Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01522:Jcad'

89449

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Jcad

Ensembl Gene

ENSMUSG00000033960

Gene Name

junctional cadherin 5 associated

Synonyms

9430020K01Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL01522

Quality Score

Status

Chromosome

Chromosomal Location

4634878-4682869 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 4673312 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Serine at position 358 (N358S)

Ref Sequence

ENSEMBL: ENSMUSP00000038613 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000037029]

AlphaFold

Q5DTX6

Predicted Effect

probably damaging
Transcript: ENSMUST00000037029
AA Change: N358S

PolyPhen 2 Score 0.974 (Sensitivity: 0.76; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000038613
Gene: ENSMUSG00000033960
AA Change: N358S

Domain	Start	End	E-Value	Type
Pfam:JCAD	1	1309	N/A	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 41 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts12	T	C	15: 11,065,245 (GRCm39)		probably null	Het
Adamts3	T	C	5: 89,850,802 (GRCm39)	N579S	probably benign	Het
Akr1c19	A	G	13: 4,289,098 (GRCm39)		probably benign	Het
Ankrd39	T	A	1: 36,581,142 (GRCm39)	H69L	probably damaging	Het
Apcdd1	T	A	18: 63,085,186 (GRCm39)	M461K	possibly damaging	Het
Bpifa3	G	A	2: 153,979,502 (GRCm39)	C209Y	probably damaging	Het
Cep131	T	C	11: 119,957,989 (GRCm39)	E779G	probably benign	Het
Cep85	T	C	4: 133,879,566 (GRCm39)	Q394R	probably damaging	Het
Cep85	G	T	4: 133,879,567 (GRCm39)	Q394K	probably damaging	Het
Clcn6	T	C	4: 148,101,992 (GRCm39)	Y364C	probably benign	Het
Fetub	G	A	16: 22,748,391 (GRCm39)	M1I	probably null	Het
Greb1	T	C	12: 16,751,202 (GRCm39)	I1003V	probably damaging	Het
Hsf3	A	G	X: 95,364,200 (GRCm39)		probably benign	Het
Kndc1	T	C	7: 139,493,888 (GRCm39)		probably benign	Het
Lama1	A	T	17: 68,059,769 (GRCm39)		probably benign	Het
Mark2	A	G	19: 7,258,603 (GRCm39)	V50A	probably benign	Het
Mmp7	T	C	9: 7,692,229 (GRCm39)	W35R	probably damaging	Het
Ndc80	A	G	17: 71,806,320 (GRCm39)	V578A	probably benign	Het
Nfyc	T	C	4: 120,638,721 (GRCm39)	E42G	probably damaging	Het
Or1j15	A	G	2: 36,459,233 (GRCm39)	T208A	probably benign	Het
Or52b4	A	T	7: 102,184,391 (GRCm39)	I146F	probably damaging	Het
Or5d37	T	C	2: 87,923,360 (GRCm39)	K307E	possibly damaging	Het
Or8g21	A	T	9: 38,906,396 (GRCm39)	C112S	probably benign	Het
Or9i16	A	T	19: 13,864,722 (GRCm39)	L284*	probably null	Het
Pcdha11	T	C	18: 37,318,061 (GRCm39)	F925L	probably damaging	Het
Pdcd1	T	G	1: 93,968,571 (GRCm39)	R154S	probably benign	Het
Pepd	T	A	7: 34,623,865 (GRCm39)	D87E	probably benign	Het
Pfn4	A	G	12: 4,820,240 (GRCm39)	T30A	probably benign	Het
Pgpep1l	A	G	7: 67,887,456 (GRCm39)	M48T	possibly damaging	Het
Pla2g15	A	G	8: 106,889,748 (GRCm39)	N340S	probably benign	Het
Plcb4	A	G	2: 135,844,547 (GRCm39)	D155G	probably damaging	Het
Plg	G	A	17: 12,622,956 (GRCm39)	G499S	probably damaging	Het
Plin3	C	T	17: 56,587,799 (GRCm39)	W305*	probably null	Het
Polq	C	A	16: 36,848,265 (GRCm39)	L291I	probably damaging	Het
Sanbr	A	G	11: 23,532,865 (GRCm39)		probably null	Het
Sdf2l1	T	A	16: 16,950,014 (GRCm39)	H54L	probably damaging	Het
Slc38a2	C	T	15: 96,590,936 (GRCm39)	D276N	possibly damaging	Het
Syk	A	G	13: 52,797,097 (GRCm39)	T576A	probably benign	Het
Tas2r119	G	A	15: 32,178,339 (GRCm39)	V302I	probably benign	Het
Uso1	T	C	5: 92,329,278 (GRCm39)	F389L	probably damaging	Het
Wwc2	T	A	8: 48,321,668 (GRCm39)	Y482F	unknown	Het

Other mutations in Jcad

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00650:Jcad	APN	18	4,675,692 (GRCm39)	missense	probably benign	0.14
IGL00672:Jcad	APN	18	4,674,835 (GRCm39)	missense	possibly damaging	0.77
IGL00782:Jcad	APN	18	4,675,073 (GRCm39)	missense	probably benign	0.00
IGL00825:Jcad	APN	18	4,673,516 (GRCm39)	missense	probably damaging	1.00
IGL01796:Jcad	APN	18	4,672,855 (GRCm39)	nonsense	probably null
IGL01973:Jcad	APN	18	4,675,514 (GRCm39)	missense	probably benign	0.21
IGL02083:Jcad	APN	18	4,680,266 (GRCm39)	utr 3 prime	probably benign
IGL02625:Jcad	APN	18	4,674,422 (GRCm39)	missense	probably benign	0.03
IGL03002:Jcad	APN	18	4,675,153 (GRCm39)	missense	probably benign	0.00
IGL03325:Jcad	APN	18	4,673,902 (GRCm39)	missense	probably benign
R0304:Jcad	UTSW	18	4,673,325 (GRCm39)	missense	possibly damaging	0.75
R0487:Jcad	UTSW	18	4,673,243 (GRCm39)	missense	probably damaging	1.00
R0519:Jcad	UTSW	18	4,649,122 (GRCm39)	start gained	probably benign
R0664:Jcad	UTSW	18	4,676,063 (GRCm39)	missense	probably damaging	0.97
R1649:Jcad	UTSW	18	4,673,309 (GRCm39)	missense	probably damaging	1.00
R1710:Jcad	UTSW	18	4,674,511 (GRCm39)	missense	probably damaging	1.00
R1734:Jcad	UTSW	18	4,674,526 (GRCm39)	missense	probably damaging	1.00
R1823:Jcad	UTSW	18	4,675,780 (GRCm39)	missense	probably damaging	1.00
R1824:Jcad	UTSW	18	4,649,293 (GRCm39)	missense	probably benign
R1850:Jcad	UTSW	18	4,675,730 (GRCm39)	missense	possibly damaging	0.95
R1872:Jcad	UTSW	18	4,673,048 (GRCm39)	missense	probably benign
R1878:Jcad	UTSW	18	4,673,857 (GRCm39)	missense	possibly damaging	0.60
R1918:Jcad	UTSW	18	4,674,292 (GRCm39)	missense	probably damaging	1.00
R1967:Jcad	UTSW	18	4,675,162 (GRCm39)	missense	probably benign	0.07
R2420:Jcad	UTSW	18	4,675,952 (GRCm39)	missense	probably damaging	1.00
R2504:Jcad	UTSW	18	4,674,026 (GRCm39)	missense	probably damaging	0.99
R2936:Jcad	UTSW	18	4,675,153 (GRCm39)	missense	probably benign	0.00
R4420:Jcad	UTSW	18	4,676,032 (GRCm39)	missense	probably benign	0.00
R4668:Jcad	UTSW	18	4,680,221 (GRCm39)	splice site	probably null
R4670:Jcad	UTSW	18	4,674,175 (GRCm39)	missense	probably benign	0.03
R4671:Jcad	UTSW	18	4,674,175 (GRCm39)	missense	probably benign	0.03
R4707:Jcad	UTSW	18	4,649,338 (GRCm39)	nonsense	probably null
R4720:Jcad	UTSW	18	4,674,055 (GRCm39)	missense	probably benign	0.03
R4815:Jcad	UTSW	18	4,675,223 (GRCm39)	missense	possibly damaging	0.94
R4906:Jcad	UTSW	18	4,673,762 (GRCm39)	missense	probably damaging	1.00
R5214:Jcad	UTSW	18	4,674,134 (GRCm39)	missense	probably damaging	1.00
R5439:Jcad	UTSW	18	4,675,790 (GRCm39)	missense	probably damaging	1.00
R5563:Jcad	UTSW	18	4,673,944 (GRCm39)	missense	possibly damaging	0.93
R5721:Jcad	UTSW	18	4,676,044 (GRCm39)	missense	possibly damaging	0.48
R5825:Jcad	UTSW	18	4,674,896 (GRCm39)	missense	probably benign	0.00
R5952:Jcad	UTSW	18	4,674,554 (GRCm39)	missense	probably damaging	1.00
R6661:Jcad	UTSW	18	4,675,256 (GRCm39)	missense	probably damaging	1.00
R6928:Jcad	UTSW	18	4,673,372 (GRCm39)	missense	probably benign	0.00
R7426:Jcad	UTSW	18	4,675,529 (GRCm39)	missense	probably benign	0.11
R7808:Jcad	UTSW	18	4,673,113 (GRCm39)	missense	probably damaging	1.00
R7943:Jcad	UTSW	18	4,672,700 (GRCm39)	missense	probably damaging	1.00
R8010:Jcad	UTSW	18	4,674,581 (GRCm39)	missense	probably benign
R8080:Jcad	UTSW	18	4,649,270 (GRCm39)	missense	probably benign	0.01
R8133:Jcad	UTSW	18	4,649,384 (GRCm39)	missense	probably benign	0.03
R8168:Jcad	UTSW	18	4,675,094 (GRCm39)	missense	probably benign	0.00
R8232:Jcad	UTSW	18	4,674,862 (GRCm39)	missense	probably benign	0.23
R8276:Jcad	UTSW	18	4,674,318 (GRCm39)	missense	probably damaging	1.00
R8408:Jcad	UTSW	18	4,649,402 (GRCm39)	missense	possibly damaging	0.55
R9173:Jcad	UTSW	18	4,675,820 (GRCm39)	missense	probably benign	0.42
R9415:Jcad	UTSW	18	4,673,912 (GRCm39)	missense	probably damaging	1.00
R9571:Jcad	UTSW	18	4,673,252 (GRCm39)	nonsense	probably null
T0722:Jcad	UTSW	18	4,675,531 (GRCm39)	missense	probably benign	0.25
X0017:Jcad	UTSW	18	4,676,044 (GRCm39)	missense	probably benign	0.01

Posted On

2013-12-03