Mutagenetix > Incidental Mutations

Incidental Mutation 'R5792:Layn'

447028

Institutional Source

Beutler Lab

Gene Symbol

Layn

Ensembl Gene

ENSMUSG00000060594

Gene Name

layilin

Synonyms

LOC244864, E030012M19Rik

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.061) question?

Stock #

R5792 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

51054640-51077094 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 51068161 bp

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Glycine at position 148 (E148G)

Ref Sequence

ENSEMBL: ENSMUSP00000150681 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000098782] [ENSMUST00000214452] [ENSMUST00000217212]

Predicted Effect

probably damaging
Transcript: ENSMUST00000098782
AA Change: E148G

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

SMART Domains

Protein: ENSMUSP00000096379
Gene: ENSMUSG00000060594
AA Change: E148G

Domain	Start	End	E-Value	Type
signal peptide	1	24	N/A	INTRINSIC
CLECT	41	185	6.18e-25	SMART
transmembrane domain	237	259	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000214090

Predicted Effect

probably benign
Transcript: ENSMUST00000214452

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000216453

Predicted Effect

probably damaging
Transcript: ENSMUST00000217212
AA Change: E148G

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

Meta Mutation Damage Score

0.5946

Coding Region Coverage

1x: 99.3%
3x: 98.7%
10x: 97.5%
20x: 95.9%

Validation Efficiency

95% (56/59)

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930433I11Rik	A	T	7: 40,993,521	I296F	possibly damaging	Het
Adamts19	C	T	18: 58,837,512	T56M	possibly damaging	Het
Armc4	T	C	18: 7,217,965	N583S	probably benign	Het
Axdnd1	T	G	1: 156,341,889	E802D	probably damaging	Het
Birc6	T	C	17: 74,631,053	V2630A	probably benign	Het
Capn5	A	T	7: 98,131,195	F323I	probably benign	Het
Cdc25b	A	G	2: 131,191,759	E206G	probably damaging	Het
Cmah	T	G	13: 24,456,915	N382K	probably benign	Het
Col11a1	A	T	3: 114,131,593	D25V	probably damaging	Het
Cyp2d41-ps	G	T	15: 82,779,220		noncoding transcript	Het
Cyp3a59	A	G	5: 146,099,851	K288E	possibly damaging	Het
Cyr61	T	C	3: 145,648,658	D166G	probably benign	Het
Dclre1a	A	C	19: 56,529,590	I1019S	probably damaging	Het
Fat2	G	T	11: 55,262,325	A3687D	possibly damaging	Het
Flg2	T	A	3: 93,203,497	V944E	unknown	Het
Galntl5	T	C	5: 25,198,463	V177A	possibly damaging	Het
Gm12695	T	C	4: 96,728,283	T438A	probably benign	Het
Gm14295	A	T	2: 176,811,014	N766Y	probably benign	Het
Gm15433	T	A	1: 84,964,112		noncoding transcript	Het
Gm2431	C	T	7: 142,258,332	G8E	unknown	Het
Gm5435	T	A	12: 82,495,426		noncoding transcript	Het
Gprc5c	G	T	11: 114,864,267	V257L	possibly damaging	Het
Grip1	T	C	10: 119,985,480	I350T	probably benign	Het
Guf1	T	A	5: 69,560,486	F196I	probably damaging	Het
Kcng4	G	T	8: 119,626,279	D297E	probably damaging	Het
Khdrbs2	G	A	1: 32,472,692	R246Q	probably damaging	Het
Lrig3	T	A	10: 126,009,919	V739E	probably damaging	Het
Lyg1	A	G	1: 37,947,267	W129R	probably benign	Het
Nup210l	C	T	3: 90,199,857	T1567I	probably damaging	Het
Nus1	T	A	10: 52,429,256	L12*	probably null	Het
Olfr2	A	T	7: 107,001,443	V139D	possibly damaging	Het
Olfr354	A	G	2: 36,907,101	I52V	probably benign	Het
Otop1	A	G	5: 38,297,916	N218S	probably benign	Het
Pcif1	T	A	2: 164,885,379	N90K	probably damaging	Het
Phf2	T	C	13: 48,820,042		probably null	Het
Piezo2	T	A	18: 63,146,856	I215F	probably damaging	Het
Pitpnm2	G	T	5: 124,130,321	C553*	probably null	Het
Prdm1	A	G	10: 44,450,228	V115A	probably damaging	Het
Prkdc	A	G	16: 15,816,752	D3587G	probably damaging	Het
Sez6l	A	T	5: 112,422,024	Y883*	probably null	Het
Sh3rf2	A	C	18: 42,111,138	H223P	probably damaging	Het
Slco1a5	C	T	6: 142,242,113	C500Y	probably damaging	Het
Slf1	T	A	13: 77,066,737	H610L	probably benign	Het
Syn3	T	C	10: 86,294,628	*244W	probably null	Het
Sytl2	A	T	7: 90,375,689	D295V	probably damaging	Het
Tnfrsf1a	T	A	6: 125,358,077	C44S	probably damaging	Het
Ttc6	T	G	12: 57,673,204	L854V	possibly damaging	Het
Ttn	T	C	2: 76,766,258	I18358V	probably benign	Het
Vmn2r108	A	G	17: 20,463,136	V602A	probably damaging	Het
Zap70	A	G	1: 36,779,009		probably benign	Het
Zfhx2	T	C	14: 55,066,846	E1227G	possibly damaging	Het
Znhit3	G	A	11: 84,916,084		probably null	Het
Zpbp2	A	G	11: 98,551,410		probably benign	Het

Other mutations in Layn

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00921:Layn	APN	9	51057408	missense	probably damaging	1.00
IGL01145:Layn	APN	9	51074046	missense	probably benign	0.01
IGL02006:Layn	APN	9	51057291	intron	probably benign
IGL02226:Layn	APN	9	51074017	missense	probably damaging	1.00
PIT4677001:Layn	UTSW	9	51057411	missense	probably damaging	0.98
R1464:Layn	UTSW	9	51057586	missense	probably damaging	1.00
R1464:Layn	UTSW	9	51057586	missense	probably damaging	1.00
R1775:Layn	UTSW	9	51059533	missense	probably benign	0.03
R2156:Layn	UTSW	9	51057397	missense	probably benign
R3732:Layn	UTSW	9	51059544	missense	probably damaging	1.00
R3732:Layn	UTSW	9	51059544	missense	probably damaging	1.00
R3733:Layn	UTSW	9	51059544	missense	probably damaging	1.00
R3757:Layn	UTSW	9	51059556	missense	probably benign	0.11
R4840:Layn	UTSW	9	51057382	missense	probably damaging	1.00
R7185:Layn	UTSW	9	51073873	missense	possibly damaging	0.58
R7216:Layn	UTSW	9	51077052	start gained	probably benign
R7404:Layn	UTSW	9	51057370	missense	possibly damaging	0.94

Predicted Primers

PCR Primer
(F):5'- AAGTTCTTGGTACCAGCAGC -3'
(R):5'- TTGTTGGCAGTGCTTCAATTCC -3'

Sequencing Primer
(F):5'- ACCAGCAGCTGTTTTTGAAATGGAG -3'
(R):5'- GCAGTGCTTCAATTCCTCCGTC -3'

Posted On

2016-12-15