Mutagenetix > Incidental Mutation

Incidental Mutation 'R7515:Lgals8'

582411

Institutional Source

Beutler Lab

Gene Symbol

Lgals8

Ensembl Gene

ENSMUSG00000057554

Gene Name

lectin, galactose binding, soluble 8

Synonyms

D13Ertd524e, Lgals-8, 1200015E08Rik

MMRRC Submission

045588-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.108) question?

Stock #

R7515 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

12454296-12479825 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to A at 12463343 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Stop codon at position 198 (R198*)

Ref Sequence

ENSEMBL: ENSMUSP00000115094 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099820] [ENSMUST00000099821] [ENSMUST00000124888] [ENSMUST00000135166] [ENSMUST00000143693] [ENSMUST00000144283]

AlphaFold

Q9JL15

Predicted Effect

probably null
Transcript: ENSMUST00000099820
AA Change: R198*

SMART Domains

Protein: ENSMUSP00000097408
Gene: ENSMUSG00000057554
AA Change: R198*

Domain	Start	End	E-Value	Type
GLECT	16	151	3.05e-50	SMART
Gal-bind_lectin	22	150	7.41e-55	SMART
GLECT	184	316	1.38e-48	SMART
Gal-bind_lectin	190	315	1.28e-49	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000099821
AA Change: R198*

SMART Domains

Protein: ENSMUSP00000097409
Gene: ENSMUSG00000057554
AA Change: R198*

Domain	Start	End	E-Value	Type
GLECT	16	151	3.05e-50	SMART
Gal-bind_lectin	22	150	7.41e-55	SMART
GLECT	184	316	1.38e-48	SMART
Gal-bind_lectin	190	315	1.28e-49	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000124888
AA Change: R198*

SMART Domains

Protein: ENSMUSP00000115094
Gene: ENSMUSG00000057554
AA Change: R198*

Domain	Start	End	E-Value	Type
GLECT	16	151	3.05e-50	SMART
Gal-bind_lectin	22	150	7.41e-55	SMART
GLECT	184	316	1.38e-48	SMART
Gal-bind_lectin	190	315	1.28e-49	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000135166
AA Change: R105*

SMART Domains

Protein: ENSMUSP00000120210
Gene: ENSMUSG00000057554
AA Change: R105*

Domain	Start	End	E-Value	Type
Pfam:Gal-bind_lectin	1	57	4e-16	PFAM
GLECT	91	223	1.38e-48	SMART
Gal-bind_lectin	97	222	1.28e-49	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000143693
AA Change: R105*

SMART Domains

Protein: ENSMUSP00000118925
Gene: ENSMUSG00000057554
AA Change: R105*

Domain	Start	End	E-Value	Type
Pfam:Gal-bind_lectin	1	57	4e-16	PFAM
GLECT	91	223	1.38e-48	SMART
Gal-bind_lectin	97	222	1.28e-49	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000144283
AA Change: R207*

SMART Domains

Protein: ENSMUSP00000114200
Gene: ENSMUSG00000057554
AA Change: R207*

Domain	Start	End	E-Value	Type
GLECT	16	151	3.05e-50	SMART
Gal-bind_lectin	22	150	7.41e-55	SMART
GLECT	193	325	1.38e-48	SMART
Gal-bind_lectin	199	324	1.28e-49	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.4%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the galectin family. Galectins are beta-galactoside-binding animal lectins with conserved carbohydrate recognition domains. The galectins have been implicated in many essential functions including development, differentiation, cell-cell adhesion, cell-matrix interaction, growth regulation, apoptosis, and RNA splicing. This gene is widely expressed in tumoral tissues and seems to be involved in integrin-like cell interactions. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit reduced VEGF-C-induced lymphangiogenesis, and ameliorated corneal pathology and lymphangiogenesis in a model of herpes simplex virus keratitis. Mice homozygous for a gene trapped allele exhibit hyperactivity. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ankrd36	A	T	11: 5,578,905 (GRCm39)	E56D	possibly damaging	Het
Ankrd44	T	C	1: 54,805,514 (GRCm39)	Y182C	probably damaging	Het
Anxa3	A	T	5: 96,986,179 (GRCm39)	N273Y	probably damaging	Het
Apobec2	T	C	17: 48,730,015 (GRCm39)	E217G	probably damaging	Het
Arhgap24	A	G	5: 102,993,882 (GRCm39)		probably benign	Het
Asap2	A	G	12: 21,279,240 (GRCm39)	H374R	possibly damaging	Het
Camsap2	T	C	1: 136,273,108 (GRCm39)	D23G	probably damaging	Het
Ccr2	T	C	9: 123,906,197 (GRCm39)	V159A	probably damaging	Het
Cfap61	T	A	2: 145,884,645 (GRCm39)	D614E	unknown	Het
Crb2	G	A	2: 37,673,412 (GRCm39)	G103R	probably damaging	Het
Cyp2b9	A	G	7: 25,898,596 (GRCm39)	Y317C	probably damaging	Het
Dhx36	A	G	3: 62,379,508 (GRCm39)	V860A	probably benign	Het
Dnah3	T	C	7: 119,672,815 (GRCm39)	D553G	probably benign	Het
Dnah7c	T	C	1: 46,496,450 (GRCm39)	S112P	probably benign	Het
Dnah9	A	G	11: 65,732,240 (GRCm39)	F4222S	probably benign	Het
Ei24	T	C	9: 36,701,211 (GRCm39)	D36G	probably damaging	Het
Etv3	G	T	3: 87,435,363 (GRCm39)	R78L	possibly damaging	Het
Fbxo34	T	C	14: 47,767,798 (GRCm39)	L437P	possibly damaging	Het
Foxn1	T	C	11: 78,261,970 (GRCm39)	D133G	possibly damaging	Het
Gabra1	T	A	11: 42,045,660 (GRCm39)	D150V	possibly damaging	Het
Gpr158	T	C	2: 21,373,092 (GRCm39)	L9P	probably damaging	Het
H2-M10.3	G	A	17: 36,677,435 (GRCm39)	T281I	probably damaging	Het
Il18r1	T	C	1: 40,537,830 (GRCm39)	S532P	not run	Het
Itpr2	T	C	6: 146,228,608 (GRCm39)	D1329G	probably damaging	Het
Jakmip2	A	T	18: 43,704,191 (GRCm39)	N384K	probably benign	Het
Kdsr	A	G	1: 106,662,290 (GRCm39)	V255A	possibly damaging	Het
Kifc1	A	G	17: 34,103,777 (GRCm39)	L182P	probably damaging	Het
Lrrk1	A	T	7: 65,912,310 (GRCm39)	M1750K	probably benign	Het
Lrsam1	A	G	2: 32,830,251 (GRCm39)		probably null	Het
Lztr1	C	T	16: 17,327,525 (GRCm39)	A76V	possibly damaging	Het
Mcc	G	T	18: 44,626,499 (GRCm39)	H366N	probably benign	Het
Mif4gd	A	G	11: 115,499,222 (GRCm39)	V220A	possibly damaging	Het
Mtmr12	T	A	15: 12,270,037 (GRCm39)	F708L	probably damaging	Het
Muc16	A	T	9: 18,550,958 (GRCm39)	W5112R	probably benign	Het
Ndrg2	A	G	14: 52,146,380 (GRCm39)	I140T	probably benign	Het
Nid2	C	A	14: 19,841,635 (GRCm39)	Q887K	probably benign	Het
Nop16	A	T	13: 54,737,550 (GRCm39)	S48T	possibly damaging	Het
Nrap	G	A	19: 56,354,859 (GRCm39)	T489I	possibly damaging	Het
Oas1e	C	T	5: 120,929,951 (GRCm39)	G189D	probably damaging	Het
Or4a39	A	G	2: 89,237,250 (GRCm39)	Y58H	possibly damaging	Het
Or7g34	A	T	9: 19,477,949 (GRCm39)	C244S	probably damaging	Het
Pcdha5	A	T	18: 37,095,171 (GRCm39)	D560V	probably damaging	Het
Peg10	GC	GCTCC	6: 4,756,452 (GRCm39)		probably benign	Het
Phldb2	C	T	16: 45,594,603 (GRCm39)	D901N	possibly damaging	Het
Piezo1	T	C	8: 123,212,035 (GRCm39)	H2058R		Het
Ptgis	T	A	2: 167,048,758 (GRCm39)	K419N	possibly damaging	Het
Ptprz1	T	C	6: 23,022,266 (GRCm39)	F1714L	probably damaging	Het
Rasa2	T	C	9: 96,434,353 (GRCm39)		probably null	Het
Recql	C	T	6: 142,320,611 (GRCm39)	D146N	probably damaging	Het
Rnf6	T	G	5: 146,148,602 (GRCm39)	S139R	probably damaging	Het
Rock1	A	G	18: 10,067,631 (GRCm39)	S1301P	probably damaging	Het
Safb2	A	G	17: 56,889,982 (GRCm39)		probably null	Het
Setd5	T	A	6: 113,087,850 (GRCm39)	I137N	probably damaging	Het
Sf3b6	G	A	12: 4,870,619 (GRCm39)	R19Q	probably damaging	Het
Slc15a5	T	A	6: 138,020,496 (GRCm39)	H279L	possibly damaging	Het
Slc26a9	A	G	1: 131,681,711 (GRCm39)	T175A	probably damaging	Het
Sspo	A	T	6: 48,470,820 (GRCm39)	N36I	probably damaging	Het
Supv3l1	A	C	10: 62,268,090 (GRCm39)	F585C	probably damaging	Het
Tnrc6c	G	T	11: 117,632,507 (GRCm39)	V1070L	probably benign	Het
Vmn2r53	T	A	7: 12,315,846 (GRCm39)	M658L	probably benign	Het
Zc3h13	A	G	14: 75,546,349 (GRCm39)	D150G	unknown	Het
Zfp607b	T	C	7: 27,402,921 (GRCm39)	V459A	probably benign	Het
Zfp653	T	C	9: 21,982,427 (GRCm39)	R71G	probably damaging	Het

Other mutations in Lgals8

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01601:Lgals8	APN	13	12,471,219 (GRCm39)	splice site	probably benign
IGL02407:Lgals8	APN	13	12,469,699 (GRCm39)	missense	probably benign	0.01
R0015:Lgals8	UTSW	13	12,462,179 (GRCm39)	missense	probably damaging	1.00
R0015:Lgals8	UTSW	13	12,462,179 (GRCm39)	missense	probably damaging	1.00
R0973:Lgals8	UTSW	13	12,466,276 (GRCm39)	splice site	probably benign
R1452:Lgals8	UTSW	13	12,468,208 (GRCm39)	nonsense	probably null
R1748:Lgals8	UTSW	13	12,469,824 (GRCm39)	missense	probably damaging	1.00
R1939:Lgals8	UTSW	13	12,474,069 (GRCm39)	missense	probably benign	0.00
R2076:Lgals8	UTSW	13	12,469,750 (GRCm39)	nonsense	probably null
R2214:Lgals8	UTSW	13	12,469,713 (GRCm39)	missense	probably benign	0.02
R4568:Lgals8	UTSW	13	12,468,254 (GRCm39)	missense	probably damaging	1.00
R4791:Lgals8	UTSW	13	12,468,203 (GRCm39)	missense	possibly damaging	0.94
R5243:Lgals8	UTSW	13	12,469,645 (GRCm39)	missense	probably benign	0.27
R6947:Lgals8	UTSW	13	12,469,682 (GRCm39)	start gained	probably benign
R7476:Lgals8	UTSW	13	12,463,362 (GRCm39)	missense	probably damaging	0.97
R7942:Lgals8	UTSW	13	12,468,137 (GRCm39)	critical splice donor site	probably null
R8208:Lgals8	UTSW	13	12,468,255 (GRCm39)	missense	probably damaging	1.00
R8674:Lgals8	UTSW	13	12,462,117 (GRCm39)	missense	probably damaging	1.00
R9232:Lgals8	UTSW	13	12,469,777 (GRCm39)	missense	probably damaging	1.00
R9727:Lgals8	UTSW	13	12,462,038 (GRCm39)	missense	possibly damaging	0.67
R9785:Lgals8	UTSW	13	12,462,051 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TTTACCTACCTGGCCAAGAGGG -3'
(R):5'- CTCAGTGAGACCGTGCTTTG -3'

Sequencing Primer
(F):5'- CCAAGAGGGGCCCCAGC -3'
(R):5'- CCAGCTGAGATGAACATAGCCATAG -3'

Posted On

2019-10-17