Mutagenetix > Incidental Mutation

Incidental Mutation 'R6111:Zdhhc8'

484871

Institutional Source

Beutler Lab

Gene Symbol

Zdhhc8

Ensembl Gene

ENSMUSG00000060166

Gene Name

zinc finger, DHHC domain containing 8

Synonyms

Op53c05, E330009O14Rik, D16H22S1738E

MMRRC Submission

044260-MU

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.728) question?

Stock #

R6111 (G1)

Quality Score

189.009

Status

Validated

Chromosome

Chromosomal Location

18038617-18053000 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 18042762 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Arginine at position 479 (S479R)

Ref Sequence

ENSEMBL: ENSMUSP00000076224 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000076957] [ENSMUST00000231369] [ENSMUST00000231860] [ENSMUST00000231965]

AlphaFold

Q5Y5T5

Predicted Effect

probably damaging
Transcript: ENSMUST00000076957
AA Change: S479R

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

SMART Domains

Protein: ENSMUSP00000076224
Gene: ENSMUSG00000060166
AA Change: S479R

Domain	Start	End	E-Value	Type
transmembrane domain	15	34	N/A	INTRINSIC
transmembrane domain	46	68	N/A	INTRINSIC
Pfam:zf-DHHC	99	224	4.8e-36	PFAM
low complexity region	304	318	N/A	INTRINSIC
low complexity region	404	417	N/A	INTRINSIC
low complexity region	509	524	N/A	INTRINSIC
low complexity region	551	563	N/A	INTRINSIC
low complexity region	619	644	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000231369

Predicted Effect

probably benign
Transcript: ENSMUST00000231412

Predicted Effect

probably benign
Transcript: ENSMUST00000231860

Predicted Effect

probably benign
Transcript: ENSMUST00000231965

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.0%
20x: 94.2%

Validation Efficiency

98% (57/58)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a four transmembrane protein that is a member of the zinc finger DHHC domain-containing protein family. The encoded protein may function as a palmitoyltransferase. Defects in this gene may be associated with a susceptibility to schizophrenia. Alternate splicing of this gene results in multiple transcript variants. A pseudogene of this gene is found on chromosome 22.[provided by RefSeq, May 2010]
PHENOTYPE: Homozygous null females display impaired prepulse inhibition and reduced exploration in new environments. Homozygous null males display normal prepulse inhibition and only a slight decrease in exploration. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2210408I21Rik	A	G	13: 77,476,021 (GRCm39)	E1110G	possibly damaging	Het
Abcd4	G	A	12: 84,661,888 (GRCm39)	T79I	probably damaging	Het
Acd	A	G	8: 106,424,919 (GRCm39)	M407T	probably benign	Het
Adcy2	T	A	13: 68,877,360 (GRCm39)	H460L	probably damaging	Het
Atad2	G	A	15: 57,971,487 (GRCm39)	H752Y	probably benign	Het
Bmal2	T	C	6: 146,722,097 (GRCm39)	F223L	probably benign	Het
Camsap2	A	G	1: 136,209,036 (GRCm39)	S819P	probably benign	Het
Col24a1	C	A	3: 145,019,815 (GRCm39)	T62K	probably damaging	Het
Cpne6	G	A	14: 55,752,091 (GRCm39)	V283M	probably benign	Het
D630003M21Rik	A	G	2: 158,055,368 (GRCm39)	S590P	probably damaging	Het
Daam1	T	A	12: 71,989,038 (GRCm39)	M146K	unknown	Het
Dclk2	A	G	3: 86,712,968 (GRCm39)	Y495H	probably benign	Het
Ddx4	A	T	13: 112,757,766 (GRCm39)	C330*	probably null	Het
Dlec1	T	C	9: 118,931,692 (GRCm39)	L37P	possibly damaging	Het
Dock2	G	A	11: 34,599,614 (GRCm39)	P322S	probably damaging	Het
Espl1	A	G	15: 102,208,323 (GRCm39)	E443G	probably damaging	Het
Eya4	T	A	10: 23,015,953 (GRCm39)	D338V	possibly damaging	Het
Fcmr	A	G	1: 130,805,566 (GRCm39)	I267V	probably damaging	Het
Gfra3	T	A	18: 34,823,927 (GRCm39)	H349L	probably damaging	Het
Gm25747	A	G	12: 113,392,703 (GRCm39)		probably benign	Het
Gria4	G	A	9: 4,502,430 (GRCm39)	R368C	probably damaging	Het
H2-Q5	A	T	17: 35,613,885 (GRCm39)	I145F	possibly damaging	Het
Hace1	A	T	10: 45,465,606 (GRCm39)	K54I	possibly damaging	Het
Ift122	T	A	6: 115,852,247 (GRCm39)	I79N	probably damaging	Het
Ino80b	A	G	6: 83,101,347 (GRCm39)	V121A	probably damaging	Het
Kcnq1	A	G	7: 142,661,474 (GRCm39)	T63A	probably benign	Het
Map4k4	C	A	1: 40,050,822 (GRCm39)	Q762K	probably benign	Het
Mios	G	A	6: 8,214,836 (GRCm39)	A11T	probably benign	Het
Nfatc1	A	G	18: 80,741,125 (GRCm39)	S278P	probably damaging	Het
Notch2	T	C	3: 98,053,609 (GRCm39)	S2091P	probably benign	Het
Nudt19	T	A	7: 35,254,952 (GRCm39)	D93V	probably benign	Het
Or8b12b	T	C	9: 37,684,228 (GRCm39)	I91T	probably damaging	Het
Osbpl2	A	G	2: 179,791,994 (GRCm39)	T233A	probably benign	Het
P3h1	C	T	4: 119,098,329 (GRCm39)	R369*	probably null	Het
Pcdhb3	A	T	18: 37,435,242 (GRCm39)	I403L	probably benign	Het
Pigo	T	C	4: 43,019,724 (GRCm39)	D935G	probably benign	Het
Plpp1	A	G	13: 113,003,451 (GRCm39)	H224R	probably damaging	Het
Rai1	T	A	11: 60,078,732 (GRCm39)	M932K	probably damaging	Het
Rexo2	A	T	9: 48,384,412 (GRCm39)	F122L	probably damaging	Het
Rsf1	GCG	GCGACGGCGACG	7: 97,229,114 (GRCm39)		probably benign	Het
Sdc3	A	G	4: 130,546,153 (GRCm39)	T77A	unknown	Het
Skint5	T	C	4: 113,562,845 (GRCm39)	T786A	unknown	Het
Smok3c	C	A	5: 138,063,365 (GRCm39)	P284Q	probably damaging	Het
Spg11	A	G	2: 121,923,963 (GRCm39)	V786A	probably damaging	Het
Tmem273	T	C	14: 32,528,755 (GRCm39)	I40T	possibly damaging	Het
Tnfrsf10b	T	A	14: 70,020,007 (GRCm39)	C380S	possibly damaging	Het
Tsen54	T	C	11: 115,710,956 (GRCm39)	V176A	possibly damaging	Het
Ttll4	A	T	1: 74,736,698 (GRCm39)	K1141M	possibly damaging	Het
Ttpa	A	T	4: 20,014,772 (GRCm39)	I116F	probably damaging	Het
Tubgcp6	T	C	15: 88,985,123 (GRCm39)	D1655G	possibly damaging	Het
Usp38	A	G	8: 81,740,551 (GRCm39)	V172A	probably damaging	Het
Vmn2r73	A	G	7: 85,520,997 (GRCm39)	S324P	probably benign	Het
Wdr72	T	C	9: 74,117,607 (GRCm39)	M773T	probably benign	Het
Xirp2	T	A	2: 67,342,161 (GRCm39)	H1467Q	possibly damaging	Het
Zfp423	A	G	8: 88,509,315 (GRCm39)	V322A	probably damaging	Het
Zfp87	T	G	13: 74,520,504 (GRCm39)	E191D	probably benign	Het
Zfp933	T	C	4: 147,913,217 (GRCm39)	T14A	probably damaging	Het

Other mutations in Zdhhc8

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00338:Zdhhc8	APN	16	18,043,060 (GRCm39)	missense	possibly damaging	0.66
IGL01994:Zdhhc8	APN	16	18,045,636 (GRCm39)	unclassified	probably benign
IGL02102:Zdhhc8	APN	16	18,043,063 (GRCm39)	missense	possibly damaging	0.95
IGL02706:Zdhhc8	APN	16	18,042,758 (GRCm39)	missense	probably damaging	1.00
IGL03287:Zdhhc8	APN	16	18,042,964 (GRCm39)	missense	probably benign	0.01
IGL03296:Zdhhc8	APN	16	18,044,587 (GRCm39)	missense	possibly damaging	0.94
R0066:Zdhhc8	UTSW	16	18,043,064 (GRCm39)	missense	probably benign	0.00
R0066:Zdhhc8	UTSW	16	18,043,064 (GRCm39)	missense	probably benign	0.00
R0491:Zdhhc8	UTSW	16	18,046,254 (GRCm39)	missense	probably damaging	0.99
R0838:Zdhhc8	UTSW	16	18,042,430 (GRCm39)	missense	probably damaging	0.99
R1567:Zdhhc8	UTSW	16	18,044,984 (GRCm39)	missense	probably benign	0.36
R2057:Zdhhc8	UTSW	16	18,046,210 (GRCm39)	missense	probably damaging	1.00
R3913:Zdhhc8	UTSW	16	18,044,587 (GRCm39)	missense	possibly damaging	0.94
R4690:Zdhhc8	UTSW	16	18,044,605 (GRCm39)	missense	probably damaging	0.96
R4902:Zdhhc8	UTSW	16	18,045,030 (GRCm39)	missense	probably benign
R5111:Zdhhc8	UTSW	16	18,044,612 (GRCm39)	missense	probably benign	0.00
R5825:Zdhhc8	UTSW	16	18,046,538 (GRCm39)	missense	probably null	0.99
R6152:Zdhhc8	UTSW	16	18,041,202 (GRCm39)	missense	possibly damaging	0.90
R7296:Zdhhc8	UTSW	16	18,052,790 (GRCm39)	missense	probably benign	0.00
R7450:Zdhhc8	UTSW	16	18,043,035 (GRCm39)	missense	probably benign	0.00
R7540:Zdhhc8	UTSW	16	18,045,674 (GRCm39)	missense	probably damaging	1.00
R9015:Zdhhc8	UTSW	16	18,041,141 (GRCm39)	missense	probably damaging	1.00
R9256:Zdhhc8	UTSW	16	18,042,686 (GRCm39)	missense	probably damaging	1.00
R9448:Zdhhc8	UTSW	16	18,039,558 (GRCm39)	missense
R9520:Zdhhc8	UTSW	16	18,045,044 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- CCAAAGAGTGAGTCAGTCTGGG -3'
(R):5'- ATGCCTTCTCAGGTGCCTTG -3'

Sequencing Primer
(F):5'- ACAGGTTGTCATAGCGCAC -3'
(R):5'- TGCGCTCCCTGAGTCTCAAG -3'

Posted On

2017-08-16