Mutagenetix > Incidental Mutation

Incidental Mutation 'R7838:Igsf11'

606128

Institutional Source

Beutler Lab

Gene Symbol

Igsf11

Ensembl Gene

ENSMUSG00000022790

Gene Name

immunoglobulin superfamily, member 11

Synonyms

1700025L02Rik, BT-IgSF

MMRRC Submission

045892-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7838 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

38713033-38847521 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 38827565 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 41 (V41A)

Ref Sequence

ENSEMBL: ENSMUSP00000023478 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000023478] [ENSMUST00000114706]

AlphaFold

P0C673

Predicted Effect

possibly damaging
Transcript: ENSMUST00000023478
AA Change: V41A

PolyPhen 2 Score 0.653 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000023478
Gene: ENSMUSG00000022790
AA Change: V41A

Domain	Start	End	E-Value	Type
IG	29	143	4.32e-8	SMART
IGc2	156	222	2.54e-5	SMART
transmembrane domain	240	262	N/A	INTRINSIC
low complexity region	271	286	N/A	INTRINSIC
low complexity region	301	319	N/A	INTRINSIC
Blast:DEXDc	355	425	8e-14	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000114706

SMART Domains

Protein: ENSMUSP00000110354
Gene: ENSMUSG00000022790

Domain	Start	End	E-Value	Type
IG_like	11	84	3.12e1	SMART
IGc2	97	163	2.54e-5	SMART
transmembrane domain	181	203	N/A	INTRINSIC
low complexity region	212	227	N/A	INTRINSIC
low complexity region	242	260	N/A	INTRINSIC
Blast:DEXDc	296	366	5e-14	BLAST

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

98% (64/65)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] IGSF11 is an immunoglobulin (Ig) superfamily member that is preferentially expressed in brain and testis. It shares significant homology with coxsackievirus and adenovirus receptor (CXADR; MIM 602621) and endothelial cell-selective adhesion molecule (ESAM).[supplied by OMIM, Apr 2005]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit disrupted synaptic transmission and plasticity. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 64 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700113H08Rik	G	A	10: 87,042,061 (GRCm39)		probably null	Het
4930522H14Rik	G	A	4: 109,362,776 (GRCm39)	A181V	probably damaging	Het
Alk	A	T	17: 72,274,549 (GRCm39)	H587Q	possibly damaging	Het
Ascc3	A	G	10: 50,604,393 (GRCm39)	Y1371C	probably benign	Het
Asxl1	T	C	2: 153,238,733 (GRCm39)	F354S	probably damaging	Het
Cachd1	A	T	4: 100,824,211 (GRCm39)	I551F	possibly damaging	Het
Cacna1e	T	C	1: 154,347,149 (GRCm39)	E1068G	probably benign	Het
Cdc27	A	T	11: 104,403,830 (GRCm39)	M644K	probably damaging	Het
Chl1	T	C	6: 103,668,635 (GRCm39)	V456A	probably benign	Het
Ctxn1	A	G	8: 4,308,461 (GRCm39)	Y57H	probably damaging	Het
Cyp2c54	A	G	19: 40,058,688 (GRCm39)	I248T	probably benign	Het
Dchs2	A	G	3: 83,211,834 (GRCm39)	T1878A	probably benign	Het
Ddi2	A	G	4: 141,412,561 (GRCm39)	V117A	probably benign	Het
Dennd5a	G	T	7: 109,533,196 (GRCm39)	F191L	probably benign	Het
Dnm3	C	T	1: 161,819,619 (GRCm39)	R851H	possibly damaging	Het
Eif3l	G	A	15: 78,973,799 (GRCm39)	D405N	possibly damaging	Het
Espn	T	A	4: 152,215,738 (GRCm39)	D507V	possibly damaging	Het
Fam83f	A	T	15: 80,576,704 (GRCm39)	S452C	possibly damaging	Het
Fbxo22	A	C	9: 55,125,651 (GRCm39)	E171D	probably damaging	Het
Fgl2	T	C	5: 21,577,752 (GRCm39)	V13A	probably benign	Het
Fsip2	A	G	2: 82,807,044 (GRCm39)	H1121R	probably benign	Het
G0s2	A	T	1: 192,955,081 (GRCm39)	M1K	probably null	Het
Gnptab	G	A	10: 88,276,254 (GRCm39)		probably null	Het
Grm1	G	A	10: 10,956,096 (GRCm39)	P63S	probably benign	Het
Grsf1	G	A	5: 88,823,523 (GRCm39)		probably benign	Het
Hcfc1r1	G	A	17: 23,892,985 (GRCm39)	G10D	probably damaging	Het
Hdac1-ps	A	C	17: 78,799,447 (GRCm39)	E146A	probably damaging	Het
Il17a	C	A	1: 20,802,351 (GRCm39)	A20E	probably benign	Het
Kcnv2	A	G	19: 27,300,332 (GRCm39)	Y61C	probably damaging	Het
Kmt2c	A	G	5: 25,499,697 (GRCm39)	M481T	possibly damaging	Het
Krt40	A	T	11: 99,430,961 (GRCm39)	C263S	possibly damaging	Het
Larp1	T	C	11: 57,938,540 (GRCm39)	V441A	possibly damaging	Het
Lrwd1	T	C	5: 136,160,983 (GRCm39)	E300G	probably damaging	Het
Mcoln3	G	T	3: 145,845,230 (GRCm39)	W475C	probably damaging	Het
Mdga1	A	G	17: 30,058,796 (GRCm39)	I30T	probably benign	Het
Mmd	T	A	11: 90,158,433 (GRCm39)	V181D	probably benign	Het
Muc4	T	A	16: 32,752,558 (GRCm38)	L812*	probably null	Het
Mycbp2	T	C	14: 103,414,729 (GRCm39)	D2561G	probably benign	Het
Myh11	T	A	16: 14,027,481 (GRCm39)	E1251V		Het
Myl12a	G	T	17: 71,303,166 (GRCm39)	N95K	probably benign	Het
Myo1h	A	G	5: 114,466,872 (GRCm39)		probably null	Het
Myrf	G	A	19: 10,196,983 (GRCm39)	P266S	possibly damaging	Het
Ncf1	A	G	5: 134,250,949 (GRCm39)	V330A	possibly damaging	Het
Nfasc	T	C	1: 132,533,287 (GRCm39)	D638G	probably damaging	Het
Nkapl	T	C	13: 21,651,437 (GRCm39)	K392R	possibly damaging	Het
Or2y3	A	G	17: 38,393,293 (GRCm39)	V192A	probably benign	Het
Or6a2	A	T	7: 106,600,514 (GRCm39)	C184*	probably null	Het
Or8b50	A	G	9: 38,517,708 (GRCm39)		probably benign	Het
Pelo	T	A	13: 115,226,184 (GRCm39)	N91I	probably damaging	Het
Ptk2b	T	C	14: 66,395,850 (GRCm39)	N836D	probably benign	Het
Pwp2	A	T	10: 78,018,778 (GRCm39)		probably null	Het
Slc44a1	G	A	4: 53,517,657 (GRCm39)	V127I	probably benign	Het
Snx13	A	G	12: 35,155,174 (GRCm39)	T413A	probably benign	Het
Spaca7	C	T	8: 12,635,696 (GRCm39)	P71S	probably damaging	Het
Spef2	A	T	15: 9,609,637 (GRCm39)	M1296K	possibly damaging	Het
Suco	G	A	1: 161,656,890 (GRCm39)	A978V	probably benign	Het
Tcerg1	A	G	18: 42,670,002 (GRCm39)	E494G	probably benign	Het
Tenm2	A	G	11: 35,997,626 (GRCm39)	V821A	probably benign	Het
Tg	T	A	15: 66,565,112 (GRCm39)	D1151E	probably benign	Het
Trp53bp2	A	G	1: 182,283,384 (GRCm39)	E1040G	probably damaging	Het
Ubap2	A	T	4: 41,233,655 (GRCm39)	N79K	probably damaging	Het
Vmn2r111	T	C	17: 22,778,032 (GRCm39)	N549S	possibly damaging	Het
Yars2	T	G	16: 16,122,385 (GRCm39)		probably null	Het
Ylpm1	A	G	12: 85,095,640 (GRCm39)	I1847V	possibly damaging	Het

Other mutations in Igsf11

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00969:Igsf11	APN	16	38,829,279 (GRCm39)	missense	probably damaging	1.00
R0139:Igsf11	UTSW	16	38,829,240 (GRCm39)	missense	probably damaging	1.00
R0348:Igsf11	UTSW	16	38,829,179 (GRCm39)	missense	probably benign	0.01
R1268:Igsf11	UTSW	16	38,845,216 (GRCm39)	missense	probably benign	0.01
R4494:Igsf11	UTSW	16	38,831,703 (GRCm39)	missense	possibly damaging	0.46
R4791:Igsf11	UTSW	16	38,845,226 (GRCm39)	missense	probably damaging	0.99
R5387:Igsf11	UTSW	16	38,842,785 (GRCm39)	missense	probably damaging	1.00
R5572:Igsf11	UTSW	16	38,845,294 (GRCm39)	missense	probably damaging	0.97
R6150:Igsf11	UTSW	16	38,843,711 (GRCm39)	missense	probably damaging	0.96
R6340:Igsf11	UTSW	16	38,829,336 (GRCm39)	missense	probably benign
R6815:Igsf11	UTSW	16	38,829,243 (GRCm39)	missense	probably benign	0.02
R7521:Igsf11	UTSW	16	38,829,274 (GRCm39)	missense	probably damaging	1.00
R7533:Igsf11	UTSW	16	38,829,236 (GRCm39)	missense	probably benign	0.07
R7732:Igsf11	UTSW	16	38,829,160 (GRCm39)	missense	probably damaging	0.99
R8305:Igsf11	UTSW	16	38,827,586 (GRCm39)	missense	probably damaging	1.00
R8842:Igsf11	UTSW	16	38,829,243 (GRCm39)	missense	probably benign	0.02
R9732:Igsf11	UTSW	16	38,843,652 (GRCm39)	missense	probably benign	0.16
X0026:Igsf11	UTSW	16	38,827,648 (GRCm39)	missense	possibly damaging	0.71

Predicted Primers

PCR Primer
(F):5'- TTCCTTTGGCTCAGTAACTAGTG -3'
(R):5'- AGGTACACTGACCCTGTCAC -3'

Sequencing Primer
(F):5'- AGACTATCCTGATGTGTGTTCAGAG -3'
(R):5'- GGTACACTGACCCTGTCACCTTAC -3'

Posted On

2019-12-20