Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02398:Dcaf7'

291782

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Dcaf7

Ensembl Gene

ENSMUSG00000049354

Gene Name

DDB1 and CUL4 associated factor 7

Synonyms

1700012F10Rik, 2610037L01Rik, Wdr68

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

IGL02398

Quality Score

Status

Chromosome

Chromosomal Location

106036872-106059324 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 106053753 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 254 (V254A)

Ref Sequence

ENSEMBL: ENSMUSP00000058168 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000058438]

AlphaFold

P61963

Predicted Effect

probably benign
Transcript: ENSMUST00000058438
AA Change: V254A

PolyPhen 2 Score 0.028 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000058168
Gene: ENSMUSG00000049354
AA Change: V254A

Domain	Start	End	E-Value	Type
WD40	58	99	3.42e1	SMART
WD40	104	149	1.43e1	SMART
WD40	163	205	3.81e-5	SMART
WD40	211	251	1.1e2	SMART
WD40	255	295	8.88e-6	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000135857

Meta Mutation Damage Score

0.0724

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein with multiple WD40 repeats which facilitate protein-protein interactions and thereby enable the assembly of multiprotein complexes. This protein has been shown to function as a scaffold protein for protein complexes involved in kinase signaling. This highly conserved gene is present in eukaryotic plants, fungi, and animals. The ortholog of this gene was first identified in plants as a key regulator of anthocyanin biosynthesis and flower pigmentation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014]

Allele List at MGI

Other mutations in this stock

Total: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgre1	T	A	17: 57,402,824 (GRCm38)	C160*	probably null	Het
Alkbh8	C	T	9: 3,345,870 (GRCm38)	P197S	possibly damaging	Het
Ankef1	A	C	2: 136,555,782 (GRCm38)	N761T	probably damaging	Het
Ankrd7	A	G	6: 18,866,697 (GRCm38)	Y72C	probably damaging	Het
Cfap36	T	G	11: 29,222,833 (GRCm38)	M231L	probably benign	Het
Cog7	A	G	7: 121,964,209 (GRCm38)	C227R	probably damaging	Het
Csgalnact1	C	A	8: 68,401,492 (GRCm38)	G219V	probably damaging	Het
Cspg4	A	T	9: 56,886,686 (GRCm38)	E568D	probably benign	Het
Cwc27	G	A	13: 104,804,254 (GRCm38)	T199I	possibly damaging	Het
Cyp26a1	A	G	19: 37,700,019 (GRCm38)	I330V	probably benign	Het
Dhrs7	G	A	12: 72,664,692 (GRCm38)	R24C	probably damaging	Het
Ehmt2	T	A	17: 34,908,479 (GRCm38)	C838S	probably damaging	Het
Fn1	A	T	1: 71,618,670 (GRCm38)		probably null	Het
Gjb3	T	A	4: 127,326,062 (GRCm38)	S226C	probably benign	Het
Gm14496	A	G	2: 181,996,170 (GRCm38)	I346V	probably benign	Het
Gm8050	T	C	14: 6,717,330 (GRCm38)	E172G	probably damaging	Het
Higd1a	G	A	9: 121,852,524 (GRCm38)	R22W	probably damaging	Het
Hmcn1	A	G	1: 150,802,897 (GRCm38)	L491S	possibly damaging	Het
Igsf9b	T	C	9: 27,333,130 (GRCm38)	S794P	possibly damaging	Het
Irgm2	A	T	11: 58,219,929 (GRCm38)	I161F	probably damaging	Het
Lrp8	G	T	4: 107,847,494 (GRCm38)	V304F	probably damaging	Het
Lrp8	C	A	4: 107,869,048 (GRCm38)	S850R	probably damaging	Het
Lrrc9	A	T	12: 72,466,903 (GRCm38)	M513L	probably benign	Het
Myo18b	A	T	5: 112,830,312 (GRCm38)	V1248E	possibly damaging	Het
Myo1b	A	T	1: 51,757,891 (GRCm38)	N945K	probably damaging	Het
Nipbl	A	G	15: 8,327,090 (GRCm38)	L1604P	probably damaging	Het
Oas1f	A	T	5: 120,851,505 (GRCm38)	Y169F	probably benign	Het
Ogfod3	G	A	11: 121,203,025 (GRCm38)	T53I	probably benign	Het
Or2a56	A	T	6: 42,956,112 (GRCm38)	I205F	probably benign	Het
Or52r1c	G	A	7: 103,086,106 (GRCm38)	C191Y	probably damaging	Het
Or8k22	A	T	2: 86,332,524 (GRCm38)	Y277*	probably null	Het
Parp8	A	G	13: 116,910,863 (GRCm38)		probably null	Het
Pde4dip	T	C	3: 97,766,781 (GRCm38)	Y273C	probably benign	Het
Pgbd5	C	T	8: 124,384,518 (GRCm38)	A54T	probably damaging	Het
Pglyrp4	G	A	3: 90,739,117 (GRCm38)		probably benign	Het
Piezo1	A	T	8: 122,486,563 (GRCm38)	S1819R	probably benign	Het
Polr1a	T	C	6: 71,936,556 (GRCm38)		probably benign	Het
Polr1b	A	G	2: 129,102,966 (GRCm38)	I61V	probably benign	Het
Prlhr	G	T	19: 60,467,315 (GRCm38)	A271E	probably damaging	Het
Rad23b	C	T	4: 55,350,360 (GRCm38)		probably benign	Het
Rad51ap1	A	T	6: 126,928,151 (GRCm38)	S132R	probably damaging	Het
Ros1	T	A	10: 52,144,884 (GRCm38)		probably benign	Het
Ryr3	T	C	2: 112,847,422 (GRCm38)	D1327G	probably benign	Het
Slit1	A	C	19: 41,602,237 (GRCm38)	V1332G	probably damaging	Het
Spin2h	A	G	X: 32,651,386 (GRCm38)	D224G	probably damaging	Het
Tmem178b	A	G	6: 40,207,527 (GRCm38)	M120V	probably damaging	Het
Trim25	T	C	11: 88,999,804 (GRCm38)	C106R	probably damaging	Het
Trim35	A	G	14: 66,309,248 (GRCm38)	Y488C	probably damaging	Het
Tsc2	A	T	17: 24,621,729 (GRCm38)	H326Q	probably damaging	Het
Yap1	A	T	9: 7,950,535 (GRCm38)	I315K	probably benign	Het
Zfp654	A	G	16: 64,786,018 (GRCm38)	V607A	probably benign	Het

Other mutations in Dcaf7

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01481:Dcaf7	APN	11	106,054,746 (GRCm38)	missense	probably damaging	1.00
IGL01584:Dcaf7	APN	11	106,053,827 (GRCm38)	missense	probably benign	0.12
IGL02516:Dcaf7	APN	11	106,051,872 (GRCm38)	missense	probably damaging	1.00
IGL02672:Dcaf7	APN	11	106,054,858 (GRCm38)	utr 3 prime	probably benign
IGL02892:Dcaf7	APN	11	106,046,692 (GRCm38)	missense	possibly damaging	0.95
IGL02953:Dcaf7	APN	11	106,051,876 (GRCm38)	nonsense	probably null
Camomile	UTSW	11	106,054,722 (GRCm38)	missense	possibly damaging	0.93
Nescafe	UTSW	11	106,051,797 (GRCm38)	missense	probably damaging	0.98
R0179:Dcaf7	UTSW	11	106,051,797 (GRCm38)	missense	probably damaging	0.98
R0539:Dcaf7	UTSW	11	106,051,826 (GRCm38)	missense	probably damaging	0.98
R1471:Dcaf7	UTSW	11	106,046,747 (GRCm38)	missense	probably benign	0.01
R1647:Dcaf7	UTSW	11	106,051,802 (GRCm38)	missense	probably damaging	1.00
R1648:Dcaf7	UTSW	11	106,051,802 (GRCm38)	missense	probably damaging	1.00
R3551:Dcaf7	UTSW	11	106,054,796 (GRCm38)	missense	probably benign	0.00
R4656:Dcaf7	UTSW	11	106,053,798 (GRCm38)	missense	probably damaging	1.00
R6167:Dcaf7	UTSW	11	106,037,251 (GRCm38)	missense	probably damaging	0.99
R6192:Dcaf7	UTSW	11	106,051,758 (GRCm38)	missense	probably damaging	1.00
R6782:Dcaf7	UTSW	11	106,054,755 (GRCm38)	missense	probably damaging	1.00
R6864:Dcaf7	UTSW	11	106,046,821 (GRCm38)	missense	probably damaging	1.00
R7155:Dcaf7	UTSW	11	106,037,190 (GRCm38)	missense	probably damaging	0.97
R7253:Dcaf7	UTSW	11	106,047,843 (GRCm38)	splice site	probably null
R7446:Dcaf7	UTSW	11	106,053,735 (GRCm38)	missense	probably benign	0.04
R7631:Dcaf7	UTSW	11	106,053,753 (GRCm38)	missense	probably benign	0.03
R8109:Dcaf7	UTSW	11	106,046,778 (GRCm38)	missense	probably damaging	0.98
R8480:Dcaf7	UTSW	11	106,054,793 (GRCm38)	missense	probably benign	0.00
R8489:Dcaf7	UTSW	11	106,051,917 (GRCm38)	missense	probably damaging	1.00
R8731:Dcaf7	UTSW	11	106,054,722 (GRCm38)	missense	possibly damaging	0.93
R8927:Dcaf7	UTSW	11	106,051,926 (GRCm38)	missense	probably damaging	1.00
R8928:Dcaf7	UTSW	11	106,051,926 (GRCm38)	missense	probably damaging	1.00
R9625:Dcaf7	UTSW	11	106,051,968 (GRCm38)	critical splice donor site	probably null
Z1177:Dcaf7	UTSW	11	106,053,795 (GRCm38)	missense	probably benign	0.00

Posted On

2015-04-16