Mutagenetix > Incidental Mutation

Incidental Mutation 'R5974:Zfp296'

471617

Institutional Source

Beutler Lab

Gene Symbol

Zfp296

Ensembl Gene

ENSMUSG00000011267

Gene Name

zinc finger protein 296

Synonyms

2210018A16Rik

MMRRC Submission

044157-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.395) question?

Stock #

R5974 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

19311212-19314581 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 19311862 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Leucine to Proline at position 123 (L123P)

Ref Sequence

ENSEMBL: ENSMUSP00000104093 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000051364] [ENSMUST00000086041] [ENSMUST00000108453] [ENSMUST00000117222] [ENSMUST00000119912] [ENSMUST00000122055] [ENSMUST00000122127] [ENSMUST00000207907] [ENSMUST00000208068] [ENSMUST00000207663] [ENSMUST00000208826] [ENSMUST00000151646]

AlphaFold

E9Q6W4

Predicted Effect

probably benign
Transcript: ENSMUST00000051364

SMART Domains

Protein: ENSMUSP00000055844
Gene: ENSMUSG00000044709

Domain	Start	End	E-Value	Type
low complexity region	4	20	N/A	INTRINSIC
Pfam:Gemin7	50	129	1.9e-45	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000086041

SMART Domains

Protein: ENSMUSP00000083205
Gene: ENSMUSG00000061028

Domain	Start	End	E-Value	Type
low complexity region	19	35	N/A	INTRINSIC
DRY_EERY	39	171	1.28e-64	SMART
low complexity region	172	212	N/A	INTRINSIC
low complexity region	241	260	N/A	INTRINSIC
low complexity region	263	283	N/A	INTRINSIC
low complexity region	302	324	N/A	INTRINSIC
low complexity region	339	368	N/A	INTRINSIC
low complexity region	372	446	N/A	INTRINSIC
low complexity region	453	476	N/A	INTRINSIC
low complexity region	480	532	N/A	INTRINSIC
coiled coil region	574	630	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000108453
AA Change: L123P

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000104093
Gene: ENSMUSG00000011267
AA Change: L123P

Domain	Start	End	E-Value	Type
ZnF_C2H2	138	161	5.07e0	SMART
ZnF_C2H2	212	234	2.05e-2	SMART
ZnF_C2H2	240	262	1.1e-2	SMART
low complexity region	281	295	N/A	INTRINSIC
low complexity region	317	329	N/A	INTRINSIC
ZnF_C2H2	360	382	1.95e-3	SMART
ZnF_C2H2	388	410	3.39e-3	SMART
ZnF_C2H2	418	441	1.14e0	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000117222

SMART Domains

Protein: ENSMUSP00000113266
Gene: ENSMUSG00000044709

Domain	Start	End	E-Value	Type
low complexity region	4	20	N/A	INTRINSIC
Pfam:Gemin7	50	129	1.9e-45	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000119912

SMART Domains

Protein: ENSMUSP00000112742
Gene: ENSMUSG00000044709

Domain	Start	End	E-Value	Type
low complexity region	4	20	N/A	INTRINSIC
Pfam:Gemin7	50	129	1.9e-45	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000122055

SMART Domains

Protein: ENSMUSP00000113583
Gene: ENSMUSG00000044709

Domain	Start	End	E-Value	Type
low complexity region	4	20	N/A	INTRINSIC
Pfam:Gemin7	50	129	1.9e-45	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000122127

SMART Domains

Protein: ENSMUSP00000113709
Gene: ENSMUSG00000044709

Domain	Start	End	E-Value	Type
low complexity region	4	20	N/A	INTRINSIC
Pfam:Gemin7	50	129	1.9e-45	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000208464

Predicted Effect

probably benign
Transcript: ENSMUST00000207907

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000208314

Predicted Effect

probably benign
Transcript: ENSMUST00000208068

Predicted Effect

probably benign
Transcript: ENSMUST00000207663

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000208716

Predicted Effect

probably benign
Transcript: ENSMUST00000208826

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000208427

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000207253

Predicted Effect

probably benign
Transcript: ENSMUST00000151646

SMART Domains

Protein: ENSMUSP00000116207
Gene: ENSMUSG00000044709

Domain	Start	End	E-Value	Type
low complexity region	4	20	N/A	INTRINSIC
Pfam:Gemin7	50	81	7e-16	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.5%
10x: 97.6%
20x: 92.6%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Afg3l2	G	T	18: 67,554,329 (GRCm39)	L458M	probably damaging	Het
Anapc4	T	C	5: 53,002,742 (GRCm39)	L261P	probably damaging	Het
Aqp6	A	G	15: 99,499,317 (GRCm39)	Y10C	probably benign	Het
Ccnb1ip1	A	T	14: 51,029,662 (GRCm39)	N133K	probably benign	Het
Clip4	A	T	17: 72,138,242 (GRCm39)	H433L	probably damaging	Het
Cntnap5c	T	A	17: 58,183,480 (GRCm39)	M62K	probably benign	Het
Col12a1	A	G	9: 79,589,409 (GRCm39)	S1049P	probably damaging	Het
Col15a1	C	T	4: 47,258,683 (GRCm39)	T358I	probably benign	Het
Coro7	A	T	16: 4,449,753 (GRCm39)	D645E	possibly damaging	Het
Ctnnal1	C	A	4: 56,817,067 (GRCm39)	W585L	probably damaging	Het
Ctnnd1	C	A	2: 84,451,259 (GRCm39)	E114*	probably null	Het
Daam2	T	A	17: 49,771,501 (GRCm39)	S882C	probably damaging	Het
Des	T	A	1: 75,339,628 (GRCm39)	S329T	probably benign	Het
Dido1	T	C	2: 180,313,290 (GRCm39)	D994G	probably benign	Het
Dock3	A	G	9: 106,871,261 (GRCm39)	V547A	probably damaging	Het
Ebf4	G	A	2: 130,207,484 (GRCm39)	A643T	probably damaging	Het
Ect2	C	A	3: 27,199,112 (GRCm39)	E194*	probably null	Het
Epb41l2	A	G	10: 25,317,713 (GRCm39)	I77V	possibly damaging	Het
Fat3	A	T	9: 15,917,824 (GRCm39)		probably null	Het
Fbn2	T	G	18: 58,181,992 (GRCm39)	D1803A	probably damaging	Het
Fbxo10	T	C	4: 45,040,631 (GRCm39)	E858G	probably benign	Het
Fbxo24	C	T	5: 137,617,912 (GRCm39)	R284Q	probably benign	Het
Fsip2	T	A	2: 82,793,657 (GRCm39)	I425N	possibly damaging	Het
Fut9	A	C	4: 25,620,090 (GRCm39)	Y241*	probably null	Het
Galr2	A	G	11: 116,173,852 (GRCm39)	S161G	possibly damaging	Het
Gcc2	T	A	10: 58,094,065 (GRCm39)	L14I	probably damaging	Het
H2-T15	A	T	17: 36,367,677 (GRCm39)	D220E	probably benign	Het
Hdac11	G	A	6: 91,150,196 (GRCm39)	V332I	probably benign	Het
Hdac7	T	C	15: 97,699,953 (GRCm39)		probably null	Het
Kif16b	C	T	2: 142,699,301 (GRCm39)	G93D	probably damaging	Het
Krtap11-1	C	A	16: 89,367,656 (GRCm39)	C121F	possibly damaging	Het
Lacc1	T	C	14: 77,272,517 (GRCm39)	Q93R	probably damaging	Het
Lama1	T	C	17: 68,080,722 (GRCm39)	F1250S	probably benign	Het
Lmbrd2	A	G	15: 9,172,202 (GRCm39)	E332G	probably benign	Het
Lrp2	C	A	2: 69,289,892 (GRCm39)	C3649F	probably damaging	Het
Map1a	T	C	2: 121,134,857 (GRCm39)	V1653A	probably benign	Het
Mrpl1	T	C	5: 96,379,653 (GRCm39)		probably null	Het
Myo1b	A	G	1: 51,817,532 (GRCm39)	S577P	probably damaging	Het
Nedd4	T	A	9: 72,650,920 (GRCm39)		probably null	Het
Negr1	T	A	3: 156,774,923 (GRCm39)	V213E	probably damaging	Het
Nlk	T	G	11: 78,481,792 (GRCm39)	Q223P	probably benign	Het
Ntn5	A	G	7: 45,340,848 (GRCm39)	H162R	probably damaging	Het
Nup42	T	C	5: 24,372,400 (GRCm39)	S63P	probably damaging	Het
Obscn	C	A	11: 58,967,373 (GRCm39)	D477Y	probably damaging	Het
Or12d12	A	T	17: 37,611,229 (GRCm39)	I28N	possibly damaging	Het
Or5an1	T	C	19: 12,261,200 (GRCm39)	S263P	probably damaging	Het
Or8u10	T	C	2: 85,915,225 (GRCm39)	S299G	probably benign	Het
Pabpn1	A	G	14: 55,134,617 (GRCm39)	T280A	probably damaging	Het
Per3	A	T	4: 151,127,194 (GRCm39)	V109E	possibly damaging	Het
Pira2	A	C	7: 3,844,576 (GRCm39)	V485G	probably benign	Het
Pknox2	A	G	9: 36,847,618 (GRCm39)	L133P	probably damaging	Het
Pros1	A	C	16: 62,721,030 (GRCm39)	N195T	probably damaging	Het
Rffl	T	C	11: 82,696,977 (GRCm39)	K289E	probably damaging	Het
Ripk1	T	A	13: 34,214,084 (GRCm39)	Y475*	probably null	Het
Ryr2	A	G	13: 11,729,397 (GRCm39)		probably null	Het
Sgk1	T	A	10: 21,872,148 (GRCm39)	N241K	probably damaging	Het
Skint1	T	A	4: 111,876,516 (GRCm39)	S146T	probably benign	Het
Sox30	G	T	11: 45,871,900 (GRCm39)	D252Y	probably damaging	Het
Syngap1	A	G	17: 27,182,012 (GRCm39)	Y1002C	probably damaging	Het
Tiam2	A	G	17: 3,465,084 (GRCm39)	D271G	possibly damaging	Het
Ticam1	T	C	17: 56,578,178 (GRCm39)	T306A	probably benign	Het
Tmem252	A	G	19: 24,651,632 (GRCm39)	E67G	probably benign	Het
Tnxb	T	G	17: 34,904,681 (GRCm39)	F1149V	probably damaging	Het
Ubr4	A	G	4: 139,148,389 (GRCm39)		probably null	Het
Unc50	A	G	1: 37,476,290 (GRCm39)	D150G	probably benign	Het
Ywhag	A	C	5: 135,940,483 (GRCm39)	L37R	probably damaging	Het
Zfp418	G	T	7: 7,185,199 (GRCm39)	Q387H	possibly damaging	Het
Zfp882	T	C	8: 72,666,999 (GRCm39)	F53L	probably damaging	Het

Other mutations in Zfp296

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00590:Zfp296	APN	7	19,311,760 (GRCm39)	missense	possibly damaging	0.85
IGL01098:Zfp296	APN	7	19,311,845 (GRCm39)	missense	possibly damaging	0.72
R0359:Zfp296	UTSW	7	19,313,864 (GRCm39)	missense	possibly damaging	0.68
R0510:Zfp296	UTSW	7	19,311,831 (GRCm39)	missense	probably benign	0.01
R0707:Zfp296	UTSW	7	19,313,661 (GRCm39)	missense	probably benign	0.00
R4931:Zfp296	UTSW	7	19,313,637 (GRCm39)	missense	possibly damaging	0.73
R4932:Zfp296	UTSW	7	19,313,637 (GRCm39)	missense	possibly damaging	0.73
R4933:Zfp296	UTSW	7	19,313,637 (GRCm39)	missense	possibly damaging	0.73
R5190:Zfp296	UTSW	7	19,311,332 (GRCm39)	missense	probably benign	0.33
R9694:Zfp296	UTSW	7	19,314,227 (GRCm39)	missense	possibly damaging	0.71

Predicted Primers

PCR Primer
(F):5'- TAGTATCGGGACCTTCGGTG -3'
(R):5'- ATTAGGGGTGTATGGCAAAACC -3'

Sequencing Primer
(F):5'- GGGACCTTCGGTGCTTCTC -3'
(R):5'- TGTATGGCAAAACCCCGGG -3'

Posted On

2017-03-31