Mutagenetix > Incidental Mutation

Incidental Mutation 'R4280:Zfp429'

322861

Institutional Source

Beutler Lab

Gene Symbol

Zfp429

Ensembl Gene

ENSMUSG00000078994

Gene Name

zinc finger protein 429

Synonyms

2810487A22Rik

MMRRC Submission

041648-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.069) question?

Stock #

R4280 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

67536024-67547938 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 67538914 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Glycine at position 177 (C177G)

Ref Sequence

ENSEMBL: ENSMUSP00000105354 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000109732] [ENSMUST00000181071] [ENSMUST00000224684] [ENSMUST00000224825]

AlphaFold

Q7M6Y0

Predicted Effect

probably damaging
Transcript: ENSMUST00000109732
AA Change: C177G

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000105354
Gene: ENSMUSG00000078994
AA Change: C177G

Domain	Start	End	E-Value	Type
KRAB	15	75	7.16e-34	SMART
ZnF_C2H2	119	141	5.12e1	SMART
ZnF_C2H2	147	169	2.27e-4	SMART
ZnF_C2H2	175	197	1.28e-3	SMART
ZnF_C2H2	203	225	1.56e-2	SMART
ZnF_C2H2	259	281	4.62e1	SMART
ZnF_C2H2	287	309	5.14e-3	SMART
ZnF_C2H2	315	337	6.78e-3	SMART
ZnF_C2H2	343	365	3.11e-2	SMART
ZnF_C2H2	371	393	1.25e-1	SMART
ZnF_C2H2	399	421	6.32e-3	SMART
ZnF_C2H2	427	449	1.47e-3	SMART
ZnF_C2H2	455	477	5.42e-2	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000181071

SMART Domains

Protein: ENSMUSP00000137755
Gene: ENSMUSG00000078994

Domain	Start	End	E-Value	Type
KRAB	15	75	7.16e-34	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000224684

Predicted Effect

probably benign
Transcript: ENSMUST00000224825

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000225810

Meta Mutation Damage Score

0.7424

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.4%
20x: 95.4%

Validation Efficiency

100% (51/51)

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Arhgap32	T	C	9: 32,171,185 (GRCm39)	C1322R	probably damaging	Het
Arl6ip1	AAAATAAATAAATAAATAAATAAATA	AAAATAAATAAATAAATAAATAAATAAATA	7: 117,721,122 (GRCm39)		probably benign	Het
Arvcf	G	A	16: 18,216,741 (GRCm39)	R292H	probably damaging	Het
Ccdc102a	C	A	8: 95,634,444 (GRCm39)	G382*	probably null	Het
Cd274	A	T	19: 29,357,871 (GRCm39)	M188L	probably benign	Het
Cep76	T	A	18: 67,773,229 (GRCm39)	D23V	probably benign	Het
Cimip3	T	C	17: 47,724,780 (GRCm39)	M17V	probably benign	Het
Clec12a	A	G	6: 129,340,892 (GRCm39)	Y224C	probably damaging	Het
Cplx2	A	G	13: 54,527,377 (GRCm39)	E87G	probably damaging	Het
Ctr9	A	G	7: 110,645,930 (GRCm39)		probably benign	Het
Dgat2	A	G	7: 98,808,204 (GRCm39)	I157T	probably damaging	Het
Epha1	G	T	6: 42,341,986 (GRCm39)	P355T	probably damaging	Het
Fabp3	C	T	4: 130,206,245 (GRCm39)		probably null	Het
Gmip	T	A	8: 70,266,251 (GRCm39)		probably benign	Het
Hephl1	A	G	9: 15,023,330 (GRCm39)	V24A	probably benign	Het
Itgb4	T	A	11: 115,881,761 (GRCm39)	M771K	probably damaging	Het
Mov10	A	C	3: 104,707,095 (GRCm39)	F635V	probably damaging	Het
Mtres1	A	T	10: 43,408,905 (GRCm39)	F79L	probably benign	Het
Or10ag60	A	G	2: 87,438,595 (GRCm39)	T288A	possibly damaging	Het
Or5an9	A	G	19: 12,187,302 (GRCm39)	Y124C	probably damaging	Het
Pbrm1	T	C	14: 30,829,269 (GRCm39)		probably null	Het
Plscr1l1	T	C	9: 92,225,701 (GRCm39)	Y8H	possibly damaging	Het
Plxnd1	A	T	6: 115,933,056 (GRCm39)		probably null	Het
Plxnd1	C	A	6: 115,933,055 (GRCm39)		probably benign	Het
Pnma5	T	C	X: 72,079,036 (GRCm39)	M549V	probably benign	Het
Polq	C	A	16: 36,902,419 (GRCm39)	Q2205K	probably damaging	Het
Ppp4r3c1	A	T	X: 88,976,105 (GRCm39)	W31R	probably damaging	Het
Pramel24	A	G	4: 143,452,592 (GRCm39)	T8A	possibly damaging	Het
Psma8	T	A	18: 14,854,292 (GRCm39)	D57E	probably benign	Het
Rbm47	T	C	5: 66,183,520 (GRCm39)	Y361C	probably damaging	Het
Rec8	A	G	14: 55,856,091 (GRCm39)	H11R	probably damaging	Het
Ric1	A	G	19: 29,563,950 (GRCm39)	Y568C	probably damaging	Het
Rrp36	G	A	17: 46,983,302 (GRCm39)	T104I	probably damaging	Het
Rrs1	G	A	1: 9,616,364 (GRCm39)	G206S	probably damaging	Het
Scgb2b6	A	G	7: 31,318,367 (GRCm39)		noncoding transcript	Het
Skint5	T	A	4: 113,799,749 (GRCm39)	K126I	probably damaging	Het
Slc38a10	C	T	11: 120,028,704 (GRCm39)	G202D	probably damaging	Het
Supt5	G	A	7: 28,016,498 (GRCm39)	R761W	probably damaging	Het
Tmtc2	A	G	10: 105,184,294 (GRCm39)		probably null	Het
Tob1	T	C	11: 94,105,148 (GRCm39)	V228A	probably benign	Het
Traj44	T	C	14: 54,411,148 (GRCm39)		probably benign	Het
Trps1	G	A	15: 50,709,478 (GRCm39)	L291F	probably benign	Het
Ttn	T	A	2: 76,585,168 (GRCm39)	I22042F	probably damaging	Het
Ush2a	A	G	1: 188,310,658 (GRCm39)	Q2078R	probably benign	Het
Zbtb24	T	C	10: 41,340,916 (GRCm39)	S649P	probably benign	Het
Zfp28	A	T	7: 6,396,700 (GRCm39)	Q378H	probably benign	Het

Other mutations in Zfp429

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01160:Zfp429	APN	13	67,539,132 (GRCm39)	missense	probably damaging	0.96
IGL01913:Zfp429	APN	13	67,544,793 (GRCm39)	missense	probably damaging	1.00
IGL02343:Zfp429	APN	13	67,538,844 (GRCm39)	missense	probably damaging	0.98
IGL02679:Zfp429	APN	13	67,547,855 (GRCm39)	intron	probably benign
IGL03396:Zfp429	APN	13	67,544,159 (GRCm39)	splice site	probably benign
FR4342:Zfp429	UTSW	13	67,544,769 (GRCm39)	missense	probably benign	0.02
R0012:Zfp429	UTSW	13	67,538,796 (GRCm39)	missense	probably benign	0.01
R1232:Zfp429	UTSW	13	67,538,751 (GRCm39)	missense	possibly damaging	0.47
R1330:Zfp429	UTSW	13	67,544,262 (GRCm39)	splice site	probably null
R1653:Zfp429	UTSW	13	67,538,043 (GRCm39)	missense	possibly damaging	0.87
R1761:Zfp429	UTSW	13	67,544,195 (GRCm39)	missense	probably benign	0.28
R1813:Zfp429	UTSW	13	67,538,505 (GRCm39)	missense	possibly damaging	0.55
R2356:Zfp429	UTSW	13	67,538,746 (GRCm39)	missense	probably benign
R4283:Zfp429	UTSW	13	67,538,914 (GRCm39)	missense	probably damaging	1.00
R4464:Zfp429	UTSW	13	67,538,617 (GRCm39)	missense	probably benign	0.13
R4789:Zfp429	UTSW	13	67,538,523 (GRCm39)	missense	probably benign	0.06
R5187:Zfp429	UTSW	13	67,538,959 (GRCm39)	missense	probably damaging	0.99
R5250:Zfp429	UTSW	13	67,538,638 (GRCm39)	missense	probably benign	0.00
R6688:Zfp429	UTSW	13	67,544,249 (GRCm39)	missense	probably damaging	0.98
R6772:Zfp429	UTSW	13	67,538,317 (GRCm39)	missense	probably damaging	1.00
R6989:Zfp429	UTSW	13	67,538,080 (GRCm39)	missense	probably benign	0.00
R7041:Zfp429	UTSW	13	67,538,830 (GRCm39)	missense	probably damaging	1.00
R7101:Zfp429	UTSW	13	67,538,931 (GRCm39)	missense	possibly damaging	0.88
R7593:Zfp429	UTSW	13	67,538,410 (GRCm39)	missense	probably damaging	1.00
R7792:Zfp429	UTSW	13	67,538,558 (GRCm39)	nonsense	probably null
R8500:Zfp429	UTSW	13	67,538,828 (GRCm39)	nonsense	probably null
R8721:Zfp429	UTSW	13	67,538,331 (GRCm39)	missense	probably damaging	0.98
R8891:Zfp429	UTSW	13	67,538,830 (GRCm39)	missense	probably damaging	1.00
R9364:Zfp429	UTSW	13	67,538,531 (GRCm39)	missense	probably benign	0.12
R9554:Zfp429	UTSW	13	67,538,531 (GRCm39)	missense	probably benign	0.12

Predicted Primers

PCR Primer
(F):5'- TTCCTGAAGCGGTAGAGGAG -3'
(R):5'- GCAAACTGACTAATTGTAAATCGCTCC -3'

Sequencing Primer
(F):5'- GAGGGGGAAATCTTTTGACACATTC -3'
(R):5'- GAAACCCTACAAGTGTGGAGAATTTG -3'

Posted On

2015-06-20