Mutagenetix > Incidental Mutation

Incidental Mutation 'R7430:Zfp763'

576427

Institutional Source

Beutler Lab

Gene Symbol

Zfp763

Ensembl Gene

ENSMUSG00000067430

Gene Name

zinc finger protein 763

Synonyms

1700065O13Rik

MMRRC Submission

045508-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7430 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

33235838-33252355 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 33238506 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Phenylalanine at position 213 (Y213F)

Ref Sequence

ENSEMBL: ENSMUSP00000084936 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000087654]

AlphaFold

Q8BIC7

Predicted Effect

possibly damaging
Transcript: ENSMUST00000087654
AA Change: Y213F

PolyPhen 2 Score 0.682 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000084936
Gene: ENSMUSG00000067430
AA Change: Y213F

Domain	Start	End	E-Value	Type
KRAB	10	60	7.47e-14	SMART
ZnF_C2H2	223	245	2.53e-2	SMART
ZnF_C2H2	251	273	4.54e-4	SMART
ZnF_C2H2	279	301	1.69e-3	SMART
ZnF_C2H2	307	329	5.72e-1	SMART
ZnF_C2H2	335	357	1.64e-1	SMART
ZnF_C2H2	363	385	1.56e-2	SMART
ZnF_C2H2	391	413	1.82e-3	SMART
ZnF_C2H2	419	441	1.64e-1	SMART
ZnF_C2H2	447	469	5.9e-3	SMART
ZnF_C2H2	475	497	2.02e-1	SMART
ZnF_C2H2	503	525	7.15e-2	SMART
ZnF_C2H2	531	553	1.79e-2	SMART
ZnF_C2H2	559	581	5.14e-3	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.6%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca3	G	C	17: 24,583,932 (GRCm39)		probably null	Het
Ankrd17	C	G	5: 90,443,516 (GRCm39)	E384Q	possibly damaging	Het
Atp8b4	A	T	2: 126,245,291 (GRCm39)	V286E	possibly damaging	Het
BC028528	CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT	CTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTTCTGTGGTCACTGGTT	3: 95,795,448 (GRCm39)		probably benign	Het
BC028528	ACTGGTTCTGTGGTC	ACTGGTTCTGTGGTCTCTGGTTCTGTGGTC	3: 95,795,481 (GRCm39)		probably benign	Het
Brms1l	T	C	12: 55,892,084 (GRCm39)	L126P	probably damaging	Het
C2cd4d	G	A	3: 94,271,657 (GRCm39)	V308M	possibly damaging	Het
Calcr	A	G	6: 3,708,586 (GRCm39)	L200S	probably damaging	Het
Card6	G	T	15: 5,128,682 (GRCm39)	Q905K	probably benign	Het
Chka	A	G	19: 3,942,787 (GRCm39)	Y415C	probably damaging	Het
Cimap3	T	C	3: 105,921,834 (GRCm39)	R30G	probably benign	Het
Cnih1	C	T	14: 47,017,679 (GRCm39)	V52I	possibly damaging	Het
Cox4i1	T	A	8: 121,400,770 (GRCm39)	M145K	probably damaging	Het
Cubn	G	T	2: 13,327,804 (GRCm39)	R2674S	possibly damaging	Het
Cyfip1	A	G	7: 55,550,341 (GRCm39)	E692G	probably damaging	Het
Dnah8	T	C	17: 30,925,363 (GRCm39)	F1266S	probably damaging	Het
Edc4	T	C	8: 106,618,216 (GRCm39)	S1245P	probably damaging	Het
Enpp1	G	T	10: 24,587,848 (GRCm39)	H14Q	probably benign	Het
Fam181b	G	A	7: 92,729,403 (GRCm39)	V59M	probably benign	Het
Fat4	T	A	3: 38,941,599 (GRCm39)	I164N	probably damaging	Het
Fat4	A	G	3: 39,063,793 (GRCm39)	D4583G	probably damaging	Het
Fgb	C	T	3: 82,954,014 (GRCm39)	V75I	probably benign	Het
Fign	T	C	2: 63,809,404 (GRCm39)	D622G	probably damaging	Het
Frmd3	A	G	4: 74,063,342 (GRCm39)	D223G	probably damaging	Het
Gclm	G	A	3: 122,039,729 (GRCm39)	R32Q	probably benign	Het
Grsf1	A	T	5: 88,811,086 (GRCm39)	I428N	possibly damaging	Het
Hnrnpll	T	A	17: 80,357,276 (GRCm39)	I247F	probably damaging	Het
Hscb	T	A	5: 110,977,024 (GRCm39)	I223L	probably benign	Het
Ifi204	C	T	1: 173,583,247 (GRCm39)	A324T	probably benign	Het
Itgav	G	A	2: 83,624,602 (GRCm39)	V731M	probably damaging	Het
Loricrin	C	T	3: 91,989,206 (GRCm39)	G27S	unknown	Het
Lpin3	A	G	2: 160,740,586 (GRCm39)	D377G	probably benign	Het
Marveld3	A	G	8: 110,675,100 (GRCm39)	S239P	possibly damaging	Het
Mast3	A	C	8: 71,232,947 (GRCm39)	C1122G	probably damaging	Het
Ms4a4d	A	G	19: 11,535,297 (GRCm39)	I198M	probably benign	Het
Mup14	C	T	4: 61,259,447 (GRCm39)	G35E	probably damaging	Het
Myh1	C	T	11: 67,096,393 (GRCm39)	Q291*	probably null	Het
Myo1a	T	A	10: 127,542,716 (GRCm39)	V118E	probably damaging	Het
Nfatc3	A	G	8: 106,835,035 (GRCm39)	T794A	probably benign	Het
Nkx6-2	T	C	7: 139,161,916 (GRCm39)	T154A	probably damaging	Het
Or51g2	A	T	7: 102,622,969 (GRCm39)	S77T	probably damaging	Het
Or7g16	T	C	9: 18,726,650 (GRCm39)	*313W	probably null	Het
Ovgp1	G	C	3: 105,893,618 (GRCm39)	A464P	probably damaging	Het
Ovgp1	C	T	3: 105,893,619 (GRCm39)	A464V	possibly damaging	Het
Pde6c	T	A	19: 38,129,887 (GRCm39)	Y266N	probably damaging	Het
Per2	C	A	1: 91,351,705 (GRCm39)	E934*	probably null	Het
Pgm1	T	A	4: 99,813,192 (GRCm39)	M1K	probably null	Het
Plcb4	T	C	2: 135,810,242 (GRCm39)	Y626H	probably damaging	Het
Postn	T	A	3: 54,277,623 (GRCm39)	V206D	probably damaging	Het
Prss29	T	A	17: 25,540,113 (GRCm39)		probably null	Het
Ptges3l	C	A	11: 101,314,641 (GRCm39)	V85L	possibly damaging	Het
Riok2	T	C	17: 17,607,802 (GRCm39)	L450S	probably benign	Het
Rpap3	A	T	15: 97,586,031 (GRCm39)	L320Q	possibly damaging	Het
Rptor	T	C	11: 119,737,654 (GRCm39)	W576R	probably damaging	Het
Sgk3	A	G	1: 9,942,483 (GRCm39)	D85G	probably benign	Het
Slc2a1	A	G	4: 118,993,510 (GRCm39)	Y449C	probably damaging	Het
Slco1a5	A	T	6: 142,194,438 (GRCm39)	S402T	probably benign	Het
Smad2	T	A	18: 76,421,151 (GRCm39)	V160E	probably damaging	Het
Snx13	T	C	12: 35,183,357 (GRCm39)	V760A	possibly damaging	Het
Sugt1	T	A	14: 79,857,241 (GRCm39)		probably null	Het
Syne2	C	T	12: 75,980,770 (GRCm39)	T1509M	probably damaging	Het
Syne2	T	A	12: 76,087,184 (GRCm39)	L214*	probably null	Het
Tmem120a	T	A	5: 135,764,990 (GRCm39)		probably null	Het
Tmem161b	A	G	13: 84,430,866 (GRCm39)		probably null	Het
Trim33	T	C	3: 103,218,219 (GRCm39)	I256T	possibly damaging	Het
Tspan17	G	A	13: 54,943,785 (GRCm39)	E213K	probably benign	Het
Ttc6	T	A	12: 57,704,888 (GRCm39)	I631N	probably benign	Het
Ttn	T	A	2: 76,641,283 (GRCm39)	L13574F	probably damaging	Het
Tufm	A	G	7: 126,088,299 (GRCm39)	D228G	probably benign	Het
Usf1	T	A	1: 171,245,295 (GRCm39)	S236T	probably benign	Het
Usp39	T	C	6: 72,319,900 (GRCm39)	Y106C	probably damaging	Het
Usp46	T	A	5: 74,163,849 (GRCm39)	Y296F	probably damaging	Het
Vmn2r82	A	G	10: 79,217,087 (GRCm39)	N473S	probably damaging	Het
Washc5	A	T	15: 59,241,762 (GRCm39)	Y51*	probably null	Het
Zbtb47	G	A	9: 121,592,732 (GRCm39)	D351N	probably benign	Het
Zswim5	A	G	4: 116,833,054 (GRCm39)	T596A	possibly damaging	Het

Other mutations in Zfp763

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02638:Zfp763	APN	17	33,238,908 (GRCm39)	missense	probably benign	0.41
IGL03291:Zfp763	APN	17	33,238,860 (GRCm39)	missense	probably damaging	0.96
R0346:Zfp763	UTSW	17	33,238,721 (GRCm39)	missense	probably benign	0.26
R0675:Zfp763	UTSW	17	33,238,774 (GRCm39)	missense	possibly damaging	0.92
R0683:Zfp763	UTSW	17	33,237,892 (GRCm39)	missense	probably damaging	1.00
R1494:Zfp763	UTSW	17	33,240,477 (GRCm39)	missense	probably damaging	0.99
R1521:Zfp763	UTSW	17	33,252,276 (GRCm39)	start codon destroyed	probably benign	0.03
R1607:Zfp763	UTSW	17	33,238,881 (GRCm39)	missense	probably benign	0.08
R1627:Zfp763	UTSW	17	33,240,758 (GRCm39)	missense	probably damaging	1.00
R1714:Zfp763	UTSW	17	33,238,591 (GRCm39)	missense	probably damaging	0.99
R1993:Zfp763	UTSW	17	33,237,413 (GRCm39)	missense	probably damaging	1.00
R2109:Zfp763	UTSW	17	33,238,752 (GRCm39)	missense	probably benign
R4420:Zfp763	UTSW	17	33,237,455 (GRCm39)	missense	probably benign	0.43
R4612:Zfp763	UTSW	17	33,237,922 (GRCm39)	missense	probably benign	0.05
R5114:Zfp763	UTSW	17	33,237,949 (GRCm39)	missense	probably damaging	0.99
R5426:Zfp763	UTSW	17	33,238,569 (GRCm39)	missense	probably benign
R5503:Zfp763	UTSW	17	33,238,507 (GRCm39)	missense	possibly damaging	0.95
R5534:Zfp763	UTSW	17	33,240,768 (GRCm39)	missense	probably damaging	0.97
R6133:Zfp763	UTSW	17	33,237,675 (GRCm39)	missense	possibly damaging	0.75
R7141:Zfp763	UTSW	17	33,237,769 (GRCm39)	missense	probably damaging	0.97
R7365:Zfp763	UTSW	17	33,252,352 (GRCm39)	start gained	probably benign
R7552:Zfp763	UTSW	17	33,237,625 (GRCm39)	missense	probably benign
R8277:Zfp763	UTSW	17	33,252,294 (GRCm39)	start gained	probably benign
R8446:Zfp763	UTSW	17	33,238,473 (GRCm39)	missense	probably benign	0.28
R8964:Zfp763	UTSW	17	33,240,710 (GRCm39)	missense	probably benign	0.25
R9662:Zfp763	UTSW	17	33,240,787 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AAGGTGTATCTCCACTGTGAATTC -3'
(R):5'- AGTATGAGACACGTTATGCAGATG -3'

Sequencing Primer
(F):5'- CACTGTGAATTCTTTCATGTTTCTGG -3'
(R):5'- GAGACACGTTATGCAGATGTCACTTC -3'

Posted On

2019-10-07