Mutagenetix > Incidental Mutation

Incidental Mutation 'R5245:Zfp322a'

401122

Institutional Source

Beutler Lab

Gene Symbol

Zfp322a

Ensembl Gene

ENSMUSG00000046351

Gene Name

zinc finger protein 322A

Synonyms

9630054P07Rik

MMRRC Submission

042816-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.107) question?

Stock #

R5245 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

23537273-23553378 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 23541156 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Stop codon at position 195 (C195*)

Ref Sequence

ENSEMBL: ENSMUSP00000061524 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000050101] [ENSMUST00000125328] [ENSMUST00000145451] [ENSMUST00000152557]

AlphaFold

Q8BZ89

Predicted Effect

probably null
Transcript: ENSMUST00000050101
AA Change: C195*

SMART Domains

Protein: ENSMUSP00000061524
Gene: ENSMUSG00000046351
AA Change: C195*

Domain	Start	End	E-Value	Type
ZnF_C2H2	81	103	6.42e-4	SMART
ZnF_C2H2	109	131	3.34e-2	SMART
ZnF_C2H2	137	159	1.28e-3	SMART
ZnF_C2H2	165	187	2.95e-3	SMART
ZnF_C2H2	193	215	1.95e-3	SMART
ZnF_C2H2	221	243	4.79e-3	SMART
ZnF_C2H2	249	271	5.14e-3	SMART
ZnF_C2H2	277	299	8.94e-3	SMART
ZnF_C2H2	303	325	5.68e1	SMART
ZnF_C2H2	361	383	1.89e-1	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000122940

Predicted Effect

probably benign
Transcript: ENSMUST00000125328

SMART Domains

Protein: ENSMUSP00000120804
Gene: ENSMUSG00000046351

Domain	Start	End	E-Value	Type
ZnF_C2H2	81	103	6.42e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000145451

SMART Domains

Protein: ENSMUSP00000119883
Gene: ENSMUSG00000046351

Domain	Start	End	E-Value	Type
ZnF_C2H2	81	103	6.42e-4	SMART
ZnF_C2H2	109	131	3.34e-2	SMART
ZnF_C2H2	137	159	1.28e-3	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000152557

SMART Domains

Protein: ENSMUSP00000118754
Gene: ENSMUSG00000046351

Domain	Start	End	E-Value	Type
ZnF_C2H2	81	103	6.42e-4	SMART
ZnF_C2H2	109	131	3.34e-2	SMART
ZnF_C2H2	137	159	1.28e-3	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000224779

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.2%
20x: 95.3%

Validation Efficiency

100% (51/51)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] ZNF322A is a member of the zinc-finger transcription factor family and may regulate transcriptional activation in MAPK (see MAPK1; MIM 176948) signaling pathways (Li et al., 2004 [PubMed 15555580]).[supplied by OMIM, Mar 2008]

Allele List at MGI

Other mutations in this stock

Total: 45 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abhd17b	T	A	19: 21,661,624 (GRCm39)	Y270*	probably null	Het
Akap9	A	T	5: 4,026,209 (GRCm39)	Q59L	probably damaging	Het
Aloxe3	A	T	11: 69,020,502 (GRCm39)	Q182L	probably benign	Het
Arhgef5	G	T	6: 43,242,614 (GRCm39)		probably benign	Het
Bcas3	T	A	11: 85,449,912 (GRCm39)	N663K	probably damaging	Het
Cimap3	T	C	3: 105,921,770 (GRCm39)	H51R	possibly damaging	Het
Cntfr	A	T	4: 41,670,879 (GRCm39)	W95R	possibly damaging	Het
Dcun1d4	A	G	5: 73,714,657 (GRCm39)	T275A	probably benign	Het
Eps8l1	A	G	7: 4,473,873 (GRCm39)	R227G	probably damaging	Het
Ets2	G	A	16: 95,513,304 (GRCm39)	W160*	probably null	Het
Flt4	AC	ACC	11: 49,541,861 (GRCm39)		probably null	Het
Fsip2	A	G	2: 82,823,505 (GRCm39)	M6413V	probably benign	Het
Gm14401	C	T	2: 176,778,471 (GRCm39)	P186S	probably damaging	Het
Hrc	G	A	7: 44,984,855 (GRCm39)	G2D	probably damaging	Het
Kcnq3	A	G	15: 65,903,284 (GRCm39)	V142A	possibly damaging	Het
Lama3	G	A	18: 12,552,950 (GRCm39)	C454Y	probably damaging	Het
Lrrk2	A	G	15: 91,680,292 (GRCm39)	T2068A	probably damaging	Het
Mab21l2	T	C	3: 86,454,799 (GRCm39)	E67G	possibly damaging	Het
Map3k5	G	A	10: 20,016,437 (GRCm39)	V1343I	probably benign	Het
Mcm4	T	A	16: 15,448,289 (GRCm39)	T423S	probably benign	Het
Mmp16	A	G	4: 18,054,596 (GRCm39)		probably benign	Het
Nat3	C	T	8: 68,000,832 (GRCm39)	T237I	probably benign	Het
Nol4	A	T	18: 22,828,179 (GRCm39)	*484R	probably null	Het
Nsmf	A	G	2: 24,946,119 (GRCm39)	E202G	probably damaging	Het
Olfml2b	T	C	1: 170,496,443 (GRCm39)	V358A	probably benign	Het
Or2v2	T	A	11: 49,004,116 (GRCm39)	I146F	probably benign	Het
Or4b1d	T	A	2: 89,968,606 (GRCm39)	K292N	probably damaging	Het
Osbpl1a	T	C	18: 12,891,910 (GRCm39)	E466G	probably damaging	Het
Pim3	A	G	15: 88,747,404 (GRCm39)	E90G	possibly damaging	Het
Recql5	T	C	11: 115,784,385 (GRCm39)	E905G	probably damaging	Het
Rnf31	T	G	14: 55,839,163 (GRCm39)	L925R	probably damaging	Het
Secisbp2l	A	G	2: 125,589,511 (GRCm39)	V679A	probably damaging	Het
Setdb2	T	A	14: 59,663,943 (GRCm39)	E68V	probably null	Het
Shtn1	T	A	19: 59,020,652 (GRCm39)	N190I	possibly damaging	Het
Slc25a25	G	A	2: 32,311,340 (GRCm39)	Q14*	probably null	Het
Snrnp27	A	G	6: 86,659,941 (GRCm39)	S18P	unknown	Het
Srsf11	C	T	3: 157,728,981 (GRCm39)		probably benign	Het
Tbx5	T	C	5: 120,021,230 (GRCm39)	V412A	possibly damaging	Het
Tcea3	A	G	4: 135,991,813 (GRCm39)	T166A	probably benign	Het
Tdrp	A	T	8: 14,024,479 (GRCm39)		probably benign	Het
Tent5a	G	T	9: 85,208,401 (GRCm39)	Q160K	possibly damaging	Het
Tmem132e	T	C	11: 82,333,464 (GRCm39)	V624A	probably damaging	Het
Tnnt1	T	C	7: 4,513,066 (GRCm39)	D72G	probably damaging	Het
Trim80	C	A	11: 115,332,398 (GRCm39)	H197N	probably damaging	Het
Zfp335	A	G	2: 164,736,678 (GRCm39)	S986P	probably benign	Het

Other mutations in Zfp322a

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02579:Zfp322a	APN	13	23,541,613 (GRCm39)	missense	probably damaging	0.97
R1395:Zfp322a	UTSW	13	23,540,945 (GRCm39)	missense	probably benign	0.01
R1975:Zfp322a	UTSW	13	23,541,074 (GRCm39)	missense	probably damaging	1.00
R2100:Zfp322a	UTSW	13	23,541,460 (GRCm39)	missense	possibly damaging	0.85
R2332:Zfp322a	UTSW	13	23,541,494 (GRCm39)	missense	probably damaging	1.00
R2571:Zfp322a	UTSW	13	23,540,614 (GRCm39)	missense	probably damaging	1.00
R4959:Zfp322a	UTSW	13	23,541,052 (GRCm39)	missense	probably damaging	1.00
R5310:Zfp322a	UTSW	13	23,541,532 (GRCm39)	missense	possibly damaging	0.90
R5389:Zfp322a	UTSW	13	23,541,149 (GRCm39)	missense	probably damaging	1.00
R5525:Zfp322a	UTSW	13	23,541,685 (GRCm39)	missense	probably benign
R5810:Zfp322a	UTSW	13	23,541,579 (GRCm39)	nonsense	probably null
R7299:Zfp322a	UTSW	13	23,541,314 (GRCm39)	missense	probably benign	0.22
R7299:Zfp322a	UTSW	13	23,541,313 (GRCm39)	missense	probably damaging	0.97
R7301:Zfp322a	UTSW	13	23,541,314 (GRCm39)	missense	probably benign	0.22
R7301:Zfp322a	UTSW	13	23,541,313 (GRCm39)	missense	probably damaging	0.97
R8670:Zfp322a	UTSW	13	23,541,274 (GRCm39)	missense	possibly damaging	0.83
R9108:Zfp322a	UTSW	13	23,541,437 (GRCm39)	missense	probably benign	0.01
R9789:Zfp322a	UTSW	13	23,540,558 (GRCm39)	missense	possibly damaging	0.83

Predicted Primers

PCR Primer
(F):5'- GGAAGTCACTCTCACACATAGAC -3'
(R):5'- TGCCTTGAACGTGAACAAAACTTT -3'

Sequencing Primer
(F):5'- AAGGTCTGATTTCTGGCCAAAGC -3'
(R):5'- GAAGAGCTTTTGGCACCACTTAGC -3'

Posted On

2016-07-06