Mutagenetix > Incidental Mutation

Incidental Mutation 'R2223:Luc7l2'

241610

Institutional Source

Beutler Lab

Gene Symbol

Luc7l2

Ensembl Gene

ENSMUSG00000029823

Gene Name

LUC7-like 2 (S. cerevisiae)

Synonyms

CGI-59, 4930471C18Rik, CGI-74

MMRRC Submission

040224-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.305) question?

Stock #

R2223 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

38528269-38586405 bp(+) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

T to C at 38542659 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000125394 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000057692] [ENSMUST00000159936] [ENSMUST00000160511] [ENSMUST00000161227] [ENSMUST00000161538] [ENSMUST00000162386] [ENSMUST00000163047]

AlphaFold

Q7TNC4

Predicted Effect

probably benign
Transcript: ENSMUST00000057692

SMART Domains

Protein: ENSMUSP00000055254
Gene: ENSMUSG00000029823

Domain	Start	End	E-Value	Type
Pfam:LUC7	5	257	6.5e-84	PFAM
low complexity region	269	341	N/A	INTRINSIC
low complexity region	347	370	N/A	INTRINSIC
low complexity region	377	388	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000159936

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160430

SMART Domains

Protein: ENSMUSP00000124686
Gene: ENSMUSG00000029823

Domain	Start	End	E-Value	Type
Pfam:LUC7	1	211	9.9e-70	PFAM
low complexity region	217	281	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000160511

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160582

Predicted Effect

probably benign
Transcript: ENSMUST00000161227

SMART Domains

Protein: ENSMUSP00000125111
Gene: ENSMUSG00000029823

Domain	Start	End	E-Value	Type
Pfam:LUC7	1	288	6.9e-65	PFAM
low complexity region	294	317	N/A	INTRINSIC
low complexity region	324	335	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000161538

SMART Domains

Protein: ENSMUSP00000124010
Gene: ENSMUSG00000029823

Domain	Start	End	E-Value	Type
Pfam:LUC7	4	309	3.3e-93	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000162386

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000162530

Predicted Effect

probably benign
Transcript: ENSMUST00000163047

SMART Domains

Protein: ENSMUSP00000125394
Gene: ENSMUSG00000029823

Domain	Start	End	E-Value	Type
Pfam:LUC7	1	257	3.2e-66	PFAM

Coding Region Coverage

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

Validation Efficiency

100% (59/59)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that contains a C2H2-type zinc finger, coiled-coil region and arginine, serine-rich (RS) domain. A similar protein in mouse interacts with sodium channel modifier 1, and the encoded protein may be involved in the recognition of non-consensus splice donor sites in association with the U1 snRNP spliceosomal subunit. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Sep 2011]

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abhd18	A	G	3: 40,889,296 (GRCm39)		probably benign	Het
Acvr1b	C	T	15: 101,100,924 (GRCm39)	A362V	probably benign	Het
Adamts5	A	C	16: 85,696,194 (GRCm39)	L321R	probably damaging	Het
Adamtsl1	A	C	4: 86,306,762 (GRCm39)	D1392A	probably benign	Het
Afdn	T	C	17: 14,103,999 (GRCm39)		probably benign	Het
Aph1b	A	T	9: 66,691,921 (GRCm39)	M121K	probably damaging	Het
Aspg	G	A	12: 112,080,868 (GRCm39)	A120T	probably damaging	Het
Atp8b1	T	A	18: 64,697,428 (GRCm39)	N472I	possibly damaging	Het
B4galt3	C	A	1: 171,101,613 (GRCm39)	H196N	probably damaging	Het
Cdcp3	A	T	7: 130,849,186 (GRCm39)		probably null	Het
Cfd	A	T	10: 79,728,039 (GRCm39)		probably null	Het
Cntnap5b	A	G	1: 100,141,412 (GRCm39)	E242G	probably damaging	Het
Col9a2	C	G	4: 120,911,455 (GRCm39)	R599G	probably damaging	Het
Cradd	A	C	10: 95,011,735 (GRCm39)	V135G	probably benign	Het
Cry1	A	G	10: 84,979,617 (GRCm39)	C460R	probably damaging	Het
Cryz	A	T	3: 154,324,191 (GRCm39)	N192I	possibly damaging	Het
Cyp2d11	T	A	15: 82,274,332 (GRCm39)	M350L	probably benign	Het
Emsy	T	C	7: 98,239,982 (GRCm39)	E1091G	possibly damaging	Het
Exoc3l4	C	G	12: 111,392,586 (GRCm39)	A471G	possibly damaging	Het
Fam184a	G	A	10: 53,531,175 (GRCm39)	T733M	probably damaging	Het
Fmo2	C	T	1: 162,725,813 (GRCm39)	C21Y	probably damaging	Het
Glul	T	A	1: 153,782,243 (GRCm39)		probably null	Het
Gm5174	T	A	10: 86,492,372 (GRCm39)		noncoding transcript	Het
Gtpbp2	A	G	17: 46,478,153 (GRCm39)	I434V	probably benign	Het
Kctd10	G	T	5: 114,505,410 (GRCm39)	R195S	probably benign	Het
Lrrc38	T	A	4: 143,096,419 (GRCm39)	C243*	probably null	Het
Magi2	T	A	5: 20,670,670 (GRCm39)	V111D	probably damaging	Het
Map3k5	T	C	10: 19,943,666 (GRCm39)	V590A	possibly damaging	Het
Megf11	G	A	9: 64,567,713 (GRCm39)	G401S	possibly damaging	Het
Mgat4d	G	A	8: 84,082,301 (GRCm39)		probably benign	Het
Mroh1	T	C	15: 76,292,245 (GRCm39)		probably null	Het
Mx1	T	C	16: 97,256,432 (GRCm39)		probably benign	Het
Nlrp1b	A	G	11: 71,046,815 (GRCm39)		probably benign	Het
Ntrk3	T	C	7: 77,848,600 (GRCm39)	I759V	probably damaging	Het
Or6c210	T	A	10: 129,495,678 (GRCm39)	M1K	probably null	Het
Pde8b	T	C	13: 95,179,955 (GRCm39)	N318S	probably damaging	Het
Pkd1l1	T	C	11: 8,839,063 (GRCm39)	T874A	probably benign	Het
Pkd1l1	T	C	11: 8,900,422 (GRCm39)	T40A	probably benign	Het
Prdm2	T	C	4: 142,861,469 (GRCm39)	N607S	possibly damaging	Het
Ptprn	A	T	1: 75,234,581 (GRCm39)		probably benign	Het
Setx	T	G	2: 29,038,549 (GRCm39)	I1678S	possibly damaging	Het
Setx	GTGGCT	GT	2: 29,044,073 (GRCm39)	1814	probably null	Het
Snap91	T	C	9: 86,674,580 (GRCm39)	T544A	possibly damaging	Het
Sp8	G	A	12: 118,813,473 (GRCm39)	G443S	probably damaging	Het
Stk39	C	T	2: 68,144,923 (GRCm39)	G384S	probably damaging	Het
Sva	T	A	6: 42,015,357 (GRCm39)	M1K	probably null	Het
Trip10	A	G	17: 57,570,039 (GRCm39)	D568G	possibly damaging	Het
Trpa1	A	T	1: 14,973,480 (GRCm39)	F279L	probably null	Het
Ttc39b	T	C	4: 83,150,999 (GRCm39)	N532S	probably benign	Het
Ube2w	A	G	1: 16,668,183 (GRCm39)	S97P	possibly damaging	Het
Uvssa	C	T	5: 33,549,407 (GRCm39)	T356I	probably damaging	Het
Vmn1r25	A	C	6: 57,956,223 (GRCm39)	L22R	probably damaging	Het
Vmn2r112	T	G	17: 22,820,214 (GRCm39)	M29R	possibly damaging	Het
Vmn2r71	T	A	7: 85,273,301 (GRCm39)	M705K	probably benign	Het
Zfp516	C	A	18: 82,973,895 (GRCm39)	A31D	possibly damaging	Het

Other mutations in Luc7l2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00089:Luc7l2	APN	6	38,585,105 (GRCm39)	unclassified	probably benign
IGL00684:Luc7l2	APN	6	38,585,111 (GRCm39)	unclassified	probably benign
IGL00785:Luc7l2	APN	6	38,575,721 (GRCm39)	missense	possibly damaging	0.73
R0004:Luc7l2	UTSW	6	38,566,169 (GRCm39)	missense	probably damaging	1.00
R0304:Luc7l2	UTSW	6	38,569,711 (GRCm39)	missense	probably damaging	0.98
R1820:Luc7l2	UTSW	6	38,575,754 (GRCm39)	splice site	probably null
R3815:Luc7l2	UTSW	6	38,547,526 (GRCm39)	missense	possibly damaging	0.83
R5016:Luc7l2	UTSW	6	38,562,036 (GRCm39)	missense	possibly damaging	0.54
R7583:Luc7l2	UTSW	6	38,528,820 (GRCm39)	missense	probably damaging	0.98
R7655:Luc7l2	UTSW	6	38,580,399 (GRCm39)	missense	unknown
R7656:Luc7l2	UTSW	6	38,580,399 (GRCm39)	missense	unknown
R7722:Luc7l2	UTSW	6	38,580,243 (GRCm39)	missense	unknown
R7761:Luc7l2	UTSW	6	38,531,999 (GRCm39)	critical splice donor site	probably null
R8105:Luc7l2	UTSW	6	38,569,588 (GRCm39)	missense	probably benign	0.29
R9222:Luc7l2	UTSW	6	38,542,633 (GRCm39)	missense	probably benign
R9420:Luc7l2	UTSW	6	38,547,489 (GRCm39)	missense	probably damaging	1.00
R9544:Luc7l2	UTSW	6	38,580,315 (GRCm39)	missense	unknown
Z1088:Luc7l2	UTSW	6	38,580,304 (GRCm39)	utr 3 prime	probably benign
Z1176:Luc7l2	UTSW	6	38,528,843 (GRCm39)	nonsense	probably null

Predicted Primers

Posted On

2014-10-15