Mutagenetix > Incidental Mutation

Incidental Mutation 'R7467:Zfp354c'

578881

Institutional Source

Beutler Lab

Gene Symbol

Zfp354c

Ensembl Gene

ENSMUSG00000044807

Gene Name

zinc finger protein 354C

Synonyms

5330421P20Rik, Kid3, AJ18

MMRRC Submission

045541-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.073) question?

Stock #

R7467 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

50701913-50718551 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 50706253 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 274 (Y274C)

Ref Sequence

ENSEMBL: ENSMUSP00000104763 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000000632] [ENSMUST00000109135]

AlphaFold

Q571J5

Predicted Effect

probably damaging
Transcript: ENSMUST00000000632
AA Change: Y274C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000000632
Gene: ENSMUSG00000044807
AA Change: Y274C

Domain	Start	End	E-Value	Type
KRAB	14	74	9.98e-33	SMART
ZnF_C2H2	218	240	5.9e-3	SMART
ZnF_C2H2	246	268	3.74e-5	SMART
ZnF_C2H2	274	296	1.72e-4	SMART
ZnF_C2H2	302	324	7.78e-3	SMART
ZnF_C2H2	330	352	1.92e-2	SMART
ZnF_C2H2	358	380	4.79e-3	SMART
ZnF_C2H2	386	408	1.1e-2	SMART
ZnF_C2H2	414	436	5.67e-5	SMART
ZnF_C2H2	442	464	9.08e-4	SMART
ZnF_C2H2	470	492	5.59e-4	SMART
ZnF_C2H2	498	520	3.39e-3	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000109135
AA Change: Y274C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000104763
Gene: ENSMUSG00000044807
AA Change: Y274C

Domain	Start	End	E-Value	Type
KRAB	14	74	9.98e-33	SMART
ZnF_C2H2	218	240	5.9e-3	SMART
ZnF_C2H2	246	268	3.74e-5	SMART
ZnF_C2H2	274	296	1.72e-4	SMART
ZnF_C2H2	302	324	7.78e-3	SMART
ZnF_C2H2	330	352	1.92e-2	SMART
ZnF_C2H2	358	380	4.79e-3	SMART
ZnF_C2H2	386	408	1.1e-2	SMART
ZnF_C2H2	414	436	5.67e-5	SMART
ZnF_C2H2	442	464	9.08e-4	SMART
ZnF_C2H2	470	492	5.59e-4	SMART
ZnF_C2H2	498	520	3.39e-3	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139465

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.4%

Validation Efficiency

98% (103/105)

Allele List at MGI

Other mutations in this stock

Total: 106 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgre4	G	A	17: 56,098,952 (GRCm39)	V153I	probably benign	Het
Akap13	G	A	7: 75,380,213 (GRCm39)	R462H	probably damaging	Het
Aldh16a1	A	G	7: 44,795,331 (GRCm39)	Y443H	probably benign	Het
Apbb1	A	G	7: 105,215,339 (GRCm39)	V434A	probably benign	Het
Atrip	A	G	9: 108,898,422 (GRCm39)	M199T	probably damaging	Het
Atxn2	T	C	5: 121,940,330 (GRCm39)		probably null	Het
AU040320	A	G	4: 126,708,103 (GRCm39)	T240A	probably benign	Het
Btf3l4	A	T	4: 108,675,589 (GRCm39)		probably null	Het
Ccdc106	A	G	7: 5,063,325 (GRCm39)	T277A	probably damaging	Het
Cdk15	G	T	1: 59,328,938 (GRCm39)	W282L	probably null	Het
Cflar	T	A	1: 58,765,597 (GRCm39)	M1K	probably null	Het
Champ1	C	A	8: 13,928,579 (GRCm39)	P246T	possibly damaging	Het
Crat	A	C	2: 30,299,994 (GRCm39)	F129V	probably damaging	Het
Csmd3	T	C	15: 47,492,640 (GRCm39)	N2256S		Het
Cwh43	C	A	5: 73,569,311 (GRCm39)	Q118K	probably damaging	Het
Daam1	A	T	12: 72,032,580 (GRCm39)	K949*	probably null	Het
Ddn	C	G	15: 98,703,247 (GRCm39)	E682Q	possibly damaging	Het
Des	T	A	1: 75,339,605 (GRCm39)	M321K	possibly damaging	Het
Dnm2	T	C	9: 21,392,672 (GRCm39)	V460A	probably damaging	Het
Dst	G	A	1: 34,230,236 (GRCm39)	E2610K	probably benign	Het
Efr3a	C	T	15: 65,729,360 (GRCm39)	T660I	possibly damaging	Het
Eogt	T	C	6: 97,119,794 (GRCm39)	E138G	probably benign	Het
Epha8	G	A	4: 136,658,399 (GRCm39)	A992V	possibly damaging	Het
Exoc2	A	T	13: 31,109,716 (GRCm39)	D217E	probably damaging	Het
Fam222b	T	C	11: 78,045,173 (GRCm39)	S245P	probably damaging	Het
Fbxo45	T	C	16: 32,057,339 (GRCm39)	Y185C	probably damaging	Het
Fbxo47	T	C	11: 97,755,993 (GRCm39)	T170A	probably benign	Het
Fbxw26	A	T	9: 109,561,765 (GRCm39)	V143E	probably benign	Het
Foxb2	T	C	19: 16,851,004 (GRCm39)	M1V	probably null	Het
Gm11596	C	A	11: 99,683,962 (GRCm39)	V53L	unknown	Het
Gm47791	A	G	1: 82,748,547 (GRCm39)	*140Q	probably null	Het
Gpr179	C	T	11: 97,226,115 (GRCm39)	M2013I	probably benign	Het
Hck	T	A	2: 152,971,850 (GRCm39)	L137*	probably null	Het
Hectd4	T	A	5: 121,462,024 (GRCm39)	C964S	possibly damaging	Het
Hexa	T	C	9: 59,464,683 (GRCm39)		probably null	Het
Ifna12	C	A	4: 88,521,502 (GRCm39)	S15I	possibly damaging	Het
Kif18b	C	A	11: 102,807,234 (GRCm39)	V34L	probably damaging	Het
Kif18b	A	T	11: 102,803,174 (GRCm39)		probably null	Het
Kifap3	A	T	1: 163,643,402 (GRCm39)	H209L	probably benign	Het
Klhl1	A	T	14: 96,360,713 (GRCm39)	D712E	probably damaging	Het
Kmt2c	T	C	5: 25,513,530 (GRCm39)	D3088G	probably damaging	Het
Mageb3	A	G	2: 121,784,953 (GRCm39)	Y250H	probably damaging	Het
Manba	G	T	3: 135,250,562 (GRCm39)	E396D	probably damaging	Het
Mapkbp1	T	A	2: 119,852,669 (GRCm39)	V997E	probably damaging	Het
Mdc1	A	G	17: 36,155,448 (GRCm39)	H41R	probably benign	Het
Mis18a	T	G	16: 90,516,866 (GRCm39)	M179L	probably benign	Het
Mmp25	C	G	17: 23,863,756 (GRCm39)	G25R	possibly damaging	Het
Mmp3	A	G	9: 7,447,621 (GRCm39)	D202G	possibly damaging	Het
Mmp3	C	T	9: 7,450,125 (GRCm39)	P286S	probably benign	Het
Mrgpra2b	G	A	7: 47,114,277 (GRCm39)	H152Y	possibly damaging	Het
Mslnl	A	T	17: 25,955,895 (GRCm39)	M1L	probably benign	Het
Myo1d	G	A	11: 80,477,743 (GRCm39)	T880I	probably damaging	Het
Ncaph	T	A	2: 126,975,795 (GRCm39)		probably benign	Het
Nln	T	C	13: 104,161,530 (GRCm39)	D680G	possibly damaging	Het
Noct	C	T	3: 51,132,622 (GRCm39)	A33V	probably benign	Het
Nolc1	A	G	19: 46,070,773 (GRCm39)	T325A	unknown	Het
Nr2e3	A	G	9: 59,856,434 (GRCm39)		probably null	Het
Nrg2	T	A	18: 36,155,459 (GRCm39)	H450L	probably benign	Het
Or13a21	T	C	7: 139,999,287 (GRCm39)	N133S	probably benign	Het
Or2t43	A	C	11: 58,457,288 (GRCm39)	N294K	possibly damaging	Het
Or5ak24	T	G	2: 85,261,171 (GRCm39)	M1L	possibly damaging	Het
Or5an1	T	A	19: 12,260,839 (GRCm39)	C142*	probably null	Het
Or6b3	T	A	1: 92,439,570 (GRCm39)	Y60F	possibly damaging	Het
Pank2	T	A	2: 131,115,967 (GRCm39)	N128K	possibly damaging	Het
Pcdha3	T	C	18: 37,080,584 (GRCm39)	V442A	probably damaging	Het
Pds5b	T	A	5: 150,659,792 (GRCm39)	S252T	probably damaging	Het
Pfpl	T	C	19: 12,405,878 (GRCm39)	L43S	probably damaging	Het
Pigu	T	A	2: 155,141,009 (GRCm39)	I295F	probably damaging	Het
Piwil4	T	C	9: 14,616,337 (GRCm39)	Y673C	probably damaging	Het
Pls1	A	G	9: 95,651,166 (GRCm39)	Y414H	possibly damaging	Het
Ppp1r13l	A	T	7: 19,105,305 (GRCm39)	Q359L	probably damaging	Het
Ppp2r5c	A	G	12: 110,519,317 (GRCm39)	Y263C	probably damaging	Het
Prrc2c	A	T	1: 162,504,932 (GRCm39)	S2638R	possibly damaging	Het
Prss39	T	A	1: 34,538,473 (GRCm39)		probably null	Het
Psmd1	G	A	1: 86,044,355 (GRCm39)	V648M	probably damaging	Het
Rad50	T	C	11: 53,545,735 (GRCm39)	D1196G	probably damaging	Het
Rfx1	T	C	8: 84,800,542 (GRCm39)	Y48H	possibly damaging	Het
Rgs20	A	G	1: 4,982,553 (GRCm39)	I305T	probably benign	Het
Rpl9	T	C	5: 65,548,310 (GRCm39)	T9A	probably benign	Het
Samd4	A	G	14: 47,325,313 (GRCm39)	N598D	probably benign	Het
Sema7a	T	C	9: 57,868,705 (GRCm39)	Y606H	probably damaging	Het
Sf3b3	A	G	8: 111,538,088 (GRCm39)	S1150P	possibly damaging	Het
Sirt1	T	C	10: 63,157,929 (GRCm39)	N495S	probably benign	Het
Slc17a3	T	C	13: 24,030,950 (GRCm39)		probably null	Het
Slc25a22	T	C	7: 141,013,889 (GRCm39)	T24A	probably benign	Het
Slc30a9	T	C	5: 67,502,987 (GRCm39)	I363T	probably benign	Het
Srbd1	A	G	17: 86,406,702 (GRCm39)	V561A	probably damaging	Het
Srgap1	C	A	10: 121,691,344 (GRCm39)	E297*	probably null	Het
Srgap2	T	C	1: 131,220,405 (GRCm39)	S896G	probably damaging	Het
Sspo	T	C	6: 48,463,237 (GRCm39)	C3730R	probably damaging	Het
Stat2	T	A	10: 128,113,772 (GRCm39)		probably null	Het
Tcof1	T	C	18: 60,964,977 (GRCm39)	K581E	unknown	Het
Tdpoz6	T	A	3: 93,600,265 (GRCm39)	T35S	probably benign	Het
Thbs1	T	C	2: 117,948,681 (GRCm39)	S446P	probably damaging	Het
Thsd7a	T	C	6: 12,331,584 (GRCm39)	Y1330C		Het
Tmem121	C	A	12: 113,152,690 (GRCm39)	P303T	probably benign	Het
Tmem87b	T	A	2: 128,691,071 (GRCm39)		probably null	Het
Tmem98	A	T	11: 80,711,011 (GRCm39)		probably null	Het
Trpm3	T	A	19: 22,955,698 (GRCm39)	I1091N	possibly damaging	Het
Urb2	A	G	8: 124,755,250 (GRCm39)	E319G	probably benign	Het
Vmn1r170	A	T	7: 23,306,320 (GRCm39)	M241L	not run	Het
Vmn1r238	T	C	18: 3,123,393 (GRCm39)	N7S	probably benign	Het
Wdr6	T	C	9: 108,450,201 (GRCm39)	H1109R	probably benign	Het
Zdhhc13	T	C	7: 48,454,156 (GRCm39)	V193A	probably benign	Het
Zfp738	T	A	13: 67,821,080 (GRCm39)	E89V	probably benign	Het
Zswim3	T	A	2: 164,661,795 (GRCm39)	F92I	possibly damaging	Het

Other mutations in Zfp354c

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00923:Zfp354c	APN	11	50,706,440 (GRCm39)	missense	probably damaging	0.97
IGL01615:Zfp354c	APN	11	50,708,732 (GRCm39)	missense	possibly damaging	0.90
IGL03019:Zfp354c	APN	11	50,708,021 (GRCm39)	missense	probably damaging	1.00
R0546:Zfp354c	UTSW	11	50,706,457 (GRCm39)	missense	probably benign	0.12
R1370:Zfp354c	UTSW	11	50,706,667 (GRCm39)	missense	probably benign
R2109:Zfp354c	UTSW	11	50,707,969 (GRCm39)	missense	probably benign	0.01
R2850:Zfp354c	UTSW	11	50,706,158 (GRCm39)	nonsense	probably null
R4010:Zfp354c	UTSW	11	50,705,771 (GRCm39)	missense	probably damaging	0.98
R5034:Zfp354c	UTSW	11	50,705,866 (GRCm39)	missense	probably benign	0.14
R5430:Zfp354c	UTSW	11	50,706,022 (GRCm39)	missense	probably benign	0.02
R5439:Zfp354c	UTSW	11	50,706,597 (GRCm39)	missense	probably benign	0.01
R5905:Zfp354c	UTSW	11	50,706,253 (GRCm39)	missense	probably damaging	1.00
R6244:Zfp354c	UTSW	11	50,705,798 (GRCm39)	missense	probably benign	0.41
R6264:Zfp354c	UTSW	11	50,706,274 (GRCm39)	missense	probably benign	0.00
R6591:Zfp354c	UTSW	11	50,705,602 (GRCm39)	missense	probably benign	0.41
R6650:Zfp354c	UTSW	11	50,705,518 (GRCm39)	missense	probably damaging	1.00
R6691:Zfp354c	UTSW	11	50,705,602 (GRCm39)	missense	probably benign	0.41
R7087:Zfp354c	UTSW	11	50,706,040 (GRCm39)	missense	probably damaging	1.00
R7313:Zfp354c	UTSW	11	50,705,483 (GRCm39)	missense	probably damaging	1.00
R7619:Zfp354c	UTSW	11	50,708,635 (GRCm39)	critical splice donor site	probably null
R7699:Zfp354c	UTSW	11	50,706,067 (GRCm39)	small deletion	probably benign
R7710:Zfp354c	UTSW	11	50,706,067 (GRCm39)	small deletion	probably benign
R7712:Zfp354c	UTSW	11	50,706,067 (GRCm39)	small deletion	probably benign
R7747:Zfp354c	UTSW	11	50,706,067 (GRCm39)	small deletion	probably benign
R7748:Zfp354c	UTSW	11	50,706,067 (GRCm39)	small deletion	probably benign
R7784:Zfp354c	UTSW	11	50,706,067 (GRCm39)	small deletion	probably benign
R7816:Zfp354c	UTSW	11	50,706,067 (GRCm39)	small deletion	probably benign
R7817:Zfp354c	UTSW	11	50,706,067 (GRCm39)	small deletion	probably benign
R7853:Zfp354c	UTSW	11	50,706,067 (GRCm39)	small deletion	probably benign
R7855:Zfp354c	UTSW	11	50,706,067 (GRCm39)	small deletion	probably benign
R7870:Zfp354c	UTSW	11	50,706,065 (GRCm39)	small deletion	probably benign
R8852:Zfp354c	UTSW	11	50,706,019 (GRCm39)	missense	probably damaging	1.00
R8860:Zfp354c	UTSW	11	50,706,019 (GRCm39)	missense	probably damaging	1.00
R8862:Zfp354c	UTSW	11	50,708,718 (GRCm39)	missense	probably benign	0.15
R9169:Zfp354c	UTSW	11	50,706,088 (GRCm39)	missense	probably damaging	1.00
R9215:Zfp354c	UTSW	11	50,706,666 (GRCm39)	missense	probably benign	0.31
R9273:Zfp354c	UTSW	11	50,706,059 (GRCm39)	missense	probably damaging	1.00
R9762:Zfp354c	UTSW	11	50,706,239 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CGTGTAAAGGTTCTCCCACATTG -3'
(R):5'- CCTGCTACGTATCACACTTCAG -3'

Sequencing Primer
(F):5'- GCAGTTAAAGGCCTTGTCAC -3'
(R):5'- GAAGCTTTCAAATGTACCCAGG -3'

Posted On

2019-10-07