Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01061:Dnajc18'

53143

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Dnajc18

Ensembl Gene

ENSMUSG00000024350

Gene Name

DnaJ heat shock protein family (Hsp40) member C18

Synonyms

2700075B01Rik

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.116) question?

Stock #

IGL01061

Quality Score

Status

Chromosome

Chromosomal Location

35804156-35841467 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

A to G at 35813995 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000025208 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000025208]

AlphaFold

Q9CZJ9

Predicted Effect

probably benign
Transcript: ENSMUST00000025208

SMART Domains

Protein: ENSMUSP00000025208
Gene: ENSMUSG00000024350

Domain	Start	End	E-Value	Type
DnaJ	81	138	6.52e-27	SMART
low complexity region	200	218	N/A	INTRINSIC
Pfam:DUF1977	243	349	1.7e-28	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 48 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aen	G	A	7: 78,557,050 (GRCm39)	M299I	probably damaging	Het
Ankfy1	T	A	11: 72,619,686 (GRCm39)	C186*	probably null	Het
Ankmy1	A	T	1: 92,798,696 (GRCm39)		probably benign	Het
B3gnt2	T	A	11: 22,786,042 (GRCm39)	E382V	probably damaging	Het
Carmil3	T	G	14: 55,736,087 (GRCm39)	S610A	possibly damaging	Het
Cfap70	T	C	14: 20,497,693 (GRCm39)		probably benign	Het
Chek1	G	A	9: 36,625,815 (GRCm39)	R277C	possibly damaging	Het
Cpb1	T	A	3: 20,320,680 (GRCm39)	I92L	probably benign	Het
Ddx56	C	T	11: 6,214,671 (GRCm39)		probably null	Het
Dicer1	A	T	12: 104,672,586 (GRCm39)	M887K	probably null	Het
Dock2	A	G	11: 34,596,653 (GRCm39)	V401A	probably damaging	Het
Dock4	A	C	12: 40,752,968 (GRCm39)	N434T	probably benign	Het
Dync2i1	C	A	12: 116,193,324 (GRCm39)	A543S	probably benign	Het
Ehbp1l1	A	T	19: 5,767,916 (GRCm39)	M1129K	probably benign	Het
Fam83a	A	T	15: 57,849,771 (GRCm39)	Y105F	possibly damaging	Het
Fnbp1	C	A	2: 30,973,054 (GRCm39)	D70Y	probably damaging	Het
Gtf3c2	A	G	5: 31,325,698 (GRCm39)	F414L	possibly damaging	Het
Kndc1	A	T	7: 139,502,610 (GRCm39)	E965D	probably benign	Het
Lrrc66	T	C	5: 73,772,842 (GRCm39)	K209E	probably benign	Het
Mcm3	A	T	1: 20,884,720 (GRCm39)	I261N	possibly damaging	Het
Mier3	T	A	13: 111,850,970 (GRCm39)		probably benign	Het
Muc6	T	C	7: 141,234,720 (GRCm39)	E669G	probably damaging	Het
Myh1	T	A	11: 67,108,688 (GRCm39)	M1368K	probably benign	Het
Nav1	A	G	1: 135,378,368 (GRCm39)	I1653T	probably damaging	Het
Nuak1	C	A	10: 84,210,998 (GRCm39)	L363F	probably damaging	Het
Or14j2	A	G	17: 37,885,795 (GRCm39)	I173T	possibly damaging	Het
Or52b1	A	G	7: 104,978,589 (GRCm39)	I270T	possibly damaging	Het
Or9i1	T	C	19: 13,840,069 (GRCm39)	V304A	possibly damaging	Het
Pkd1l3	A	G	8: 110,365,338 (GRCm39)	H1153R	probably damaging	Het
Poglut3	A	G	9: 53,299,887 (GRCm39)		probably benign	Het
Ppp6r2	A	T	15: 89,170,218 (GRCm39)		probably benign	Het
Prelid3b	T	C	2: 174,307,614 (GRCm39)		probably null	Het
Prrt3	T	C	6: 113,474,731 (GRCm39)	K164E	possibly damaging	Het
Rab22a	T	A	2: 173,530,003 (GRCm39)	D60E	probably damaging	Het
Rab32	A	G	10: 10,433,618 (GRCm39)	L72P	probably damaging	Het
Samm50	A	G	15: 84,086,455 (GRCm39)	T225A	probably benign	Het
Snx27	T	A	3: 94,436,287 (GRCm39)		probably benign	Het
Taf7	G	A	18: 37,776,486 (GRCm39)	T27M	probably damaging	Het
Tgm5	A	T	2: 120,901,977 (GRCm39)	C231S	probably benign	Het
Tll1	A	G	8: 64,491,488 (GRCm39)		probably null	Het
Tmem150a	A	G	6: 72,334,101 (GRCm39)	D61G	probably damaging	Het
Ttll8	G	A	15: 88,801,453 (GRCm39)	R412C	possibly damaging	Het
Ubr3	T	A	2: 69,813,569 (GRCm39)	D1293E	probably benign	Het
Utp20	T	C	10: 88,606,566 (GRCm39)	N1669D	probably benign	Het
Vmn2r28	A	G	7: 5,491,183 (GRCm39)	W355R	probably damaging	Het
Yars2	C	T	16: 16,124,406 (GRCm39)	R338*	probably null	Het
Zfhx2	T	A	14: 55,311,339 (GRCm39)	N452Y	possibly damaging	Het
Zfp180	T	G	7: 23,804,170 (GRCm39)	D196E	possibly damaging	Het

Other mutations in Dnajc18

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01152:Dnajc18	APN	18	35,813,926 (GRCm39)	missense	probably benign	0.02
IGL01621:Dnajc18	APN	18	35,813,893 (GRCm39)	missense	probably benign
IGL03201:Dnajc18	APN	18	35,813,972 (GRCm39)	missense	probably benign	0.19
R1464:Dnajc18	UTSW	18	35,813,900 (GRCm39)	missense	possibly damaging	0.88
R1464:Dnajc18	UTSW	18	35,813,900 (GRCm39)	missense	possibly damaging	0.88
R1801:Dnajc18	UTSW	18	35,813,857 (GRCm39)	missense	probably damaging	1.00
R3893:Dnajc18	UTSW	18	35,834,048 (GRCm39)	splice site	probably null
R4974:Dnajc18	UTSW	18	35,816,372 (GRCm39)	missense	possibly damaging	0.75
R5234:Dnajc18	UTSW	18	35,816,351 (GRCm39)	missense	probably benign	0.12
R6326:Dnajc18	UTSW	18	35,813,978 (GRCm39)	missense	possibly damaging	0.95
R6360:Dnajc18	UTSW	18	35,819,762 (GRCm39)	missense	probably damaging	1.00
R6460:Dnajc18	UTSW	18	35,833,963 (GRCm39)	missense	probably benign	0.41
R7215:Dnajc18	UTSW	18	35,815,034 (GRCm39)	missense	probably benign
R7492:Dnajc18	UTSW	18	35,819,846 (GRCm39)	missense	probably damaging	1.00
R8290:Dnajc18	UTSW	18	35,816,324 (GRCm39)	nonsense	probably null
R9364:Dnajc18	UTSW	18	35,808,260 (GRCm39)	missense	probably damaging	1.00
R9464:Dnajc18	UTSW	18	35,830,166 (GRCm39)	missense	probably damaging	0.96
X0063:Dnajc18	UTSW	18	35,819,786 (GRCm39)	missense	probably damaging	0.97

Posted On

2013-06-21