Mutagenetix > Incidental Mutation

Incidental Mutation 'R8191:Vwa7'

635191

Institutional Source

Beutler Lab

Gene Symbol

Vwa7

Ensembl Gene

ENSMUSG00000007030

Gene Name

von Willebrand factor A domain containing 7

Synonyms

G7c, D17H6S56E-3

MMRRC Submission

067614-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.056) question?

Stock #

R8191 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

35235555-35245717 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 35238712 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 267 (T267A)

Ref Sequence

ENSEMBL: ENSMUSP00000007245 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000007245] [ENSMUST00000087315] [ENSMUST00000172499] [ENSMUST00000173584]

AlphaFold

Q9JHA8

Predicted Effect

probably damaging
Transcript: ENSMUST00000007245
AA Change: T267A

PolyPhen 2 Score 0.958 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000007245
Gene: ENSMUSG00000007030
AA Change: T267A

Domain	Start	End	E-Value	Type
signal peptide	1	28	N/A	INTRINSIC
VWA	314	499	2.59e0	SMART
low complexity region	683	701	N/A	INTRINSIC
low complexity region	840	861	N/A	INTRINSIC
low complexity region	864	877	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000087315

SMART Domains

Protein: ENSMUSP00000084572
Gene: ENSMUSG00000007029

Domain	Start	End	E-Value	Type
Pfam:GST_N	2	81	5.7e-16	PFAM
Pfam:GST_C	107	198	7.3e-13	PFAM
low complexity region	234	256	N/A	INTRINSIC
low complexity region	261	271	N/A	INTRINSIC
Pfam:tRNA-synt_1	307	938	2e-197	PFAM
Pfam:tRNA-synt_1g	336	496	6e-6	PFAM
Pfam:tRNA-synt_1_2	555	623	1.9e-11	PFAM
Pfam:Anticodon_1	983	1138	2.6e-34	PFAM
low complexity region	1153	1174	N/A	INTRINSIC
low complexity region	1207	1225	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000172499
AA Change: T267A

PolyPhen 2 Score 0.958 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000133418
Gene: ENSMUSG00000007030
AA Change: T267A

Domain	Start	End	E-Value	Type
signal peptide	1	28	N/A	INTRINSIC
VWA	314	478	7.28e0	SMART
low complexity region	662	680	N/A	INTRINSIC
low complexity region	819	840	N/A	INTRINSIC
low complexity region	843	856	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000173142

SMART Domains

Protein: ENSMUSP00000134669
Gene: ENSMUSG00000007029

Domain	Start	End	E-Value	Type
SCOP:d1gaxa3	32	67	3e-7	SMART
PDB:1IYW\|B	36	122	4e-6	PDB

Predicted Effect

probably benign
Transcript: ENSMUST00000173584

SMART Domains

Protein: ENSMUSP00000133994
Gene: ENSMUSG00000007029

Domain	Start	End	E-Value	Type
low complexity region	25	38	N/A	INTRINSIC
low complexity region	44	58	N/A	INTRINSIC
low complexity region	78	89	N/A	INTRINSIC
Pfam:GST_C	96	198	7.8e-14	PFAM
low complexity region	234	256	N/A	INTRINSIC
low complexity region	261	271	N/A	INTRINSIC
Pfam:tRNA-synt_1	307	938	1.9e-200	PFAM
Pfam:tRNA-synt_1g	336	493	2.1e-7	PFAM
Pfam:tRNA-synt_1_2	555	623	1.1e-12	PFAM
Pfam:Anticodon_1	983	1138	7.2e-36	PFAM
low complexity region	1153	1174	N/A	INTRINSIC
coiled coil region	1197	1225	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.4%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700037C18Rik	G	A	16: 3,724,918 (GRCm39)	R49W	probably damaging	Het
Adamts4	T	C	1: 171,080,292 (GRCm39)	S282P		Het
Aqp4	A	G	18: 15,531,222 (GRCm39)	S180P	probably benign	Het
Armc2	T	G	10: 41,839,747 (GRCm39)	E406A	probably benign	Het
Atp13a3	A	T	16: 30,168,598 (GRCm39)	Y464N	probably damaging	Het
B3gnt3	C	A	8: 72,146,122 (GRCm39)	V136L	probably benign	Het
Cacna1s	C	T	1: 136,035,893 (GRCm39)	H1378Y	probably damaging	Het
Ccnk	A	T	12: 108,159,933 (GRCm39)	E138D	probably benign	Het
Cenpe	A	G	3: 134,957,375 (GRCm39)	K1878E	probably benign	Het
Cep57l1	T	A	10: 41,616,955 (GRCm39)	I111L	probably damaging	Het
Cfap298	G	T	16: 90,727,889 (GRCm39)	N100K	probably damaging	Het
Copg2	T	C	6: 30,790,665 (GRCm39)	I509V	probably benign	Het
Cux2	T	A	5: 122,012,217 (GRCm39)	D406V	probably benign	Het
Cyp2a12	G	T	7: 26,730,529 (GRCm39)	A165S	probably benign	Het
Dnaaf5	T	G	5: 139,167,250 (GRCm39)	S719A	probably benign	Het
Dnah7c	A	G	1: 46,646,618 (GRCm39)	I1220V	possibly damaging	Het
Dnai3	G	T	3: 145,800,066 (GRCm39)	P158H	probably damaging	Het
Dnajb8	C	T	6: 88,199,940 (GRCm39)	R159C	possibly damaging	Het
Dusp10	T	A	1: 183,769,749 (GRCm39)	D238E	possibly damaging	Het
Dync1li1	C	A	9: 114,538,253 (GRCm39)	D203E	probably benign	Het
Ecpas	A	T	4: 58,872,587 (GRCm39)		probably null	Het
Eif5b	T	C	1: 38,075,283 (GRCm39)	S587P	probably damaging	Het
Ephb2	G	A	4: 136,386,256 (GRCm39)	T832I	probably damaging	Het
Exoc1	T	A	5: 76,707,674 (GRCm39)		probably null	Het
Fam193a	T	A	5: 34,597,917 (GRCm39)	N571K	probably damaging	Het
Fem1a	T	A	17: 56,565,356 (GRCm39)	I483N	probably damaging	Het
Fgf20	C	A	8: 40,761,361 (GRCm39)		probably benign	Het
Fkbp1a	C	T	2: 151,399,356 (GRCm39)	P98S		Het
Gpsm3	A	T	17: 34,809,451 (GRCm39)	D19V	probably benign	Het
Ido2	C	A	8: 25,023,696 (GRCm39)	G381W	probably damaging	Het
Ifi204	T	C	1: 173,579,226 (GRCm39)	T540A	possibly damaging	Het
Isl1	A	T	13: 116,441,954 (GRCm39)	M93K	probably benign	Het
Map3k10	T	A	7: 27,362,671 (GRCm39)	S472C	probably damaging	Het
Mcrs1	A	T	15: 99,141,206 (GRCm39)	V432E	probably damaging	Het
Metap2	A	G	10: 93,701,267 (GRCm39)		probably null	Het
Muc5b	A	G	7: 141,421,421 (GRCm39)	S4304G	probably benign	Het
Myef2l	G	T	3: 10,153,914 (GRCm39)	V228F	probably damaging	Het
Nell1	T	C	7: 50,098,622 (GRCm39)	V308A	unknown	Het
Or10g1b	A	G	14: 52,627,987 (GRCm39)	V81A	probably benign	Het
Or4d5	A	T	9: 40,012,767 (GRCm39)	H6Q	probably benign	Het
Plxna4	C	A	6: 32,493,885 (GRCm39)	V244F	possibly damaging	Het
Pnpla6	T	C	8: 3,592,382 (GRCm39)	S1224P	probably benign	Het
Ripk4	A	G	16: 97,564,726 (GRCm39)		probably benign	Het
Rnpep	T	C	1: 135,200,172 (GRCm39)	E261G	possibly damaging	Het
Robo1	C	A	16: 72,730,142 (GRCm39)	S194R	probably damaging	Het
Rpusd1	C	G	17: 25,947,611 (GRCm39)	Y99*	probably null	Het
Scarf1	T	C	11: 75,413,065 (GRCm39)	M437T	probably benign	Het
Sh3tc2	G	T	18: 62,106,429 (GRCm39)	D153Y	probably damaging	Het
Siglec1	T	C	2: 130,927,599 (GRCm39)	Y69C	probably damaging	Het
Slc25a34	T	C	4: 141,347,895 (GRCm39)	Y262C	probably damaging	Het
Srrm2	T	A	17: 24,039,219 (GRCm39)	N1954K	probably damaging	Het
St6galnac2	T	C	11: 116,572,748 (GRCm39)	Y236C	probably damaging	Het
Stac3	T	A	10: 127,344,068 (GRCm39)	I322N	probably damaging	Het
Tcaf1	T	C	6: 42,652,190 (GRCm39)	Q764R	probably damaging	Het
Tcf20	G	A	15: 82,737,606 (GRCm39)	R1282*	probably null	Het
Tlr2	T	A	3: 83,743,821 (GRCm39)	K754M	probably damaging	Het
Tlr2	T	G	3: 83,743,822 (GRCm39)	K754Q	probably damaging	Het
Tnn	C	T	1: 159,953,088 (GRCm39)	V651M	probably damaging	Het
Ttn	T	C	2: 76,701,083 (GRCm39)	H9622R	unknown	Het
Tubgcp6	C	T	15: 89,004,843 (GRCm39)	G259S	probably damaging	Het
Ubr5	C	A	15: 38,006,751 (GRCm39)	C1174F		Het
Ugt2b35	T	A	5: 87,149,302 (GRCm39)	S184R	probably damaging	Het
Vit	C	T	17: 78,853,828 (GRCm39)	H25Y	probably benign	Het
Vmn1r177	G	A	7: 23,565,736 (GRCm39)	Q47*	probably null	Het
Vmn2r104	A	T	17: 20,250,465 (GRCm39)	V602D	possibly damaging	Het
Vmn2r115	A	G	17: 23,578,530 (GRCm39)	T668A	probably damaging	Het
Vmn2r125	T	G	4: 156,703,709 (GRCm39)	C362W	probably damaging	Het
Xpa	C	A	4: 46,183,225 (GRCm39)	R188L	possibly damaging	Het
Zfp143	C	T	7: 109,676,364 (GRCm39)	T249I	probably damaging	Het
Zfp607a	A	G	7: 27,578,868 (GRCm39)	E646G	possibly damaging	Het
Zfp729a	A	T	13: 67,769,838 (GRCm39)	S130R	probably benign	Het
Zswim3	C	A	2: 164,662,128 (GRCm39)	Q203K	probably damaging	Het

Other mutations in Vwa7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01103:Vwa7	APN	17	35,243,918 (GRCm39)	missense	probably damaging	1.00
IGL01736:Vwa7	APN	17	35,238,827 (GRCm39)	missense	probably damaging	1.00
IGL01868:Vwa7	APN	17	35,240,235 (GRCm39)	missense	probably null	0.96
IGL01920:Vwa7	APN	17	35,243,579 (GRCm39)	missense	probably benign	0.01
IGL02227:Vwa7	APN	17	35,239,060 (GRCm39)	missense	probably damaging	1.00
IGL02947:Vwa7	APN	17	35,242,476 (GRCm39)	splice site	probably null
IGL03259:Vwa7	APN	17	35,239,002 (GRCm39)	splice site	probably null
IGL03263:Vwa7	APN	17	35,240,575 (GRCm39)	missense	probably benign	0.16
R0008:Vwa7	UTSW	17	35,238,781 (GRCm39)	missense	probably benign	0.33
R0057:Vwa7	UTSW	17	35,243,523 (GRCm39)	missense	possibly damaging	0.85
R0057:Vwa7	UTSW	17	35,243,523 (GRCm39)	missense	possibly damaging	0.85
R0418:Vwa7	UTSW	17	35,236,933 (GRCm39)	missense	possibly damaging	0.57
R0538:Vwa7	UTSW	17	35,241,627 (GRCm39)	missense	probably damaging	1.00
R1121:Vwa7	UTSW	17	35,236,770 (GRCm39)	missense	probably damaging	1.00
R1659:Vwa7	UTSW	17	35,238,047 (GRCm39)	missense	probably benign	0.04
R1766:Vwa7	UTSW	17	35,242,919 (GRCm39)	critical splice donor site	probably null
R1777:Vwa7	UTSW	17	35,243,924 (GRCm39)	missense	probably damaging	1.00
R1793:Vwa7	UTSW	17	35,243,388 (GRCm39)	nonsense	probably null
R1874:Vwa7	UTSW	17	35,236,088 (GRCm39)	missense	probably benign	0.00
R2139:Vwa7	UTSW	17	35,242,406 (GRCm39)	missense	probably benign	0.00
R2248:Vwa7	UTSW	17	35,238,019 (GRCm39)	missense	probably benign	0.04
R2290:Vwa7	UTSW	17	35,236,187 (GRCm39)	missense	probably damaging	1.00
R2869:Vwa7	UTSW	17	35,240,218 (GRCm39)	missense	probably damaging	1.00
R2869:Vwa7	UTSW	17	35,240,218 (GRCm39)	missense	probably damaging	1.00
R2870:Vwa7	UTSW	17	35,240,218 (GRCm39)	missense	probably damaging	1.00
R2870:Vwa7	UTSW	17	35,240,218 (GRCm39)	missense	probably damaging	1.00
R2871:Vwa7	UTSW	17	35,240,218 (GRCm39)	missense	probably damaging	1.00
R2871:Vwa7	UTSW	17	35,240,218 (GRCm39)	missense	probably damaging	1.00
R2873:Vwa7	UTSW	17	35,240,218 (GRCm39)	missense	probably damaging	1.00
R2874:Vwa7	UTSW	17	35,240,218 (GRCm39)	missense	probably damaging	1.00
R3038:Vwa7	UTSW	17	35,241,637 (GRCm39)	missense	probably damaging	1.00
R3792:Vwa7	UTSW	17	35,244,135 (GRCm39)	splice site	probably null
R3970:Vwa7	UTSW	17	35,236,684 (GRCm39)	missense	probably damaging	1.00
R4612:Vwa7	UTSW	17	35,242,426 (GRCm39)	missense	probably damaging	0.96
R5013:Vwa7	UTSW	17	35,241,709 (GRCm39)	missense	probably damaging	1.00
R5068:Vwa7	UTSW	17	35,243,166 (GRCm39)	missense	probably benign	0.25
R5069:Vwa7	UTSW	17	35,243,166 (GRCm39)	missense	probably benign	0.25
R5070:Vwa7	UTSW	17	35,243,166 (GRCm39)	missense	probably benign	0.25
R5137:Vwa7	UTSW	17	35,236,822 (GRCm39)	missense	probably damaging	1.00
R5384:Vwa7	UTSW	17	35,243,902 (GRCm39)	splice site	probably null
R6170:Vwa7	UTSW	17	35,240,186 (GRCm39)	missense	possibly damaging	0.56
R6229:Vwa7	UTSW	17	35,243,241 (GRCm39)	missense	probably benign	0.00
R6249:Vwa7	UTSW	17	35,242,365 (GRCm39)	missense	probably benign	0.00
R6401:Vwa7	UTSW	17	35,236,286 (GRCm39)	splice site	probably null
R6429:Vwa7	UTSW	17	35,243,175 (GRCm39)	missense	probably benign	0.32
R6678:Vwa7	UTSW	17	35,238,776 (GRCm39)	missense	probably damaging	1.00
R6793:Vwa7	UTSW	17	35,243,867 (GRCm39)	missense	probably benign	0.06
R6966:Vwa7	UTSW	17	35,236,072 (GRCm39)	missense	probably benign
R7492:Vwa7	UTSW	17	35,238,020 (GRCm39)	missense	possibly damaging	0.86
R7903:Vwa7	UTSW	17	35,236,763 (GRCm39)	missense	probably damaging	1.00
R7922:Vwa7	UTSW	17	35,243,409 (GRCm39)	missense	possibly damaging	0.81
R8728:Vwa7	UTSW	17	35,236,133 (GRCm39)	missense	probably damaging	1.00
R8961:Vwa7	UTSW	17	35,238,086 (GRCm39)	missense	probably damaging	1.00
R9037:Vwa7	UTSW	17	35,236,268 (GRCm39)	missense	probably benign	0.00
R9275:Vwa7	UTSW	17	35,238,712 (GRCm39)	missense	probably damaging	0.96

Predicted Primers

PCR Primer
(F):5'- GCTGATGCTATCGTGCTGAG -3'
(R):5'- TGAAGTTTCCGCATTCGTCC -3'

Sequencing Primer
(F):5'- CGTGCTGAGGGGTGGAAAAATC -3'
(R):5'- AATGCCTCAGTTCCCGCAG -3'

Posted On

2020-07-13