Mutagenetix > Incidental Mutation

Incidental Mutation 'R1908:Dcaf17'

210023

Institutional Source

Beutler Lab

Gene Symbol

Dcaf17

Ensembl Gene

ENSMUSG00000041966

Gene Name

DDB1 and CUL4 associated factor 17

Synonyms

4833418A01Rik, 2810055O12Rik, A030004A10Rik, A930009G19Rik

MMRRC Submission

039927-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.180) question?

Stock #

R1908 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

70885672-70929486 bp(+) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 70890713 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Stop codon at position 83 (R83*)

Ref Sequence

ENSEMBL: ENSMUSP00000120016 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000064141] [ENSMUST00000090849] [ENSMUST00000100037] [ENSMUST00000102701] [ENSMUST00000112159] [ENSMUST00000112167] [ENSMUST00000112179] [ENSMUST00000154704] [ENSMUST00000135357] [ENSMUST00000112186] [ENSMUST00000148876]

AlphaFold

Q3TUL7

Predicted Effect

probably null
Transcript: ENSMUST00000064141
AA Change: R83*

Predicted Effect

probably benign
Transcript: ENSMUST00000090849

Predicted Effect

probably benign
Transcript: ENSMUST00000100037

SMART Domains

Protein: ENSMUSP00000097615
Gene: ENSMUSG00000041975

Domain	Start	End	E-Value	Type
Pfam:Methyltransf_23	115	304	1.4e-14	PFAM
Pfam:Ubie_methyltran	126	265	1.4e-7	PFAM
Pfam:Methyltransf_31	137	304	5.6e-10	PFAM
Pfam:Methyltransf_26	140	251	4.2e-8	PFAM
Pfam:Methyltransf_25	143	246	5.3e-13	PFAM
Pfam:Methyltransf_12	144	248	1e-12	PFAM
Pfam:Methyltransf_11	144	250	7.4e-14	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000102701
AA Change: R83*

Predicted Effect

probably null
Transcript: ENSMUST00000112159
AA Change: R83*

Predicted Effect

probably null
Transcript: ENSMUST00000112167
AA Change: R83*

Predicted Effect

probably benign
Transcript: ENSMUST00000112179

SMART Domains

Protein: ENSMUSP00000107800
Gene: ENSMUSG00000041975

Domain	Start	End	E-Value	Type
low complexity region	190	206	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000154704
AA Change: R83*

Predicted Effect

probably null
Transcript: ENSMUST00000130292
AA Change: R97*

SMART Domains

Protein: ENSMUSP00000117830
Gene: ENSMUSG00000041966
AA Change: R97*

Domain	Start	End	E-Value	Type
Pfam:DCAF17	55	405	6.6e-166	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000135357

SMART Domains

Protein: ENSMUSP00000118011
Gene: ENSMUSG00000041966

Domain	Start	End	E-Value	Type
transmembrane domain	98	117	N/A	INTRINSIC
transmembrane domain	132	151	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000124208

Predicted Effect

probably benign
Transcript: ENSMUST00000112186

SMART Domains

Protein: ENSMUSP00000107804
Gene: ENSMUSG00000041975

Domain	Start	End	E-Value	Type
Pfam:Methyltransf_23	158	349	5.1e-15	PFAM
Pfam:Ubie_methyltran	173	312	8.7e-8	PFAM
Pfam:Methyltransf_31	184	348	3.7e-9	PFAM
Pfam:Methyltransf_25	190	293	3.9e-13	PFAM
Pfam:Methyltransf_12	191	295	7e-13	PFAM
Pfam:Methyltransf_11	191	297	6.2e-13	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000136299

Predicted Effect

probably benign
Transcript: ENSMUST00000148876

SMART Domains

Protein: ENSMUSP00000115855
Gene: ENSMUSG00000041975

Domain	Start	End	E-Value	Type
Pfam:Methyltransf_25	190	281	1.9e-8	PFAM
Pfam:Methyltransf_11	191	280	2.8e-8	PFAM

Coding Region Coverage

1x: 97.3%
3x: 96.8%
10x: 95.4%
20x: 93.0%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a nuclear transmembrane protein that associates with cullin 4A/damaged DNA binding protein 1 ubiquitin ligase complex. Mutations in this gene are associated with Woodhouse-Sakati syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]

Allele List at MGI

Other mutations in this stock

Total: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca8b	C	A	11: 109,847,924 (GRCm39)	L852F	possibly damaging	Het
Abcc6	T	C	7: 45,669,558 (GRCm39)		probably null	Het
Alg11	T	G	8: 22,555,584 (GRCm39)	C240G	probably damaging	Het
Aox1	A	G	1: 58,141,783 (GRCm39)	I1190V	probably damaging	Het
Apc2	T	G	10: 80,150,678 (GRCm39)	S1911A	probably benign	Het
Arfgef3	T	C	10: 18,528,511 (GRCm39)	D292G	possibly damaging	Het
Arhgef4	C	A	1: 34,763,340 (GRCm39)	S865R	probably benign	Het
Ass1	T	A	2: 31,383,160 (GRCm39)	Y190*	probably null	Het
B4galnt3	A	T	6: 120,187,051 (GRCm39)		probably null	Het
Btnl10	C	A	11: 58,811,367 (GRCm39)	P230Q	possibly damaging	Het
C3	A	G	17: 57,516,489 (GRCm39)	Y1348H	probably damaging	Het
Ccdc198	G	T	14: 49,464,032 (GRCm39)	D292E	probably damaging	Het
Cebpz	A	T	17: 79,242,336 (GRCm39)	Y439*	probably null	Het
Cic	C	A	7: 24,986,265 (GRCm39)	T1229K	probably damaging	Het
Clip4	T	C	17: 72,144,744 (GRCm39)	S524P	probably damaging	Het
Col6a3	A	C	1: 90,739,421 (GRCm39)	I269R	probably damaging	Het
Dbh	C	T	2: 27,071,506 (GRCm39)	T533I	possibly damaging	Het
Dennd2b	G	A	7: 109,124,533 (GRCm39)	Q686*	probably null	Het
Dnah1	A	G	14: 30,984,515 (GRCm39)	L3923P	probably damaging	Het
Dnah7a	A	T	1: 53,670,721 (GRCm39)	D510E	probably benign	Het
Dock6	A	G	9: 21,752,925 (GRCm39)	F296S	probably damaging	Het
Eif4enif1	T	C	11: 3,177,455 (GRCm39)	S341P	probably damaging	Het
Epb41l1	G	T	2: 156,352,737 (GRCm39)	G461V	possibly damaging	Het
Epg5	T	A	18: 78,002,247 (GRCm39)	D555E	probably benign	Het
Fes	T	C	7: 80,036,609 (GRCm39)	R113G	probably damaging	Het
Garre1	T	A	7: 33,957,461 (GRCm39)	I59L	probably benign	Het
Gm10684	A	G	9: 45,021,511 (GRCm39)		probably benign	Het
Gm12185	T	C	11: 48,806,231 (GRCm39)	E320G	probably benign	Het
Gm14412	G	T	2: 177,007,269 (GRCm39)	H209N	probably damaging	Het
Gm14412	A	C	2: 177,007,630 (GRCm39)	S88R	probably benign	Het
Grhl1	T	A	12: 24,658,555 (GRCm39)	L400Q	probably damaging	Het
Havcr1	T	A	11: 46,664,511 (GRCm39)	Y216*	probably null	Het
Hephl1	A	C	9: 14,985,420 (GRCm39)	Y745*	probably null	Het
Hmcn2	T	G	2: 31,301,922 (GRCm39)		probably null	Het
Hs3st6	A	G	17: 24,977,110 (GRCm39)	K197E	possibly damaging	Het
Ifi214	C	T	1: 173,357,077 (GRCm39)	V9I	probably benign	Het
Jakmip2	T	C	18: 43,700,209 (GRCm39)	T450A	probably benign	Het
Lrp4	T	A	2: 91,328,753 (GRCm39)	V1551D	possibly damaging	Het
Macf1	A	T	4: 123,351,634 (GRCm39)	H1634Q	possibly damaging	Het
Mcpt8	T	A	14: 56,321,291 (GRCm39)	I58F	probably benign	Het
Mga	T	A	2: 119,757,075 (GRCm39)	H1018Q	possibly damaging	Het
Myo10	T	A	15: 25,801,308 (GRCm39)	V1499E	probably damaging	Het
Myom2	G	T	8: 15,131,023 (GRCm39)	D320Y	probably damaging	Het
Or11g7	T	A	14: 50,691,295 (GRCm39)	M262K	probably damaging	Het
Or13a27	T	C	7: 139,925,378 (GRCm39)	I175V	probably benign	Het
Or2r11	C	T	6: 42,437,360 (GRCm39)	V198M	probably benign	Het
Or2t26	A	C	11: 49,039,101 (GRCm39)	N6H	possibly damaging	Het
Or4c115	G	A	2: 88,927,888 (GRCm39)	P128S	probably damaging	Het
Or5d47	A	T	2: 87,804,403 (GRCm39)	V202D	possibly damaging	Het
Pabpc4	G	T	4: 123,182,861 (GRCm39)	R166L	possibly damaging	Het
Pcdhb8	A	G	18: 37,489,015 (GRCm39)	E231G	possibly damaging	Het
Pomgnt2	A	T	9: 121,811,257 (GRCm39)	I508N	possibly damaging	Het
Ppp2r5e	C	G	12: 75,516,341 (GRCm39)	A239P	probably damaging	Het
Prdm15	G	T	16: 97,638,885 (GRCm39)	D58E	probably benign	Het
Rgl2	A	G	17: 34,151,122 (GRCm39)	T117A	probably benign	Het
Rp1	A	G	1: 4,418,943 (GRCm39)	I723T	probably damaging	Het
Serpina3g	A	G	12: 104,207,536 (GRCm39)	E233G	probably damaging	Het
Skint6	T	A	4: 112,749,187 (GRCm39)	S798C	probably benign	Het
Slc35f1	T	C	10: 52,898,000 (GRCm39)	L137P	possibly damaging	Het
Slc6a20a	T	C	9: 123,485,373 (GRCm39)	N246S	probably damaging	Het
Slc7a2	T	C	8: 41,369,534 (GRCm39)	L663S	probably benign	Het
Slco1a4	A	G	6: 141,761,173 (GRCm39)		probably null	Het
Slit2	A	G	5: 48,439,330 (GRCm39)	T41A	probably damaging	Het
Smc2	T	C	4: 52,450,863 (GRCm39)	I227T	probably damaging	Het
Smg1	A	G	7: 117,753,422 (GRCm39)		probably benign	Het
Ssu2	A	T	6: 112,361,388 (GRCm39)	L23M	probably benign	Het
Syne2	A	G	12: 76,141,053 (GRCm39)		probably null	Het
Tekt1	T	C	11: 72,242,761 (GRCm39)	T249A	probably benign	Het
Tfr2	T	C	5: 137,569,954 (GRCm39)	V120A	probably benign	Het
Thsd7b	C	T	1: 129,605,846 (GRCm39)	P529L	probably damaging	Het
Tll1	C	T	8: 64,478,141 (GRCm39)	D871N	probably damaging	Het
Tlr11	A	C	14: 50,598,664 (GRCm39)	I217L	probably benign	Het
Tmem87b	T	A	2: 128,673,479 (GRCm39)	V241D	probably damaging	Het
Tshz2	T	A	2: 169,727,465 (GRCm39)	I218N	possibly damaging	Het
Vmn1r18	A	T	6: 57,367,026 (GRCm39)	I176N	possibly damaging	Het
Vmn2r68	T	A	7: 84,883,260 (GRCm39)	H164L	probably benign	Het
Vmn2r74	T	C	7: 85,601,650 (GRCm39)	T663A	probably benign	Het
Vmn2r8	T	C	5: 108,945,436 (GRCm39)	T724A	probably benign	Het
Wdr11	T	C	7: 129,206,954 (GRCm39)	V289A	possibly damaging	Het
Zfp62	T	A	11: 49,107,047 (GRCm39)	D379E	probably damaging	Het
Zfp78	C	T	7: 6,381,897 (GRCm39)	P316S	probably damaging	Het
Zfyve27	T	G	19: 42,159,987 (GRCm39)	M1R	probably null	Het
Zkscan8	G	A	13: 21,709,325 (GRCm39)	P191L	probably damaging	Het

Other mutations in Dcaf17

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00093:Dcaf17	APN	2	70,908,503 (GRCm39)	missense	probably benign	0.03
IGL01125:Dcaf17	APN	2	70,920,149 (GRCm39)	missense	probably benign	0.03
IGL01761:Dcaf17	APN	2	70,886,881 (GRCm39)	missense	probably damaging	1.00
IGL02641:Dcaf17	APN	2	70,912,375 (GRCm39)	missense	probably damaging	1.00
R0081:Dcaf17	UTSW	2	70,908,812 (GRCm39)	splice site	probably benign
R0388:Dcaf17	UTSW	2	70,908,915 (GRCm39)	missense	probably benign	0.02
R0593:Dcaf17	UTSW	2	70,917,744 (GRCm39)	critical splice donor site	probably null
R0637:Dcaf17	UTSW	2	70,890,763 (GRCm39)	missense	probably damaging	0.99
R0661:Dcaf17	UTSW	2	70,918,779 (GRCm39)	missense	probably damaging	1.00
R1281:Dcaf17	UTSW	2	70,908,500 (GRCm39)	missense	probably damaging	1.00
R1454:Dcaf17	UTSW	2	70,903,517 (GRCm39)	missense	probably damaging	1.00
R1501:Dcaf17	UTSW	2	70,912,332 (GRCm39)	missense	probably damaging	1.00
R1919:Dcaf17	UTSW	2	70,908,516 (GRCm39)	splice site	probably null
R2882:Dcaf17	UTSW	2	70,912,371 (GRCm39)	missense	possibly damaging	0.96
R4585:Dcaf17	UTSW	2	70,918,924 (GRCm39)	missense	probably benign	0.00
R4586:Dcaf17	UTSW	2	70,918,924 (GRCm39)	missense	probably benign	0.00
R6093:Dcaf17	UTSW	2	70,912,356 (GRCm39)	missense	possibly damaging	0.51
R7070:Dcaf17	UTSW	2	70,918,857 (GRCm39)	missense	probably benign	0.00
R8289:Dcaf17	UTSW	2	70,885,718 (GRCm39)	missense
R8418:Dcaf17	UTSW	2	70,918,717 (GRCm39)	missense	probably damaging	1.00
R8681:Dcaf17	UTSW	2	70,886,913 (GRCm39)	nonsense	probably null
R8786:Dcaf17	UTSW	2	70,917,744 (GRCm39)	critical splice donor site	probably null
R8879:Dcaf17	UTSW	2	70,893,746 (GRCm39)	missense	possibly damaging	0.85
R9072:Dcaf17	UTSW	2	70,920,136 (GRCm39)	missense	probably benign	0.01
R9312:Dcaf17	UTSW	2	70,908,458 (GRCm39)	missense	probably benign	0.01
R9460:Dcaf17	UTSW	2	70,917,695 (GRCm39)	missense	possibly damaging	0.89

Predicted Primers

PCR Primer
(F):5'- AGCAATCTCCAGGTGACTTTAC -3'
(R):5'- TCAAGATGAAGCCAAGAACTCG -3'

Sequencing Primer
(F):5'- GTAGGAACCAAACTTGAGTCCTCTG -3'
(R):5'- CCAAGAACTCGAGATAAAGTGTG -3'

Posted On

2014-06-30