Mutagenetix > Incidental Mutation

Incidental Mutation 'R9269:Zfp386'

702788

Institutional Source

Beutler Lab

Gene Symbol

Zfp386

Ensembl Gene

ENSMUSG00000042063

Gene Name

zinc finger protein 386 (Kruppel-like)

Synonyms

MMRRC Submission

Accession Numbers

Genbank: NM_001004066, NM_019565

Essential gene?

Probably non essential (E-score: 0.064) question?

Stock #

R9269 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

116047724-116063360 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 116059663 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 334 (T334A)

Ref Sequence

ENSEMBL: ENSMUSP00000138305 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073551] [ENSMUST00000183125]

AlphaFold

Q1WWJ5

Predicted Effect

probably benign
Transcript: ENSMUST00000073551
AA Change: T299A

PolyPhen 2 Score 0.013 (Sensitivity: 0.96; Specificity: 0.78)

SMART Domains

Protein: ENSMUSP00000073241
Gene: ENSMUSG00000042063
AA Change: T299A

Domain	Start	End	E-Value	Type
KRAB	6	66	1.88e-19	SMART
ZnF_C2H2	379	401	4.72e-2	SMART
ZnF_C2H2	407	429	6.42e-4	SMART
ZnF_C2H2	435	457	5.14e-3	SMART
ZnF_C2H2	463	485	2.09e-3	SMART
ZnF_C2H2	491	513	6.42e-4	SMART
ZnF_C2H2	519	541	4.87e-4	SMART
ZnF_C2H2	547	569	1.28e-3	SMART
ZnF_C2H2	575	597	2.2e-2	SMART
ZnF_C2H2	603	625	5.99e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000183125
AA Change: T334A

PolyPhen 2 Score 0.008 (Sensitivity: 0.96; Specificity: 0.76)

SMART Domains

Protein: ENSMUSP00000138305
Gene: ENSMUSG00000042063
AA Change: T334A

Domain	Start	End	E-Value	Type
KRAB	6	66	1.88e-19	SMART
ZnF_C2H2	379	401	4.72e-2	SMART
ZnF_C2H2	407	429	6.42e-4	SMART
ZnF_C2H2	435	457	5.14e-3	SMART
ZnF_C2H2	463	485	2.09e-3	SMART
ZnF_C2H2	491	513	6.42e-4	SMART
ZnF_C2H2	519	541	4.87e-4	SMART
ZnF_C2H2	547	569	1.28e-3	SMART
ZnF_C2H2	575	597	2.2e-2	SMART
ZnF_C2H2	603	625	5.99e-4	SMART

Coding Region Coverage

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

Validation Efficiency

Allele List at MGI

All alleles(4) : Gene trapped(4)

Other mutations in this stock

Total: 90 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2410089E03Rik	A	C	15: 8,219,016	Q1683P	probably damaging	Het
A2m	T	C	6: 121,660,906	S845P	probably benign	Het
Actn1	T	A	12: 80,172,971	N709Y	probably benign	Het
Alox5ap	A	G	5: 149,279,196	Y64C	probably damaging	Het
Anapc4	T	A	5: 52,861,278	S521T	possibly damaging	Het
Ap3b1	C	A	13: 94,404,062	P164Q	probably damaging	Het
Arhgef26	A	G	3: 62,340,499	N335D	probably damaging	Het
Arrdc2	G	A	8: 70,836,329	A354V	probably benign	Het
Atg2b	A	G	12: 105,652,100	S898P	probably damaging	Het
Atxn1	T	A	13: 45,557,204	T751S	probably benign	Het
Begain	T	A	12: 109,033,193	R551W	possibly damaging	Het
Borcs8	C	A	8: 70,141,871	D15E	probably benign	Het
Btbd16	C	T	7: 130,815,786	R344C	probably damaging	Het
Card11	A	T	5: 140,906,761	M183K	probably damaging	Het
Cldn3	T	C	5: 134,986,725	L94P	probably damaging	Het
Clvs2	A	T	10: 33,543,426	Y211N	probably damaging	Het
Col15a1	G	C	4: 47,288,200		probably benign	Het
Cop1	C	T	1: 159,288,983	P409L	probably benign	Het
Crhbp	C	A	13: 95,436,516	A241S	probably benign	Het
Cyfip1	C	A	7: 55,907,431	S794*	probably null	Het
D17Wsu92e	A	C	17: 27,786,075	Y169*	probably null	Het
Dlg5	T	A	14: 24,192,813	H172L	probably damaging	Het
Doc2a	T	A	7: 126,850,987	I199N	probably benign	Het
Dock3	T	C	9: 106,941,323	T1191A	probably benign	Het
Efcab8	G	C	2: 153,804,941	V397L	unknown	Het
Fcgr1	C	T	3: 96,285,838	R281H	probably benign	Het
Fndc10	T	C	4: 155,694,748	V83A	possibly damaging	Het
Galnt2	T	A	8: 124,338,463	I444K	probably benign	Het
Gcnt3	T	C	9: 70,034,008	Y426C	probably damaging	Het
Gm5580	C	T	6: 116,552,356	T398I	probably damaging	Het
Gtpbp1	C	T	15: 79,717,654	R533C	probably damaging	Het
Hid1	T	C	11: 115,361,676	E60G	probably damaging	Het
Ighv1-81	A	T	12: 115,920,541	L30Q	possibly damaging	Het
Ighv5-8	TATATATATATATATATATATA	TATATATATATATATATATATATA	12: 113,654,945		probably null	Het
Klf10	A	G	15: 38,297,758	L44P	probably damaging	Het
Lamc3	T	C	2: 31,923,005	V1001A	probably benign	Het
Lamc3	C	A	2: 31,928,896	S1211*	probably null	Het
Lmx1a	T	A	1: 167,830,625	H192Q	probably benign	Het
Nkx2-4	T	C	2: 147,084,264	H226R	possibly damaging	Het
Olfr1046	T	C	2: 86,216,903	H269R	probably damaging	Het
Olfr1179	G	A	2: 88,402,242	R231C	probably benign	Het
Olfr1240	T	A	2: 89,439,932	M116L	probably damaging	Het
Olfr1281	T	C	2: 111,328,952	F178L	probably damaging	Het
Olfr1453	T	C	19: 13,027,630	H233R	probably benign	Het
Olfr1468-ps1	A	T	19: 13,375,640	N226I	unknown	Het
Olfr472	T	A	7: 107,903,320	I201N	possibly damaging	Het
Olfr715	T	C	7: 107,128,626	I256V	probably benign	Het
Olfr869	T	C	9: 20,137,461	M115T	probably damaging	Het
Orai3	G	T	7: 127,774,022	A232S	probably benign	Het
Pak1ip1	G	A	13: 41,009,251	G177R	probably benign	Het
Pcp4l1	T	C	1: 171,174,406	R62G	possibly damaging	Het
Phox2b	T	A	5: 67,098,721	Q74L	probably benign	Het
Pi4kb	A	G	3: 94,984,486	Y159C	probably damaging	Het
Pkd1l3	GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA	GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA	8: 109,624,195		probably benign	Het
Plxna1	T	C	6: 89,329,559	R1430G	probably null	Het
Plxna4	T	C	6: 32,178,380	H1543R	probably benign	Het
Prcc	A	T	3: 87,869,731	F312Y	probably damaging	Het
Ranbp6	A	G	19: 29,809,988	L988P	probably damaging	Het
Rbm27	A	G	18: 42,327,507	T840A	probably benign	Het
Rchy1	G	T	5: 91,957,972	T39N	probably benign	Het
Rmi1	C	T	13: 58,409,026	T363I	probably benign	Het
Rnpc3	A	C	3: 113,611,246	I420S	probably damaging	Het
Rsph4a	T	A	10: 33,909,398	V435E	probably benign	Het
Rwdd1	T	C	10: 34,012,099	T38A	probably damaging	Het
S100a13	G	T	3: 90,515,863	D54Y	unknown	Het
Sel1l3	T	C	5: 53,154,286	Y619C	probably damaging	Het
Sf3b3	T	C	8: 110,812,026	T1121A	probably damaging	Het
Sgk3	T	C	1: 9,872,309	V102A	probably benign	Het
Sh2b1	T	C	7: 126,469,182	T486A	probably damaging	Het
Slc22a5	C	T	11: 53,876,155	R169H	probably damaging	Het
Slc4a5	T	C	6: 83,289,241	V889A	possibly damaging	Het
Spast	C	A	17: 74,339,074	S13*	probably null	Het
Srek1	T	C	13: 103,753,146		probably null	Het
Sugp1	G	T	8: 70,056,570	E164D	probably benign	Het
Synpo2	T	C	3: 123,117,324	D224G	probably benign	Het
Tanc1	A	G	2: 59,800,088	D804G	probably damaging	Het
Tep1	C	T	14: 50,844,309	C1228Y	probably damaging	Het
Tes	T	A	6: 17,100,342	C325S	probably benign	Het
Themis	T	C	10: 28,863,394	V620A	probably benign	Het
Trim17	T	C	11: 58,971,431	S430P	probably damaging	Het
Tubgcp5	T	C	7: 55,795,945	I65T	possibly damaging	Het
Unc13b	T	C	4: 43,171,955	S928P	unknown	Het
Vat1l	C	T	8: 114,289,432	A354V	probably damaging	Het
Vmn1r170	T	A	7: 23,606,838	S222T	probably benign	Het
Vmn2r112	A	T	17: 22,601,232	M29L	probably benign	Het
Vmn2r72	T	C	7: 85,751,203	I213V	probably benign	Het
Wdr89	T	A	12: 75,632,790	Q230L	possibly damaging	Het
Zfp442	T	A	2: 150,409,367	H205L	probably benign	Het
Zfyve26	A	T	12: 79,276,302	I890N	possibly damaging	Het
Zic1	T	C	9: 91,364,320	E233G	probably damaging	Het

Other mutations in Zfp386

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01982:Zfp386	APN	12	116059168	missense	probably benign
IGL02692:Zfp386	APN	12	116059235	missense	probably damaging	0.96
IGL03071:Zfp386	APN	12	116059140	missense	probably benign	0.08
F5493:Zfp386	UTSW	12	116060302	missense	probably damaging	0.99
R0098:Zfp386	UTSW	12	116059214	nonsense	probably null
R0098:Zfp386	UTSW	12	116059214	nonsense	probably null
R0372:Zfp386	UTSW	12	116054816	missense	possibly damaging	0.71
R0784:Zfp386	UTSW	12	116059920	nonsense	probably null
R0866:Zfp386	UTSW	12	116054709	splice site	probably benign
R0947:Zfp386	UTSW	12	116059778	missense	probably benign	0.11
R1080:Zfp386	UTSW	12	116059806	nonsense	probably null
R1517:Zfp386	UTSW	12	116059605	missense	possibly damaging	0.67
R1597:Zfp386	UTSW	12	116060089	missense	probably damaging	0.99
R1722:Zfp386	UTSW	12	116059906	missense	probably damaging	0.99
R2043:Zfp386	UTSW	12	116059161	missense	probably benign	0.22
R3741:Zfp386	UTSW	12	116059550	nonsense	probably null
R3742:Zfp386	UTSW	12	116059550	nonsense	probably null
R3902:Zfp386	UTSW	12	116060155	missense	probably damaging	1.00
R5012:Zfp386	UTSW	12	116059244	missense	probably benign
R5590:Zfp386	UTSW	12	116059727	missense	probably benign	0.41
R5709:Zfp386	UTSW	12	116059685	missense	probably benign	0.23
R6156:Zfp386	UTSW	12	116059906	missense	probably damaging	0.99
R6184:Zfp386	UTSW	12	116060513	missense	possibly damaging	0.64
R6423:Zfp386	UTSW	12	116060113	missense	probably damaging	0.96
R8015:Zfp386	UTSW	12	116059407	missense	probably damaging	0.96
R8120:Zfp386	UTSW	12	116054953	missense	unknown
R8137:Zfp386	UTSW	12	116059648	missense	possibly damaging	0.91
R9093:Zfp386	UTSW	12	116060258	nonsense	probably null
R9320:Zfp386	UTSW	12	116059897	missense	probably damaging	1.00
R9331:Zfp386	UTSW	12	116047813	start gained	probably benign
R9536:Zfp386	UTSW	12	116060066	missense	probably damaging	1.00
R9641:Zfp386	UTSW	12	116059710	missense	probably benign	0.03
Z1088:Zfp386	UTSW	12	116054773	missense	possibly damaging	0.95

Predicted Primers

PCR Primer
(F):5'- CTGCTACTGATCCATTATTGCATAGC -3'
(R):5'- TGCACACTGGGTAAAGGATTTTC -3'

Sequencing Primer
(F):5'- TTGCATAGCCAAAATCTAGATACAG -3'
(R):5'- TCTCTCCTGTGTGAATTATGCTG -3'

Posted On

2022-03-25