Mutagenetix > Incidental Mutation

Incidental Mutation 'R8943:Zfp446'

681097

Institutional Source

Beutler Lab

Gene Symbol

Zfp446

Ensembl Gene

ENSMUSG00000033961

Gene Name

zinc finger protein 446

Synonyms

A630035I11Rik

MMRRC Submission

068782-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.080) question?

Stock #

R8943 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

12711726-12718323 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

C to T at 12713564 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Stop codon at position 177 (Q177*)

Ref Sequence

ENSEMBL: ENSMUSP00000104176 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000045810] [ENSMUST00000108535] [ENSMUST00000108536] [ENSMUST00000108537]

AlphaFold

Q8C9M8

Predicted Effect

probably null
Transcript: ENSMUST00000045810
AA Change: Q277*

SMART Domains

Protein: ENSMUSP00000039073
Gene: ENSMUSG00000033961
AA Change: Q277*

Domain	Start	End	E-Value	Type
low complexity region	67	79	N/A	INTRINSIC
SCAN	122	234	1.29e-53	SMART
KRAB	299	360	3.96e-2	SMART
ZnF_C2H2	419	441	2.95e-3	SMART
ZnF_C2H2	468	490	8.47e-4	SMART
ZnF_C2H2	496	518	5.34e-1	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000108535
AA Change: Q177*

SMART Domains

Protein: ENSMUSP00000104175
Gene: ENSMUSG00000033961
AA Change: Q177*

Domain	Start	End	E-Value	Type
SCAN	22	134	1.29e-53	SMART
KRAB	199	254	1.14e0	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000108536
AA Change: Q177*

SMART Domains

Protein: ENSMUSP00000104176
Gene: ENSMUSG00000033961
AA Change: Q177*

Domain	Start	End	E-Value	Type
SCAN	22	134	1.29e-53	SMART
KRAB	199	260	3.96e-2	SMART
ZnF_C2H2	319	341	2.95e-3	SMART
ZnF_C2H2	368	390	8.47e-4	SMART
ZnF_C2H2	396	418	5.34e-1	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000108537

SMART Domains

Protein: ENSMUSP00000104177
Gene: ENSMUSG00000033961

Domain	Start	End	E-Value	Type
SCAN	22	128	7.37e-49	SMART
KRAB	124	185	3.96e-2	SMART
ZnF_C2H2	244	266	2.95e-3	SMART
ZnF_C2H2	293	315	8.47e-4	SMART
ZnF_C2H2	321	343	5.34e-1	SMART

Meta Mutation Damage Score

0.9757

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.5%

Validation Efficiency

98% (50/51)

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610021A01Rik	T	C	7: 41,275,667 (GRCm39)	S457P	probably damaging	Het
Aak1	A	G	6: 86,964,234 (GRCm39)	N945S	unknown	Het
Actr1a	C	A	19: 46,369,438 (GRCm39)	R192L	possibly damaging	Het
Adgrl2	T	A	3: 148,534,119 (GRCm39)	N1036I	probably damaging	Het
Ak5	A	G	3: 152,361,511 (GRCm39)	V137A	probably damaging	Het
Aldh1a2	T	C	9: 71,169,055 (GRCm39)	V179A	probably damaging	Het
Ap2b1	A	T	11: 83,237,579 (GRCm39)	I548F	probably damaging	Het
Arhgef10l	A	G	4: 140,292,550 (GRCm39)	Y352H	probably damaging	Het
Atad5	C	T	11: 79,986,524 (GRCm39)	T537M	possibly damaging	Het
Atoh7	A	G	10: 62,935,938 (GRCm39)	K2E	possibly damaging	Het
BC061237	A	G	14: 44,741,658 (GRCm39)	I134V	probably benign	Het
Cadm1	T	C	9: 47,701,136 (GRCm39)	I141T	probably damaging	Het
Capn10	T	C	1: 92,871,454 (GRCm39)	S351P	probably damaging	Het
Cct6b	T	C	11: 82,654,959 (GRCm39)		probably benign	Het
Cd19	T	C	7: 126,011,330 (GRCm39)	T284A	probably benign	Het
Cfap53	A	G	18: 74,432,253 (GRCm39)	Y47C	probably damaging	Het
Cldn18	T	C	9: 99,578,162 (GRCm39)	M194V	probably benign	Het
Dgkb	T	A	12: 38,652,777 (GRCm39)	Y721N	probably damaging	Het
Dmbt1	A	G	7: 130,721,372 (GRCm39)	Q1880R	possibly damaging	Het
Dock2	T	C	11: 34,599,646 (GRCm39)	N311S	possibly damaging	Het
Dpysl5	G	T	5: 30,935,375 (GRCm39)	M159I	probably benign	Het
Eif2b3	G	A	4: 116,901,778 (GRCm39)	G147E	probably damaging	Het
Fam193a	A	G	5: 34,597,796 (GRCm39)	D531G	probably benign	Het
Fndc3b	T	C	3: 27,555,329 (GRCm39)		probably benign	Het
Foxe3	C	A	4: 114,782,523 (GRCm39)	A230S	unknown	Het
Gm5591	A	T	7: 38,219,727 (GRCm39)	V382E	probably benign	Het
Gm7995	A	T	14: 42,132,228 (GRCm39)	N21I	probably damaging	Het
Ipo8	G	A	6: 148,676,547 (GRCm39)	P981S	probably benign	Het
Kcnh8	A	G	17: 53,104,486 (GRCm39)	D161G	probably benign	Het
Krt71	A	G	15: 101,645,180 (GRCm39)	I377T	possibly damaging	Het
Krt75	A	T	15: 101,476,767 (GRCm39)	M374K	probably benign	Het
Krt9	TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC	TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC	11: 100,079,903 (GRCm39)		probably benign	Het
Lpcat1	A	G	13: 73,662,029 (GRCm39)	T409A	probably benign	Het
Lrch1	A	T	14: 75,032,808 (GRCm39)	I514K	probably benign	Het
Mc4r	A	C	18: 66,993,110 (GRCm39)	M1R	probably null	Het
Mthfd1l	A	T	10: 3,978,466 (GRCm39)	H442L	probably damaging	Het
Or5d38	T	A	2: 87,954,718 (GRCm39)	I204F	probably damaging	Het
Pdcd1lg2	T	C	19: 29,423,553 (GRCm39)	M199T	probably benign	Het
Pigg	G	A	5: 108,484,066 (GRCm39)	V438M	probably damaging	Het
Pira12	T	C	7: 3,898,365 (GRCm39)	E319G	probably benign	Het
Ppfibp1	T	A	6: 146,920,681 (GRCm39)		probably null	Het
Rbm15	T	A	3: 107,239,372 (GRCm39)	Y342F	possibly damaging	Het
Rhbdl1	A	T	17: 26,054,116 (GRCm39)	V278E	probably damaging	Het
Ryr3	T	C	2: 112,465,669 (GRCm39)	N4781S	probably damaging	Het
Scn7a	A	T	2: 66,525,206 (GRCm39)		silent	Het
Sfswap	A	G	5: 129,581,168 (GRCm39)	R114G	probably damaging	Het
Sohlh2	C	A	3: 55,104,282 (GRCm39)	A258D	possibly damaging	Het
Sstr4	T	A	2: 148,237,782 (GRCm39)	V131D	possibly damaging	Het
Tenm2	T	C	11: 36,834,861 (GRCm39)	T45A	probably damaging	Het
Tmem131l	A	T	3: 83,831,479 (GRCm39)	F818I	probably damaging	Het
Trappc6b	A	G	12: 59,097,149 (GRCm39)	F58L	probably damaging	Het
Vmn1r229	A	T	17: 21,035,418 (GRCm39)	H221L	possibly damaging	Het
Vmn1r33	T	A	6: 66,588,783 (GRCm39)	Y257F	probably damaging	Het
Wdfy3	T	C	5: 101,993,231 (GRCm39)		probably benign	Het
Zup1	A	G	10: 33,795,301 (GRCm39)	*552Q	probably null	Het

Other mutations in Zfp446

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01486:Zfp446	APN	7	12,713,307 (GRCm39)	critical splice donor site	probably null
IGL01534:Zfp446	APN	7	12,713,493 (GRCm39)	missense	probably damaging	1.00
IGL02471:Zfp446	APN	7	12,716,181 (GRCm39)	missense	probably benign	0.41
IGL02888:Zfp446	APN	7	12,713,255 (GRCm39)	missense	probably damaging	1.00
IGL03153:Zfp446	APN	7	12,711,834 (GRCm39)	missense	probably benign	0.01
IGL03185:Zfp446	APN	7	12,712,925 (GRCm39)	missense	probably null	0.43
IGL03242:Zfp446	APN	7	12,713,252 (GRCm39)	missense	probably damaging	1.00
R0538:Zfp446	UTSW	7	12,713,516 (GRCm39)	missense	possibly damaging	0.94
R1809:Zfp446	UTSW	7	12,713,048 (GRCm39)	missense	probably damaging	1.00
R3686:Zfp446	UTSW	7	12,716,580 (GRCm39)	missense	probably damaging	0.97
R3701:Zfp446	UTSW	7	12,712,079 (GRCm39)	unclassified	probably benign
R5256:Zfp446	UTSW	7	12,713,231 (GRCm39)	nonsense	probably null
R5363:Zfp446	UTSW	7	12,711,984 (GRCm39)	missense	probably benign	0.20
R5377:Zfp446	UTSW	7	12,716,178 (GRCm39)	missense	possibly damaging	0.88
R6806:Zfp446	UTSW	7	12,713,043 (GRCm39)	missense	probably damaging	1.00
R7167:Zfp446	UTSW	7	12,712,049 (GRCm39)	unclassified	probably benign
R7988:Zfp446	UTSW	7	12,712,970 (GRCm39)	missense	possibly damaging	0.93
R8288:Zfp446	UTSW	7	12,711,885 (GRCm39)	missense	probably benign	0.00
R8487:Zfp446	UTSW	7	12,716,555 (GRCm39)	missense	possibly damaging	0.68
R9315:Zfp446	UTSW	7	12,713,397 (GRCm39)	missense	probably benign	0.28
Z1177:Zfp446	UTSW	7	12,712,093 (GRCm39)	unclassified	probably benign

Predicted Primers

PCR Primer
(F):5'- TCCTGAAGCCAAAGATGCTTCC -3'
(R):5'- CACTGCATTGACCTTTGGCC -3'

Sequencing Primer
(F):5'- ATGCTTCCTCTAGTCCAGAAGGAG -3'
(R):5'- GGGAAGTGACCCCATTCTTCTCAG -3'

Posted On

2021-08-31