Mutagenetix > Incidental Mutation

Incidental Mutation 'R5775:Zfp354b'

448739

Institutional Source

Beutler Lab

Gene Symbol

Zfp354b

Ensembl Gene

ENSMUSG00000020335

Gene Name

zinc finger protein 354B

Synonyms

Kid2

MMRRC Submission

043374-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.059) question?

Stock #

R5775 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

50812650-50822460 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 50813647 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Tyrosine at position 426 (F426Y)

Ref Sequence

ENSEMBL: ENSMUSP00000127671 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000109124] [ENSMUST00000164280]

AlphaFold

Q9QXT9

Predicted Effect

probably benign
Transcript: ENSMUST00000109124
AA Change: F426Y

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)

SMART Domains

Protein: ENSMUSP00000104752
Gene: ENSMUSG00000020335
AA Change: F426Y

Domain	Start	End	E-Value	Type
KRAB	14	74	1.85e-36	SMART
ZnF_C2H2	206	228	4.47e-3	SMART
ZnF_C2H2	234	256	3.16e-3	SMART
ZnF_C2H2	262	284	7.37e-4	SMART
ZnF_C2H2	290	312	1.3e-4	SMART
ZnF_C2H2	343	365	1.47e-3	SMART
ZnF_C2H2	371	393	4.24e-4	SMART
ZnF_C2H2	399	421	2.79e-4	SMART
ZnF_C2H2	427	449	9.58e-3	SMART
ZnF_C2H2	455	477	2.4e-3	SMART
ZnF_C2H2	483	505	1.2e-3	SMART
ZnF_C2H2	511	533	3.95e-4	SMART
ZnF_C2H2	539	561	2.99e-4	SMART
ZnF_C2H2	567	589	4.87e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000164280
AA Change: F426Y

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)

SMART Domains

Protein: ENSMUSP00000127671
Gene: ENSMUSG00000020335
AA Change: F426Y

Domain	Start	End	E-Value	Type
KRAB	14	74	1.85e-36	SMART
ZnF_C2H2	206	228	4.47e-3	SMART
ZnF_C2H2	234	256	3.16e-3	SMART
ZnF_C2H2	262	284	7.37e-4	SMART
ZnF_C2H2	290	312	1.3e-4	SMART
ZnF_C2H2	343	365	1.47e-3	SMART
ZnF_C2H2	371	393	4.24e-4	SMART
ZnF_C2H2	399	421	2.79e-4	SMART
ZnF_C2H2	427	449	9.58e-3	SMART
ZnF_C2H2	455	477	2.4e-3	SMART
ZnF_C2H2	483	505	1.2e-3	SMART
ZnF_C2H2	511	533	3.95e-4	SMART
ZnF_C2H2	539	561	2.99e-4	SMART
ZnF_C2H2	567	589	4.87e-4	SMART

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.4%
20x: 95.7%

Validation Efficiency

97% (59/61)

Allele List at MGI

Other mutations in this stock

Total: 56 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam6a	A	G	12: 113,509,886 (GRCm39)	D753G	possibly damaging	Het
Arpc2	T	A	1: 74,295,108 (GRCm39)		probably null	Het
Atxn2	C	T	5: 121,951,512 (GRCm39)	T619M	probably damaging	Het
Cacna1s	T	C	1: 136,035,860 (GRCm39)	Y1120H	probably damaging	Het
Calm5	T	C	13: 3,904,435 (GRCm39)	L20S	probably damaging	Het
Carmil1	T	C	13: 24,460,520 (GRCm39)	I20V	probably benign	Het
Cd177	T	C	7: 24,451,693 (GRCm39)	E441G	probably damaging	Het
Cd63	T	A	10: 128,746,299 (GRCm39)	C9S	probably damaging	Het
Cep250	A	C	2: 155,811,294 (GRCm39)	D380A	possibly damaging	Het
Col5a3	G	T	9: 20,712,368 (GRCm39)	P509Q	unknown	Het
Cyp11b2	A	G	15: 74,725,327 (GRCm39)	V264A	probably benign	Het
Dennd6a	T	A	14: 26,340,528 (GRCm39)	L214*	probably null	Het
Dna2	A	G	10: 62,785,021 (GRCm39)	N46S	possibly damaging	Het
Elovl1	G	A	4: 118,288,094 (GRCm39)	V77I	probably benign	Het
Eml1	A	T	12: 108,472,813 (GRCm39)	Y207F	probably damaging	Het
Epha6	C	T	16: 59,639,357 (GRCm39)	R839Q	possibly damaging	Het
Erlec1	A	T	11: 30,893,848 (GRCm39)	S105T	probably benign	Het
Esp3	T	A	17: 40,944,468 (GRCm39)	S37T	possibly damaging	Het
Foxh1	G	A	15: 76,554,049 (GRCm39)	A8V	probably benign	Het
Fut1	A	C	7: 45,268,886 (GRCm39)	D280A	probably damaging	Het
Gm13998	G	T	2: 119,708,892 (GRCm39)		noncoding transcript	Het
Gm7247	C	T	14: 51,601,805 (GRCm39)	S26F	probably benign	Het
H2az1	T	C	3: 137,571,380 (GRCm39)	Y61H	probably damaging	Het
Kcns1	T	C	2: 164,006,686 (GRCm39)	I426V	probably damaging	Het
Kdm4c	T	G	4: 74,277,668 (GRCm39)	V774G	probably damaging	Het
Mrc2	G	A	11: 105,228,639 (GRCm39)	V673I	probably benign	Het
Mtnr1b	G	A	9: 15,774,168 (GRCm39)	A297V	possibly damaging	Het
Or5d43	A	T	2: 88,105,045 (GRCm39)	M116K	probably damaging	Het
Or8b40	A	T	9: 38,027,423 (GRCm39)	E110D	probably damaging	Het
Osbpl5	A	T	7: 143,258,266 (GRCm39)	V346D	probably benign	Het
Pdzrn4	A	T	15: 92,655,562 (GRCm39)	E485V	probably damaging	Het
Pgpep1	G	A	8: 71,105,101 (GRCm39)	T53M	probably damaging	Het
Pigo	T	C	4: 43,023,475 (GRCm39)	D233G	probably damaging	Het
Pmm1	A	T	15: 81,836,156 (GRCm39)	I152N	probably benign	Het
Pot1a	A	T	6: 25,757,297 (GRCm39)		probably null	Het
Ppp1r12b	G	T	1: 134,803,780 (GRCm39)	L460I	probably benign	Het
Prrc2a	T	C	17: 35,377,463 (GRCm39)	D565G	unknown	Het
Psd	C	A	19: 46,303,211 (GRCm39)	E724*	probably null	Het
Rasa2	C	T	9: 96,459,521 (GRCm39)		probably null	Het
Rsbn1	A	T	3: 103,869,888 (GRCm39)	Q783L	possibly damaging	Het
Ryr2	T	C	13: 11,784,848 (GRCm39)	Y1035C	probably damaging	Het
Sec24d	C	T	3: 123,084,109 (GRCm39)	A96V	probably benign	Het
Sec61a2	A	T	2: 5,887,585 (GRCm39)		probably null	Het
Sec62	A	G	3: 30,847,436 (GRCm39)		probably benign	Het
Tcstv2a	T	A	13: 120,725,475 (GRCm39)	C46*	probably null	Het
Tmem132b	T	A	5: 125,715,394 (GRCm39)		probably null	Het
Tnip3	A	G	6: 65,591,741 (GRCm39)	S247G	probably benign	Het
Traf3	A	G	12: 111,219,162 (GRCm39)	K263R	possibly damaging	Het
Tubgcp3	A	T	8: 12,675,056 (GRCm39)	I713N	probably damaging	Het
Unc5c	A	G	3: 141,534,281 (GRCm39)	E860G	probably damaging	Het
Usp44	A	G	10: 93,681,840 (GRCm39)	S97G	possibly damaging	Het
Vmn2r129	G	T	4: 156,686,692 (GRCm39)		noncoding transcript	Het
Vps37a	A	G	8: 40,982,160 (GRCm39)	H109R	probably damaging	Het
Wfikkn2	G	T	11: 94,129,114 (GRCm39)	D342E	probably benign	Het
Zfp462	C	A	4: 55,010,590 (GRCm39)	T852N	probably damaging	Het
Zfp987	T	G	4: 146,061,505 (GRCm39)	S312R	probably benign	Het

Other mutations in Zfp354b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02029:Zfp354b	APN	11	50,814,664 (GRCm39)	missense	probably benign
R1299:Zfp354b	UTSW	11	50,814,297 (GRCm39)	missense	probably benign	0.04
R1353:Zfp354b	UTSW	11	50,814,240 (GRCm39)	missense	probably damaging	0.96
R1860:Zfp354b	UTSW	11	50,814,369 (GRCm39)	missense	probably benign
R2072:Zfp354b	UTSW	11	50,813,279 (GRCm39)	nonsense	probably null
R5221:Zfp354b	UTSW	11	50,813,917 (GRCm39)	missense	probably benign	0.00
R5231:Zfp354b	UTSW	11	50,813,917 (GRCm39)	missense	probably benign	0.00
R5258:Zfp354b	UTSW	11	50,813,917 (GRCm39)	missense	probably benign	0.00
R5847:Zfp354b	UTSW	11	50,814,043 (GRCm39)	missense	probably damaging	0.96
R5929:Zfp354b	UTSW	11	50,813,282 (GRCm39)	missense	probably damaging	0.99
R6443:Zfp354b	UTSW	11	50,813,581 (GRCm39)	missense	possibly damaging	0.93
R6748:Zfp354b	UTSW	11	50,813,659 (GRCm39)	missense	probably damaging	1.00
R7439:Zfp354b	UTSW	11	50,813,224 (GRCm39)	missense	probably damaging	1.00
R7706:Zfp354b	UTSW	11	50,819,390 (GRCm39)	critical splice donor site	probably null
R7819:Zfp354b	UTSW	11	50,814,632 (GRCm39)	nonsense	probably null
R7830:Zfp354b	UTSW	11	50,814,136 (GRCm39)	missense	probably benign	0.28
R8508:Zfp354b	UTSW	11	50,814,297 (GRCm39)	missense	probably benign	0.04
R9157:Zfp354b	UTSW	11	50,813,887 (GRCm39)	missense	possibly damaging	0.95
R9170:Zfp354b	UTSW	11	50,814,362 (GRCm39)	missense	probably benign
R9303:Zfp354b	UTSW	11	50,820,256 (GRCm39)	missense	probably damaging	0.97
R9462:Zfp354b	UTSW	11	50,814,523 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- ATGCAAATCTATGTTCAAGGCG -3'
(R):5'- GCATCCACGTCCCTTTCAG -3'

Sequencing Primer
(F):5'- CCCGCACGTGTTACATTTAAAGGG -3'
(R):5'- GACCTACTTGTGCAACGAATGTG -3'

Posted On

2016-12-15