084,558 (GRCm38)		probably null	Het
Frem2	T	C	3: 53,655,407 (GRCm38)	T560A	possibly damaging	Het
Gabra4	G	A	5: 71,633,632 (GRCm38)	T289M	probably damaging	Het
Gcnt1	A	G	19: 17,329,833 (GRCm38)	V176A	probably damaging	Het
Gemin8	G	A	X: 166,180,648 (GRCm38)	S100N	probably benign	Het
Gm1527	T	C	3: 28,920,418 (GRCm38)	I460T	probably damaging	Het
Gm6729	A	G	10: 86,540,175 (GRCm38)		noncoding transcript	Het
Gprin2	T	C	14: 34,195,079 (GRCm38)	S245G	probably benign	Het
Gsdmc	A	T	15: 63,803,630 (GRCm38)	I112N	probably damaging	Het
Hspb6	A	G	7: 30,553,423 (GRCm38)	D30G	probably benign	Het
Hydin	A	G	8: 110,533,271 (GRCm38)	D2625G	probably benign	Het
Iqca	C	A	1: 90,142,731 (GRCm38)	G133V	probably null	Het
Irf2	T	A	8: 46,837,840 (GRCm38)		probably null	Het
Kdm3b	T	C	18: 34,793,173 (GRCm38)		probably null	Het
Khdc3	G	A	9: 73,103,491 (GRCm38)	E208K	possibly damaging	Het
Kifc1	A	T	17: 33,883,662 (GRCm38)	S263T	probably benign	Het
Lrig3	C	A	10: 126,008,698 (GRCm38)	T677K	probably damaging	Het
Mapkapk3	A	T	9: 107,263,623 (GRCm38)		probably null	Het
Mertk	T	C	2: 128,790,328 (GRCm38)		probably null	Het
Metrn	A	G	17: 25,794,977 (GRCm38)	*292R	probably null	Het
Mllt6	G	T	11: 97,665,023 (GRCm38)	A60S	probably damaging	Het
Mmp21	T	C	7: 133,679,045 (GRCm38)	I65M	probably benign	Het
Nhsl1	A	G	10: 18,408,355 (GRCm38)	S15G	probably benign	Het
Nos1ap	T	C	1: 170,338,118 (GRCm38)	D192G	probably benign	Het
Nrcam	A	G	12: 44,572,249 (GRCm38)	T844A	probably damaging	Het
Pax4	A	G	6: 28,444,841 (GRCm38)	L203P	probably damaging	Het
Pbld2	T	C	10: 63,076,433 (GRCm38)	I280T	probably benign	Het
Pclo	A	G	5: 14,788,406 (GRCm38)	Y4681C	unknown	Het
Phyhip	T	A	14: 70,461,760 (GRCm38)	M1K	probably null	Het
Plppr4	T	C	3: 117,322,841 (GRCm38)	N456D	probably damaging	Het
Prpf31	T	C	7: 3,640,857 (GRCm38)	Y473H	probably damaging	Het
Rapgef2	A	T	3: 79,092,749 (GRCm38)	V564D	probably damaging	Het
Rexo1	T	C	10: 80,542,751 (GRCm38)	S1123G	probably benign	Het
Rnasel	C	A	1: 153,756,013 (GRCm38)	Q513K	probably damaging	Het
Rnf165	G	A	18: 77,462,938 (GRCm38)	T98I	probably benign	Het
Rnf213	T	C	11: 119,441,888 (GRCm38)	V2641A	probably damaging	Het
Rnf40	G	T	7: 127,590,615 (GRCm38)	R184L	probably damaging	Het
Rnf8	A	G	17: 29,626,972 (GRCm38)	K179R	probably damaging	Het
Sipa1l2	C	T	8: 125,447,613 (GRCm38)	D1309N	possibly damaging	Het
Slc25a38	T	A	9: 120,123,703 (GRCm38)	M307K	possibly damaging	Het
Snx33	T	C	9: 56,926,182 (GRCm38)	D201G	possibly damaging	Het
Sulf1	T	A	1: 12,817,350 (GRCm38)	Y249*	probably null	Het
Sult2a4	G	A	7: 13,909,860 (GRCm38)	Q261*	probably null	Het
Syndig1	G	A	2: 150,003,234 (GRCm38)	A226T	probably damaging	Het
Tcaf2	C	T	6: 42,624,451 (GRCm38)	W891*	probably null	Het
Tcf15	C	A	2: 152,143,888 (GRCm38)	T88K	probably damaging	Het
Tmem19	A	T	10: 115,347,217 (GRCm38)	M117K	probably damaging	Het
Trim32	T	C	4: 65,614,004 (GRCm38)	L266P	probably benign	Het
Vmn2r11	T	C	5: 109,053,841 (GRCm38)	I266V	probably benign	Het
Vmn2r73	A	T	7: 85,870,278 (GRCm38)	Y491N	probably benign	Het
Wrn	C	T	8: 33,292,716 (GRCm38)	E486K	probably benign	Het
Zfp457	T	C	13: 67,293,437 (GRCm38)	E262G	probably damaging	Het
Zfp598	A	G	17: 24,678,629 (GRCm38)	D308G	probably null	Het
Zufsp	T	C	10: 33,927,440 (GRCm38)	I549M	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
R0138:Myo7b	UTSW	18	32,010,151 (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
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'- ACTGACCTTTGACCCAGGCTCATAC -3'
(R):5'- GATCAGCTCACAGAGTCGCCATAC -3'

Sequencing Primer
(F):5'- ATATGGACATTTCCAGGCCC -3'
(R):5'- ACCAGTTCTTCAGGTGCG -3'

Posted On

2014-04-13