Mutagenetix > Incidental Mutation

Incidental Mutation 'R7269:Slc22a28'

565194

Institutional Source

Beutler Lab

Gene Symbol

Slc22a28

Ensembl Gene

ENSMUSG00000063590

Gene Name

solute carrier family 22, member 28

Synonyms

Gm5631

MMRRC Submission

045320-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.299) question?

Stock #

R7269 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

8039574-8109346 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 8094491 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Serine at position 177 (T177S)

Ref Sequence

ENSEMBL: ENSMUSP00000067114 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000065651]

AlphaFold

B2RT89

Predicted Effect

probably benign
Transcript: ENSMUST00000065651
AA Change: T177S

PolyPhen 2 Score 0.059 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000067114
Gene: ENSMUSG00000063590
AA Change: T177S

Domain	Start	End	E-Value	Type
transmembrane domain	13	35	N/A	INTRINSIC
Pfam:Sugar_tr	99	527	1.4e-26	PFAM
Pfam:MFS_1	140	375	1.1e-15	PFAM

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

98% (85/87)

Allele List at MGI

Other mutations in this stock

Total: 87 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2700062C07Rik	A	T	18: 24,606,013 (GRCm39)	N36I	probably damaging	Het
A430033K04Rik	T	A	5: 138,645,014 (GRCm39)	Y300N	possibly damaging	Het
Adipor2	T	C	6: 119,347,205 (GRCm39)	Q26R	probably benign	Het
Ahnak	T	A	19: 8,983,981 (GRCm39)	M1755K	probably damaging	Het
Ahnak2	A	T	12: 112,780,802 (GRCm38)	V70E		Het
AI837181	C	A	19: 5,476,462 (GRCm39)	S208R	probably damaging	Het
Arhgap35	T	G	7: 16,295,652 (GRCm39)	M1138L	probably benign	Het
Card14	T	G	11: 119,228,573 (GRCm39)	L633R	probably damaging	Het
Carmil3	A	G	14: 55,731,352 (GRCm39)	T144A	probably benign	Het
Cbfa2t2	T	A	2: 154,357,895 (GRCm39)	N223K	probably benign	Het
Ccdc39	T	C	3: 33,884,254 (GRCm39)	I363V	probably benign	Het
Ccng2	C	G	5: 93,421,202 (GRCm39)	S237R	probably benign	Het
Ccpg1	G	T	9: 72,920,609 (GRCm39)	R741S	probably benign	Het
Cenpc1	A	G	5: 86,161,366 (GRCm39)	F855L	probably damaging	Het
Cenpc1	A	T	5: 86,180,277 (GRCm39)	M665K	probably benign	Het
Cp	A	G	3: 20,037,641 (GRCm39)	H832R	probably damaging	Het
Defa24	A	G	8: 22,224,565 (GRCm39)	I5V	probably benign	Het
Dlc1	A	C	8: 37,046,407 (GRCm39)	L730R	probably damaging	Het
Dmbt1	A	T	7: 130,668,351 (GRCm39)	I536F	unknown	Het
Dscam	G	A	16: 96,479,601 (GRCm39)	T1182I	probably benign	Het
Eea1	A	T	10: 95,854,000 (GRCm39)	I553F	probably damaging	Het
Far1	T	C	7: 113,160,654 (GRCm39)	V400A	probably benign	Het
Fbrsl1	A	T	5: 110,580,880 (GRCm39)	S126T	probably benign	Het
Frmpd2	A	T	14: 33,244,838 (GRCm39)	E552V	possibly damaging	Het
Gm5431	T	A	11: 48,779,237 (GRCm39)	T562S	probably benign	Het
Gm5475	T	C	15: 100,324,890 (GRCm39)	F106S	unknown	Het
Gpr12	T	C	5: 146,520,188 (GRCm39)	T245A	probably damaging	Het
Gsta2	A	G	9: 78,239,419 (GRCm39)	Y166H	probably benign	Het
H6pd	A	G	4: 150,067,369 (GRCm39)	V347A	probably benign	Het
Ifih1	T	C	2: 62,475,977 (GRCm39)	T100A	probably benign	Het
Ift70b	A	G	2: 75,767,838 (GRCm39)	F305S	probably damaging	Het
Itga2	C	T	13: 115,023,225 (GRCm39)	W59*	probably null	Het
Knstrn	T	A	2: 118,661,869 (GRCm39)		probably null	Het
Kprp	A	G	3: 92,731,178 (GRCm39)	V624A	probably damaging	Het
Lmbrd2	A	G	15: 9,194,771 (GRCm39)	Y591C	probably damaging	Het
Map7d1	A	G	4: 126,126,666 (GRCm39)	V842A	unknown	Het
Mboat2	A	T	12: 24,881,708 (GRCm39)	T4S	probably benign	Het
Mcph1	T	A	8: 18,657,288 (GRCm39)		probably null	Het
Mrtfb	A	T	16: 13,218,898 (GRCm39)	M515L	possibly damaging	Het
Muc5b	A	G	7: 141,411,272 (GRCm39)	D1406G	unknown	Het
Mylk	G	A	16: 34,605,381 (GRCm39)	G3D	probably damaging	Het
Ndst4	A	G	3: 125,232,007 (GRCm39)	D192G	probably damaging	Het
Nemp1	G	T	10: 127,531,345 (GRCm39)	R361L	probably damaging	Het
Nol4	A	C	18: 23,172,846 (GRCm39)	V85G	probably benign	Het
Nrbf2	G	A	10: 67,103,605 (GRCm39)	T166M	probably damaging	Het
Obscn	T	C	11: 58,933,838 (GRCm39)	E5342G	probably damaging	Het
Or10al7	C	A	17: 38,366,442 (GRCm39)	C5F	probably damaging	Het
Or4f47	T	A	2: 111,972,905 (GRCm39)	F205Y	probably damaging	Het
Or4p19	C	T	2: 88,242,839 (GRCm39)	M54I	possibly damaging	Het
Or51d1	T	G	7: 102,348,252 (GRCm39)	L269R	probably damaging	Het
Or7d10	A	G	9: 19,831,631 (GRCm39)	N42S	possibly damaging	Het
Pakap	G	T	4: 57,855,217 (GRCm39)	R182L	probably damaging	Het
Pde4dip	A	G	3: 97,674,275 (GRCm39)	S214P	probably damaging	Het
Per3	A	T	4: 151,116,393 (GRCm39)	C278*	probably null	Het
Pi4k2a	T	C	19: 42,079,125 (GRCm39)	L62P	probably damaging	Het
Plekha7	C	A	7: 115,780,447 (GRCm39)	G126W	probably damaging	Het
Ppp1r13b	T	C	12: 111,801,353 (GRCm39)	K567E	probably damaging	Het
Pradc1	T	A	6: 85,424,548 (GRCm39)	Q134L	probably benign	Het
Pwp2	A	G	10: 78,012,170 (GRCm39)	F628L	probably benign	Het
Rab5c	C	T	11: 100,606,928 (GRCm39)	G217D	probably benign	Het
Rad51ap2	G	T	12: 11,506,807 (GRCm39)	S243I	possibly damaging	Het
Rasgrp4	C	A	7: 28,847,855 (GRCm39)	R432S	probably damaging	Het
Rhot2	C	T	17: 26,061,402 (GRCm39)		probably null	Het
Scn2a	T	A	2: 65,594,113 (GRCm39)	L1654Q	probably damaging	Het
Skint6	A	T	4: 112,711,686 (GRCm39)		probably null	Het
Slc25a24	G	T	3: 109,065,960 (GRCm39)	Q272H	probably null	Het
Slc3a1	A	T	17: 85,339,873 (GRCm39)	I144F	probably damaging	Het
Smg9	C	T	7: 24,105,495 (GRCm39)	R176C	possibly damaging	Het
Sorl1	A	T	9: 41,948,499 (GRCm39)	L762Q	probably damaging	Het
Srebf2	C	A	15: 82,088,270 (GRCm39)	P1079T	probably benign	Het
Sub1	A	T	15: 11,993,937 (GRCm39)	S4T	probably benign	Het
Tacr1	A	T	6: 82,469,692 (GRCm39)	Y192F	probably benign	Het
Tm4sf19	A	T	16: 32,224,814 (GRCm39)	H54L	probably damaging	Het
Tnxb	T	C	17: 34,914,428 (GRCm39)	L1838P	probably damaging	Het
Trmt1l	T	C	1: 151,333,539 (GRCm39)	S681P	possibly damaging	Het
Ttn	A	G	2: 76,738,176 (GRCm39)	V4167A	unknown	Het
Unc13d	T	A	11: 115,959,056 (GRCm39)	M702L	probably benign	Het
Vgll3	A	G	16: 65,636,404 (GRCm39)	H240R	probably benign	Het
Vmn1r189	C	G	13: 22,286,737 (GRCm39)	W33C	probably benign	Het
Vmn2r17	G	A	5: 109,576,337 (GRCm39)	A403T	possibly damaging	Het
Vmn2r2	G	A	3: 64,033,998 (GRCm39)	T508I	probably benign	Het
Vps54	T	A	11: 21,227,670 (GRCm39)		probably null	Het
Wfs1	G	A	5: 37,125,134 (GRCm39)	Q586*	probably null	Het
Zbp1	A	T	2: 173,055,665 (GRCm39)	H166Q	unknown	Het
Zcchc3	G	A	2: 152,256,294 (GRCm39)	A135V	probably benign	Het
Zfp51	T	C	17: 21,683,960 (GRCm39)	Y192H	probably benign	Het
Zkscan2	T	C	7: 123,088,994 (GRCm39)	T426A	probably benign	Het

Other mutations in Slc22a28

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00155:Slc22a28	APN	19	8,107,567 (GRCm39)	missense	possibly damaging	0.89
IGL00515:Slc22a28	APN	19	8,094,428 (GRCm39)	missense	probably benign	0.34
IGL01025:Slc22a28	APN	19	8,094,272 (GRCm39)	splice site	probably benign
IGL02697:Slc22a28	APN	19	8,094,491 (GRCm39)	missense	probably benign	0.06
PIT4378001:Slc22a28	UTSW	19	8,049,279 (GRCm39)	missense	probably damaging	0.96
R0744:Slc22a28	UTSW	19	8,094,197 (GRCm39)	missense	possibly damaging	0.94
R0836:Slc22a28	UTSW	19	8,094,197 (GRCm39)	missense	possibly damaging	0.94
R1398:Slc22a28	UTSW	19	8,107,566 (GRCm39)	nonsense	probably null
R1456:Slc22a28	UTSW	19	8,049,223 (GRCm39)	missense	possibly damaging	0.50
R1603:Slc22a28	UTSW	19	8,040,674 (GRCm39)	missense	probably damaging	1.00
R1993:Slc22a28	UTSW	19	8,094,488 (GRCm39)	missense	possibly damaging	0.79
R2254:Slc22a28	UTSW	19	8,041,858 (GRCm39)	missense	probably benign
R2262:Slc22a28	UTSW	19	8,048,573 (GRCm39)	missense	probably benign	0.00
R4078:Slc22a28	UTSW	19	8,078,777 (GRCm39)	missense	probably benign	0.15
R4165:Slc22a28	UTSW	19	8,040,773 (GRCm39)	missense	possibly damaging	0.95
R4612:Slc22a28	UTSW	19	8,078,770 (GRCm39)	missense	probably damaging	1.00
R4947:Slc22a28	UTSW	19	8,108,816 (GRCm39)	missense	probably benign	0.03
R5573:Slc22a28	UTSW	19	8,048,462 (GRCm39)	missense	possibly damaging	0.50
R5611:Slc22a28	UTSW	19	8,040,698 (GRCm39)	missense	probably damaging	1.00
R5621:Slc22a28	UTSW	19	8,048,376 (GRCm39)	missense	probably benign	0.00
R5671:Slc22a28	UTSW	19	8,108,795 (GRCm39)	missense	probably damaging	1.00
R6063:Slc22a28	UTSW	19	8,094,386 (GRCm39)	missense	probably benign	0.01
R6358:Slc22a28	UTSW	19	8,049,253 (GRCm39)	missense	probably damaging	0.99
R6385:Slc22a28	UTSW	19	8,078,844 (GRCm39)	missense	probably damaging	0.99
R6680:Slc22a28	UTSW	19	8,078,757 (GRCm39)	missense	probably benign	0.07
R6767:Slc22a28	UTSW	19	8,094,409 (GRCm39)	missense	probably damaging	1.00
R6865:Slc22a28	UTSW	19	8,041,856 (GRCm39)	nonsense	probably null
R6947:Slc22a28	UTSW	19	8,041,875 (GRCm39)	missense	possibly damaging	0.58
R7049:Slc22a28	UTSW	19	8,049,270 (GRCm39)	missense	probably benign
R7484:Slc22a28	UTSW	19	8,048,492 (GRCm39)	missense	probably benign
R7823:Slc22a28	UTSW	19	8,041,890 (GRCm39)	missense	probably benign	0.38
R7856:Slc22a28	UTSW	19	8,040,698 (GRCm39)	missense	probably damaging	1.00
R7980:Slc22a28	UTSW	19	8,078,837 (GRCm39)	missense	probably damaging	0.99
R8323:Slc22a28	UTSW	19	8,108,788 (GRCm39)	missense	probably damaging	1.00
R8404:Slc22a28	UTSW	19	8,108,793 (GRCm39)	nonsense	probably null
R8435:Slc22a28	UTSW	19	8,048,565 (GRCm39)	missense	probably benign	0.13
R8529:Slc22a28	UTSW	19	8,040,778 (GRCm39)	missense	probably benign	0.01
R9149:Slc22a28	UTSW	19	8,049,205 (GRCm39)	missense	probably benign	0.00
R9727:Slc22a28	UTSW	19	8,108,818 (GRCm39)	missense	probably benign
R9782:Slc22a28	UTSW	19	8,041,813 (GRCm39)	missense	probably null	1.00
Z1088:Slc22a28	UTSW	19	8,039,763 (GRCm39)	missense	probably damaging	0.96
Z1176:Slc22a28	UTSW	19	8,039,748 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- CAAGACCTAAGTTTGAGCAAGG -3'
(R):5'- TGGCATGAGTTAGTCAAATTTCTGG -3'

Sequencing Primer
(F):5'- CTAAGTTTGAGCAAGGGCCCATTTC -3'
(R):5'- GCAAACCGAATTGTTCCTC -3'

Posted On

2019-06-26