Mutagenetix > Incidental Mutation

Incidental Mutation 'R6502:Zdhhc13'

519794

Institutional Source

Beutler Lab

Gene Symbol

Zdhhc13

Ensembl Gene

ENSMUSG00000030471

Gene Name

zinc finger, DHHC domain containing 13

Synonyms

Hip14l, kojak, skc4, 2410004E01Rik

MMRRC Submission

044634-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R6502 (G1)

Quality Score

216.009

Status

Not validated

Chromosome

Chromosomal Location

48438751-48477188 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 48465308 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 406 (E406G)

Ref Sequence

ENSEMBL: ENSMUSP00000112498 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000118927] [ENSMUST00000125280]

AlphaFold

Q9CWU2

Predicted Effect

possibly damaging
Transcript: ENSMUST00000118927
AA Change: E406G

PolyPhen 2 Score 0.953 (Sensitivity: 0.79; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000112498
Gene: ENSMUSG00000030471
AA Change: E406G

Domain	Start	End	E-Value	Type
Blast:ANK	48	77	1e-9	BLAST
ANK	81	110	3.08e-1	SMART
ANK	115	144	4.39e-6	SMART
ANK	148	177	2.37e-2	SMART
ANK	181	211	5.19e2	SMART
ANK	216	245	8.07e-5	SMART
ANK	249	277	1.09e3	SMART
transmembrane domain	292	310	N/A	INTRINSIC
transmembrane domain	317	339	N/A	INTRINSIC
transmembrane domain	344	366	N/A	INTRINSIC
transmembrane domain	373	392	N/A	INTRINSIC
Pfam:zf-DHHC	421	558	1.1e-30	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000125280
AA Change: E276G

PolyPhen 2 Score 0.908 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000123603
Gene: ENSMUSG00000030471
AA Change: E276G

Domain	Start	End	E-Value	Type
ANK	18	47	2.37e-2	SMART
ANK	51	81	5.19e2	SMART
ANK	86	115	8.07e-5	SMART
ANK	119	147	1.09e3	SMART
transmembrane domain	160	182	N/A	INTRINSIC
transmembrane domain	187	209	N/A	INTRINSIC
transmembrane domain	214	236	N/A	INTRINSIC
Pfam:zf-DHHC	258	428	1.1e-35	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.2%
20x: 94.7%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for an ENU mutation display wasting, weight loss, hair loss (alopecia), reduced bone mineral density (osteoporosis), and generalized amyloid deposition, which resulted in early death. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 78 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700013D24Rik	A	T	6: 124,333,908 (GRCm39)	I24K	probably benign	Het
Adamts9	A	T	6: 92,849,316 (GRCm39)	C467S	probably damaging	Het
Adcy7	G	A	8: 89,052,107 (GRCm39)	R925Q	probably damaging	Het
Akap6	G	A	12: 53,186,998 (GRCm39)	G1471S	probably damaging	Het
Ap2b1	T	C	11: 83,233,505 (GRCm39)	V506A	probably damaging	Het
Apob	A	G	12: 8,051,814 (GRCm39)	I1113M	probably damaging	Het
Arsg	A	T	11: 109,408,162 (GRCm39)	N105Y	probably damaging	Het
Blm	T	A	7: 80,131,223 (GRCm39)	Y872F	probably damaging	Het
Btaf1	A	T	19: 36,961,017 (GRCm39)	N797Y	probably benign	Het
Camsap1	T	C	2: 25,846,320 (GRCm39)	E201G	probably damaging	Het
Ccdc122	T	A	14: 77,279,509 (GRCm39)		probably null	Homo
Ccdc141	A	G	2: 77,000,745 (GRCm39)	V29A	probably damaging	Het
Cd244a	T	A	1: 171,405,447 (GRCm39)	D277E	probably benign	Het
Cfap157	T	C	2: 32,670,690 (GRCm39)	Y186C	probably damaging	Het
Ciita	C	T	16: 10,329,774 (GRCm39)	A686V	probably damaging	Het
Clptm1l	T	C	13: 73,765,884 (GRCm39)		probably null	Het
Col16a1	C	T	4: 129,949,787 (GRCm39)	P50L	probably damaging	Het
Crisp3	A	T	17: 40,546,804 (GRCm39)	V38D	probably damaging	Het
Cyfip2	T	C	11: 46,112,173 (GRCm39)	E1010G	probably damaging	Het
Dvl3	G	A	16: 20,346,133 (GRCm39)	E488K	probably damaging	Het
Eed	C	A	7: 89,626,237 (GRCm39)	E45D	probably benign	Het
Eln	A	G	5: 134,754,628 (GRCm39)		probably benign	Het
Fah	T	A	7: 84,244,043 (GRCm39)	I239F	probably damaging	Het
Fbxw5	T	A	2: 25,392,448 (GRCm39)	Y77N	possibly damaging	Het
Garnl3	T	C	2: 32,896,833 (GRCm39)	E602G	possibly damaging	Het
Gkn3	A	T	6: 87,365,786 (GRCm39)	M11K	probably benign	Het
Glt1d1	A	G	5: 127,784,045 (GRCm39)	Y333C	probably damaging	Het
Gm10762	A	T	2: 128,809,090 (GRCm39)	Y86*	probably null	Het
Gm14496	A	G	2: 181,642,386 (GRCm39)	M686V	probably benign	Het
Gse1	T	A	8: 121,280,428 (GRCm39)		probably null	Het
Herc4	C	A	10: 63,153,197 (GRCm39)	T1035K	probably benign	Het
Hmcn2	T	A	2: 31,272,490 (GRCm39)	N1323K	probably damaging	Het
Hnrnpd	T	A	5: 100,114,025 (GRCm39)	E3D	probably damaging	Het
Htr7	T	A	19: 35,947,010 (GRCm39)	I335F	probably damaging	Het
Ift70b	T	A	2: 75,767,448 (GRCm39)	N435I	possibly damaging	Het
Itgae	A	T	11: 73,036,418 (GRCm39)	I1119F	probably benign	Het
Lcn11	T	C	2: 25,669,103 (GRCm39)	F137S	probably benign	Het
Lrp3	T	G	7: 34,903,413 (GRCm39)	D311A	possibly damaging	Het
Lrrc1	G	T	9: 77,349,473 (GRCm39)	D364E	probably damaging	Het
Lrrc37a	T	A	11: 103,383,005 (GRCm39)	E2456V	unknown	Het
Lrriq1	T	C	10: 103,063,045 (GRCm39)	Y87C	probably damaging	Het
Mcc	A	T	18: 44,601,457 (GRCm39)	L449*	probably null	Het
Mcc	A	T	18: 44,601,458 (GRCm39)	L624M	probably damaging	Het
Mcm9	T	C	10: 53,488,935 (GRCm39)	T496A	probably damaging	Het
Myef2	T	A	2: 124,958,602 (GRCm39)	D109V	probably damaging	Het
Myom3	C	T	4: 135,489,824 (GRCm39)		probably benign	Het
Nanos1	G	T	19: 60,744,977 (GRCm39)	G92W	possibly damaging	Het
Ncor1	T	A	11: 62,272,240 (GRCm39)	K84*	probably null	Het
Neb	T	A	2: 52,181,094 (GRCm39)	D1171V	probably benign	Het
Notch3	A	G	17: 32,377,191 (GRCm39)	W267R	probably damaging	Het
Or5d39	A	T	2: 87,980,360 (GRCm39)	M1K	probably null	Het
Or8d1	A	C	9: 38,766,933 (GRCm39)	T192P	probably damaging	Het
Per2	A	G	1: 91,355,485 (GRCm39)	S758P	probably benign	Het
Pi4k2a	A	G	19: 42,079,371 (GRCm39)	Q144R	probably benign	Het
Pirb	A	T	7: 3,720,392 (GRCm39)	V327E	probably benign	Het
Pla2g4a	C	T	1: 149,748,367 (GRCm39)	W272*	probably null	Het
Plekha4	T	A	7: 45,180,000 (GRCm39)	M1K	probably null	Het
Ppt2	A	G	17: 34,844,894 (GRCm39)	C117R	probably damaging	Het
Prph	A	T	15: 98,954,267 (GRCm39)	I222F	probably damaging	Het
Rbm43	T	C	2: 51,815,588 (GRCm39)	D211G	probably damaging	Het
Rims2	A	G	15: 39,398,251 (GRCm39)	D1072G	probably benign	Het
Rnf123	G	T	9: 107,945,531 (GRCm39)	Q380K	possibly damaging	Het
Rnf145	T	C	11: 44,415,932 (GRCm39)	F49S	probably damaging	Het
Sall4	A	G	2: 168,597,628 (GRCm39)	I404T	probably damaging	Het
Slc25a39	G	A	11: 102,295,286 (GRCm39)	P228L	probably damaging	Het
Tbc1d14	T	C	5: 36,677,825 (GRCm39)	T377A	possibly damaging	Het
Tbc1d17	A	G	7: 44,491,049 (GRCm39)	I555T	probably benign	Het
Tmem131l	A	T	3: 83,829,715 (GRCm39)	S980T	probably damaging	Het
Tmem14a	G	T	1: 21,299,662 (GRCm39)	L97F	possibly damaging	Het
Tmem98	T	C	11: 80,703,461 (GRCm39)	V26A	probably benign	Het
Tmppe	G	T	9: 114,234,720 (GRCm39)	G340W	probably damaging	Het
Tsc1	T	C	2: 28,555,613 (GRCm39)	S237P	probably damaging	Het
Ubr4	C	T	4: 139,171,982 (GRCm39)	R2992W	probably damaging	Het
Ugt2a2	A	G	5: 87,608,318 (GRCm39)	V673A	possibly damaging	Het
Vmn2r19	T	C	6: 123,293,067 (GRCm39)	Y370H	possibly damaging	Het
Vmn2r20	A	G	6: 123,373,342 (GRCm39)	F500S	possibly damaging	Het
Zc3h7b	A	G	15: 81,653,252 (GRCm39)	Y47C	probably benign	Het
Zfp418	T	C	7: 7,185,599 (GRCm39)	S521P	possibly damaging	Het

Other mutations in Zdhhc13

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00852:Zdhhc13	APN	7	48,455,349 (GRCm39)	missense	probably benign	0.00
IGL01820:Zdhhc13	APN	7	48,458,613 (GRCm39)	missense	probably damaging	1.00
IGL02941:Zdhhc13	APN	7	48,466,886 (GRCm39)	splice site	probably benign
bernard	UTSW	7	48,476,621 (GRCm39)	missense	probably damaging	1.00
brindle	UTSW	7	48,474,479 (GRCm39)	missense	possibly damaging	0.47
oxidized	UTSW	7	48,466,175 (GRCm39)	missense	probably benign	0.04
rusty	UTSW	7	48,474,392 (GRCm39)	missense	possibly damaging	0.95
zephiro	UTSW	7	48,461,103 (GRCm39)	nonsense	probably null
PIT4445001:Zdhhc13	UTSW	7	48,445,697 (GRCm39)	missense	probably benign	0.00
R0456:Zdhhc13	UTSW	7	48,458,602 (GRCm39)	missense	probably benign	0.03
R1398:Zdhhc13	UTSW	7	48,476,621 (GRCm39)	missense	probably damaging	1.00
R1785:Zdhhc13	UTSW	7	48,474,392 (GRCm39)	missense	possibly damaging	0.95
R1786:Zdhhc13	UTSW	7	48,474,392 (GRCm39)	missense	possibly damaging	0.95
R2066:Zdhhc13	UTSW	7	48,466,175 (GRCm39)	missense	probably benign	0.04
R2131:Zdhhc13	UTSW	7	48,474,392 (GRCm39)	missense	possibly damaging	0.95
R2133:Zdhhc13	UTSW	7	48,474,392 (GRCm39)	missense	possibly damaging	0.95
R2405:Zdhhc13	UTSW	7	48,472,478 (GRCm39)	splice site	probably null
R3770:Zdhhc13	UTSW	7	48,452,692 (GRCm39)	missense	probably damaging	1.00
R4374:Zdhhc13	UTSW	7	48,458,589 (GRCm39)	missense	probably damaging	1.00
R4772:Zdhhc13	UTSW	7	48,449,621 (GRCm39)	missense	probably benign	0.24
R5052:Zdhhc13	UTSW	7	48,474,479 (GRCm39)	missense	possibly damaging	0.47
R5455:Zdhhc13	UTSW	7	48,455,323 (GRCm39)	missense	possibly damaging	0.95
R6418:Zdhhc13	UTSW	7	48,461,149 (GRCm39)	missense	possibly damaging	0.94
R7136:Zdhhc13	UTSW	7	48,451,080 (GRCm39)	missense	probably benign
R7467:Zdhhc13	UTSW	7	48,454,156 (GRCm39)	missense	probably benign	0.02
R7485:Zdhhc13	UTSW	7	48,461,103 (GRCm39)	nonsense	probably null
R7723:Zdhhc13	UTSW	7	48,458,567 (GRCm39)	missense	probably benign
R8297:Zdhhc13	UTSW	7	48,465,257 (GRCm39)	missense	probably damaging	0.96
R8356:Zdhhc13	UTSW	7	48,452,747 (GRCm39)	missense	probably damaging	1.00
R8385:Zdhhc13	UTSW	7	48,455,444 (GRCm39)	critical splice donor site	probably null
R8456:Zdhhc13	UTSW	7	48,452,747 (GRCm39)	missense	probably damaging	1.00
R9346:Zdhhc13	UTSW	7	48,472,328 (GRCm39)	missense	probably benign	0.18
R9397:Zdhhc13	UTSW	7	48,476,628 (GRCm39)	missense	probably benign
X0021:Zdhhc13	UTSW	7	48,454,963 (GRCm39)	missense	possibly damaging	0.79

Predicted Primers

PCR Primer
(F):5'- TTGCTTGCTTCACACATGATG -3'
(R):5'- GGCAGGCATTCAAGACTAAAATTG -3'

Sequencing Primer
(F):5'- CACACATGATGCTTTTCTCAGTAGAG -3'
(R):5'- GATTGATGAGGGATCACTTTTTACAG -3'

Posted On

2018-06-06