Mutagenetix > Incidental Mutation

Incidental Mutation 'R8098:Sidt2'

630325

Institutional Source

Beutler Lab

Gene Symbol

Sidt2

Ensembl Gene

ENSMUSG00000034908

Gene Name

SID1 transmembrane family, member 2

Synonyms

CGI-40

MMRRC Submission

067530-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.180) question?

Stock #

R8098 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

45849155-45866556 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 45857028 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 426 (V426A)

Ref Sequence

ENSEMBL: ENSMUSP00000110220 (fasta)

Gene Model

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

AlphaFold

Q8CIF6

Predicted Effect

probably benign
Transcript: ENSMUST00000038488
AA Change: V405A

PolyPhen 2 Score 0.304 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000044290
Gene: ENSMUSG00000034908
AA Change: V405A

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 benign
Transcript: ENSMUST00000114573
AA Change: V426A

PolyPhen 2 Score 0.051 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000110220
Gene: ENSMUSG00000034908
AA Change: V426A

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

possibly damaging
Transcript: ENSMUST00000160138
AA Change: V128A

PolyPhen 2 Score 0.908 (Sensitivity: 0.81; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000124945
Gene: ENSMUSG00000034908
AA Change: V128A

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

Predicted Effect

probably benign
Transcript: ENSMUST00000160618
AA Change: V33A

PolyPhen 2 Score 0.304 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000125037
Gene: ENSMUSG00000034908
AA Change: V33A

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

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

SMART Domains

Protein: ENSMUSP00000125660
Gene: ENSMUSG00000034908
AA Change: V200A

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

Predicted Effect

possibly damaging
Transcript: ENSMUST00000162072
AA Change: V449A

PolyPhen 2 Score 0.824 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000124750
Gene: ENSMUSG00000034908
AA Change: V449A

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 damaging
Transcript: ENSMUST00000162529
AA Change: V199A

PolyPhen 2 Score 0.989 (Sensitivity: 0.72; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000125060
Gene: ENSMUSG00000034908
AA Change: V199A

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: 99.9%
3x: 99.8%
10x: 99.3%
20x: 98.4%

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: 92 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3425401B19Rik	A	G	14: 32,384,618 (GRCm39)	L449P	probably damaging	Het
Abca15	A	G	7: 119,960,619 (GRCm39)	S694G	probably benign	Het
Abcc6	A	G	7: 45,646,089 (GRCm39)	L800P	probably damaging	Het
Adam15	T	A	3: 89,251,193 (GRCm39)	D504V	probably damaging	Het
Adnp	T	C	2: 168,024,452 (GRCm39)	T948A	probably benign	Het
Akap11	T	C	14: 78,750,362 (GRCm39)	D675G		Het
Atp13a3	A	C	16: 30,173,115 (GRCm39)	V254G	possibly damaging	Het
Atp1a1	A	G	3: 101,489,365 (GRCm39)	I749T	probably damaging	Het
B3glct	T	A	5: 149,673,965 (GRCm39)	Y369*	probably null	Het
Bms1	C	T	6: 118,361,219 (GRCm39)	R1204H	probably damaging	Het
Btla	T	A	16: 45,064,612 (GRCm39)	L188*	probably null	Het
Btn2a2	A	G	13: 23,666,058 (GRCm39)	V258A	probably benign	Het
C1ra	G	A	6: 124,494,684 (GRCm39)	E316K	probably benign	Het
Cacna1g	T	C	11: 94,307,338 (GRCm39)	H1782R	probably benign	Het
Calcoco1	T	C	15: 102,624,759 (GRCm39)	D172G	probably benign	Het
Ccdc192	A	T	18: 57,800,403 (GRCm39)	I185L	probably benign	Het
Ciart	G	A	3: 95,788,656 (GRCm39)	P61L	probably damaging	Het
Ckap4	A	G	10: 84,369,499 (GRCm39)	S78P	probably damaging	Het
Col6a3	A	T	1: 90,731,383 (GRCm39)	D1623E	probably benign	Het
Col7a1	A	G	9: 108,785,763 (GRCm39)	T411A	unknown	Het
Cpt1a	A	C	19: 3,420,849 (GRCm39)	I436L	probably benign	Het
Cyp2c23	T	A	19: 44,004,242 (GRCm39)	I173F	probably benign	Het
Dcun1d2	T	C	8: 13,311,396 (GRCm39)	T198A	probably benign	Het
Ddx50	A	C	10: 62,460,922 (GRCm39)		probably null	Het
Depdc1b	A	G	13: 108,460,593 (GRCm39)	T68A	probably damaging	Het
Dgkq	G	A	5: 108,800,334 (GRCm39)	R546W	probably damaging	Het
Dmbt1	G	A	7: 130,710,188 (GRCm39)	W1493*	probably null	Het
Dnah17	A	G	11: 117,941,193 (GRCm39)	S3219P	probably damaging	Het
Egf	T	A	3: 129,484,486 (GRCm39)	Y986F	probably benign	Het
Ell3	TCTCCTC	TCTC	2: 121,269,937 (GRCm39)		probably benign	Het
Ep400	A	T	5: 110,841,117 (GRCm39)	M1805K	unknown	Het
Exoc3	A	G	13: 74,320,271 (GRCm39)	M730T	probably benign	Het
Fbxl13	T	A	5: 21,825,716 (GRCm39)	M129L	probably benign	Het
Fem1al	A	G	11: 29,774,450 (GRCm39)	S336P	possibly damaging	Het
Gins4	T	A	8: 23,727,037 (GRCm39)	M19L	probably benign	Het
Gm3238	T	C	10: 77,606,474 (GRCm39)	N229S	unknown	Het
Gpd2	T	A	2: 57,180,020 (GRCm39)	V89D	possibly damaging	Het
Hectd4	G	A	5: 121,459,461 (GRCm39)	V777I	possibly damaging	Het
Hgf	T	A	5: 16,766,059 (GRCm39)	V65E	probably benign	Het
Hnrnpdl	A	G	5: 100,185,779 (GRCm39)	S169P	probably benign	Het
Igfbp3	T	C	11: 7,160,104 (GRCm39)	D183G	possibly damaging	Het
Il16	A	G	7: 83,295,767 (GRCm39)	V1134A	probably damaging	Het
Kcnn4	A	G	7: 24,083,504 (GRCm39)	D395G	probably damaging	Het
Kctd17	CAGCTGGAGGAGC	CAGC	15: 78,321,113 (GRCm39)		probably benign	Het
Kif13a	T	C	13: 46,968,780 (GRCm39)	N354S	probably damaging	Het
Lrp1	C	T	10: 127,410,324 (GRCm39)	R1474Q	possibly damaging	Het
Map3k9	T	C	12: 81,780,888 (GRCm39)	Q424R	probably damaging	Het
Mkx	A	C	18: 6,992,784 (GRCm39)	S167A	possibly damaging	Het
Ms4a14	A	G	19: 11,281,979 (GRCm39)	F193S	possibly damaging	Het
Myo18a	A	T	11: 77,736,227 (GRCm39)	D1508V	probably damaging	Het
Nek4	T	A	14: 30,685,908 (GRCm39)	N273K	probably benign	Het
Nipal3	A	T	4: 135,179,709 (GRCm39)	V403D	possibly damaging	Het
Nlrp6	G	A	7: 140,503,168 (GRCm39)	V425M	probably damaging	Het
Or13p4	A	T	4: 118,547,406 (GRCm39)	V81E	possibly damaging	Het
Or14j6	A	G	17: 38,215,250 (GRCm39)	D271G	probably damaging	Het
Or4c122	T	A	2: 89,079,652 (GRCm39)	M117L	possibly damaging	Het
Or9k2	T	C	10: 129,998,916 (GRCm39)	K93R	probably benign	Het
Otub1	A	T	19: 7,181,794 (GRCm39)	D27E	probably damaging	Het
Pcnx2	T	C	8: 126,495,040 (GRCm39)	D1607G	probably damaging	Het
Pde2a	A	G	7: 101,071,178 (GRCm39)	Y16C	probably benign	Het
Pkd1l3	GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA	GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA	8: 110,350,827 (GRCm39)		probably benign	Het
Prph2	A	T	17: 47,230,892 (GRCm39)	M262L	probably benign	Het
Pxdn	C	T	12: 30,056,601 (GRCm39)	L1271F	probably damaging	Het
Rnf10	A	C	5: 115,389,438 (GRCm39)	I243S	probably damaging	Het
Samd9l	T	C	6: 3,375,549 (GRCm39)	I571V	probably damaging	Het
Scube1	C	T	15: 83,543,289 (GRCm39)	G183D	probably damaging	Het
Slc20a1	T	C	2: 129,051,041 (GRCm39)	L566P	probably damaging	Het
Slc22a3	A	G	17: 12,642,619 (GRCm39)		probably null	Het
Snx11	G	T	11: 96,661,500 (GRCm39)	S168R	probably benign	Het
Snx5	T	C	2: 144,097,482 (GRCm39)	N218D	probably benign	Het
Snx7	A	T	3: 117,632,583 (GRCm39)	D169E	probably benign	Het
Soat1	A	G	1: 156,274,180 (GRCm39)	L77P	probably damaging	Het
Sucnr1	T	A	3: 59,994,162 (GRCm39)	V230E	probably damaging	Het
Supv3l1	T	C	10: 62,265,282 (GRCm39)	K753E	probably benign	Het
Tango6	T	G	8: 107,468,990 (GRCm39)	L829V	possibly damaging	Het
Tek	T	C	4: 94,715,907 (GRCm39)	V443A	probably benign	Het
Tet1	A	T	10: 62,714,859 (GRCm39)	L312Q	probably damaging	Het
Tgm1	A	T	14: 55,947,991 (GRCm39)	N269K	probably damaging	Het
Thrb	A	T	14: 18,008,645 (GRCm38)	D168V	probably damaging	Het
Tk2	C	T	8: 104,957,804 (GRCm39)	V181I	probably benign	Het
Tm6sf2	T	C	8: 70,526,972 (GRCm39)	L47P	probably damaging	Het
Tmcc3	T	A	10: 94,415,078 (GRCm39)	M291K	probably benign	Het
Tnfrsf21	A	G	17: 43,350,790 (GRCm39)	E318G	probably benign	Het
Ttc7	T	C	17: 87,641,756 (GRCm39)	V451A	probably benign	Het
Ugt2b36	A	T	5: 87,240,252 (GRCm39)	D44E	probably benign	Het
Usp17la	G	T	7: 104,510,138 (GRCm39)	V248L	probably damaging	Het
Utp20	A	C	10: 88,588,810 (GRCm39)	I2453S	probably benign	Het
Wdr91	A	T	6: 34,863,817 (GRCm39)	I566N	possibly damaging	Het
Zfp282	A	G	6: 47,867,652 (GRCm39)	D276G	probably benign	Het
Zfp764l1	C	T	7: 126,992,496 (GRCm39)	C38Y	probably null	Het
Zfp866	T	C	8: 70,218,628 (GRCm39)	K331E	probably benign	Het
Zkscan17	A	T	11: 59,394,410 (GRCm39)	W64R	possibly damaging	Het

Other mutations in Sidt2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00325:Sidt2	APN	9	45,853,534 (GRCm39)	missense	possibly damaging	0.84
IGL00586:Sidt2	APN	9	45,854,350 (GRCm39)	missense	possibly damaging	0.78
IGL00786:Sidt2	APN	9	45,861,101 (GRCm39)	missense	possibly damaging	0.69
IGL01069:Sidt2	APN	9	45,854,375 (GRCm39)	missense	possibly damaging	0.73
IGL01160:Sidt2	APN	9	45,854,024 (GRCm39)	missense	probably damaging	1.00
IGL01474:Sidt2	APN	9	45,858,280 (GRCm39)	critical splice donor site	probably null
IGL02068:Sidt2	APN	9	45,856,962 (GRCm39)	critical splice donor site	probably null
IGL02171:Sidt2	APN	9	45,864,068 (GRCm39)	missense	possibly damaging	0.81
IGL02312:Sidt2	APN	9	45,858,299 (GRCm39)	missense	probably benign	0.27
IGL02344:Sidt2	APN	9	45,856,590 (GRCm39)	missense	probably null	1.00
IGL03030:Sidt2	APN	9	45,850,803 (GRCm39)	missense	probably damaging	1.00
IGL03062:Sidt2	APN	9	45,853,981 (GRCm39)	critical splice donor site	probably null
R0157:Sidt2	UTSW	9	45,850,565 (GRCm39)	missense	probably damaging	1.00
R0330:Sidt2	UTSW	9	45,866,200 (GRCm39)	missense	probably benign	0.09
R0549:Sidt2	UTSW	9	45,864,417 (GRCm39)	splice site	probably null
R0714:Sidt2	UTSW	9	45,858,358 (GRCm39)	splice site	probably benign
R1241:Sidt2	UTSW	9	45,857,002 (GRCm39)	missense	probably damaging	0.97
R1511:Sidt2	UTSW	9	45,861,387 (GRCm39)	missense	probably damaging	1.00
R1558:Sidt2	UTSW	9	45,863,098 (GRCm39)	missense	probably damaging	1.00
R1677:Sidt2	UTSW	9	45,864,517 (GRCm39)	missense	probably benign	0.01
R2152:Sidt2	UTSW	9	45,856,638 (GRCm39)	missense	probably damaging	1.00
R2153:Sidt2	UTSW	9	45,856,638 (GRCm39)	missense	probably damaging	1.00
R2154:Sidt2	UTSW	9	45,856,638 (GRCm39)	missense	probably damaging	1.00
R4210:Sidt2	UTSW	9	45,854,073 (GRCm39)	missense	probably benign	0.00
R4349:Sidt2	UTSW	9	45,857,011 (GRCm39)	missense	possibly damaging	0.94
R4855:Sidt2	UTSW	9	45,863,327 (GRCm39)	missense	probably benign
R5069:Sidt2	UTSW	9	45,850,759 (GRCm39)	splice site	probably null
R5175:Sidt2	UTSW	9	45,863,086 (GRCm39)	missense	probably damaging	1.00
R5276:Sidt2	UTSW	9	45,866,075 (GRCm39)	missense	probably damaging	0.97
R5544:Sidt2	UTSW	9	45,855,753 (GRCm39)	missense	probably damaging	1.00
R5805:Sidt2	UTSW	9	45,853,497 (GRCm39)	missense	probably damaging	0.97
R5927:Sidt2	UTSW	9	45,855,752 (GRCm39)	missense	probably damaging	1.00
R6954:Sidt2	UTSW	9	45,864,148 (GRCm39)	missense	probably benign	0.01
R7060:Sidt2	UTSW	9	45,864,544 (GRCm39)	missense	possibly damaging	0.91
R7117:Sidt2	UTSW	9	45,864,517 (GRCm39)	missense	probably benign	0.01
R7207:Sidt2	UTSW	9	45,856,449 (GRCm39)	missense	probably damaging	1.00
R7317:Sidt2	UTSW	9	45,854,988 (GRCm39)	nonsense	probably null
R7765:Sidt2	UTSW	9	45,852,873 (GRCm39)	splice site	probably null
R9039:Sidt2	UTSW	9	45,856,648 (GRCm39)	missense	probably benign	0.05
R9157:Sidt2	UTSW	9	45,852,658 (GRCm39)	missense	possibly damaging	0.58
R9160:Sidt2	UTSW	9	45,858,280 (GRCm39)	critical splice donor site	probably null
R9261:Sidt2	UTSW	9	45,861,396 (GRCm39)	missense	probably damaging	0.99
R9313:Sidt2	UTSW	9	45,852,658 (GRCm39)	missense	possibly damaging	0.58
R9641:Sidt2	UTSW	9	45,864,495 (GRCm39)	missense	probably benign	0.00
R9792:Sidt2	UTSW	9	45,850,563 (GRCm39)	missense	probably damaging	0.97
R9793:Sidt2	UTSW	9	45,850,563 (GRCm39)	missense	probably damaging	0.97
R9803:Sidt2	UTSW	9	45,854,912 (GRCm39)	missense	probably damaging	1.00
X0026:Sidt2	UTSW	9	45,850,597 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AATTAGTCCCGATCTCCCCAG -3'
(R):5'- AGTACGTTTCCTGCCAGCAC -3'

Sequencing Primer
(F):5'- GACTTCTCCTGGAGTCGGTC -3'
(R):5'- TACCGCTCTGAGCTCTGG -3'

Posted On

2020-06-30