Mutagenetix > Incidental Mutation

Incidental Mutation 'R4471:Slc5a4b'

329443

Institutional Source

Beutler Lab

Gene Symbol

Slc5a4b

Ensembl Gene

ENSMUSG00000020226

Gene Name

solute carrier family 5 (neutral amino acid transporters, system A), member 4b

Synonyms

SGLT3b, pSGLT2, 2010104G07Rik, SAAT1

MMRRC Submission

041728-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.116) question?

Stock #

R4471 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

75894452-75946852 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to A at 75894725 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Stop codon at position 594 (Q594*)

Ref Sequence

ENSEMBL: ENSMUSP00000113582 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000120757]

AlphaFold

Q91ZP4

Predicted Effect

probably null
Transcript: ENSMUST00000120757
AA Change: Q594*

SMART Domains

Protein: ENSMUSP00000113582
Gene: ENSMUSG00000020226
AA Change: Q594*

Domain	Start	End	E-Value	Type
low complexity region	16	21	N/A	INTRINSIC
Pfam:SSF	58	492	1.4e-163	PFAM
transmembrane domain	526	548	N/A	INTRINSIC
transmembrane domain	640	659	N/A	INTRINSIC

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.4%

Validation Efficiency

99% (69/70)

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Alpk1	A	G	3: 127,473,175 (GRCm39)	S943P	probably damaging	Het
Ankdd1a	T	C	9: 65,410,791 (GRCm39)	D398G	probably damaging	Het
Ankrd13b	T	A	11: 77,367,040 (GRCm39)	K49M	probably damaging	Het
Asah1	A	G	8: 41,796,761 (GRCm39)		probably null	Het
Cdc34b	A	G	11: 94,633,064 (GRCm39)	E88G	probably benign	Het
Cdh2	T	C	18: 16,907,533 (GRCm39)		probably null	Het
Ceacam1	T	A	7: 25,174,025 (GRCm39)	N210I	possibly damaging	Het
Celf3	A	G	3: 94,395,585 (GRCm39)		probably null	Het
Cfap20dc	A	G	14: 8,536,571 (GRCm38)	L212P	probably damaging	Het
Cmya5	A	T	13: 93,228,833 (GRCm39)	M2085K	probably benign	Het
Cpne6	G	A	14: 55,754,089 (GRCm39)	V469M	probably damaging	Het
Cyp2j12	A	G	4: 96,021,306 (GRCm39)	V100A	probably benign	Het
Dnajb4	A	T	3: 151,890,799 (GRCm39)	H333Q	probably benign	Het
Eif3f	T	C	7: 108,540,153 (GRCm39)	V316A	possibly damaging	Het
Eml1	T	C	12: 108,472,894 (GRCm39)		probably benign	Het
Ern1	C	A	11: 106,310,868 (GRCm39)	V302L	possibly damaging	Het
Fam110b	A	T	4: 5,799,092 (GRCm39)	H170L	probably benign	Het
Fn3krp	T	G	11: 121,317,499 (GRCm39)	D146E	probably benign	Het
Git1	A	G	11: 77,390,650 (GRCm39)	T129A	probably benign	Het
Glrp1	T	A	1: 88,431,196 (GRCm39)	Q58L	unknown	Het
Gpatch2	A	G	1: 186,965,337 (GRCm39)	E281G	probably damaging	Het
Hipk2	T	A	6: 38,713,857 (GRCm39)		probably benign	Het
Hydin	A	G	8: 111,313,764 (GRCm39)	N4214S	probably damaging	Het
Icam5	T	A	9: 20,946,802 (GRCm39)	C443*	probably null	Het
Impdh1	G	A	6: 29,204,631 (GRCm39)	Q307*	probably null	Het
Ivns1abp	C	T	1: 151,236,990 (GRCm39)	T447M	probably benign	Het
Lman1	A	T	18: 66,124,797 (GRCm39)		probably benign	Het
Mdn1	A	G	4: 32,668,860 (GRCm39)	E306G	probably benign	Het
Msc	G	C	1: 14,825,902 (GRCm39)	P24R	probably damaging	Het
Mtif2	T	C	11: 29,490,053 (GRCm39)		probably benign	Het
Mvp	C	T	7: 126,601,130 (GRCm39)	M1I	probably null	Het
Myh7	A	T	14: 55,229,311 (GRCm39)	Y162*	probably null	Het
Nemf	G	A	12: 69,361,216 (GRCm39)	H956Y	probably benign	Het
Nktr	T	C	9: 121,577,962 (GRCm39)		probably benign	Het
Nrxn3	T	C	12: 90,171,515 (GRCm39)	S276P	probably damaging	Het
Or8d1	T	C	9: 38,766,927 (GRCm39)	S190P	probably damaging	Het
Patj	A	G	4: 98,423,816 (GRCm39)	K621E	probably damaging	Het
Prss2	A	G	6: 41,499,780 (GRCm39)	I24V	probably damaging	Het
R3hcc1l	T	C	19: 42,571,259 (GRCm39)		probably benign	Het
Rest	T	C	5: 77,429,027 (GRCm39)	V482A	probably benign	Het
Rexo1	A	T	10: 80,378,492 (GRCm39)	S476T	probably damaging	Het
Rin2	C	T	2: 145,702,366 (GRCm39)	T354I	probably benign	Het
Slc16a3	T	C	11: 120,846,774 (GRCm39)		probably benign	Het
Slk	T	G	19: 47,603,862 (GRCm39)	V202G	probably damaging	Het
Smarca2	T	A	19: 26,597,277 (GRCm39)	V53D	possibly damaging	Het
Snrnp200	T	A	2: 127,080,673 (GRCm39)	V2036E	probably benign	Het
Sox5	A	G	6: 143,790,491 (GRCm39)	M523T	possibly damaging	Het
Syt17	A	G	7: 118,036,040 (GRCm39)		probably null	Het
Taf2	T	C	15: 54,922,276 (GRCm39)	D337G	possibly damaging	Het
Tcstv2a	G	T	13: 120,725,579 (GRCm39)	R81L	probably benign	Het
Tecrl	A	G	5: 83,461,134 (GRCm39)	Y108H	probably benign	Het
Tln1	A	T	4: 43,551,018 (GRCm39)	F409L	probably benign	Het
Tmem59l	A	G	8: 70,939,951 (GRCm39)	L6S	unknown	Het
Ttc23	G	A	7: 67,319,904 (GRCm39)	R187Q	probably benign	Het
Ttl	T	C	2: 128,923,977 (GRCm39)	V230A	probably benign	Het
Ube2u	G	A	4: 100,338,843 (GRCm39)	W36*	probably null	Het
Ube4a	A	T	9: 44,857,830 (GRCm39)		probably benign	Het
Ulk1	C	T	5: 110,937,223 (GRCm39)	R691Q	probably benign	Het
Unc45a	A	G	7: 79,982,728 (GRCm39)	I399T	possibly damaging	Het
Utp25	C	T	1: 192,812,445 (GRCm39)	R5Q	possibly damaging	Het
Wdr59	A	C	8: 112,193,419 (GRCm39)		probably null	Het
Zfp24	A	G	18: 24,151,172 (GRCm39)		probably benign	Het
Zfp777	A	T	6: 48,019,041 (GRCm39)	W342R	probably damaging	Het
Zfp979	A	T	4: 147,697,913 (GRCm39)	C265*	probably null	Het
Zzef1	T	A	11: 72,804,157 (GRCm39)	L2633Q	probably damaging	Het

Other mutations in Slc5a4b

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01348:Slc5a4b	APN	10	75,906,422 (GRCm39)	missense	probably damaging	1.00
IGL01433:Slc5a4b	APN	10	75,906,329 (GRCm39)	splice site	probably benign
IGL01754:Slc5a4b	APN	10	75,906,449 (GRCm39)	missense	probably damaging	1.00
IGL01904:Slc5a4b	APN	10	75,896,260 (GRCm39)	missense	probably damaging	0.98
IGL01990:Slc5a4b	APN	10	75,896,188 (GRCm39)	missense	probably benign	0.01
IGL02211:Slc5a4b	APN	10	75,896,297 (GRCm39)	splice site	probably benign
IGL02254:Slc5a4b	APN	10	75,896,264 (GRCm39)	missense	probably benign
IGL02389:Slc5a4b	APN	10	75,908,299 (GRCm39)	nonsense	probably null
IGL02427:Slc5a4b	APN	10	75,894,713 (GRCm39)	missense	possibly damaging	0.47
IGL02493:Slc5a4b	APN	10	75,910,849 (GRCm39)	missense	probably damaging	1.00
IGL02554:Slc5a4b	APN	10	75,946,685 (GRCm39)	missense	possibly damaging	0.75
IGL02670:Slc5a4b	APN	10	75,910,934 (GRCm39)	missense	probably damaging	1.00
R0254:Slc5a4b	UTSW	10	75,906,462 (GRCm39)	missense	possibly damaging	0.55
R0285:Slc5a4b	UTSW	10	75,898,117 (GRCm39)	missense	probably damaging	0.99
R0294:Slc5a4b	UTSW	10	75,917,161 (GRCm39)	missense	probably damaging	1.00
R0522:Slc5a4b	UTSW	10	75,926,534 (GRCm39)	missense	probably damaging	0.99
R0601:Slc5a4b	UTSW	10	75,899,870 (GRCm39)	missense	possibly damaging	0.81
R0714:Slc5a4b	UTSW	10	75,917,341 (GRCm39)	missense	probably benign	0.09
R0975:Slc5a4b	UTSW	10	75,917,241 (GRCm39)	missense	probably benign	0.09
R1934:Slc5a4b	UTSW	10	75,917,307 (GRCm39)	missense	possibly damaging	0.51
R2339:Slc5a4b	UTSW	10	75,944,383 (GRCm39)	missense	probably damaging	1.00
R2886:Slc5a4b	UTSW	10	75,910,907 (GRCm39)	missense	probably damaging	0.98
R3552:Slc5a4b	UTSW	10	75,917,358 (GRCm39)	missense	probably damaging	0.99
R3890:Slc5a4b	UTSW	10	75,898,094 (GRCm39)	missense	probably benign	0.01
R4012:Slc5a4b	UTSW	10	75,910,826 (GRCm39)	missense	probably damaging	1.00
R4259:Slc5a4b	UTSW	10	75,939,686 (GRCm39)	missense	probably damaging	1.00
R4260:Slc5a4b	UTSW	10	75,939,686 (GRCm39)	missense	probably damaging	1.00
R4667:Slc5a4b	UTSW	10	75,910,879 (GRCm39)	missense	possibly damaging	0.78
R4846:Slc5a4b	UTSW	10	75,898,073 (GRCm39)	missense	probably damaging	0.99
R4939:Slc5a4b	UTSW	10	75,917,301 (GRCm39)	missense	probably benign	0.44
R5181:Slc5a4b	UTSW	10	75,896,221 (GRCm39)	nonsense	probably null
R5319:Slc5a4b	UTSW	10	75,898,233 (GRCm39)	missense	probably benign	0.08
R6306:Slc5a4b	UTSW	10	75,917,185 (GRCm39)	missense	probably benign	0.01
R6422:Slc5a4b	UTSW	10	75,939,696 (GRCm39)	missense	probably damaging	0.97
R6837:Slc5a4b	UTSW	10	75,898,220 (GRCm39)	missense	possibly damaging	0.49
R6997:Slc5a4b	UTSW	10	75,925,812 (GRCm39)	missense	probably damaging	0.97
R7140:Slc5a4b	UTSW	10	75,910,943 (GRCm39)	missense	probably damaging	1.00
R7527:Slc5a4b	UTSW	10	75,946,742 (GRCm39)	missense	probably benign	0.01
R7683:Slc5a4b	UTSW	10	75,899,906 (GRCm39)	missense	probably damaging	0.96
R7718:Slc5a4b	UTSW	10	75,906,407 (GRCm39)	missense	probably damaging	1.00
R7794:Slc5a4b	UTSW	10	75,898,133 (GRCm39)	missense	probably benign	0.19
R7877:Slc5a4b	UTSW	10	75,910,886 (GRCm39)	missense	probably damaging	1.00
R8150:Slc5a4b	UTSW	10	75,939,680 (GRCm39)	missense	possibly damaging	0.93
R8843:Slc5a4b	UTSW	10	75,910,925 (GRCm39)	missense	probably damaging	1.00
R9111:Slc5a4b	UTSW	10	75,925,827 (GRCm39)	splice site	probably benign
R9163:Slc5a4b	UTSW	10	75,917,165 (GRCm39)	nonsense	probably null
R9195:Slc5a4b	UTSW	10	75,898,149 (GRCm39)	missense	probably damaging	1.00
R9600:Slc5a4b	UTSW	10	75,896,239 (GRCm39)	missense	probably damaging	1.00
R9643:Slc5a4b	UTSW	10	75,945,896 (GRCm39)	missense	probably benign	0.01
R9656:Slc5a4b	UTSW	10	75,944,391 (GRCm39)	missense	probably damaging	0.98
R9699:Slc5a4b	UTSW	10	75,946,674 (GRCm39)	missense	probably damaging	0.99
X0019:Slc5a4b	UTSW	10	75,946,685 (GRCm39)	missense	possibly damaging	0.75

Predicted Primers

PCR Primer
(F):5'- AGTTTCTGCTTCCTTCAGGG -3'
(R):5'- ATGTGATCCGCTGTACTATTGG -3'

Sequencing Primer
(F):5'- CTTCCTTCAGGGTTCAGGCAAAATAG -3'
(R):5'- GAAGGTCCGGAGTTCAAATCCC -3'

Posted On

2015-07-21