Mutagenetix > Incidental Mutation

Incidental Mutation 'R5431:Dcaf13'

428068

Institutional Source

Beutler Lab

Gene Symbol

Dcaf13

Ensembl Gene

ENSMUSG00000022300

Gene Name

DDB1 and CUL4 associated factor 13

Synonyms

Wdsof1, LOC223499

MMRRC Submission

042847-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.955) question?

Stock #

R5431 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

38976300-39010251 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

C to A at 38986619 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glutamic Acid at position 130 (D130E)

Ref Sequence

ENSEMBL: ENSMUSP00000022909 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000022909]

AlphaFold

Q6PAC3

Predicted Effect

probably benign
Transcript: ENSMUST00000022909
AA Change: D130E

PolyPhen 2 Score 0.161 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000022909
Gene: ENSMUSG00000022300
AA Change: D130E

Domain	Start	End	E-Value	Type
WD40	55	95	5.77e-5	SMART
WD40	98	137	4.38e-5	SMART
WD40	185	225	5.97e-1	SMART
Blast:WD40	228	267	1e-18	BLAST
WD40	271	310	2.69e-5	SMART
WD40	312	353	2.96e-2	SMART
Pfam:Sof1	354	440	7.2e-38	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000228436

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 95.1%

Validation Efficiency

Allele List at MGI

All alleles(9) : Targeted, other(2) Gene trapped(7)

Other mutations in this stock

Total: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2310061N02Rik	T	C	16: 88,504,426 (GRCm39)	S124G	possibly damaging	Het
4921539E11Rik	T	C	4: 103,128,045 (GRCm39)	T27A	probably benign	Het
Aspg	T	A	12: 112,089,846 (GRCm39)	N461K	probably benign	Het
B4galnt3	T	A	6: 120,195,928 (GRCm39)	T300S	probably damaging	Het
BC035044	A	G	6: 128,861,970 (GRCm39)		probably benign	Het
Bmp5	C	T	9: 75,800,991 (GRCm39)	P374S	probably damaging	Het
C330018D20Rik	A	T	18: 57,090,928 (GRCm39)	F78L	probably benign	Het
Cds2	T	A	2: 132,144,090 (GRCm39)	S289T	probably benign	Het
Cerkl	C	T	2: 79,171,679 (GRCm39)	C393Y	probably damaging	Het
Cibar2	C	A	8: 120,894,042 (GRCm39)		probably null	Het
Ciita	C	T	16: 10,341,656 (GRCm39)	R1020C	probably damaging	Het
Dnal4	C	T	15: 79,646,648 (GRCm39)	G50R	probably damaging	Het
Elfn1	A	G	5: 139,957,323 (GRCm39)	N109S	probably damaging	Het
Ep400	A	G	5: 110,824,420 (GRCm39)	V2435A	unknown	Het
Fam178b	T	C	1: 36,671,566 (GRCm39)	E185G	probably damaging	Het
Fam227b	C	A	2: 125,968,851 (GRCm39)	L74F	probably benign	Het
Fgfr4	G	A	13: 55,304,464 (GRCm39)	V138I	probably benign	Het
Flnc	A	G	6: 29,456,383 (GRCm39)	I2161V	possibly damaging	Het
Frmd5	T	C	2: 121,393,390 (GRCm39)	N235S	probably damaging	Het
Gad1-ps	G	A	10: 99,281,009 (GRCm39)		noncoding transcript	Het
Ggt6	A	G	11: 72,328,564 (GRCm39)	T355A	possibly damaging	Het
Gm14393	G	A	2: 174,905,669 (GRCm39)	T41I	probably damaging	Het
Gpr151	A	C	18: 42,711,932 (GRCm39)	S249A	probably damaging	Het
Gpr152	T	A	19: 4,193,746 (GRCm39)	V429D	probably benign	Het
Grm7	G	A	6: 111,335,387 (GRCm39)	M599I	probably benign	Het
Hdac4	T	A	1: 91,900,512 (GRCm39)	R54*	probably null	Het
Ice1	A	G	13: 70,740,769 (GRCm39)	L2146S	probably damaging	Het
Igfbpl1	C	T	4: 45,815,588 (GRCm39)	V183I	probably benign	Het
Kel	G	A	6: 41,675,354 (GRCm39)	S299F	probably benign	Het
Kif14	T	C	1: 136,424,433 (GRCm39)	I1016T	possibly damaging	Het
Lhx3	T	C	2: 26,091,130 (GRCm39)	D395G	probably damaging	Het
Micu1	T	C	10: 59,586,343 (GRCm39)	Y140H	possibly damaging	Het
Myt1l	G	A	12: 29,882,331 (GRCm39)	G509R	unknown	Het
Nbn	C	T	4: 15,986,593 (GRCm39)	H665Y	probably benign	Het
Pkhd1	G	T	1: 20,188,060 (GRCm39)	T3416K	probably benign	Het
Plxnb1	T	C	9: 108,929,840 (GRCm39)	F232S	probably damaging	Het
Pus7l	T	C	15: 94,427,367 (GRCm39)	N472D	probably damaging	Het
Rfx1	C	T	8: 84,809,349 (GRCm39)	Q225*	probably null	Het
Rnase2a	T	C	14: 51,493,020 (GRCm39)	Y115C	possibly damaging	Het
Ryr1	T	A	7: 28,809,237 (GRCm39)	D386V	probably benign	Het
Sfi1	A	ATCTTCCCAAAGCCAGTGC	11: 3,103,384 (GRCm39)		probably benign	Homo
Sgcz	T	A	8: 38,107,138 (GRCm39)	T125S	probably damaging	Het
Sntb1	C	G	15: 55,506,191 (GRCm39)	G461R	probably damaging	Het
Syt2	A	G	1: 134,668,695 (GRCm39)	S36G	probably benign	Het
Tcaf3	A	G	6: 42,574,119 (GRCm39)	L31P	probably damaging	Het
Tenm3	C	A	8: 48,820,412 (GRCm39)	E142*	probably null	Het
Tgfbr2	G	T	9: 115,960,669 (GRCm39)	S94R	probably damaging	Het
Tut4	T	A	4: 108,348,609 (GRCm39)	I297N	probably damaging	Het
Vmn2r12	A	G	5: 109,239,684 (GRCm39)	I293T	probably damaging	Het
Wrap73	G	A	4: 154,229,731 (GRCm39)	R34Q	probably damaging	Het
Zc3h14	A	G	12: 98,746,324 (GRCm39)	D511G	possibly damaging	Het

Other mutations in Dcaf13

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00787:Dcaf13	APN	15	39,007,027 (GRCm39)	nonsense	probably null
IGL01081:Dcaf13	APN	15	38,982,201 (GRCm39)	missense	probably damaging	1.00
IGL01766:Dcaf13	APN	15	38,982,145 (GRCm39)	missense	probably benign	0.00
IGL02174:Dcaf13	APN	15	39,001,544 (GRCm39)	missense	probably damaging	1.00
IGL02262:Dcaf13	APN	15	38,982,102 (GRCm39)	splice site	probably benign
IGL02740:Dcaf13	APN	15	39,008,495 (GRCm39)	nonsense	probably null
IGL03092:Dcaf13	APN	15	38,991,371 (GRCm39)	splice site	probably benign
IGL03374:Dcaf13	APN	15	39,008,543 (GRCm39)	nonsense	probably null
R0590:Dcaf13	UTSW	15	39,008,480 (GRCm39)	splice site	probably benign
R0594:Dcaf13	UTSW	15	38,986,663 (GRCm39)	missense	probably benign	0.00
R0711:Dcaf13	UTSW	15	39,001,484 (GRCm39)	missense	probably damaging	1.00
R1036:Dcaf13	UTSW	15	39,007,113 (GRCm39)	missense	probably damaging	1.00
R1770:Dcaf13	UTSW	15	38,993,633 (GRCm39)	missense	probably damaging	1.00
R1826:Dcaf13	UTSW	15	38,982,294 (GRCm39)	missense	probably damaging	1.00
R1933:Dcaf13	UTSW	15	39,001,483 (GRCm39)	missense	probably damaging	0.99
R2508:Dcaf13	UTSW	15	39,008,547 (GRCm39)	missense	probably benign
R4113:Dcaf13	UTSW	15	38,993,615 (GRCm39)	missense	probably damaging	0.98
R4595:Dcaf13	UTSW	15	38,982,288 (GRCm39)	missense	probably damaging	1.00
R4649:Dcaf13	UTSW	15	39,001,637 (GRCm39)	missense	possibly damaging	0.54
R5454:Dcaf13	UTSW	15	38,987,759 (GRCm39)	missense	probably benign
R5834:Dcaf13	UTSW	15	39,007,037 (GRCm39)	nonsense	probably null
R5929:Dcaf13	UTSW	15	39,007,048 (GRCm39)	missense	possibly damaging	0.89
R5944:Dcaf13	UTSW	15	39,010,072 (GRCm39)	missense	probably benign
R6319:Dcaf13	UTSW	15	39,007,067 (GRCm39)	missense	probably benign	0.00
R6394:Dcaf13	UTSW	15	39,007,132 (GRCm39)	missense	probably benign	0.04
R6664:Dcaf13	UTSW	15	38,982,283 (GRCm39)	missense	probably damaging	1.00
R6884:Dcaf13	UTSW	15	38,986,635 (GRCm39)	missense	probably damaging	1.00
R7419:Dcaf13	UTSW	15	38,993,615 (GRCm39)	missense	probably damaging	0.98
R8750:Dcaf13	UTSW	15	38,982,836 (GRCm39)	missense	probably damaging	1.00
R8944:Dcaf13	UTSW	15	39,001,612 (GRCm39)	missense	possibly damaging	0.79
R9294:Dcaf13	UTSW	15	38,993,687 (GRCm39)	missense	possibly damaging	0.92
R9300:Dcaf13	UTSW	15	39,010,102 (GRCm39)	missense	probably damaging	1.00
R9663:Dcaf13	UTSW	15	38,982,178 (GRCm39)	missense	possibly damaging	0.88
R9696:Dcaf13	UTSW	15	39,001,496 (GRCm39)	missense	possibly damaging	0.80
R9778:Dcaf13	UTSW	15	39,008,586 (GRCm39)	missense	probably damaging	0.99
Z1088:Dcaf13	UTSW	15	39,008,642 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CTTTTGCTTTACTCATACTGGGGAG -3'
(R):5'- TTTAAACCTTGTTTTAGCGGCC -3'

Sequencing Primer
(F):5'- CTTTACTCATACTGGGGAGTTTTG -3'
(R):5'- AACCTTGTTTTAGCGGCCAATTATTC -3'

Posted On

2016-09-01