Mutagenetix > Incidental Mutation

Incidental Mutation 'R2223:Lrrc38'

241606

Institutional Source

Beutler Lab

Gene Symbol

Lrrc38

Ensembl Gene

ENSMUSG00000028584

Gene Name

leucine rich repeat containing 38

Synonyms

MMRRC Submission

040224-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.057) question?

Stock #

R2223 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

143349757-143371032 bp(+) (GRCm38)

Type of Mutation

nonsense

DNA Base Change (assembly)

T to A at 143369849 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Stop codon at position 243 (C243*)

Ref Sequence

ENSEMBL: ENSMUSP00000053597 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000052458]

AlphaFold

A2VDH3

Predicted Effect

probably null
Transcript: ENSMUST00000052458
AA Change: C243*

SMART Domains

Protein: ENSMUSP00000053597
Gene: ENSMUSG00000028584
AA Change: C243*

Domain	Start	End	E-Value	Type
low complexity region	12	27	N/A	INTRINSIC
LRRNT	31	64	2.82e-4	SMART
LRR	84	106	1.37e1	SMART
LRR	108	130	5.26e0	SMART
LRR	132	154	2.27e1	SMART
LRR	155	178	8.09e-1	SMART
LRRCT	190	244	8.63e-6	SMART
transmembrane domain	252	274	N/A	INTRINSIC
low complexity region	288	298	N/A	INTRINSIC

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 94.8%

Validation Efficiency

100% (59/59)

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5430419D17Rik	A	T	7: 131,247,457		probably null	Het
Abhd18	A	G	3: 40,934,861		probably benign	Het
Acvr1b	C	T	15: 101,203,043	A362V	probably benign	Het
Adamts5	A	C	16: 85,899,306	L321R	probably damaging	Het
Adamtsl1	A	C	4: 86,388,525	D1392A	probably benign	Het
Afdn	T	C	17: 13,883,737		probably benign	Het
Aph1b	A	T	9: 66,784,639	M121K	probably damaging	Het
Aspg	G	A	12: 112,114,434	A120T	probably damaging	Het
Atp8b1	T	A	18: 64,564,357	N472I	possibly damaging	Het
B4galt3	C	A	1: 171,274,043	H196N	probably damaging	Het
Cfd	A	T	10: 79,892,205		probably null	Het
Cntnap5b	A	G	1: 100,213,687	E242G	probably damaging	Het
Col9a2	C	G	4: 121,054,258	R599G	probably damaging	Het
Cradd	A	C	10: 95,175,873	V135G	probably benign	Het
Cry1	A	G	10: 85,143,753	C460R	probably damaging	Het
Cryz	A	T	3: 154,618,554	N192I	possibly damaging	Het
Cyp2d11	T	A	15: 82,390,131	M350L	probably benign	Het
Emsy	T	C	7: 98,590,775	E1091G	possibly damaging	Het
Exoc3l4	C	G	12: 111,426,152	A471G	possibly damaging	Het
Fam184a	G	A	10: 53,655,079	T733M	probably damaging	Het
Fmo2	C	T	1: 162,898,244	C21Y	probably damaging	Het
Glul	T	A	1: 153,906,497		probably null	Het
Gm5174	T	A	10: 86,656,508		noncoding transcript	Het
Gtpbp2	A	G	17: 46,167,227	I434V	probably benign	Het
Kctd10	G	T	5: 114,367,349	R195S	probably benign	Het
Luc7l2	T	C	6: 38,565,724		probably benign	Het
Magi2	T	A	5: 20,465,672	V111D	probably damaging	Het
Map3k5	T	C	10: 20,067,920	V590A	possibly damaging	Het
Megf11	G	A	9: 64,660,431	G401S	possibly damaging	Het
Mgat4d	G	A	8: 83,355,672		probably benign	Het
Mroh1	T	C	15: 76,408,045		probably null	Het
Mx1	T	C	16: 97,455,232		probably benign	Het
Nlrp1b	A	G	11: 71,155,989		probably benign	Het
Ntrk3	T	C	7: 78,198,852	I759V	probably damaging	Het
Olfr800	T	A	10: 129,659,809	M1K	probably null	Het
Pde8b	T	C	13: 95,043,447	N318S	probably damaging	Het
Pkd1l1	T	C	11: 8,889,063	T874A	probably benign	Het
Pkd1l1	T	C	11: 8,950,422	T40A	probably benign	Het
Prdm2	T	C	4: 143,134,899	N607S	possibly damaging	Het
Ptprn	A	T	1: 75,257,937		probably benign	Het
Setx	T	G	2: 29,148,537	I1678S	possibly damaging	Het
Setx	GTGGCT	GT	2: 29,154,061	1814	probably null	Het
Snap91	T	C	9: 86,792,527	T544A	possibly damaging	Het
Sp8	G	A	12: 118,849,738	G443S	probably damaging	Het
Stk39	C	T	2: 68,314,579	G384S	probably damaging	Het
Sva	T	A	6: 42,038,423	M1K	probably null	Het
Trip10	A	G	17: 57,263,039	D568G	possibly damaging	Het
Trpa1	A	T	1: 14,903,256	F279L	probably null	Het
Ttc39b	T	C	4: 83,232,762	N532S	probably benign	Het
Ube2w	A	G	1: 16,597,959	S97P	possibly damaging	Het
Uvssa	C	T	5: 33,392,063	T356I	probably damaging	Het
Vmn1r25	A	C	6: 57,979,238	L22R	probably damaging	Het
Vmn2r112	T	G	17: 22,601,233	M29R	possibly damaging	Het
Vmn2r71	T	A	7: 85,624,093	M705K	probably benign	Het
Zfp516	C	A	18: 82,955,770	A31D	possibly damaging	Het

Other mutations in Lrrc38

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0281:Lrrc38	UTSW	4	143350409	missense	probably damaging	0.99
R0545:Lrrc38	UTSW	4	143350758	missense	probably benign	0.41
R1078:Lrrc38	UTSW	4	143350518	missense	probably benign	0.06
R1467:Lrrc38	UTSW	4	143369880	missense	probably damaging	1.00
R1467:Lrrc38	UTSW	4	143369880	missense	probably damaging	1.00
R1967:Lrrc38	UTSW	4	143369983	missense	unknown
R2221:Lrrc38	UTSW	4	143369849	nonsense	probably null
R4061:Lrrc38	UTSW	4	143350506	missense	probably damaging	1.00
R4930:Lrrc38	UTSW	4	143369868	missense	probably damaging	0.98
R5585:Lrrc38	UTSW	4	143350391	missense	probably damaging	0.96
R6787:Lrrc38	UTSW	4	143369794	missense	probably benign	0.18
R7046:Lrrc38	UTSW	4	143350169	start codon destroyed	probably null
R7706:Lrrc38	UTSW	4	143350275	missense	probably damaging	1.00
R8189:Lrrc38	UTSW	4	143350733	missense	probably damaging	1.00
R8190:Lrrc38	UTSW	4	143350733	missense	probably damaging	1.00
R8192:Lrrc38	UTSW	4	143350733	missense	probably damaging	1.00
R8219:Lrrc38	UTSW	4	143350733	missense	probably damaging	1.00
R8221:Lrrc38	UTSW	4	143350733	missense	probably damaging	1.00
R8223:Lrrc38	UTSW	4	143350733	missense	probably damaging	1.00
R8226:Lrrc38	UTSW	4	143350733	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TGTTGTGAGAACTCCTCCCTGG -3'
(R):5'- TCAGCATCAGTCTCCCTTGG -3'

Sequencing Primer
(F):5'- CTCCCTGGAGGTACTTCTGAG -3'
(R):5'- CTTGGAGAGGTGCCACTG -3'

Posted On

2014-10-15