Mutagenetix > Incidental Mutation

Incidental Mutation 'R1321:Zfp251'

157697

Institutional Source

Beutler Lab

Gene Symbol

Zfp251

Ensembl Gene

ENSMUSG00000022526

Gene Name

zinc finger protein 251

Synonyms

9130001M19Rik

MMRRC Submission

039387-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.081) question?

Stock #

R1321 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

76736331-76755635 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to T at 76738436 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glutamine at position 219 (R219Q)

Ref Sequence

ENSEMBL: ENSMUSP00000079268 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080406] [ENSMUST00000229494]

AlphaFold

Q6PCX8

Predicted Effect

possibly damaging
Transcript: ENSMUST00000080406
AA Change: R219Q

PolyPhen 2 Score 0.730 (Sensitivity: 0.86; Specificity: 0.92)

SMART Domains

Protein: ENSMUSP00000079268
Gene: ENSMUSG00000022526
AA Change: R219Q

Domain	Start	End	E-Value	Type
KRAB	15	75	3.24e-32	SMART
ZnF_C2H2	202	224	3.69e-4	SMART
ZnF_C2H2	230	252	3.34e-2	SMART
ZnF_C2H2	258	280	1.69e-3	SMART
ZnF_C2H2	286	308	1.18e-2	SMART
ZnF_C2H2	314	336	4.94e-5	SMART
ZnF_C2H2	342	364	1.82e-3	SMART
ZnF_C2H2	370	392	2.71e-2	SMART
ZnF_C2H2	398	420	1.56e-2	SMART
ZnF_C2H2	426	448	1.2e-3	SMART
ZnF_C2H2	454	476	1.28e-3	SMART
ZnF_C2H2	482	504	1.3e-4	SMART
PDB:1MEY\|G	551	610	2e-8	PDB
Blast:PHD	556	610	2e-6	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000229494
AA Change: R214Q

PolyPhen 2 Score 0.180 (Sensitivity: 0.92; Specificity: 0.87)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000230315

Meta Mutation Damage Score

0.1795

Coding Region Coverage

1x: 98.8%
3x: 97.8%
10x: 95.0%
20x: 89.1%

Validation Efficiency

100% (41/41)

Allele List at MGI

Other mutations in this stock

Total: 35 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930447C04Rik	A	G	12: 72,945,318 (GRCm39)		probably benign	Het
Aco2	C	T	15: 81,779,394 (GRCm39)	S33L	probably damaging	Het
C2cd2l	A	G	9: 44,228,878 (GRCm39)		probably null	Het
Cass4	T	A	2: 172,266,572 (GRCm39)	L205Q	probably benign	Het
Ccn3	G	T	15: 54,612,642 (GRCm39)	C217F	probably damaging	Het
Celsr3	G	A	9: 108,713,069 (GRCm39)	D1834N	probably damaging	Het
Col12a1	A	T	9: 79,524,991 (GRCm39)	C2723*	probably null	Het
Cps1	A	G	1: 67,182,178 (GRCm39)		probably benign	Het
Dolpp1	A	G	2: 30,285,748 (GRCm39)	I49V	possibly damaging	Het
Dppa2	A	G	16: 48,131,999 (GRCm39)	E32G	possibly damaging	Het
Eif2b5	C	T	16: 20,323,439 (GRCm39)	R397*	probably null	Het
Far2	G	T	6: 148,075,034 (GRCm39)		probably benign	Het
Fbxo42	C	T	4: 140,895,160 (GRCm39)	T41I	probably benign	Het
Fbxw15	G	A	9: 109,387,314 (GRCm39)	S227F	probably damaging	Het
Galnt13	G	A	2: 54,988,606 (GRCm39)	R476Q	probably damaging	Het
Galnt18	A	T	7: 111,378,639 (GRCm39)	V39E	probably benign	Het
Gm10801	C	T	2: 98,494,252 (GRCm39)		probably benign	Het
Gm21954	C	T	3: 55,379,627 (GRCm39)		probably benign	Het
Lct	A	C	1: 128,227,759 (GRCm39)	L1245V	probably benign	Het
Lgr5	T	C	10: 115,314,362 (GRCm39)	T192A	probably damaging	Het
Mrpl42	C	T	10: 95,329,573 (GRCm39)	V46M	probably damaging	Het
Mybpc1	C	T	10: 88,365,403 (GRCm39)	V907M	possibly damaging	Het
Mybpc1	T	A	10: 88,406,463 (GRCm39)	Y127F	probably damaging	Het
Nrbp1	T	A	5: 31,403,157 (GRCm39)	I210N	probably damaging	Het
Otud4	T	C	8: 80,396,579 (GRCm39)	S613P	probably benign	Het
P2ry12	T	C	3: 59,124,646 (GRCm39)	E343G	possibly damaging	Het
Pbrm1	A	C	14: 30,789,459 (GRCm39)	K670T	probably damaging	Het
Prl2c2	G	C	13: 13,176,786 (GRCm39)	T47R	probably damaging	Het
Reg3b	A	G	6: 78,349,936 (GRCm39)		probably null	Het
Sppl3	TGG	TG	5: 115,226,352 (GRCm39)		probably null	Het
Ssr2	T	C	3: 88,484,261 (GRCm39)		probably benign	Het
Syne3	A	C	12: 104,942,055 (GRCm39)	V29G	probably benign	Het
Ubr4	T	C	4: 139,187,434 (GRCm39)	V3834A	possibly damaging	Het
Vmn2r112	C	T	17: 22,837,500 (GRCm39)	Q654*	probably null	Het
Vmn2r14	C	T	5: 109,364,117 (GRCm39)	V600I	probably benign	Het

Other mutations in Zfp251

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01433:Zfp251	APN	15	76,738,755 (GRCm39)	missense	probably benign	0.33
IGL02868:Zfp251	APN	15	76,738,734 (GRCm39)	missense	probably damaging	1.00
R0011:Zfp251	UTSW	15	76,738,754 (GRCm39)	missense	probably benign	0.42
R0011:Zfp251	UTSW	15	76,738,754 (GRCm39)	missense	probably benign	0.42
R1199:Zfp251	UTSW	15	76,738,436 (GRCm39)	missense	possibly damaging	0.73
R1201:Zfp251	UTSW	15	76,738,436 (GRCm39)	missense	possibly damaging	0.73
R1322:Zfp251	UTSW	15	76,738,436 (GRCm39)	missense	possibly damaging	0.73
R1565:Zfp251	UTSW	15	76,737,239 (GRCm39)	missense	possibly damaging	0.81
R1565:Zfp251	UTSW	15	76,737,238 (GRCm39)	missense	probably damaging	0.96
R1587:Zfp251	UTSW	15	76,754,484 (GRCm39)	missense	probably damaging	0.98
R1752:Zfp251	UTSW	15	76,737,863 (GRCm39)	missense	possibly damaging	0.71
R3771:Zfp251	UTSW	15	76,737,836 (GRCm39)	missense	possibly damaging	0.67
R3772:Zfp251	UTSW	15	76,737,836 (GRCm39)	missense	possibly damaging	0.67
R3773:Zfp251	UTSW	15	76,737,836 (GRCm39)	missense	possibly damaging	0.67
R4684:Zfp251	UTSW	15	76,738,607 (GRCm39)	missense	possibly damaging	0.85
R5733:Zfp251	UTSW	15	76,754,527 (GRCm39)	missense	probably damaging	1.00
R6341:Zfp251	UTSW	15	76,738,337 (GRCm39)	missense	probably damaging	1.00
R7050:Zfp251	UTSW	15	76,738,496 (GRCm39)	missense	possibly damaging	0.53
R7605:Zfp251	UTSW	15	76,738,557 (GRCm39)	missense	possibly damaging	0.53
R8783:Zfp251	UTSW	15	76,737,413 (GRCm39)	missense	probably damaging	1.00
R9662:Zfp251	UTSW	15	76,737,520 (GRCm39)	missense	possibly damaging	0.53

Predicted Primers

PCR Primer
(F):5'- AGCCTTTCCACACCAAGTGCAG -3'
(R):5'- TAGGGAGCAGTTTCCCAAGAACGC -3'

Sequencing Primer
(F):5'- ccttcccacactccttacac -3'
(R):5'- AGAACGCCCAGACTTCTGTG -3'

Posted On

2014-02-18