Mutagenetix > Incidental Mutation

Incidental Mutation 'R5054:Zfp444'

390702

Institutional Source

Beutler Lab

Gene Symbol

Zfp444

Ensembl Gene

ENSMUSG00000044876

Gene Name

zinc finger protein 444

Synonyms

2810031J10Rik, 6230401O10Rik

MMRRC Submission

042644-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.090) question?

Stock #

R5054 (G1)

Quality Score

121

Status

Validated

Chromosome

Chromosomal Location

6175429-6196103 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 6192792 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glutamic Acid at position 270 (V270E)

Ref Sequence

ENSEMBL: ENSMUSP00000104207 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000054680] [ENSMUST00000108565] [ENSMUST00000108566] [ENSMUST00000108567] [ENSMUST00000134933] [ENSMUST00000136777]

AlphaFold

Q3TDV8

Predicted Effect

probably damaging
Transcript: ENSMUST00000054680
AA Change: V270E

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000050797
Gene: ENSMUSG00000044876
AA Change: V270E

Domain	Start	End	E-Value	Type
SCAN	21	132	4.18e-39	SMART
low complexity region	167	183	N/A	INTRINSIC
ZnF_C2H2	186	208	9.3e-1	SMART
ZnF_C2H2	214	236	8.47e-4	SMART
ZnF_C2H2	254	276	5.81e-2	SMART
ZnF_C2H2	282	304	1.45e-2	SMART
low complexity region	316	329	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000108565

SMART Domains

Protein: ENSMUSP00000104205
Gene: ENSMUSG00000044876

Domain	Start	End	E-Value	Type
SCAN	21	129	9.98e-37	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000108566
AA Change: V270E

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000104206
Gene: ENSMUSG00000044876
AA Change: V270E

Domain	Start	End	E-Value	Type
SCAN	21	132	4.18e-39	SMART
low complexity region	167	183	N/A	INTRINSIC
ZnF_C2H2	186	208	9.3e-1	SMART
ZnF_C2H2	214	236	8.47e-4	SMART
ZnF_C2H2	254	276	5.81e-2	SMART
ZnF_C2H2	282	304	1.45e-2	SMART
low complexity region	316	329	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000108567
AA Change: V270E

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000104207
Gene: ENSMUSG00000044876
AA Change: V270E

Domain	Start	End	E-Value	Type
SCAN	21	132	4.18e-39	SMART
low complexity region	167	183	N/A	INTRINSIC
ZnF_C2H2	186	208	9.3e-1	SMART
ZnF_C2H2	214	236	8.47e-4	SMART
ZnF_C2H2	254	276	5.81e-2	SMART
ZnF_C2H2	282	304	1.45e-2	SMART
low complexity region	316	329	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000134933

SMART Domains

Protein: ENSMUSP00000120003
Gene: ENSMUSG00000044876

Domain	Start	End	E-Value	Type
SCAN	21	112	2.13e-31	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000136777

SMART Domains

Protein: ENSMUSP00000121948
Gene: ENSMUSG00000044876

Domain	Start	End	E-Value	Type
SCAN	21	132	4.18e-39	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000208192

Meta Mutation Damage Score

0.4701

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.9%
20x: 94.1%

Validation Efficiency

94% (67/71)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a zinc finger protein which activates transcription of a scavenger receptor gene involved in the degradation of acetylated low density lipoprotein (Ac-LDL) (PMID: 11978792). This gene is located in a cluster of zinc finger genes on chromosome 19 at q13.4. A pseudogene of this gene is located on chromosome 15. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2011]

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921517D22Rik	A	G	13: 59,837,315 (GRCm39)	Y257H	probably damaging	Het
Adam28	C	T	14: 68,855,164 (GRCm39)	C659Y	probably damaging	Het
Adamtsl2	G	A	2: 26,991,732 (GRCm39)	E627K	probably damaging	Het
Atad5	T	A	11: 79,985,502 (GRCm39)	S196R	probably benign	Het
Bcam	T	A	7: 19,490,785 (GRCm39)		probably benign	Het
Birc6	A	G	17: 74,962,320 (GRCm39)	H3978R	probably damaging	Het
Btbd7	T	C	12: 102,804,471 (GRCm39)	I190V	probably benign	Het
Ccdc8	T	C	7: 16,728,970 (GRCm39)	V153A	probably damaging	Het
Cyp2a5	C	G	7: 26,540,529 (GRCm39)	R68G	probably damaging	Het
Dock3	T	C	9: 106,815,105 (GRCm39)	Y1254C	probably damaging	Het
Dync2h1	T	C	9: 7,085,007 (GRCm39)	E2794G	possibly damaging	Het
Dytn	C	A	1: 63,700,318 (GRCm39)	V271L	possibly damaging	Het
Eif1ad15	T	C	12: 88,288,071 (GRCm39)	I61V	probably benign	Het
Eif2s2	A	C	2: 154,734,590 (GRCm39)		probably null	Het
Fndc7	A	G	3: 108,788,663 (GRCm39)	S193P	probably damaging	Het
Fzr1	G	A	10: 81,207,253 (GRCm39)		probably benign	Het
Gm17472	T	C	6: 42,957,938 (GRCm39)	I69T	probably damaging	Het
Gmppa	C	A	1: 75,416,015 (GRCm39)	Y137*	probably null	Het
Gpr45	A	G	1: 43,071,809 (GRCm39)	I151V	probably benign	Het
H1f0	G	A	15: 78,912,973 (GRCm39)	A18T	probably damaging	Het
Hbb-bh1	C	T	7: 103,491,063 (GRCm39)	V114I	probably benign	Het
Impa2	C	A	18: 67,439,797 (GRCm39)	P98Q	probably damaging	Het
Kazn	T	C	4: 141,835,957 (GRCm39)	N573D	unknown	Het
Kcna2	A	T	3: 107,011,656 (GRCm39)	D79V	probably damaging	Het
Kcna7	G	A	7: 45,056,015 (GRCm39)	R77H	probably damaging	Het
Kif13a	A	G	13: 46,956,122 (GRCm39)	Y561H	probably damaging	Het
Klk14	G	A	7: 43,341,501 (GRCm39)	C51Y	probably damaging	Het
Klra1	T	A	6: 130,352,247 (GRCm39)	Q165L	probably damaging	Het
Mat2b	T	A	11: 40,570,869 (GRCm39)	R318S	probably damaging	Het
Mgat4d	G	A	8: 84,094,837 (GRCm39)		probably null	Het
Mtor	T	A	4: 148,641,312 (GRCm39)		probably null	Het
Nostrin	A	T	2: 69,006,057 (GRCm39)	Q247L	possibly damaging	Het
Obi1	C	T	14: 104,745,466 (GRCm39)	G70E	probably damaging	Het
Obscn	T	C	11: 58,964,443 (GRCm39)	E3033G	probably damaging	Het
Pam	C	A	1: 97,749,642 (GRCm39)	D839Y	probably damaging	Het
Pds5a	A	G	5: 65,795,157 (GRCm39)	V693A	probably damaging	Het
Pigo	A	T	4: 43,021,337 (GRCm39)	L535Q	probably damaging	Het
Ppp1r12b	G	T	1: 134,883,471 (GRCm39)	A17E	probably benign	Het
Ptar1	G	T	19: 23,671,729 (GRCm39)	R44L	probably damaging	Het
Rad51c	T	C	11: 87,288,580 (GRCm39)	H201R	probably benign	Het
Rims2	A	T	15: 39,381,265 (GRCm39)		probably null	Het
Rpl22l1	T	G	3: 28,860,985 (GRCm39)	S67A	possibly damaging	Het
Rps10	A	G	17: 27,849,454 (GRCm39)	S143P	probably damaging	Het
Rundc1	T	C	11: 101,315,967 (GRCm39)	V13A	probably benign	Het
Sephs2	C	A	7: 126,872,564 (GRCm39)	M176I	probably benign	Het
Serpina16	C	T	12: 103,641,189 (GRCm39)	V179I	probably benign	Het
Serpini2	T	A	3: 75,166,784 (GRCm39)	T158S	probably damaging	Het
Slc12a3	A	G	8: 95,072,979 (GRCm39)	R701G	probably damaging	Het
Slc1a6	A	G	10: 78,650,436 (GRCm39)	E558G	probably damaging	Het
Ssx2ip	T	C	3: 146,136,672 (GRCm39)		probably benign	Het
Tbr1	A	T	2: 61,636,346 (GRCm39)	I241F	possibly damaging	Het
Tgfa	G	C	6: 86,247,064 (GRCm39)		probably null	Het
Tlr12	T	A	4: 128,511,063 (GRCm39)	K396*	probably null	Het
Tmppe	A	G	9: 114,235,026 (GRCm39)	I442V	probably benign	Het
Tubb3	T	C	8: 124,147,607 (GRCm39)	V180A	probably damaging	Het
Vmn1r222	A	G	13: 23,416,901 (GRCm39)	V104A	probably damaging	Het
Vmn2r95	G	T	17: 18,671,708 (GRCm39)	V482L	possibly damaging	Het
Zfp184	G	T	13: 22,143,452 (GRCm39)	R386L	possibly damaging	Het
Zfp985	A	T	4: 147,667,438 (GRCm39)	Y102F	probably damaging	Het

Other mutations in Zfp444

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0437:Zfp444	UTSW	7	6,192,408 (GRCm39)	missense	probably benign	0.37
R0519:Zfp444	UTSW	7	6,191,172 (GRCm39)	missense	probably benign	0.37
R1929:Zfp444	UTSW	7	6,192,554 (GRCm39)	missense	probably damaging	0.99
R2270:Zfp444	UTSW	7	6,192,554 (GRCm39)	missense	probably damaging	0.99
R2271:Zfp444	UTSW	7	6,192,554 (GRCm39)	missense	probably damaging	0.99
R6209:Zfp444	UTSW	7	6,192,948 (GRCm39)	unclassified	probably benign
R7951:Zfp444	UTSW	7	6,191,185 (GRCm39)	missense	probably benign	0.00
R8018:Zfp444	UTSW	7	6,191,142 (GRCm39)	missense	probably benign	0.00
R8910:Zfp444	UTSW	7	6,187,026 (GRCm39)	missense	probably damaging	1.00
R9138:Zfp444	UTSW	7	6,192,690 (GRCm39)	missense	probably damaging	1.00
R9147:Zfp444	UTSW	7	6,192,678 (GRCm39)	missense	probably damaging	1.00
R9178:Zfp444	UTSW	7	6,191,157 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- AAAGCCACTCCGGTGAGAAG -3'
(R):5'- GGGTGAAAGCTGAGAACTCC -3'

Sequencing Primer
(F):5'- CGGTGAGAAGCCGCACG -3'
(R):5'- CCTGCAGCAGGTGTTTAGAAC -3'

Posted On

2016-06-06