Mutagenetix > Incidental Mutation

Incidental Mutation 'R7038:Zfp467'

546850

Institutional Source

Beutler Lab

Gene Symbol

Zfp467

Ensembl Gene

ENSMUSG00000068551

Gene Name

zinc finger protein 467

Synonyms

EZI, MNCb-3350, 1190001I08Rik

MMRRC Submission

045138-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.170) question?

Stock #

R7038 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

48404631-48422759 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 48415072 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 527 (T527A)

Ref Sequence

ENSEMBL: ENSMUSP00000110208 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000101443] [ENSMUST00000114556] [ENSMUST00000114558] [ENSMUST00000114559] [ENSMUST00000114560] [ENSMUST00000114561] [ENSMUST00000114563] [ENSMUST00000114564] [ENSMUST00000114566] [ENSMUST00000141449]

AlphaFold

Q8JZL0

Predicted Effect

probably benign
Transcript: ENSMUST00000101443

Predicted Effect

probably benign
Transcript: ENSMUST00000114556

Predicted Effect

probably benign
Transcript: ENSMUST00000114558

Predicted Effect

probably benign
Transcript: ENSMUST00000114559

Predicted Effect

probably damaging
Transcript: ENSMUST00000114560
AA Change: T527A

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

SMART Domains

Protein: ENSMUSP00000110207
Gene: ENSMUSG00000068551
AA Change: T527A

Domain	Start	End	E-Value	Type
low complexity region	98	110	N/A	INTRINSIC
ZnF_C2H2	160	182	1.26e-2	SMART
ZnF_C2H2	188	210	1.67e-2	SMART
ZnF_C2H2	216	238	2.12e-4	SMART
ZnF_C2H2	244	266	5.9e-3	SMART
ZnF_C2H2	272	294	1.47e-3	SMART
ZnF_C2H2	300	322	1.82e-3	SMART
ZnF_C2H2	355	377	9.58e-3	SMART
ZnF_C2H2	430	452	7.26e-3	SMART
ZnF_C2H2	458	480	1.56e-2	SMART
ZnF_C2H2	486	508	1.18e-2	SMART
ZnF_C2H2	514	536	3.11e-2	SMART
ZnF_C2H2	542	564	2.43e-4	SMART
low complexity region	567	585	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000114561
AA Change: T527A

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

SMART Domains

Protein: ENSMUSP00000110208
Gene: ENSMUSG00000068551
AA Change: T527A

Domain	Start	End	E-Value	Type
low complexity region	98	110	N/A	INTRINSIC
ZnF_C2H2	160	182	1.26e-2	SMART
ZnF_C2H2	188	210	1.67e-2	SMART
ZnF_C2H2	216	238	2.12e-4	SMART
ZnF_C2H2	244	266	5.9e-3	SMART
ZnF_C2H2	272	294	1.47e-3	SMART
ZnF_C2H2	300	322	1.82e-3	SMART
ZnF_C2H2	355	377	9.58e-3	SMART
ZnF_C2H2	430	452	7.26e-3	SMART
ZnF_C2H2	458	480	1.56e-2	SMART
ZnF_C2H2	486	508	1.18e-2	SMART
ZnF_C2H2	514	536	3.11e-2	SMART
ZnF_C2H2	542	564	2.43e-4	SMART
low complexity region	567	585	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000114563

Predicted Effect

probably benign
Transcript: ENSMUST00000114564

Predicted Effect

probably benign
Transcript: ENSMUST00000114566

Predicted Effect

probably benign
Transcript: ENSMUST00000141449

Meta Mutation Damage Score

0.3043

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.1%

Validation Efficiency

99% (101/102)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a zinc finger protein whose function has not yet been elucidated in humans. However, the mouse ortholog of this protein enhances adipocyte differentiation and suppresses osteoblast differentiation in bone marrow. The mouse protein also is a transcription factor for several genes and can help recruit histone deacetylase complexes. [provided by RefSeq, Aug 2016]

Allele List at MGI

Other mutations in this stock

Total: 102 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abl2	T	C	1: 156,468,979 (GRCm39)	S748P	possibly damaging	Het
Alppl2	T	C	1: 87,016,833 (GRCm39)	D104G	probably damaging	Het
Als2	C	A	1: 59,206,673 (GRCm39)	W1590L	possibly damaging	Het
Aopep	G	T	13: 63,338,339 (GRCm39)	V571F	possibly damaging	Het
Aplf	C	T	6: 87,630,805 (GRCm39)	W210*	probably null	Het
Ash1l	A	T	3: 88,889,978 (GRCm39)	H619L	probably benign	Het
Baiap3	G	A	17: 25,462,814 (GRCm39)	R1075C	probably benign	Het
Bpifb1	G	T	2: 154,044,589 (GRCm39)	V19F	probably damaging	Het
Capn1	A	T	19: 6,064,349 (GRCm39)	L50Q	probably benign	Het
Carmil1	A	G	13: 24,323,318 (GRCm39)	S245P	probably damaging	Het
Cavin4	A	G	4: 48,672,479 (GRCm39)	H308R	probably benign	Het
Cd4	C	T	6: 124,847,217 (GRCm39)	V316M	probably damaging	Het
Cdcp1	T	C	9: 123,002,662 (GRCm39)	Y803C	probably damaging	Het
Cep295nl	A	G	11: 118,223,815 (GRCm39)	I343T	probably benign	Het
Cgn	T	G	3: 94,670,392 (GRCm39)	T1021P	possibly damaging	Het
Cilk1	C	T	9: 78,016,484 (GRCm39)		probably benign	Het
Col6a5	A	G	9: 105,822,937 (GRCm39)	V140A	unknown	Het
Cops8	T	C	1: 90,531,320 (GRCm39)		probably benign	Het
Crhbp	A	G	13: 95,580,699 (GRCm39)	Y54H	probably damaging	Het
Cyp2c29	G	A	19: 39,275,571 (GRCm39)	V4I	probably benign	Het
Cyp2j6	T	A	4: 96,423,708 (GRCm39)	Y220F	probably benign	Het
D130043K22Rik	A	G	13: 25,077,391 (GRCm39)	D1008G	probably damaging	Het
Ddx47	T	A	6: 135,000,336 (GRCm39)	V444E	possibly damaging	Het
Dnttip2	T	A	3: 122,070,181 (GRCm39)	C465*	probably null	Het
Dst	C	A	1: 34,221,879 (GRCm39)	S2561*	probably null	Het
Dstyk	T	C	1: 132,381,847 (GRCm39)	S534P	probably benign	Het
Eif4e	A	G	3: 138,232,943 (GRCm39)		probably benign	Het
Eipr1	C	T	12: 28,801,817 (GRCm39)		probably benign	Het
Fastkd2	T	A	1: 63,771,032 (GRCm39)	D129E	possibly damaging	Het
Fndc3b	C	T	3: 27,555,618 (GRCm39)	G312D	probably benign	Het
Gab2	T	A	7: 96,952,290 (GRCm39)	I562N	probably damaging	Het
Gata5	C	A	2: 179,975,685 (GRCm39)	D160Y	possibly damaging	Het
Gcn1	G	A	5: 115,749,203 (GRCm39)	V1912I	probably damaging	Het
Gdf5	C	A	2: 155,786,655 (GRCm39)	Q107H	probably damaging	Het
Gdpd1	A	G	11: 86,926,118 (GRCm39)	Y276H	probably damaging	Het
Gins1	A	G	2: 150,759,791 (GRCm39)	Y81C	probably damaging	Het
Gm28360	T	C	1: 117,781,329 (GRCm39)	C107R	probably damaging	Het
Hadha	T	C	5: 30,324,998 (GRCm39)		probably null	Het
Hcn4	A	T	9: 58,730,867 (GRCm39)	I25F	unknown	Het
Hectd4	A	G	5: 121,437,660 (GRCm39)	Y1095C	possibly damaging	Het
Hsp90b1	A	T	10: 86,531,730 (GRCm39)	L73Q	probably damaging	Het
Hspa12a	A	G	19: 58,793,132 (GRCm39)	V351A	probably damaging	Het
Htr1b	T	A	9: 81,514,296 (GRCm39)	M104L	probably benign	Het
Igf2r	T	C	17: 12,917,212 (GRCm39)	T1563A	probably benign	Het
Kif13a	C	T	13: 46,905,931 (GRCm39)	V671M	possibly damaging	Het
Liph	A	T	16: 21,795,009 (GRCm39)	V201E	probably damaging	Het
Ltn1	T	C	16: 87,221,759 (GRCm39)	D196G	probably damaging	Het
Med15	C	T	16: 17,470,591 (GRCm39)	D589N	possibly damaging	Het
Mknk1	A	G	4: 115,714,307 (GRCm39)	D26G	probably damaging	Het
Mpi	T	C	9: 57,452,500 (GRCm39)	D344G	probably damaging	Het
Mrc2	A	G	11: 105,223,062 (GRCm39)	E435G	possibly damaging	Het
Mrps5	A	G	2: 127,442,786 (GRCm39)	E285G	probably damaging	Het
Ms4a20	A	T	19: 11,087,675 (GRCm39)	F85L	probably benign	Het
Muc16	T	A	9: 18,531,764 (GRCm39)	M6197L	probably damaging	Het
Myo3b	A	T	2: 69,925,552 (GRCm39)	E34D	probably benign	Het
Nsd3	T	C	8: 26,131,279 (GRCm39)	S215P	probably damaging	Het
Nsmce2	T	A	15: 59,368,679 (GRCm39)		probably benign	Het
Ntan1	T	C	16: 13,644,774 (GRCm39)	S37P	probably benign	Het
Nup210l	T	A	3: 90,067,254 (GRCm39)	Y765N	probably damaging	Het
Or10q12	A	T	19: 13,745,715 (GRCm39)	D3V	probably benign	Het
Or2aa1	T	C	11: 59,480,408 (GRCm39)	Y169C	possibly damaging	Het
Or4s2b	A	T	2: 88,509,085 (GRCm39)	R288S	probably damaging	Het
Or7g30	A	C	9: 19,352,888 (GRCm39)	L226F	possibly damaging	Het
Pald1	T	C	10: 61,175,078 (GRCm39)	H724R	probably benign	Het
Pcdhb7	A	T	18: 37,475,257 (GRCm39)	D131V	possibly damaging	Het
Pds5b	G	T	5: 150,724,225 (GRCm39)	R1269S	probably benign	Het
Pikfyve	T	C	1: 65,273,520 (GRCm39)	V645A	probably damaging	Het
Plag1	G	T	4: 3,904,676 (GRCm39)	H172N	probably damaging	Het
Plch2	G	C	4: 155,074,489 (GRCm39)		probably null	Het
Plxnb1	T	A	9: 108,929,453 (GRCm39)	V103E	probably damaging	Het
Prpf8	T	A	11: 75,386,984 (GRCm39)	M1143K	probably benign	Het
Ptpn18	T	A	1: 34,498,906 (GRCm39)	M1K	probably null	Het
Rasgrf2	G	A	13: 92,130,952 (GRCm39)	T703I	possibly damaging	Het
Rassf6	A	T	5: 90,757,584 (GRCm39)	H125Q	probably benign	Het
Sdad1	A	G	5: 92,446,049 (GRCm39)		probably null	Het
Sf3a3	T	A	4: 124,622,219 (GRCm39)	F426L	probably benign	Het
Sgsm3	T	C	15: 80,892,576 (GRCm39)	F6L	possibly damaging	Het
Slc14a2	A	T	18: 78,202,252 (GRCm39)	I626N	probably damaging	Het
Slc17a8	T	C	10: 89,436,083 (GRCm39)	N165S	probably benign	Het
Slc41a1	C	A	1: 131,769,795 (GRCm39)	A305D	possibly damaging	Het
Smyd4	C	A	11: 75,281,340 (GRCm39)	P271Q	probably damaging	Het
Spag17	C	A	3: 99,891,925 (GRCm39)	H260N	probably benign	Het
Spata2	A	T	2: 167,327,283 (GRCm39)	V38E	possibly damaging	Het
Sprr2b	CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC	CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC	3: 92,224,826 (GRCm39)		probably benign	Het
Syt14	T	A	1: 192,665,966 (GRCm39)		probably benign	Het
Tbx21	A	G	11: 96,990,597 (GRCm39)	S329P	probably damaging	Het
Tex2	A	T	11: 106,402,726 (GRCm39)		probably null	Het
Tmem62	A	G	2: 120,824,058 (GRCm39)	I244M	possibly damaging	Het
Tnks	A	T	8: 35,318,790 (GRCm39)	N830K	probably damaging	Het
Tox2	A	G	2: 163,156,264 (GRCm39)	E145G	probably damaging	Het
Tpcn1	T	C	5: 120,723,342 (GRCm39)	D7G	probably damaging	Het
Ttc28	T	A	5: 111,414,445 (GRCm39)	M1320K	probably benign	Het
Tubgcp5	T	G	7: 55,455,114 (GRCm39)	V270G	probably damaging	Het
Unc5a	A	G	13: 55,152,297 (GRCm39)	R62G	probably damaging	Het
Unc5d	A	G	8: 29,205,749 (GRCm39)		probably null	Het
Utrn	T	C	10: 12,558,082 (GRCm39)	H1459R	probably damaging	Het
Vmn2r100	T	A	17: 19,725,263 (GRCm39)	L64Q	possibly damaging	Het
Wdr55	T	G	18: 36,893,473 (GRCm39)	L45R	probably damaging	Het
Zfp292	A	G	4: 34,816,357 (GRCm39)	Y306H	probably damaging	Het
Zfp398	G	T	6: 47,843,243 (GRCm39)	D300Y	probably damaging	Het
Zfp407	A	G	18: 84,579,982 (GRCm39)	V377A	probably damaging	Het
Zfp457	G	A	13: 67,441,997 (GRCm39)	H97Y	probably benign	Het

Other mutations in Zfp467

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0166:Zfp467	UTSW	6	48,415,615 (GRCm39)	missense	probably benign	0.00
R0234:Zfp467	UTSW	6	48,415,689 (GRCm39)	missense	probably damaging	1.00
R0234:Zfp467	UTSW	6	48,415,689 (GRCm39)	missense	probably damaging	1.00
R1509:Zfp467	UTSW	6	48,415,621 (GRCm39)	missense	possibly damaging	0.95
R1517:Zfp467	UTSW	6	48,415,170 (GRCm39)	missense	probably damaging	1.00
R1656:Zfp467	UTSW	6	48,416,013 (GRCm39)	missense	possibly damaging	0.87
R2131:Zfp467	UTSW	6	48,419,595 (GRCm39)	missense	probably damaging	0.98
R2912:Zfp467	UTSW	6	48,416,010 (GRCm39)	missense	possibly damaging	0.95
R4696:Zfp467	UTSW	6	48,416,291 (GRCm39)	unclassified	probably benign
R4714:Zfp467	UTSW	6	48,404,751 (GRCm39)	missense	unknown
R4993:Zfp467	UTSW	6	48,415,963 (GRCm39)	missense	probably damaging	1.00
R7224:Zfp467	UTSW	6	48,421,903 (GRCm39)	critical splice donor site	probably null
R7855:Zfp467	UTSW	6	48,416,115 (GRCm39)	missense	probably damaging	0.99
R8073:Zfp467	UTSW	6	48,414,959 (GRCm39)	missense	probably damaging	0.99
R8093:Zfp467	UTSW	6	48,420,366 (GRCm39)	missense	possibly damaging	0.95
R8139:Zfp467	UTSW	6	48,416,268 (GRCm39)	missense	probably damaging	1.00
R8920:Zfp467	UTSW	6	48,415,414 (GRCm39)	missense	probably benign	0.06
R9418:Zfp467	UTSW	6	48,415,990 (GRCm39)	missense	probably damaging	1.00
R9608:Zfp467	UTSW	6	48,404,776 (GRCm39)	missense	unknown
R9656:Zfp467	UTSW	6	48,419,603 (GRCm39)	missense	possibly damaging	0.82

Predicted Primers

PCR Primer
(F):5'- GAGGGTCAGAACTTCGCTTAG -3'
(R):5'- GCTCACGACCCAATCTAGTC -3'

Sequencing Primer
(F):5'- TACCACCTCGGAGGGATTG -3'
(R):5'- AATCTAGTCGCCCACTCCCG -3'

Posted On

2019-05-13