Mutagenetix > Incidental Mutation

Incidental Mutation 'R9230:Slc38a10'

700186

Institutional Source

Beutler Lab

Gene Symbol

Slc38a10

Ensembl Gene

ENSMUSG00000061306

Gene Name

solute carrier family 38, member 10

Synonyms

1810073N04Rik

MMRRC Submission

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R9230 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

119994786-120042172 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 119996781 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Valine at position 772 (D772V)

Ref Sequence

ENSEMBL: ENSMUSP00000099307 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000045402] [ENSMUST00000103018] [ENSMUST00000179094]

AlphaFold

Q5I012

Predicted Effect

probably benign
Transcript: ENSMUST00000045402
AA Change: D764V

PolyPhen 2 Score 0.305 (Sensitivity: 0.90; Specificity: 0.89)

SMART Domains

Protein: ENSMUSP00000048675
Gene: ENSMUSG00000061306
AA Change: D764V

Domain	Start	End	E-Value	Type
Pfam:Aa_trans	4	398	1.5e-54	PFAM
low complexity region	546	563	N/A	INTRINSIC
low complexity region	654	667	N/A	INTRINSIC
coiled coil region	699	735	N/A	INTRINSIC
low complexity region	827	837	N/A	INTRINSIC
low complexity region	1011	1019	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000103018
AA Change: D772V

PolyPhen 2 Score 0.203 (Sensitivity: 0.92; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000099307
Gene: ENSMUSG00000061306
AA Change: D772V

Domain	Start	End	E-Value	Type
Pfam:Aa_trans	4	398	8.5e-55	PFAM
low complexity region	546	563	N/A	INTRINSIC
low complexity region	654	667	N/A	INTRINSIC
coiled coil region	707	743	N/A	INTRINSIC
low complexity region	835	845	N/A	INTRINSIC
low complexity region	1019	1027	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000179094
AA Change: D772V

PolyPhen 2 Score 0.183 (Sensitivity: 0.92; Specificity: 0.87)

SMART Domains

Protein: ENSMUSP00000136719
Gene: ENSMUSG00000061306
AA Change: D772V

Domain	Start	End	E-Value	Type
Pfam:Aa_trans	4	398	1e-54	PFAM
low complexity region	546	563	N/A	INTRINSIC
low complexity region	654	667	N/A	INTRINSIC
coiled coil region	707	743	N/A	INTRINSIC
low complexity region	835	845	N/A	INTRINSIC
low complexity region	1019	1027	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

100% (68/68)

MGI Phenotype

PHENOTYPE: Homozygous null mice exhibit a fragile skeleton, reduced adiposity, lean body mass, body weight/length, long bone length and bone mineral density, increased creatinine levels, reduced amylase and serum albumin levels, increased energy efficiency and oxygen consumption, and altered liver physiology. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 68 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adarb1	A	T	10: 77,157,626 (GRCm39)	F274I	probably damaging	Het
Aen	T	A	7: 78,552,107 (GRCm39)	D22E	probably damaging	Het
Appl1	T	C	14: 26,645,692 (GRCm39)	E706G	unknown	Het
Arhgap21	T	C	2: 20,860,469 (GRCm39)	T1313A	possibly damaging	Het
Armc2	T	C	10: 41,823,935 (GRCm39)	Y511C	probably damaging	Het
Bsn	T	C	9: 107,989,459 (GRCm39)	T2098A	probably damaging	Het
Cacna1h	T	C	17: 25,599,856 (GRCm39)	Y1659C	probably damaging	Het
Catsperb	T	C	12: 101,516,053 (GRCm39)	I563T	probably benign	Het
Cblif	G	A	19: 11,737,748 (GRCm39)	W386*	probably null	Het
Cd180	TA	TAA	13: 102,841,514 (GRCm39)		probably null	Het
Cd55b	A	T	1: 130,350,619 (GRCm39)	L26*	probably null	Het
Cdc42bpa	A	G	1: 179,933,638 (GRCm39)	N759S	probably benign	Het
Chrm3	C	A	13: 9,928,479 (GRCm39)	V186L	probably benign	Het
Clrn2	A	G	5: 45,621,283 (GRCm39)	T226A	probably damaging	Het
Col3a1	C	T	1: 45,383,138 (GRCm39)	P1071S	unknown	Het
Csgalnact2	A	G	6: 118,103,212 (GRCm39)	L250P	probably damaging	Het
Cyp4a31	G	T	4: 115,428,281 (GRCm39)	E326*	probably null	Het
Def8	A	G	8: 124,186,317 (GRCm39)	E352G	probably benign	Het
Dmbt1	A	G	7: 130,639,642 (GRCm39)	D60G	probably benign	Het
Dock3	A	G	9: 106,807,223 (GRCm39)	L1368P	probably damaging	Het
Dytn	A	T	1: 63,686,611 (GRCm39)	V353D	probably benign	Het
Egfem1	G	A	3: 29,411,317 (GRCm39)	E155K	probably benign	Het
Eif3m	A	T	2: 104,831,705 (GRCm39)	M285K	probably damaging	Het
Fam135b	T	C	15: 71,335,856 (GRCm39)	K446R	probably benign	Het
Fbxo22	T	C	9: 55,116,442 (GRCm39)	L36P	probably damaging	Het
Frmd4a	T	C	2: 4,612,844 (GRCm39)	S1025P	possibly damaging	Het
Gja8	C	T	3: 96,826,664 (GRCm39)	V333M	possibly damaging	Het
Glis1	T	C	4: 107,425,327 (GRCm39)	S313P	probably benign	Het
Grid2ip	G	A	5: 143,359,194 (GRCm39)	R270Q	probably damaging	Het
Hps4	G	A	5: 112,525,905 (GRCm39)	S642N	possibly damaging	Het
Hspa4	T	C	11: 53,171,466 (GRCm39)	E246G	probably benign	Het
Ibtk	A	G	9: 85,585,702 (GRCm39)		probably null	Het
Ifit1	A	G	19: 34,625,236 (GRCm39)	E124G	possibly damaging	Het
Ifna14	T	C	4: 88,489,752 (GRCm39)	D95G	probably benign	Het
Igsf10	G	A	3: 59,243,843 (GRCm39)	R164W	probably damaging	Het
Ilkap	A	C	1: 91,314,937 (GRCm39)	I142S	probably benign	Het
Insyn2a	A	T	7: 134,520,439 (GRCm39)	Y30*	probably null	Het
Kctd14	C	G	7: 97,104,104 (GRCm39)	P53R	unknown	Het
Kndc1	A	T	7: 139,500,600 (GRCm39)	D655V	probably damaging	Het
Krt1c	A	C	15: 101,725,948 (GRCm39)	S197A	probably benign	Het
Lpin1	A	T	12: 16,588,483 (GRCm39)	S902R	unknown	Het
Mapk13	T	C	17: 28,994,532 (GRCm39)	I141T	probably damaging	Het
Micall2	A	G	5: 139,701,827 (GRCm39)	V472A	unknown	Het
Mmp15	T	C	8: 96,092,959 (GRCm39)	F113L	probably benign	Het
Msantd5f6	C	T	4: 73,319,685 (GRCm39)	A264T	probably benign	Het
Msh2	T	G	17: 88,026,717 (GRCm39)	S738A	probably benign	Het
Muc20	T	G	16: 32,613,584 (GRCm39)	T598P	probably damaging	Het
Myo1f	T	C	17: 33,795,424 (GRCm39)	V53A	probably damaging	Het
Ncf1	A	T	5: 134,250,718 (GRCm39)	N367K	probably benign	Het
Nme8	T	G	13: 19,874,384 (GRCm39)	I139L	probably benign	Het
Odam	T	C	5: 88,034,457 (GRCm39)	F46L	probably benign	Het
Or51a25	C	A	7: 102,372,795 (GRCm39)	V301F	possibly damaging	Het
Or7a42	G	A	10: 78,791,929 (GRCm39)	D297N	possibly damaging	Het
Pcare	A	G	17: 72,057,217 (GRCm39)	L820P	probably damaging	Het
Pi4ka	A	G	16: 17,099,788 (GRCm39)	I1945T		Het
Rbmyf9	T	G	Y: 3,774,819 (GRCm39)	D5E	probably damaging	Het
Rell1	T	C	5: 64,097,105 (GRCm39)		probably benign	Het
Ripk3	A	G	14: 56,023,303 (GRCm39)	F134S	probably benign	Het
Sclt1	A	T	3: 41,665,631 (GRCm39)	W146R	probably benign	Het
Slc18a2	T	C	19: 59,261,647 (GRCm39)	M178T	probably benign	Het
Slc24a5	G	T	2: 124,922,568 (GRCm39)	G110V	probably damaging	Het
Slc9c1	T	C	16: 45,398,275 (GRCm39)	L680P	possibly damaging	Het
Tll2	T	A	19: 41,093,436 (GRCm39)	Y477F	probably benign	Het
Tmco1	C	T	1: 167,136,132 (GRCm39)		probably benign	Het
Tnrc18	G	T	5: 142,773,392 (GRCm39)	A479D		Het
Topaz1	T	A	9: 122,596,097 (GRCm39)	M956K	probably benign	Het
Vmn2r56	T	A	7: 12,444,237 (GRCm39)	D465V	possibly damaging	Het
Xndc1	T	A	7: 101,722,476 (GRCm39)	V47E	probably damaging	Het

Other mutations in Slc38a10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00228:Slc38a10	APN	11	120,029,814 (GRCm39)	missense	probably damaging	1.00
IGL00236:Slc38a10	APN	11	119,997,428 (GRCm39)	missense	probably damaging	0.96
IGL01420:Slc38a10	APN	11	119,997,286 (GRCm39)	missense	probably damaging	0.99
IGL01704:Slc38a10	APN	11	120,041,913 (GRCm39)	utr 5 prime	probably benign
IGL01747:Slc38a10	APN	11	120,025,600 (GRCm39)	splice site	probably benign
IGL02295:Slc38a10	APN	11	120,007,684 (GRCm39)	splice site	probably benign
IGL02300:Slc38a10	APN	11	120,001,116 (GRCm39)	missense	probably benign	0.00
IGL02429:Slc38a10	APN	11	120,025,714 (GRCm39)	splice site	probably benign
IGL03155:Slc38a10	APN	11	119,995,945 (GRCm39)	missense	probably damaging	0.96
IGL03396:Slc38a10	APN	11	120,019,301 (GRCm39)	missense	probably damaging	1.00
Cascade	UTSW	11	120,038,645 (GRCm39)	missense	probably damaging	1.00
cherries	UTSW	11	120,041,903 (GRCm39)	start codon destroyed	probably null	1.00
Ore	UTSW	11	120,025,679 (GRCm39)	missense	probably damaging	1.00
rainier	UTSW	11	120,020,138 (GRCm39)	nonsense	probably null
slag	UTSW	11	120,023,567 (GRCm39)	missense	probably damaging	1.00
R0048:Slc38a10	UTSW	11	120,001,138 (GRCm39)	missense	probably benign	0.11
R0068:Slc38a10	UTSW	11	120,025,679 (GRCm39)	missense	probably damaging	1.00
R0068:Slc38a10	UTSW	11	120,025,679 (GRCm39)	missense	probably damaging	1.00
R0069:Slc38a10	UTSW	11	119,997,328 (GRCm39)	missense	probably damaging	1.00
R0101:Slc38a10	UTSW	11	120,041,903 (GRCm39)	start codon destroyed	probably null	1.00
R0743:Slc38a10	UTSW	11	120,031,469 (GRCm39)	missense	probably damaging	1.00
R1159:Slc38a10	UTSW	11	119,996,301 (GRCm39)	missense	probably benign
R2101:Slc38a10	UTSW	11	120,023,567 (GRCm39)	missense	probably damaging	1.00
R2367:Slc38a10	UTSW	11	120,001,087 (GRCm39)	missense	probably benign	0.12
R4280:Slc38a10	UTSW	11	120,028,704 (GRCm39)	missense	probably damaging	1.00
R4282:Slc38a10	UTSW	11	120,020,090 (GRCm39)	missense	probably damaging	1.00
R5206:Slc38a10	UTSW	11	119,995,888 (GRCm39)	missense	probably damaging	0.99
R5658:Slc38a10	UTSW	11	119,996,218 (GRCm39)	missense	probably benign	0.11
R6114:Slc38a10	UTSW	11	120,020,138 (GRCm39)	nonsense	probably null
R6118:Slc38a10	UTSW	11	120,023,669 (GRCm39)	missense	probably damaging	1.00
R6306:Slc38a10	UTSW	11	120,038,645 (GRCm39)	missense	probably damaging	1.00
R6395:Slc38a10	UTSW	11	120,015,208 (GRCm39)	missense	probably benign	0.01
R6428:Slc38a10	UTSW	11	119,996,298 (GRCm39)	missense	probably benign	0.09
R7764:Slc38a10	UTSW	11	119,995,905 (GRCm39)	missense	probably damaging	1.00
R7835:Slc38a10	UTSW	11	120,007,822 (GRCm39)	missense	possibly damaging	0.95
R8790:Slc38a10	UTSW	11	120,023,519 (GRCm39)	missense	possibly damaging	0.95
R9151:Slc38a10	UTSW	11	120,007,762 (GRCm39)	missense	probably benign	0.00
R9227:Slc38a10	UTSW	11	119,996,781 (GRCm39)	missense	probably benign	0.20
X0062:Slc38a10	UTSW	11	120,007,726 (GRCm39)	missense	possibly damaging	0.75

Predicted Primers

PCR Primer
(F):5'- CTTCTCTCAGATCAATCGGGGC -3'
(R):5'- GGAGGTTTCAGTCTTGATCATCC -3'

Sequencing Primer
(F):5'- ATCAATCGGGGCCCCCTG -3'
(R):5'- GCAGGCATTCACACATGTTG -3'

Posted On

2022-02-07