Mutagenetix > Incidental Mutation

Incidental Mutation 'R6887:Lrrc61'

536991

Institutional Source

Beutler Lab

Gene Symbol

Lrrc61

Ensembl Gene

ENSMUSG00000073096

Gene Name

leucine rich repeat containing 61

Synonyms

MMRRC Submission

044981-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.050) question?

Stock #

R6887 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

48554796-48570722 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 48568432 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Asparagine to Threonine at position 63 (N63T)

Ref Sequence

ENSEMBL: ENSMUSP00000145141 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000009425] [ENSMUST00000101436] [ENSMUST00000114545] [ENSMUST00000153222] [ENSMUST00000203627] [ENSMUST00000204071] [ENSMUST00000204182] [ENSMUST00000204267] [ENSMUST00000204930]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000009425

SMART Domains

Protein: ENSMUSP00000009425
Gene: ENSMUSG00000009281

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000101436
AA Change: N63T

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

SMART Domains

Protein: ENSMUSP00000098979
Gene: ENSMUSG00000073096
AA Change: N63T

Domain	Start	End	E-Value	Type
low complexity region	2	13	N/A	INTRINSIC
Pfam:LRR_1	54	75	1.5e-3	PFAM
Pfam:LRR_8	54	109	8.5e-9	PFAM
low complexity region	113	124	N/A	INTRINSIC
low complexity region	177	191	N/A	INTRINSIC
low complexity region	236	249	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000114545
AA Change: N63T

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

SMART Domains

Protein: ENSMUSP00000110192
Gene: ENSMUSG00000073096
AA Change: N63T

Domain	Start	End	E-Value	Type
low complexity region	2	13	N/A	INTRINSIC
Pfam:LRR_8	32	87	3.1e-9	PFAM
Pfam:LRR_6	52	76	1.8e-4	PFAM
Pfam:LRR_4	53	95	1.7e-12	PFAM
Pfam:LRR_1	54	74	8.6e-5	PFAM
Pfam:LRR_8	75	131	7.8e-9	PFAM
low complexity region	177	191	N/A	INTRINSIC
low complexity region	236	249	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000153222

Predicted Effect

probably damaging
Transcript: ENSMUST00000203627
AA Change: N63T

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

SMART Domains

Protein: ENSMUSP00000145141
Gene: ENSMUSG00000073096
AA Change: N63T

Domain	Start	End	E-Value	Type
low complexity region	2	13	N/A	INTRINSIC
Pfam:LRR_8	30	87	1.2e-6	PFAM
Pfam:LRR_4	53	95	1.1e-6	PFAM
Pfam:LRR_1	54	75	2.1e-1	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000204071

Predicted Effect

probably benign
Transcript: ENSMUST00000204182

SMART Domains

Protein: ENSMUSP00000145257
Gene: ENSMUSG00000009281

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000204267

SMART Domains

Protein: ENSMUSP00000144793
Gene: ENSMUSG00000009281

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000204930

SMART Domains

Protein: ENSMUSP00000144799
Gene: ENSMUSG00000009281

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.4%
20x: 98.1%

Validation Efficiency

100% (39/39)

Allele List at MGI

Other mutations in this stock

Total: 39 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acan	G	A	7: 79,092,483 (GRCm38)	V543I	probably damaging	Het
Adcy5	A	G	16: 35,298,590 (GRCm38)	I1104V	possibly damaging	Het
Adgrl4	A	T	3: 151,542,733 (GRCm38)	I681F	possibly damaging	Het
Adgrv1	T	A	13: 81,528,701 (GRCm38)	M2004L	probably benign	Het
Anapc1	A	G	2: 128,659,768 (GRCm38)	S785P	possibly damaging	Het
Ap3d1	A	T	10: 80,723,698 (GRCm38)	I242N	probably damaging	Het
Arhgap5	T	C	12: 52,519,144 (GRCm38)	L966P	probably benign	Het
Atp8a1	T	C	5: 67,738,451 (GRCm38)	T547A	probably benign	Het
Cadps	A	G	14: 12,505,811 (GRCm38)	F753S	probably damaging	Het
Cdc20b	T	C	13: 113,078,653 (GRCm38)	S252P	possibly damaging	Het
Cep63	A	G	9: 102,625,927 (GRCm38)		probably benign	Het
Chrna5	G	T	9: 55,005,133 (GRCm38)	V302L	probably benign	Het
Crtc2	A	G	3: 90,261,071 (GRCm38)	T374A	probably damaging	Het
Dmtf1	T	G	5: 9,137,149 (GRCm38)	D140A	probably damaging	Het
Exosc8	C	T	3: 54,733,699 (GRCm38)	V39M	probably damaging	Het
Fam135b	A	C	15: 71,463,315 (GRCm38)	S677A	probably damaging	Het
Hif1an	T	C	19: 44,563,389 (GRCm38)	Y93H	probably damaging	Het
Hrc	T	C	7: 45,335,664 (GRCm38)	F80L	probably benign	Het
Jmjd1c	A	G	10: 67,189,820 (GRCm38)	T139A	possibly damaging	Het
Kdr	T	G	5: 75,968,451 (GRCm38)	R178S	probably benign	Het
Mrc1	C	T	2: 14,325,237 (GRCm38)	A1219V	possibly damaging	Het
Neto1	T	C	18: 86,498,635 (GRCm38)	V359A	probably benign	Het
Ngly1	T	C	14: 16,281,836 (GRCm38)	I364T	probably benign	Het
Nisch	C	T	14: 31,185,344 (GRCm38)		probably benign	Het
Olfr1373	C	A	11: 52,145,352 (GRCm38)	M59I	probably benign	Het
Prrc2a	T	C	17: 35,155,675 (GRCm38)	D1333G	probably damaging	Het
Raly	G	T	2: 154,861,910 (GRCm38)	V134F	probably damaging	Het
Rbm6	T	C	9: 107,852,231 (GRCm38)	Y406C	probably damaging	Het
Robo4	G	C	9: 37,402,067 (GRCm38)	E6Q	possibly damaging	Het
Scnn1g	C	A	7: 121,760,444 (GRCm38)	S383R	probably benign	Het
Sgtb	T	C	13: 104,111,151 (GRCm38)	W13R	probably benign	Het
Slit3	T	C	11: 35,544,806 (GRCm38)		probably null	Het
Tbc1d32	G	A	10: 56,151,811 (GRCm38)	Q732*	probably null	Het
Tek	T	A	4: 94,804,944 (GRCm38)	C247S	probably damaging	Het
Tmf1	A	T	6: 97,176,838 (GRCm38)	D91E	probably damaging	Het
Usp39	A	G	6: 72,333,157 (GRCm38)	L326P	probably damaging	Het
Vmn2r7	A	T	3: 64,690,827 (GRCm38)	C770S	probably damaging	Het
Wdr31	C	T	4: 62,457,565 (GRCm38)	G58R	probably benign	Het
Zfyve26	A	G	12: 79,266,449 (GRCm38)	I54T	probably damaging	Het

Other mutations in Lrrc61

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R1675:Lrrc61	UTSW	6	48,568,774 (GRCm38)	missense	possibly damaging	0.64
R1713:Lrrc61	UTSW	6	48,568,774 (GRCm38)	missense	possibly damaging	0.64
R2352:Lrrc61	UTSW	6	48,568,872 (GRCm38)	missense	probably benign	0.02
R5337:Lrrc61	UTSW	6	48,568,374 (GRCm38)	missense	probably damaging	0.96
R5774:Lrrc61	UTSW	6	48,568,199 (GRCm38)	unclassified	probably benign
R6208:Lrrc61	UTSW	6	48,568,905 (GRCm38)	nonsense	probably null
R7835:Lrrc61	UTSW	6	48,568,572 (GRCm38)	missense	probably benign	0.00
R9319:Lrrc61	UTSW	6	48,568,294 (GRCm38)	missense	probably damaging	0.99
R9368:Lrrc61	UTSW	6	48,568,311 (GRCm38)	missense	possibly damaging	0.87
R9492:Lrrc61	UTSW	6	48,568,827 (GRCm38)	nonsense	probably null
R9581:Lrrc61	UTSW	6	48,568,719 (GRCm38)	missense	possibly damaging	0.68

Predicted Primers

PCR Primer
(F):5'- TATCATGGAGCCTCCTGGAG -3'
(R):5'- AGGAAGCATTTGCACAGAGC -3'

Sequencing Primer
(F):5'- TATCATGGAGCCTCCTGGAGAGAAG -3'
(R):5'- AGCCTCAGGTGCTCCAG -3'

Posted On

2018-10-18