Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02801:Zdhhc14'

360223

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Zdhhc14

Ensembl Gene

ENSMUSG00000034265

Gene Name

zinc finger, DHHC domain containing 14

Synonyms

New1cp, B530001K09Rik

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.080) question?

Stock #

IGL02801

Quality Score

Status

Chromosome

Chromosomal Location

5542832-5804086 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to G at 5777094 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000086589 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000089185]

AlphaFold

Q8BQQ1

Predicted Effect

probably null
Transcript: ENSMUST00000089185

SMART Domains

Protein: ENSMUSP00000086589
Gene: ENSMUSG00000034265

Domain	Start	End	E-Value	Type
transmembrane domain	62	81	N/A	INTRINSIC
transmembrane domain	91	110	N/A	INTRINSIC
Pfam:zf-DHHC	160	289	1.8e-38	PFAM
low complexity region	351	365	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Akap5	A	T	12: 76,375,769 (GRCm39)	K400N	probably benign	Het
Aox1	A	T	1: 58,393,336 (GRCm39)	I1193F	probably damaging	Het
Arhgef16	A	T	4: 154,375,964 (GRCm39)	L10Q	probably damaging	Het
Arl10	T	C	13: 54,723,696 (GRCm39)	V106A	probably benign	Het
Bmi1	T	C	2: 18,686,692 (GRCm39)	Y24H	probably damaging	Het
Cd163	T	A	6: 124,297,488 (GRCm39)	I878K	probably benign	Het
Col12a1	A	G	9: 79,515,696 (GRCm39)		probably null	Het
Csmd2	T	C	4: 128,445,868 (GRCm39)		probably null	Het
Dcp2	G	T	18: 44,550,778 (GRCm39)	M417I	probably damaging	Het
Ddx11	T	A	17: 66,455,028 (GRCm39)	C662S	probably benign	Het
Dhx29	G	A	13: 113,101,180 (GRCm39)	C1241Y	probably damaging	Het
Dnajc6	C	T	4: 101,455,010 (GRCm39)	P37L	probably benign	Het
Dqx1	A	G	6: 83,037,476 (GRCm39)		probably null	Het
Dzip1	T	A	14: 119,123,067 (GRCm39)	K643*	probably null	Het
Ecel1	A	G	1: 87,079,725 (GRCm39)	S463P	probably damaging	Het
Eml5	A	G	12: 98,784,104 (GRCm39)	V1361A	possibly damaging	Het
Fads2	C	A	19: 10,060,009 (GRCm39)	A222S	possibly damaging	Het
Fancd2	A	G	6: 113,570,278 (GRCm39)	N1410D	probably benign	Het
Fbxw16	A	G	9: 109,270,144 (GRCm39)	F199S	possibly damaging	Het
Frem2	A	G	3: 53,559,596 (GRCm39)	V1637A	possibly damaging	Het
Gabrg2	A	G	11: 41,803,220 (GRCm39)	S442P	probably damaging	Het
Gprin3	T	C	6: 59,331,966 (GRCm39)	T114A	possibly damaging	Het
Hoxd8	A	G	2: 74,536,912 (GRCm39)	E27G	probably damaging	Het
Isl2	A	G	9: 55,452,816 (GRCm39)		probably null	Het
Lamc2	T	A	1: 153,012,529 (GRCm39)	H715L	probably benign	Het
Lrif1	T	C	3: 106,641,930 (GRCm39)	V102A	possibly damaging	Het
Lrrc39	A	G	3: 116,371,995 (GRCm39)	N254S	possibly damaging	Het
Med13l	T	C	5: 118,883,178 (GRCm39)	W1346R	probably damaging	Het
Melk	T	C	4: 44,360,930 (GRCm39)	I570T	probably damaging	Het
Mlkl	G	A	8: 112,043,064 (GRCm39)	T361M	probably benign	Het
Myo1f	T	A	17: 33,797,111 (GRCm39)	M94K	probably damaging	Het
Naip1	A	G	13: 100,580,876 (GRCm39)	C124R	probably damaging	Het
Nek1	G	A	8: 61,574,095 (GRCm39)		probably null	Het
Nrn1	C	A	13: 36,914,080 (GRCm39)		probably null	Het
Pde1c	G	T	6: 56,150,651 (GRCm39)	N289K	probably damaging	Het
Pfas	G	A	11: 68,879,103 (GRCm39)		probably benign	Het
Pms2	A	T	5: 143,862,653 (GRCm39)	I587F	probably benign	Het
Ppargc1b	T	C	18: 61,440,755 (GRCm39)	E721G	possibly damaging	Het
Ppp2r1b	A	G	9: 50,790,127 (GRCm39)	I435V	probably benign	Het
Psip1	C	T	4: 83,376,357 (GRCm39)	S494N	probably benign	Het
Ranbp3	T	C	17: 57,017,766 (GRCm39)	V474A	probably benign	Het
Rnf220	C	T	4: 117,130,448 (GRCm39)	C259Y	probably damaging	Het
Sdr16c6	T	C	4: 4,076,603 (GRCm39)	I99V	probably benign	Het
Slc36a1	A	T	11: 55,116,879 (GRCm39)	I303F	probably benign	Het
Slc4a1	C	T	11: 102,249,972 (GRCm39)		probably null	Het
Syncrip	A	T	9: 88,361,862 (GRCm39)	D84E	probably damaging	Het
Tbc1d9b	T	C	11: 50,043,657 (GRCm39)	Y593H	probably damaging	Het
Tenm2	G	T	11: 35,937,857 (GRCm39)	Y1605*	probably null	Het
Tmem135	T	A	7: 88,803,333 (GRCm39)	H280L	probably benign	Het
Tmem229a	T	A	6: 24,955,121 (GRCm39)	Q211L	probably benign	Het
Txlna	T	C	4: 129,534,201 (GRCm39)	D5G	probably damaging	Het
Vmn2r57	T	C	7: 41,098,056 (GRCm39)	I4V	probably benign	Het
Wdfy3	A	G	5: 102,055,453 (GRCm39)	L1539S	probably damaging	Het

Other mutations in Zdhhc14

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00419:Zdhhc14	APN	17	5,802,959 (GRCm39)	splice site	probably benign
IGL00909:Zdhhc14	APN	17	5,803,067 (GRCm39)	missense	probably benign
IGL00964:Zdhhc14	APN	17	5,762,756 (GRCm39)	missense	probably damaging	1.00
IGL01398:Zdhhc14	APN	17	5,762,738 (GRCm39)	missense	possibly damaging	0.90
IGL01483:Zdhhc14	APN	17	5,762,733 (GRCm39)	missense	probably benign	0.01
IGL02185:Zdhhc14	APN	17	5,803,157 (GRCm39)	missense	probably benign	0.01
R0189:Zdhhc14	UTSW	17	5,775,539 (GRCm39)	missense	possibly damaging	0.90
R0304:Zdhhc14	UTSW	17	5,775,611 (GRCm39)	splice site	probably benign
R0648:Zdhhc14	UTSW	17	5,543,877 (GRCm39)	missense	probably benign	0.01
R1017:Zdhhc14	UTSW	17	5,543,924 (GRCm39)	missense	probably damaging	0.99
R1595:Zdhhc14	UTSW	17	5,543,831 (GRCm39)	missense	probably benign	0.00
R2416:Zdhhc14	UTSW	17	5,803,283 (GRCm39)	missense	probably benign
R3420:Zdhhc14	UTSW	17	5,803,366 (GRCm39)	makesense	probably null
R3421:Zdhhc14	UTSW	17	5,803,366 (GRCm39)	makesense	probably null
R4063:Zdhhc14	UTSW	17	5,802,983 (GRCm39)	missense	probably damaging	1.00
R4088:Zdhhc14	UTSW	17	5,777,131 (GRCm39)	missense	probably benign	0.01
R5359:Zdhhc14	UTSW	17	5,543,821 (GRCm39)	missense	probably benign
R6236:Zdhhc14	UTSW	17	5,543,918 (GRCm39)	missense	probably damaging	1.00
R7029:Zdhhc14	UTSW	17	5,698,186 (GRCm39)	missense	probably damaging	0.97
R7350:Zdhhc14	UTSW	17	5,777,151 (GRCm39)	missense	probably benign	0.44
R7873:Zdhhc14	UTSW	17	5,762,729 (GRCm39)	missense	probably benign	0.37
R8247:Zdhhc14	UTSW	17	5,736,031 (GRCm39)	missense	probably damaging	1.00
R8492:Zdhhc14	UTSW	17	5,762,689 (GRCm39)	missense	probably damaging	0.98
R8865:Zdhhc14	UTSW	17	5,775,570 (GRCm39)	missense	possibly damaging	0.58
R8969:Zdhhc14	UTSW	17	5,775,555 (GRCm39)	missense	probably benign	0.12
R9133:Zdhhc14	UTSW	17	5,803,283 (GRCm39)	missense	probably benign
R9291:Zdhhc14	UTSW	17	5,698,237 (GRCm39)	missense	probably benign	0.02
R9433:Zdhhc14	UTSW	17	5,781,779 (GRCm39)	missense	probably benign	0.03

Posted On

2015-12-18