Mutagenetix > Incidental Mutation

Incidental Mutation 'R6784:Jkampl'

531558

Institutional Source

Beutler Lab

Gene Symbol

Jkampl

Ensembl Gene

ENSMUSG00000056197

Gene Name

JNK1/MAPK8 associated membrane protein like

Synonyms

4931417E11Rik

MMRRC Submission

044898-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.111) question?

Stock #

R6784 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

73445563-73446621 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 73445918 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 210 (Y210*)

Ref Sequence

ENSEMBL: ENSMUSP00000068770 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000070163]

AlphaFold

Q9CR05

Predicted Effect

probably null
Transcript: ENSMUST00000070163
AA Change: Y210*

SMART Domains

Protein: ENSMUSP00000068770
Gene: ENSMUSG00000056197
AA Change: Y210*

Domain	Start	End	E-Value	Type
Pfam:DUF766	3	294	3.1e-113	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000204006

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000204961

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000205241

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.9%
3x: 99.7%
10x: 98.5%
20x: 96.2%

Validation Efficiency

98% (46/47)

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aass	C	T	6: 23,093,895 (GRCm39)	S142N	probably null	Het
Aida	A	G	1: 183,103,346 (GRCm39)	Y275C	probably damaging	Het
Arrdc4	A	G	7: 68,398,594 (GRCm39)	I74T	probably benign	Het
C1ql4	A	G	15: 98,985,290 (GRCm39)	V107A	probably benign	Het
Ccnh	T	C	13: 85,360,884 (GRCm39)	V284A	probably benign	Het
Cd180	A	G	13: 102,839,213 (GRCm39)	E32G	probably damaging	Het
Chd6	T	C	2: 160,808,174 (GRCm39)	D1680G	probably damaging	Het
Cog7	A	T	7: 121,563,516 (GRCm39)		probably null	Het
Cyp2j6	T	A	4: 96,423,741 (GRCm39)	Q209L	possibly damaging	Het
Dars1	A	T	1: 128,319,084 (GRCm39)	V116E	probably damaging	Het
Dnah10	A	G	5: 124,854,890 (GRCm39)	K1932E	probably damaging	Het
Dock9	A	G	14: 121,780,926 (GRCm39)	S2086P	probably damaging	Het
Espl1	C	G	15: 102,207,660 (GRCm39)	R375G	probably benign	Het
Fer1l6	C	T	15: 58,443,275 (GRCm39)	S526L	possibly damaging	Het
Galnt9	G	A	5: 110,768,465 (GRCm39)	R587H	probably damaging	Het
Gigyf2	G	T	1: 87,371,396 (GRCm39)	V1170L	probably damaging	Het
Gm14412	G	T	2: 177,009,133 (GRCm39)	T41K	probably benign	Het
Gm45861	A	G	8: 27,990,086 (GRCm39)		probably null	Het
H2bc4	T	C	13: 23,868,483 (GRCm39)	I90T	probably damaging	Het
Hoxc5	A	G	15: 102,922,322 (GRCm39)		probably benign	Het
Klra1	T	C	6: 130,349,817 (GRCm39)	D207G	probably benign	Het
Lancl2	A	G	6: 57,680,240 (GRCm39)	N57D	probably benign	Het
Map2k4	T	C	11: 65,582,577 (GRCm39)		probably benign	Het
Mgat3	G	T	15: 80,096,401 (GRCm39)	Q409H	probably damaging	Het
Mpp3	T	A	11: 101,892,974 (GRCm39)		probably null	Het
Myh1	T	A	11: 67,105,396 (GRCm39)	L1062Q	probably damaging	Het
Nebl	T	A	2: 17,439,725 (GRCm39)	K183*	probably null	Het
Npat	G	C	9: 53,469,458 (GRCm39)	D315H	probably damaging	Het
Nt5c2	A	G	19: 46,912,766 (GRCm39)	V63A	probably damaging	Het
Opn1sw	T	A	6: 29,379,846 (GRCm39)	E129D	probably damaging	Het
Or10ag2	C	T	2: 87,248,796 (GRCm39)	R135C	probably benign	Het
Or1e29	T	G	11: 73,667,676 (GRCm39)	H159P	probably damaging	Het
Or51t4	A	T	7: 102,597,722 (GRCm39)	T17S	possibly damaging	Het
Or5p1	A	T	7: 107,916,989 (GRCm39)	D296V	probably damaging	Het
Prdm16	T	C	4: 154,407,764 (GRCm39)	Y1153C	probably damaging	Het
Prdm6	T	A	18: 53,669,698 (GRCm39)	D105E	probably benign	Het
Pwwp4c	C	T	X: 73,684,021 (GRCm39)	R355H	probably damaging	Homo
Rbm27	T	C	18: 42,434,929 (GRCm39)	M331T	probably benign	Het
S1pr1	A	G	3: 115,505,710 (GRCm39)	Y295H	probably damaging	Het
Sgpp1	G	C	12: 75,782,243 (GRCm39)	P32R	probably benign	Het
Sla2	C	T	2: 156,725,589 (GRCm39)	S3N	unknown	Het
Slc10a6	A	G	5: 103,776,896 (GRCm39)	I68T	probably damaging	Het
Slc5a1	T	C	5: 33,315,460 (GRCm39)	F493S	probably benign	Het
Snx14	A	T	9: 88,263,845 (GRCm39)	Y847N	probably benign	Het
Tmc1	A	G	19: 20,805,015 (GRCm39)		probably null	Het
Vps8	C	A	16: 21,381,957 (GRCm39)	Q1130K	probably benign	Het

Other mutations in Jkampl

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01566:Jkampl	APN	6	73,445,673 (GRCm39)	missense	probably damaging	1.00
IGL01768:Jkampl	APN	6	73,445,899 (GRCm39)	missense	possibly damaging	0.83
IGL02903:Jkampl	APN	6	73,446,103 (GRCm39)	missense	probably damaging	1.00
R0084:Jkampl	UTSW	6	73,445,918 (GRCm39)	nonsense	probably null
R0123:Jkampl	UTSW	6	73,446,402 (GRCm39)	missense	possibly damaging	0.49
R0225:Jkampl	UTSW	6	73,446,402 (GRCm39)	missense	possibly damaging	0.49
R1478:Jkampl	UTSW	6	73,446,039 (GRCm39)	missense	probably damaging	1.00
R1640:Jkampl	UTSW	6	73,445,869 (GRCm39)	missense	probably benign	0.13
R4616:Jkampl	UTSW	6	73,446,252 (GRCm39)	missense	probably benign	0.02
R5451:Jkampl	UTSW	6	73,445,850 (GRCm39)	missense	probably benign	0.00
R5875:Jkampl	UTSW	6	73,446,028 (GRCm39)	missense	possibly damaging	0.50
R5911:Jkampl	UTSW	6	73,445,674 (GRCm39)	missense	probably damaging	0.99
R6982:Jkampl	UTSW	6	73,446,527 (GRCm39)	nonsense	probably null
R7990:Jkampl	UTSW	6	73,446,528 (GRCm39)	missense	probably damaging	1.00
R8365:Jkampl	UTSW	6	73,446,329 (GRCm39)	missense	probably benign	0.02
R8381:Jkampl	UTSW	6	73,445,895 (GRCm39)	missense	probably damaging	1.00
R9098:Jkampl	UTSW	6	73,446,517 (GRCm39)	missense	probably benign	0.18
R9363:Jkampl	UTSW	6	73,446,487 (GRCm39)	missense	possibly damaging	0.54
X0024:Jkampl	UTSW	6	73,446,033 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- AGATCTTGCTCAAGTTGCTGCC -3'
(R):5'- ATTACATCACCACCGTGCACTG -3'

Sequencing Primer
(F):5'- CCCCTGGAGAGTGCCATTAAG -3'
(R):5'- TGCACTGCACTCAGGAAG -3'

Posted On

2018-08-29