Mutagenetix > Incidental Mutation

Incidental Mutation 'R8194:Zfp266'

635350

Institutional Source

Beutler Lab

Gene Symbol

Zfp266

Ensembl Gene

ENSMUSG00000060510

Gene Name

zinc finger protein 266

Synonyms

5330440G10Rik, 5730601F06Rik

MMRRC Submission

067617-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.091) question?

Stock #

R8194 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

20406364-20432713 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 20411610 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 189 (D189G)

Ref Sequence

ENSEMBL: ENSMUSP00000066012 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000068296] [ENSMUST00000174462]

AlphaFold

E9Q2S7

Predicted Effect

probably benign
Transcript: ENSMUST00000068296
AA Change: D189G

PolyPhen 2 Score 0.050 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000066012
Gene: ENSMUSG00000060510
AA Change: D189G

Domain	Start	End	E-Value	Type
KRAB	41	101	1.4e-27	SMART
internal_repeat_1	138	318	2.7e-16	PROSPERO
ZnF_C2H2	343	365	7.78e-3	SMART
ZnF_C2H2	371	393	1.98e-4	SMART
ZnF_C2H2	399	421	2.27e-4	SMART
ZnF_C2H2	427	449	2.47e-5	SMART
ZnF_C2H2	455	477	2.99e-4	SMART
ZnF_C2H2	483	505	1.47e-3	SMART
ZnF_C2H2	511	533	5.81e-2	SMART
ZnF_C2H2	539	561	2.79e-4	SMART
ZnF_C2H2	567	589	2.09e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000174462
AA Change: D189G

PolyPhen 2 Score 0.050 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000134217
Gene: ENSMUSG00000060510
AA Change: D189G

Domain	Start	End	E-Value	Type
KRAB	41	101	1.4e-27	SMART
internal_repeat_1	138	318	2.7e-16	PROSPERO
ZnF_C2H2	343	365	7.78e-3	SMART
ZnF_C2H2	371	393	1.98e-4	SMART
ZnF_C2H2	399	421	2.27e-4	SMART
ZnF_C2H2	427	449	2.47e-5	SMART
ZnF_C2H2	455	477	2.99e-4	SMART
ZnF_C2H2	483	505	1.47e-3	SMART
ZnF_C2H2	511	533	5.81e-2	SMART
ZnF_C2H2	539	561	2.79e-4	SMART
ZnF_C2H2	567	589	2.09e-3	SMART

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.4%
20x: 98.1%

Validation Efficiency

100% (51/51)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein containing many tandem zinc-finger motifs. Zinc fingers are protein or nucleic acid-binding domains, and may be involved in a variety of functions, including regulation of transcription. This gene is located in a cluster of similar genes encoding zinc finger proteins on chromosome 19. Alternative splicing results in multiple transcript variants for this gene. [provided by RefSeq, Sep 2012]

Allele List at MGI

Other mutations in this stock

Total: 52 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Arid4a	T	A	12: 71,106,889 (GRCm39)	Y320*	probably null	Het
Ash1l	T	A	3: 88,960,062 (GRCm39)	C2265S	probably damaging	Het
Atg4b	T	A	1: 93,713,694 (GRCm39)	C55*	probably null	Het
Cacna1s	A	T	1: 136,005,430 (GRCm39)	N405I	probably benign	Het
Capn11	A	T	17: 45,944,325 (GRCm39)	D526E	probably damaging	Het
Ccdc188	A	G	16: 18,036,244 (GRCm39)	R71G	probably benign	Het
Ccser2	G	A	14: 36,618,220 (GRCm39)	R772W	probably damaging	Het
Cenpf	T	A	1: 189,414,600 (GRCm39)	E172D	probably benign	Het
Cep85	T	C	4: 133,861,400 (GRCm39)	M627V	probably null	Het
Chd1	G	A	17: 17,594,737 (GRCm39)		probably benign	Het
Cnst	A	G	1: 179,437,759 (GRCm39)	H441R	probably benign	Het
Cyp2d11	G	T	15: 82,274,638 (GRCm39)	T313N	probably damaging	Het
Cyp2g1	A	G	7: 26,514,159 (GRCm39)	N255S	possibly damaging	Het
Dnah5	A	G	15: 28,453,414 (GRCm39)	D4395G	probably damaging	Het
Fam83h	ACTCCCCTTGCGCTCAGGGTAAGCTGGGGTAGGGCTCCCCTTGCGCTCAGGGTAAGCTGGGGTAGGGCTCCCCTTGCGCTCAGGGTAAGCTGGGGTAGGGCTCCCCTTGCGCTCAGGGTAAGCTGGGGT	ACTCCCCTTGCGCTCAGGGTAAGCTGGGGTAGGGCTCCCCTTGCGCTCAGGGTAAGCTGGGGTAGGGCTCCCCTTGCGCTCAGGGTAAGCTGGGGT	15: 75,874,624 (GRCm39)		probably benign	Het
Fcnb	C	T	2: 27,968,330 (GRCm39)	S209N	possibly damaging	Het
Gpsm1	CT	CTT	2: 26,217,364 (GRCm39)		probably null	Het
Lama4	A	G	10: 38,954,716 (GRCm39)	S1090G	probably damaging	Het
Malrd1	A	G	2: 15,929,931 (GRCm39)	D1479G	unknown	Het
Man2a2	T	C	7: 80,010,766 (GRCm39)	K742E	probably benign	Het
Mapk8	A	T	14: 33,104,241 (GRCm39)	S392T	probably benign	Het
Mark3	T	C	12: 111,559,117 (GRCm39)	I53T	probably damaging	Het
Mcmdc2	A	G	1: 9,986,867 (GRCm39)	I219V	probably benign	Het
Mlycd	A	T	8: 120,134,332 (GRCm39)	E278V	probably benign	Het
Muc2	G	T	7: 141,290,801 (GRCm39)	C29F		Het
Mup20	T	C	4: 61,971,721 (GRCm39)	I77V	probably benign	Het
Myh3	A	G	11: 66,982,828 (GRCm39)	E849G	probably damaging	Het
Nedd4	A	G	9: 72,593,389 (GRCm39)	N154S	probably damaging	Het
Odad4	G	A	11: 100,454,502 (GRCm39)	G429E	probably benign	Het
Or1e1f	A	T	11: 73,856,240 (GRCm39)	I269F	probably benign	Het
Pcdh7	A	T	5: 57,877,678 (GRCm39)	N411I	probably damaging	Het
Plekhm1	A	G	11: 103,285,886 (GRCm39)	I183T	possibly damaging	Het
Prkar2a	G	A	9: 108,569,710 (GRCm39)	V19M	probably damaging	Het
Prss35	T	G	9: 86,637,666 (GRCm39)	N145K	possibly damaging	Het
Ranbp2	T	A	10: 58,291,747 (GRCm39)	D251E	possibly damaging	Het
Rnf169	C	A	7: 99,575,651 (GRCm39)	V315F	probably damaging	Het
Slc32a1	T	C	2: 158,455,761 (GRCm39)	Y139H	probably damaging	Het
Slc5a2	T	C	7: 127,870,328 (GRCm39)	V522A	probably benign	Het
Slc6a6	A	T	6: 91,717,952 (GRCm39)	Q297L	probably damaging	Het
Sos2	A	C	12: 69,645,598 (GRCm39)	Y914D	probably damaging	Het
Spata1	G	T	3: 146,195,614 (GRCm39)	T32N	possibly damaging	Het
Srcap	C	T	7: 127,138,369 (GRCm39)	R1180C	probably damaging	Het
St14	A	T	9: 31,042,921 (GRCm39)	M1K	probably null	Het
Tcaf1	T	C	6: 42,652,236 (GRCm39)	T749A	probably benign	Het
Tcp1	T	C	17: 13,141,621 (GRCm39)		probably null	Het
Tle6	A	G	10: 81,426,888 (GRCm39)	V576A	probably damaging	Het
Usp17lc	T	A	7: 103,067,407 (GRCm39)	M234K	probably benign	Het
Washc4	A	G	10: 83,416,163 (GRCm39)	I818V	possibly damaging	Het
Zdhhc18	A	G	4: 133,341,165 (GRCm39)	L236P	probably damaging	Het
Zfp474	A	T	18: 52,772,229 (GRCm39)	D294V	probably damaging	Het
Zfp568	T	C	7: 29,722,758 (GRCm39)	F568L	probably damaging	Het
Zfp93	A	G	7: 23,975,479 (GRCm39)	K488R	probably benign	Het

Other mutations in Zfp266

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
PIT4453001:Zfp266	UTSW	9	20,417,299 (GRCm39)	missense	probably benign
R0744:Zfp266	UTSW	9	20,411,095 (GRCm39)	missense	probably damaging	1.00
R0836:Zfp266	UTSW	9	20,411,095 (GRCm39)	missense	probably damaging	1.00
R2180:Zfp266	UTSW	9	20,410,975 (GRCm39)	missense	probably damaging	1.00
R2422:Zfp266	UTSW	9	20,410,558 (GRCm39)	missense	possibly damaging	0.89
R3085:Zfp266	UTSW	9	20,412,240 (GRCm39)	missense	probably damaging	0.99
R3791:Zfp266	UTSW	9	20,410,777 (GRCm39)	missense	probably damaging	0.99
R3972:Zfp266	UTSW	9	20,411,446 (GRCm39)	missense	probably damaging	1.00
R5378:Zfp266	UTSW	9	20,410,659 (GRCm39)	missense	probably damaging	1.00
R5529:Zfp266	UTSW	9	20,418,030 (GRCm39)	missense	probably damaging	0.99
R5788:Zfp266	UTSW	9	20,417,332 (GRCm39)	missense	probably damaging	0.98
R6476:Zfp266	UTSW	9	20,410,577 (GRCm39)	missense	probably damaging	1.00
R6901:Zfp266	UTSW	9	20,410,895 (GRCm39)	nonsense	probably null
R7326:Zfp266	UTSW	9	20,413,391 (GRCm39)	missense	probably benign	0.03
R7417:Zfp266	UTSW	9	20,412,232 (GRCm39)	missense	probably benign
R7783:Zfp266	UTSW	9	20,411,626 (GRCm39)	missense	probably benign	0.04
R7917:Zfp266	UTSW	9	20,416,423 (GRCm39)	missense	probably benign	0.00
R7947:Zfp266	UTSW	9	20,410,548 (GRCm39)	missense	probably benign	0.00
R8174:Zfp266	UTSW	9	20,418,110 (GRCm39)	start gained	probably benign
R8776:Zfp266	UTSW	9	20,411,509 (GRCm39)	missense	probably benign	0.03
R8776-TAIL:Zfp266	UTSW	9	20,411,509 (GRCm39)	missense	probably benign	0.03
R8872:Zfp266	UTSW	9	20,411,275 (GRCm39)	missense	probably benign	0.22
R9096:Zfp266	UTSW	9	20,416,440 (GRCm39)	missense	probably damaging	1.00
R9220:Zfp266	UTSW	9	20,413,337 (GRCm39)	nonsense	probably null
R9284:Zfp266	UTSW	9	20,411,300 (GRCm39)	nonsense	probably null
R9502:Zfp266	UTSW	9	20,413,413 (GRCm39)	nonsense	probably null
R9547:Zfp266	UTSW	9	20,411,746 (GRCm39)	missense	probably benign	0.40
R9550:Zfp266	UTSW	9	20,410,482 (GRCm39)	missense	probably damaging	1.00
R9752:Zfp266	UTSW	9	20,411,496 (GRCm39)	missense	probably benign	0.15

Predicted Primers

PCR Primer
(F):5'- CCCGTATTTACTCCAGTCAAAGG -3'
(R):5'- TTCTCAGGTGGGTGACTCATCTC -3'

Sequencing Primer
(F):5'- GCCTCATATCTGGCTGAAAGTAAGAC -3'
(R):5'- ATCTCTTCACGAGCAGTCAGG -3'

Posted On

2020-07-13