Mutagenetix > Incidental Mutations

Incidental Mutation 'R2152:Sidt2'

234406

Institutional Source

Beutler Lab

Gene Symbol

Sidt2

Ensembl Gene

ENSMUSG00000034908

Gene Name

SID1 transmembrane family, member 2

Synonyms

CGI-40

MMRRC Submission

040155-MU

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.115) question?

Stock #

R2152 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

45937857-45955258 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 45945340 bp

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 477 (D477G)

Ref Sequence

ENSEMBL: ENSMUSP00000124750 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000038488] [ENSMUST00000114573] [ENSMUST00000160138] [ENSMUST00000160618] [ENSMUST00000162072] [ENSMUST00000162379] [ENSMUST00000162529]

Predicted Effect

probably damaging
Transcript: ENSMUST00000038488
AA Change: D433G

PolyPhen 2 Score 0.983 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000044290
Gene: ENSMUSG00000034908
AA Change: D433G

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:SID-1_RNA_chan	169	832	8.5e-214	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000114573
AA Change: D454G

PolyPhen 2 Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000110220
Gene: ENSMUSG00000034908
AA Change: D454G

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:SID-1_RNA_chan	169	853	9e-290	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000159033

SMART Domains

Protein: ENSMUSP00000125273
Gene: ENSMUSG00000034908

Domain	Start	End	E-Value	Type
low complexity region	12	29	N/A	INTRINSIC
Pfam:SID-1_RNA_chan	30	74	1e-23	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000160138
AA Change: D156G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000124945
Gene: ENSMUSG00000034908
AA Change: D156G

Domain	Start	End	E-Value	Type
low complexity region	131	142	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160598

Predicted Effect

probably damaging
Transcript: ENSMUST00000160618
AA Change: D61G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000125037
Gene: ENSMUSG00000034908
AA Change: D61G

Domain	Start	End	E-Value	Type
low complexity region	36	47	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160670

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000160927

Predicted Effect

probably benign
Transcript: ENSMUST00000161042

SMART Domains

Protein: ENSMUSP00000124577
Gene: ENSMUSG00000034908

Domain	Start	End	E-Value	Type
transmembrane domain	5	27	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000161606

SMART Domains

Protein: ENSMUSP00000125660
Gene: ENSMUSG00000034908

Domain	Start	End	E-Value	Type
Pfam:SID-1_RNA_chan	1	221	4.7e-29	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000162072
AA Change: D477G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000124750
Gene: ENSMUSG00000034908
AA Change: D477G

Domain	Start	End	E-Value	Type
signal peptide	1	18	N/A	INTRINSIC
Pfam:SID-1_RNA_chan	169	338	2.3e-34	PFAM
low complexity region	452	463	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000162379

SMART Domains

Protein: ENSMUSP00000124503
Gene: ENSMUSG00000034908

Domain	Start	End	E-Value	Type
Pfam:SID-1_RNA_chan	1	135	3.3e-29	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000162529

SMART Domains

Protein: ENSMUSP00000125060
Gene: ENSMUSG00000034908

Domain	Start	End	E-Value	Type
Pfam:SID-1_RNA_chan	1	135	9.2e-20	PFAM
low complexity region	202	213	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.4%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a targeted allele exhibit male-specific decreased body weight and size, impaired glucose tolerance, increased serum glucose, decreased serum insulin and decreased insule granule release from beta cells. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 108 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4921501E09Rik	T	A	17: 33,066,934	D298V	probably damaging	Het
Ackr3	A	T	1: 90,213,843	Y8F	probably benign	Het
Acy1	T	C	9: 106,435,617	E175G	probably damaging	Het
Add2	T	C	6: 86,098,598	L243P	probably damaging	Het
Adsl	A	G	15: 80,967,662	D407G	probably damaging	Het
Afg3l1	T	G	8: 123,494,836	I478S	probably damaging	Het
Arfrp1	T	C	2: 181,359,694	T108A	probably benign	Het
Art5	A	G	7: 102,098,200	L124P	possibly damaging	Het
Asap2	A	T	12: 21,112,083	T14S	probably damaging	Het
Atp2c2	A	G	8: 119,756,102	N901S	probably benign	Het
Bbs12	G	T	3: 37,321,160	E586*	probably null	Het
Bicd2	G	T	13: 49,379,576	C546F	probably damaging	Het
Bid	A	T	6: 120,900,254	L42Q	probably damaging	Het
Bpifb9a	A	G	2: 154,260,135	K51E	probably benign	Het
Calcr	G	T	6: 3,687,615	T424K	probably benign	Het
Cd46	A	G	1: 195,062,413	I339T	probably benign	Het
Chek1	C	A	9: 36,723,983	V35F	probably damaging	Het
Cntn3	A	G	6: 102,206,537	I719T	probably damaging	Het
Cyb5r1	T	C	1: 134,409,625	I163T	possibly damaging	Het
Cyp2d26	A	T	15: 82,792,706		probably null	Het
Dclk1	A	G	3: 55,247,212	Y21C	probably damaging	Het
Dgcr2	G	A	16: 17,891,487		probably null	Het
Dhx38	T	C	8: 109,560,674	S221G	probably benign	Het
Dis3l	T	A	9: 64,307,263	N981I	probably benign	Het
Dnah3	C	T	7: 119,952,013	V3028I	probably benign	Het
Dnah6	T	C	6: 73,049,166	Y3448C	probably benign	Het
Dok5	G	A	2: 170,800,896	G38D	probably damaging	Het
Doxl2	T	A	6: 48,976,539	I466N	probably damaging	Het
Epb41l1	A	G	2: 156,514,128	D528G	probably damaging	Het
Fat4	A	T	3: 38,983,395	Y3732F	probably damaging	Het
Fgfr4	A	T	13: 55,166,964	Y640F	probably damaging	Het
Foxo6	T	A	4: 120,268,614	D328V	probably benign	Het
Foxp1	A	G	6: 99,016,541	L134P	probably damaging	Het
Frem2	G	A	3: 53,517,029	R2996*	probably null	Het
Fuk	T	A	8: 110,889,072	T542S	probably benign	Het
Garem2	T	C	5: 30,108,299	S54P	probably damaging	Het
Gcn1l1	T	A	5: 115,609,829	I1765N	probably benign	Het
Gm4787	T	A	12: 81,377,219	I722F	probably benign	Het
Gpc6	G	T	14: 116,926,092	A53S	probably benign	Het
Gtpbp8	A	G	16: 44,740,027		probably null	Het
H2-Q2	T	C	17: 35,345,276		probably null	Het
Hapln2	C	A	3: 88,023,613	R157L	probably benign	Het
Hemgn	C	A	4: 46,396,607	E210*	probably null	Het
Hpse	T	A	5: 100,691,403	K360*	probably null	Het
Iqcj	A	T	3: 68,055,310	E68V	probably damaging	Het
Kat2a	T	C	11: 100,712,346		probably benign	Het
Kat6b	A	T	14: 21,668,667	H1138L	probably benign	Het
Kcnab1	A	T	3: 65,371,440	I371F	probably damaging	Het
Klhl30	C	A	1: 91,357,824	A356D	probably benign	Het
Klra3	G	C	6: 130,333,144	R138G	probably benign	Het
Mgea5	A	T	19: 45,758,022	Y779*	probably null	Het
Micu1	G	T	10: 59,863,288	M468I	probably benign	Het
Mrc1	A	G	2: 14,327,864	T1292A	probably damaging	Het
Myh8	G	A	11: 67,294,469	E849K	probably damaging	Het
Myom3	G	T	4: 135,803,233	R1152L	probably benign	Het
Nedd4l	T	A	18: 65,210,330	H820Q	probably damaging	Het
Nlrp4g	T	A	9: 124,353,339		noncoding transcript	Het
Olfr1339	C	T	4: 118,735,249	A240V	possibly damaging	Het
Olfr1413	T	C	1: 92,573,908	S246P	probably damaging	Het
Olfr24	T	C	9: 18,755,095	D180G	probably damaging	Het
Olfr33	G	T	7: 102,713,581	H277Q	probably benign	Het
Olfr435	A	G	6: 43,202,069	I142V	probably benign	Het
Olfr592	A	T	7: 103,186,640	D13V	probably benign	Het
Olfr913	G	T	9: 38,594,411	L63F	probably damaging	Het
Olfr969	A	T	9: 39,795,647	I91F	probably benign	Het
Otop1	T	A	5: 38,302,851	M587K	probably damaging	Het
Pgm5	T	A	19: 24,834,815	I118F	probably damaging	Het
Phc2	A	G	4: 128,745,066	*41W	probably null	Het
Piezo2	A	T	18: 63,114,041	M532K	probably damaging	Het
Pjvk	A	T	2: 76,658,369	I295F	probably benign	Het
Popdc2	A	G	16: 38,363,120	N155S	possibly damaging	Het
Ppp4r3a	G	T	12: 101,042,567	N684K	probably damaging	Het
Prpf4b	T	A	13: 34,900,419	M930K	probably benign	Het
Ptpn12	C	A	5: 21,002,468	Q297H	probably damaging	Het
Ptprz1	C	A	6: 23,030,671	L1010I	probably damaging	Het
Rabepk	A	T	2: 34,784,550	D232E	possibly damaging	Het
Rad51ap2	A	G	12: 11,457,985	H636R	probably benign	Het
Rb1	T	C	14: 73,288,725	T169A	probably benign	Het
Rcc2	T	C	4: 140,717,117	L373P	probably damaging	Het
Rif1	GCCACCA	GCCA	2: 52,110,324		probably benign	Het
Rrbp1	A	G	2: 143,954,198	L1200P	possibly damaging	Het
Sdk1	A	G	5: 141,792,944	N226D	probably damaging	Het
Selenbp1	G	A	3: 94,944,130	R398H	probably damaging	Het
Selenoo	A	G	15: 89,099,282	M509V	probably benign	Het
Slc2a5	T	G	4: 150,125,638	S27A	probably damaging	Het
Slc30a5	A	T	13: 100,803,949	H619Q	probably damaging	Het
Slc5a9	A	G	4: 111,893,223	I146T	possibly damaging	Het
Slc6a1	G	T	6: 114,307,770	G263V	probably damaging	Het
Slmap	A	G	14: 26,418,247	Y771H	probably damaging	Het
Snx29	A	G	16: 11,400,843	D181G	possibly damaging	Het
Spata31d1c	G	A	13: 65,033,965		probably null	Het
Stat5a	C	A	11: 100,874,090	T213N	probably benign	Het
Stt3a	A	T	9: 36,747,996	V349D	probably damaging	Het
Tcf20	A	T	15: 82,855,602	D549E	probably damaging	Het
Thbs2	T	A	17: 14,673,209	D903V	probably damaging	Het
Tln2	T	C	9: 67,302,560	T432A	probably damaging	Het
Tmc1	A	T	19: 20,856,675	N241K	probably benign	Het
Tmem260	G	T	14: 48,477,609	R240L	possibly damaging	Het
Tnfaip6	A	T	2: 52,043,730	E32D	probably damaging	Het
Trpa1	A	T	1: 14,899,401	H381Q	probably damaging	Het
Tsen2	T	C	6: 115,547,975	I45T	possibly damaging	Het
Ttc6	G	A	12: 57,705,552	V1415I	probably damaging	Het
Ttll7	G	T	3: 146,930,189	R426L	probably damaging	Het
Ttn	A	C	2: 76,740,138	S26804A	probably damaging	Het
Ubqlnl	A	T	7: 104,148,683	C536S	probably benign	Het
Vmn2r73	A	G	7: 85,857,728	V792A	probably benign	Het
Zfp345	T	C	2: 150,472,658	T320A	probably benign	Het
Zfp407	T	C	18: 84,209,649	D1945G	possibly damaging	Het

Other mutations in Sidt2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00325:Sidt2	APN	9	45942236	missense	possibly damaging	0.84
IGL00586:Sidt2	APN	9	45943052	missense	possibly damaging	0.78
IGL00786:Sidt2	APN	9	45949803	missense	possibly damaging	0.69
IGL01069:Sidt2	APN	9	45943077	missense	possibly damaging	0.73
IGL01160:Sidt2	APN	9	45942726	missense	probably damaging	1.00
IGL01474:Sidt2	APN	9	45946982	critical splice donor site	probably null
IGL02068:Sidt2	APN	9	45945664	critical splice donor site	probably null
IGL02171:Sidt2	APN	9	45952770	missense	possibly damaging	0.81
IGL02312:Sidt2	APN	9	45947001	missense	probably benign	0.27
IGL02344:Sidt2	APN	9	45945292	missense	probably null	1.00
IGL03030:Sidt2	APN	9	45939505	missense	probably damaging	1.00
IGL03062:Sidt2	APN	9	45942683	critical splice donor site	probably null
R0157:Sidt2	UTSW	9	45939267	missense	probably damaging	1.00
R0330:Sidt2	UTSW	9	45954902	missense	probably benign	0.09
R0549:Sidt2	UTSW	9	45953119	splice site	probably null
R0714:Sidt2	UTSW	9	45947060	splice site	probably benign
R1241:Sidt2	UTSW	9	45945704	missense	probably damaging	0.97
R1511:Sidt2	UTSW	9	45950089	missense	probably damaging	1.00
R1558:Sidt2	UTSW	9	45951800	missense	probably damaging	1.00
R1677:Sidt2	UTSW	9	45953219	missense	probably benign	0.01
R2153:Sidt2	UTSW	9	45945340	missense	probably damaging	1.00
R2154:Sidt2	UTSW	9	45945340	missense	probably damaging	1.00
R4210:Sidt2	UTSW	9	45942775	missense	probably benign	0.00
R4349:Sidt2	UTSW	9	45945713	missense	possibly damaging	0.94
R4855:Sidt2	UTSW	9	45952029	missense	probably benign
R5069:Sidt2	UTSW	9	45939461	splice site	probably null
R5175:Sidt2	UTSW	9	45951788	missense	probably damaging	1.00
R5276:Sidt2	UTSW	9	45954777	missense	probably damaging	0.97
R5544:Sidt2	UTSW	9	45944455	missense	probably damaging	1.00
R5805:Sidt2	UTSW	9	45942199	missense	probably damaging	0.97
R5927:Sidt2	UTSW	9	45944454	missense	probably damaging	1.00
R6954:Sidt2	UTSW	9	45952850	missense	probably benign	0.01
R7060:Sidt2	UTSW	9	45953246	missense	possibly damaging	0.91
R7117:Sidt2	UTSW	9	45953219	missense	probably benign	0.01
R7207:Sidt2	UTSW	9	45945151	missense	probably damaging	1.00
R7317:Sidt2	UTSW	9	45943690	nonsense	probably null
R7765:Sidt2	UTSW	9	45941575	splice site	probably null
R8098:Sidt2	UTSW	9	45945730	missense	probably benign	0.05
X0026:Sidt2	UTSW	9	45939299	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GGCAGAGTTACAGACCAAGACC -3'
(R):5'- TGGCGAATCACTGTGCTGTG -3'

Sequencing Primer
(F):5'- GTGATCACCAGCTGCACC -3'
(R):5'- GACCGACTCCAGGAGAAGTC -3'

Posted On

2014-10-01