Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02220:Samsn1'

285126

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Samsn1

Ensembl Gene

ENSMUSG00000022876

Gene Name

SAM domain, SH3 domain and nuclear localization signals, 1

Synonyms

4930571B16Rik, Hacs1

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL02220

Quality Score

Status

Chromosome

Chromosomal Location

75655682-75706154 bp(-) (GRCm39)

Type of Mutation

critical splice donor site (2 bp from exon)

DNA Base Change (assembly)

A to G at 75680763 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000109877 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000114239] [ENSMUST00000114239] [ENSMUST00000114240] [ENSMUST00000114240]

AlphaFold

P57725

PDB Structure

Solution structure of the Sterile Alpha Motif (SAM) domain of mouse SAMSN1 [SOLUTION NMR]

Predicted Effect

probably null
Transcript: ENSMUST00000114239

SMART Domains

Protein: ENSMUSP00000109877
Gene: ENSMUSG00000022876

Domain	Start	End	E-Value	Type
Pfam:SLY	17	164	4.7e-57	PFAM
SH3	166	223	8.78e-4	SMART
SAM	238	305	7.6e-9	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000114239

SMART Domains

Protein: ENSMUSP00000109877
Gene: ENSMUSG00000022876

Domain	Start	End	E-Value	Type
Pfam:SLY	17	164	4.7e-57	PFAM
SH3	166	223	8.78e-4	SMART
SAM	238	305	7.6e-9	SMART

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: 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: ENSMUST00000139691

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000147447

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150248

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000226794

Coding Region Coverage

Validation Efficiency

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: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acsm4	A	G	7: 119,310,395 (GRCm39)	D460G	probably damaging	Het
Ankrd9	T	C	12: 110,943,933 (GRCm39)	M1V	probably null	Het
Anks1	T	C	17: 28,273,681 (GRCm39)	I977T	probably damaging	Het
Bcar1	T	C	8: 112,437,839 (GRCm39)	D767G	possibly damaging	Het
Bcl6	A	T	16: 23,793,641 (GRCm39)	I102N	probably damaging	Het
Cacna2d2	G	A	9: 107,392,078 (GRCm39)	G473D	probably damaging	Het
Cdh23	G	T	10: 60,140,903 (GRCm39)	H3148Q	probably damaging	Het
Col6a4	A	G	9: 105,940,141 (GRCm39)	V1263A	possibly damaging	Het
Crtc2	T	C	3: 90,166,455 (GRCm39)		probably benign	Het
D130043K22Rik	G	A	13: 25,067,738 (GRCm39)	G825S	possibly damaging	Het
Dera	T	A	6: 137,757,815 (GRCm39)		probably null	Het
Dnah17	G	T	11: 117,963,793 (GRCm39)	Y2506*	probably null	Het
Enam	T	A	5: 88,652,418 (GRCm39)	L1309*	probably null	Het
Fbxo15	G	A	18: 84,982,317 (GRCm39)		probably null	Het
Fgfbp1	T	C	5: 44,136,828 (GRCm39)	K155E	probably damaging	Het
Foxj2	C	T	6: 122,815,540 (GRCm39)		probably benign	Het
Fuca1	A	G	4: 135,666,530 (GRCm39)		probably benign	Het
Gad1-ps	T	A	10: 99,281,184 (GRCm39)		noncoding transcript	Het
H2-Eb2	C	T	17: 34,544,661 (GRCm39)		probably benign	Het
Insr	A	T	8: 3,209,578 (GRCm39)	F1168L	probably damaging	Het
Isx	T	A	8: 75,619,333 (GRCm39)	V175E	possibly damaging	Het
Kansl3	T	C	1: 36,407,070 (GRCm39)		probably benign	Het
Lin9	T	C	1: 180,494,932 (GRCm39)	I218T	probably damaging	Het
Llgl2	C	A	11: 115,736,205 (GRCm39)	A126D	possibly damaging	Het
Ltbp2	T	C	12: 84,876,083 (GRCm39)	E488G	possibly damaging	Het
Maml3	A	G	3: 51,597,639 (GRCm39)	V369A	possibly damaging	Het
Mthfsl	A	G	9: 88,597,708 (GRCm39)	I14T	probably damaging	Het
Myo3b	A	G	2: 70,119,923 (GRCm39)		probably benign	Het
Nfkbil1	T	C	17: 35,439,722 (GRCm39)	R264G	possibly damaging	Het
Or4c3d	A	G	2: 89,882,038 (GRCm39)	L210P	probably damaging	Het
Pde5a	G	T	3: 122,542,031 (GRCm39)	A174S	probably benign	Het
Plch1	A	T	3: 63,606,382 (GRCm39)	I1173N	probably damaging	Het
Ppfia1	C	A	7: 144,035,512 (GRCm39)	R1171L	probably damaging	Het
Prom1	T	C	5: 44,172,131 (GRCm39)	D595G	probably damaging	Het
Ptprz1	T	C	6: 23,042,742 (GRCm39)		probably benign	Het
Sbno2	T	A	10: 79,908,202 (GRCm39)	T66S	probably benign	Het
Serpina1c	T	A	12: 103,862,338 (GRCm39)	I326F	probably damaging	Het
Slc12a1	T	C	2: 125,030,190 (GRCm39)		probably null	Het
Slc18a2	A	G	19: 59,264,988 (GRCm39)	E324G	probably benign	Het
Slc40a1	A	T	1: 45,950,495 (GRCm39)	M319K	probably damaging	Het
Slc44a5	T	C	3: 153,956,608 (GRCm39)	Y287H	possibly damaging	Het
Stx4a	A	G	7: 127,441,672 (GRCm39)	E63G	possibly damaging	Het
Sv2a	T	C	3: 96,098,032 (GRCm39)	F545S	probably benign	Het
Svop	T	C	5: 114,203,589 (GRCm39)	D65G	probably benign	Het
Tex30	A	T	1: 44,126,182 (GRCm39)	S182R	probably benign	Het
Tmem121b	T	C	6: 120,469,298 (GRCm39)	D473G	probably damaging	Het
Tnfrsf19	C	A	14: 61,210,941 (GRCm39)		probably benign	Het
Tnrc6a	T	C	7: 122,769,679 (GRCm39)	S490P	probably benign	Het
Ubr4	A	G	4: 139,115,746 (GRCm39)	T82A	probably benign	Het
Vps16	A	G	2: 130,283,573 (GRCm39)	D589G	possibly damaging	Het
Zscan29	A	C	2: 120,997,170 (GRCm39)	S184A	probably damaging	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
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
R4725:Samsn1	UTSW	16	75,742,217 (GRCm39)	unclassified	noncoding transcript
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

Posted On

2015-04-16