Mutagenetix > Incidental Mutation

Incidental Mutation 'R5743:Zfp141'

445667

Institutional Source

Beutler Lab

Gene Symbol

Zfp141

Ensembl Gene

ENSMUSG00000092416

Gene Name

zinc finger protein 141

Synonyms

MMRRC Submission

043353-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5743 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

42122810-42155164 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to G at 42125855 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Leucine at position 206 (I206L)

Ref Sequence

ENSEMBL: ENSMUSP00000133899 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000173489] [ENSMUST00000174407]

AlphaFold

G3UY09

Predicted Effect

probably benign
Transcript: ENSMUST00000173489

Predicted Effect

possibly damaging
Transcript: ENSMUST00000174407
AA Change: I206L

PolyPhen 2 Score 0.678 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000133899
Gene: ENSMUSG00000092416
AA Change: I206L

Domain	Start	End	E-Value	Type
KRAB	18	78	4.41e-34	SMART
internal_repeat_1	146	405	8.73e-7	PROSPERO
ZnF_C2H2	410	432	4.54e-4	SMART
ZnF_C2H2	438	460	2.2e-2	SMART
ZnF_C2H2	466	488	2.95e-3	SMART
ZnF_C2H2	494	516	4.24e-4	SMART
ZnF_C2H2	522	544	9.58e-3	SMART
ZnF_C2H2	550	572	4.01e-5	SMART
ZnF_C2H2	578	600	3.21e-4	SMART
ZnF_C2H2	606	628	4.87e-4	SMART
ZnF_C2H2	634	656	5.99e-4	SMART
ZnF_C2H2	662	684	4.87e-4	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000174489

Coding Region Coverage

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

Validation Efficiency

MGI Phenotype

PHENOTYPE: Homozygous mutation of this gene results in abnormal skin pigmentation. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 60 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acss2	A	G	2: 155,416,536 (GRCm39)		probably benign	Het
Ankef1	A	G	2: 136,391,629 (GRCm39)		probably null	Het
Arhgap20	T	A	9: 51,728,027 (GRCm39)	M80K	probably benign	Het
Arhgap29	T	G	3: 121,775,560 (GRCm39)	L37R	probably damaging	Het
Baiap3	G	A	17: 25,463,759 (GRCm39)	P906S	probably benign	Het
Caskin2	T	A	11: 115,693,115 (GRCm39)	N603I	possibly damaging	Het
Catspere2	G	T	1: 177,950,328 (GRCm39)		silent	Het
Ccdc159	A	T	9: 21,840,686 (GRCm39)	E84D	probably benign	Het
Ccl1	T	G	11: 82,067,712 (GRCm39)	S73R	possibly damaging	Het
Cdh20	G	T	1: 110,036,575 (GRCm39)	C585F	probably damaging	Het
Cga	T	C	4: 34,904,108 (GRCm39)		probably null	Het
Coq5	A	C	5: 115,417,941 (GRCm39)	E57A	probably benign	Het
Cstf1	T	A	2: 172,219,753 (GRCm39)	L288Q	probably damaging	Het
Ctsll3	G	T	13: 60,948,815 (GRCm39)	Q47K	probably benign	Het
Dchs1	T	A	7: 105,420,803 (GRCm39)	Q539L	probably benign	Het
Fbxo46	C	A	7: 18,870,420 (GRCm39)	D346E	probably damaging	Het
Frem3	A	T	8: 81,342,407 (GRCm39)	T1567S	probably damaging	Het
Glce	T	A	9: 61,977,822 (GRCm39)	T21S	probably damaging	Het
Gm19402	C	T	10: 77,526,516 (GRCm39)	D26N	probably damaging	Het
Gm20830	A	G	Y: 6,916,664 (GRCm39)	Y152H	probably damaging	Het
Herc3	T	C	6: 58,895,784 (GRCm39)	Y1011H	probably benign	Het
Igkv6-29	C	A	6: 70,115,584 (GRCm39)	G70V	possibly damaging	Het
Il31ra	G	T	13: 112,664,021 (GRCm39)	T552K	possibly damaging	Het
Itga2	A	G	13: 115,021,042 (GRCm39)	V86A	probably damaging	Het
Kcnk4	A	T	19: 6,905,723 (GRCm39)	N81K	possibly damaging	Het
Lrp2	C	A	2: 69,297,221 (GRCm39)	D3247Y	probably damaging	Het
Maml3	G	T	3: 52,011,553 (GRCm39)	F4L	unknown	Het
Mcpt1	A	T	14: 56,256,072 (GRCm39)	H37L	probably benign	Het
Mpdz	T	C	4: 81,339,425 (GRCm39)	M1V	probably null	Het
Myom2	A	T	8: 15,130,914 (GRCm39)	K283N	possibly damaging	Het
Nrxn1	C	A	17: 90,950,652 (GRCm39)	R509L	probably damaging	Het
Ntng1	T	A	3: 110,042,736 (GRCm39)	Y30F	probably damaging	Het
Or52e7	A	G	7: 104,685,363 (GRCm39)		probably null	Het
Or8c13	C	A	9: 38,092,014 (GRCm39)	C35F	probably benign	Het
Or8h8	C	A	2: 86,753,549 (GRCm39)	G109V	probably benign	Het
Orc6	A	T	8: 86,029,585 (GRCm39)	Q43L	probably benign	Het
Otogl	G	A	10: 107,692,862 (GRCm39)	S874L	possibly damaging	Het
Pcdh9	T	C	14: 94,124,160 (GRCm39)	D670G	probably damaging	Het
Pcdhga9	A	T	18: 37,871,859 (GRCm39)	I563F	probably damaging	Het
Plxna1	A	T	6: 89,333,511 (GRCm39)	S373T	probably damaging	Het
Prop1	T	C	11: 50,841,836 (GRCm39)	D190G	probably damaging	Het
Qrich1	T	A	9: 108,411,314 (GRCm39)	Y280N	probably damaging	Het
Rasl10a	T	A	11: 5,009,519 (GRCm39)	D102E	probably benign	Het
Rgs1	T	C	1: 144,121,110 (GRCm39)	Y187C	probably damaging	Het
Sema5b	T	A	16: 35,478,846 (GRCm39)	W557R	probably damaging	Het
Sh2b3	A	T	5: 121,966,520 (GRCm39)	L198H	probably damaging	Het
Slc27a3	G	T	3: 90,294,379 (GRCm39)	T429K	probably benign	Het
Slc35f1	T	G	10: 52,965,546 (GRCm39)	D320E	probably benign	Het
Smug1	C	A	15: 103,066,043 (GRCm39)		probably null	Het
Spata31f3	G	A	4: 42,873,087 (GRCm39)	T68I	probably damaging	Het
Ssrp1	T	A	2: 84,871,512 (GRCm39)	Y311*	probably null	Het
Svep1	T	C	4: 58,096,223 (GRCm39)	T1466A	possibly damaging	Het
Tmem130	A	G	5: 144,687,749 (GRCm39)	S196P	probably damaging	Het
Trim30d	A	T	7: 104,121,535 (GRCm39)	C176*	probably null	Het
Ush2a	A	G	1: 188,169,159 (GRCm39)	H1100R	probably benign	Het
Vezt	A	T	10: 93,832,957 (GRCm39)	F151L	probably benign	Het
Vps35l	A	G	7: 118,396,234 (GRCm39)	T538A	possibly damaging	Het
Zc3h3	G	T	15: 75,651,380 (GRCm39)	C638*	probably null	Het
Zfp128	C	T	7: 12,618,654 (GRCm39)	R51C	probably damaging	Het
Zfp369	G	T	13: 65,443,494 (GRCm39)	K324N	probably benign	Het

Other mutations in Zfp141

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00593:Zfp141	APN	7	42,124,731 (GRCm39)	nonsense	probably null
IGL00595:Zfp141	APN	7	42,126,079 (GRCm39)	missense	probably benign	0.08
R0577:Zfp141	UTSW	7	42,125,938 (GRCm39)	missense	probably benign	0.14
R0883:Zfp141	UTSW	7	42,125,480 (GRCm39)	missense	possibly damaging	0.85
R1701:Zfp141	UTSW	7	42,125,470 (GRCm39)	missense	probably benign	0.35
R2290:Zfp141	UTSW	7	42,124,649 (GRCm39)	missense	probably damaging	1.00
R4176:Zfp141	UTSW	7	42,125,705 (GRCm39)	missense	probably benign	0.04
R4719:Zfp141	UTSW	7	42,126,111 (GRCm39)	splice site	probably null
R4897:Zfp141	UTSW	7	42,125,629 (GRCm39)	missense	probably benign	0.24
R5372:Zfp141	UTSW	7	42,126,620 (GRCm39)	missense	possibly damaging	0.91
R5438:Zfp141	UTSW	7	42,138,894 (GRCm39)	missense	probably damaging	1.00
R5447:Zfp141	UTSW	7	42,124,983 (GRCm39)	nonsense	probably null
R5969:Zfp141	UTSW	7	42,138,912 (GRCm39)	missense	probably damaging	0.98
R6731:Zfp141	UTSW	7	42,138,924 (GRCm39)	missense	probably damaging	0.99
R7127:Zfp141	UTSW	7	42,124,853 (GRCm39)	missense	probably damaging	1.00
R7474:Zfp141	UTSW	7	42,125,678 (GRCm39)	nonsense	probably null
R7572:Zfp141	UTSW	7	42,124,856 (GRCm39)	missense	probably benign	0.03
R7830:Zfp141	UTSW	7	42,124,612 (GRCm39)	missense	probably benign	0.01
R7890:Zfp141	UTSW	7	42,125,903 (GRCm39)	missense	probably damaging	0.99
R8133:Zfp141	UTSW	7	42,124,481 (GRCm39)	missense	probably damaging	1.00
R8833:Zfp141	UTSW	7	42,125,687 (GRCm39)	missense	possibly damaging	0.82
R9238:Zfp141	UTSW	7	42,125,111 (GRCm39)	nonsense	probably null
R9245:Zfp141	UTSW	7	42,124,821 (GRCm39)	nonsense	probably null
R9339:Zfp141	UTSW	7	42,125,639 (GRCm39)	missense	probably damaging	0.98
R9348:Zfp141	UTSW	7	42,124,814 (GRCm39)	nonsense	probably null
R9498:Zfp141	UTSW	7	42,125,770 (GRCm39)	missense	probably benign	0.07

Predicted Primers

PCR Primer
(F):5'- GATTCAACAGAGACTTTGCTGTAC -3'
(R):5'- CGTGAAAGCCATCATTGGTTGG -3'

Sequencing Primer
(F):5'- CAACAGAGACTTTGCTGTACTTATC -3'
(R):5'- GGGTATTTCTGAATACTGCCACAG -3'

Posted On

2016-11-21