Mutagenetix > Incidental Mutation

Incidental Mutation 'R4725:Samsn1'

358431

Institutional Source

Beutler Lab

Gene Symbol

Samsn1

Ensembl Gene

ENSMUSG00000022876

Gene Name

SAM domain, SH3 domain and nuclear localization signals, 1

Synonyms

4930571B16Rik, Hacs1

MMRRC Submission

041960-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4725 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

75655682-75706154 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

A to T at 75742217 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s): [ENSMUST00000114240]

AlphaFold

P57725

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000114240

SMART Domains

Protein: ENSMUSP00000109878
Gene: ENSMUSG00000022876

Domain	Start	End	E-Value	Type
low complexity region	69	80	N/A	INTRINSIC
Pfam:SLY	146	293	1.1e-55	PFAM
SH3	295	352	8.78e-4	SMART
SAM	367	434	7.6e-9	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000226794

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000227215

Meta Mutation Damage Score

0.0711

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 95.1%

Validation Efficiency

96% (64/67)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] SAMSN1 is a member of a novel gene family of putative adaptors and scaffold proteins containing SH3 and SAM (sterile alpha motif) domains (Claudio et al., 2001 [PubMed 11536050]).[supplied by OMIM, Mar 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit enhanced adaptive immunity. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 58 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5830454E08Rik	T	C	9: 120,406,769 (GRCm39)		probably benign	Het
Adamts20	T	C	15: 94,249,643 (GRCm39)	E458G	probably damaging	Het
Adgrl3	T	C	5: 81,914,052 (GRCm39)	I1220T	possibly damaging	Het
Aldh1a1	T	A	19: 20,617,445 (GRCm39)	M459K	probably benign	Het
Bmal1	C	A	7: 112,903,566 (GRCm39)	P454Q	possibly damaging	Het
Camta1	A	G	4: 151,232,953 (GRCm39)	V240A	probably benign	Het
Ccdc88b	C	T	19: 6,834,481 (GRCm39)	G149R	probably damaging	Het
Ceacam5	T	C	7: 17,494,602 (GRCm39)	V870A	probably benign	Het
Cep192	A	C	18: 67,949,837 (GRCm39)	Q307P	probably benign	Het
Cep63	T	C	9: 102,467,755 (GRCm39)		probably benign	Het
Cldn12	A	G	5: 5,558,385 (GRCm39)	F14S	probably damaging	Het
Ctdsp1	G	A	1: 74,433,823 (GRCm39)	V135I	possibly damaging	Het
Dcaf10	G	A	4: 45,372,769 (GRCm39)	R394Q	possibly damaging	Het
Dchs1	T	C	7: 105,404,460 (GRCm39)	D2694G	probably damaging	Het
Dchs1	C	G	7: 105,414,759 (GRCm39)	G761A	probably damaging	Het
Dennd5b	A	G	6: 148,946,277 (GRCm39)	Y445H	probably damaging	Het
Dock1	T	A	7: 134,346,743 (GRCm39)	L225*	probably null	Het
Drd3	G	T	16: 43,643,164 (GRCm39)	E467*	probably null	Het
Dysf	A	T	6: 84,074,738 (GRCm39)	N527I	probably damaging	Het
Erbb2	A	G	11: 98,315,970 (GRCm39)	T358A	possibly damaging	Het
Fhad1	A	T	4: 141,655,689 (GRCm39)		probably null	Het
Ganc	T	C	2: 120,265,754 (GRCm39)	I434T	probably damaging	Het
Gm5830	T	A	1: 78,945,549 (GRCm39)		noncoding transcript	Het
Gm6096	G	T	7: 33,950,484 (GRCm39)	E8*	probably null	Het
Gne	A	G	4: 44,066,806 (GRCm39)	F63S	probably benign	Het
Gpat2	T	C	2: 127,273,902 (GRCm39)	V315A	possibly damaging	Het
Gpr33	A	G	12: 52,070,892 (GRCm39)	L49P	probably damaging	Het
Heatr1	C	T	13: 12,439,543 (GRCm39)	Q1374*	probably null	Het
Hivep1	A	G	13: 42,316,887 (GRCm39)	I2032V	probably benign	Het
Igkv2-112	A	C	6: 68,197,450 (GRCm39)	I40L	probably benign	Het
Kcnab3	A	G	11: 69,221,294 (GRCm39)	N204D	probably benign	Het
Kcnj10	T	A	1: 172,196,726 (GRCm39)	F80Y	probably damaging	Het
Lcmt2	C	G	2: 120,969,911 (GRCm39)	V171L	probably benign	Het
Loxhd1	T	A	18: 77,483,153 (GRCm39)	Y1245N	probably damaging	Het
Lrrc7	GAAGTTGTTTGGAGATTCTTATCTTA	GA	3: 158,024,045 (GRCm39)		probably benign	Het
Mast1	A	G	8: 85,655,635 (GRCm39)	S170P	possibly damaging	Het
Mroh4	A	G	15: 74,487,956 (GRCm39)	L322P	probably damaging	Het
Npdc1	G	A	2: 25,298,957 (GRCm39)	D284N	probably damaging	Het
Nudcd3	A	T	11: 6,143,475 (GRCm39)	V1D	probably damaging	Het
Pah	T	A	10: 87,390,238 (GRCm39)	L25Q	probably damaging	Het
Pik3cg	A	T	12: 32,243,596 (GRCm39)		probably null	Het
Pira13	A	C	7: 3,824,547 (GRCm39)	S611A	probably benign	Het
Plekha6	C	A	1: 133,211,058 (GRCm39)	S625Y	probably damaging	Het
Rtn4	T	A	11: 29,658,362 (GRCm39)	S839T	probably damaging	Het
Rusc1	A	G	3: 88,998,736 (GRCm39)	S349P	possibly damaging	Het
Scimp	A	G	11: 70,691,539 (GRCm39)	V30A	probably damaging	Het
Serpinb13	C	T	1: 106,910,574 (GRCm39)	S66L	probably damaging	Het
Sgip1	A	G	4: 102,823,419 (GRCm39)	D680G	probably damaging	Het
Slc44a2	G	A	9: 21,259,691 (GRCm39)	V613M	probably damaging	Het
Smpdl3b	T	C	4: 132,472,489 (GRCm39)	T95A	probably damaging	Het
Spag6l	A	T	16: 16,610,395 (GRCm39)	L85H	probably damaging	Het
Sucla2	T	A	14: 73,806,429 (GRCm39)	Y167N	possibly damaging	Het
Svop	G	T	5: 114,203,546 (GRCm39)		probably benign	Het
Tnxb	A	T	17: 34,918,041 (GRCm39)	D2318V	probably damaging	Het
Trbv14	A	G	6: 41,112,332 (GRCm39)	D43G	probably benign	Het
Ubn2	A	G	6: 38,499,240 (GRCm39)		probably benign	Het
Ufsp1	T	C	5: 137,293,569 (GRCm39)	I173T	probably damaging	Het
Zbtb40	A	G	4: 136,746,072 (GRCm39)		probably benign	Het

Other mutations in Samsn1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00904:Samsn1	APN	16	75,706,008 (GRCm39)	splice site	probably benign
IGL02220:Samsn1	APN	16	75,680,763 (GRCm39)	critical splice donor site	probably null
R0455:Samsn1	UTSW	16	75,742,113 (GRCm39)	unclassified	noncoding transcript
R1136:Samsn1	UTSW	16	75,670,408 (GRCm39)	missense	probably null	0.00
R1140:Samsn1	UTSW	16	75,685,630 (GRCm39)	missense	possibly damaging	0.73
R1180:Samsn1	UTSW	16	75,670,536 (GRCm39)	missense	probably damaging	1.00
R1772:Samsn1	UTSW	16	75,667,663 (GRCm39)	missense	probably benign	0.01
R1968:Samsn1	UTSW	16	75,742,461 (GRCm39)	exon	noncoding transcript
R4035:Samsn1	UTSW	16	75,706,073 (GRCm39)	start codon destroyed	probably null	0.99
R4372:Samsn1	UTSW	16	75,656,344 (GRCm39)	missense	possibly damaging	0.80
R4779:Samsn1	UTSW	16	75,744,177 (GRCm39)	exon	noncoding transcript
R4795:Samsn1	UTSW	16	75,680,733 (GRCm39)	intron	probably benign
R4899:Samsn1	UTSW	16	75,675,991 (GRCm39)	missense	probably damaging	1.00
R4905:Samsn1	UTSW	16	75,673,353 (GRCm39)	missense	possibly damaging	0.94
R5050:Samsn1	UTSW	16	75,685,645 (GRCm39)	missense	probably benign
R5789:Samsn1	UTSW	16	75,673,336 (GRCm39)	missense	probably damaging	1.00
R6005:Samsn1	UTSW	16	75,670,402 (GRCm39)	missense	probably benign	0.03
R6190:Samsn1	UTSW	16	75,667,803 (GRCm39)	missense	probably damaging	1.00
R6218:Samsn1	UTSW	16	75,742,162 (GRCm39)	unclassified	noncoding transcript
R6630:Samsn1	UTSW	16	75,676,092 (GRCm39)	missense	probably benign	0.00
R7086:Samsn1	UTSW	16	75,667,794 (GRCm39)	missense	probably benign	0.00
R8289:Samsn1	UTSW	16	75,685,684 (GRCm39)	missense	probably damaging	1.00
R9189:Samsn1	UTSW	16	75,656,449 (GRCm39)	missense	probably damaging	0.99
R9330:Samsn1	UTSW	16	75,673,433 (GRCm39)	missense	probably damaging	1.00
R9635:Samsn1	UTSW	16	75,673,457 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCATCTCTGATCTTTGGAAGGTC -3'
(R):5'- AAGCAAAATCCCGAATGCTGG -3'

Sequencing Primer
(F):5'- CTTTGGAAGGTCAATGTAACACTGG -3'
(R):5'- GAATGCTGGACCACAATCCCTTTC -3'

Posted On

2015-11-11