Mutagenetix > Incidental Mutation

Incidental Mutation 'R6395:Slc38a10'

514739

Institutional Source

Beutler Lab

Gene Symbol

Slc38a10

Ensembl Gene

ENSMUSG00000061306

Gene Name

solute carrier family 38, member 10

Synonyms

1810073N04Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R6395 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

119994786-120042172 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 120015208 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 381 (S381P)

Ref Sequence

ENSEMBL: ENSMUSP00000057615 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000045402] [ENSMUST00000053692] [ENSMUST00000076697] [ENSMUST00000103018] [ENSMUST00000179094]

AlphaFold

Q5I012

Predicted Effect

probably benign
Transcript: ENSMUST00000045402

SMART Domains

Protein: ENSMUSP00000048675
Gene: ENSMUSG00000061306

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: ENSMUST00000053692
AA Change: S381P

PolyPhen 2 Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)

SMART Domains

Protein: ENSMUSP00000057615
Gene: ENSMUSG00000061306
AA Change: S381P

Domain	Start	End	E-Value	Type
Pfam:Aa_trans	4	381	8.6e-57	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000076697

SMART Domains

Protein: ENSMUSP00000075989
Gene: ENSMUSG00000061306

Domain	Start	End	E-Value	Type
Pfam:Aa_trans	4	389	4.7e-57	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000103018

SMART Domains

Protein: ENSMUSP00000099307
Gene: ENSMUSG00000061306

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

noncoding transcript
Transcript: ENSMUST00000154444

Predicted Effect

probably benign
Transcript: ENSMUST00000179094

SMART Domains

Protein: ENSMUSP00000136719
Gene: ENSMUSG00000061306

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: 99.6%
20x: 98.3%

Validation Efficiency

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: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Actc1	C	A	2: 113,879,731 (GRCm39)	E243*	probably null	Het
Ahi1	T	C	10: 20,855,491 (GRCm39)	I600T	possibly damaging	Het
Apob	A	G	12: 8,058,507 (GRCm39)	T2330A	probably benign	Het
Cabin1	A	T	10: 75,582,576 (GRCm39)	M280K	probably benign	Het
Ccdc117	T	C	11: 5,484,762 (GRCm39)		probably null	Het
Cct8	G	T	16: 87,283,364 (GRCm39)	Y292*	probably null	Het
Celf1	A	G	2: 90,834,203 (GRCm39)	I165V	probably benign	Het
Cenpc1	A	T	5: 86,183,429 (GRCm39)	N453K	probably benign	Het
Chst10	T	C	1: 38,910,770 (GRCm39)	I131M	probably damaging	Het
Cltc	A	G	11: 86,616,006 (GRCm39)	I420T	probably damaging	Het
Cspg4b	T	G	13: 113,506,003 (GRCm39)	C2377W	probably damaging	Het
Dact3	A	C	7: 16,617,086 (GRCm39)	Q95P	probably damaging	Het
Dennd2c	T	C	3: 103,056,540 (GRCm39)		probably null	Het
Dock2	G	T	11: 34,182,874 (GRCm39)	H1586Q	probably damaging	Het
Dst	T	C	1: 34,221,771 (GRCm39)	M2525T	probably benign	Het
Egflam	T	C	15: 7,261,176 (GRCm39)	H786R	probably damaging	Het
Eml6	T	C	11: 29,759,321 (GRCm39)	T811A	probably benign	Het
Epha1	T	C	6: 42,343,106 (GRCm39)	T148A	probably damaging	Het
Fsip1	A	C	2: 118,067,406 (GRCm39)	S306A	probably damaging	Het
Gga2	A	T	7: 121,607,661 (GRCm39)		probably null	Het
Gm10801	C	CGTT	2: 98,494,152 (GRCm39)		probably benign	Het
Gm9837	T	A	11: 53,360,885 (GRCm39)		probably benign	Het
Gnl2	A	T	4: 124,940,058 (GRCm39)	Q310L	probably damaging	Het
H2-M1	T	C	17: 36,982,701 (GRCm39)	D53G	probably benign	Het
Hmcn2	T	A	2: 31,259,269 (GRCm39)	D1036E	probably damaging	Het
Htr3a	A	T	9: 48,811,871 (GRCm39)	D381E	probably benign	Het
Igdcc4	G	A	9: 65,042,400 (GRCm39)	G106R	probably damaging	Het
Igfbp2	A	G	1: 72,864,078 (GRCm39)	T114A	probably damaging	Het
Ints14	A	G	9: 64,885,406 (GRCm39)		probably null	Het
Kcnt1	T	A	2: 25,799,251 (GRCm39)	M906K	possibly damaging	Het
Kif13a	C	T	13: 46,905,931 (GRCm39)	V671M	possibly damaging	Het
Lars2	A	G	9: 123,200,990 (GRCm39)	Q18R	probably benign	Het
Mndal	C	T	1: 173,698,999 (GRCm39)	C222Y	possibly damaging	Het
Msto1	C	T	3: 88,812,781 (GRCm39)	A1854V	possibly damaging	Het
Musk	G	A	4: 58,286,169 (GRCm39)	G20R	probably benign	Het
Or6c215	G	T	10: 129,638,013 (GRCm39)	P127Q	probably damaging	Het
Oxct1	G	T	15: 4,056,309 (GRCm39)	S19I	possibly damaging	Het
Papss2	G	A	19: 32,641,876 (GRCm39)	G517D	probably damaging	Het
Parp14	T	C	16: 35,676,918 (GRCm39)	S1017G	probably benign	Het
Pde2a	A	G	7: 101,150,242 (GRCm39)	Q227R	probably benign	Het
Pdlim5	G	T	3: 142,020,183 (GRCm39)	P92Q	probably damaging	Het
Pkd1l3	C	T	8: 110,350,595 (GRCm39)	T480I	probably benign	Het
Pla2g4c	C	T	7: 13,077,933 (GRCm39)	T357I	probably benign	Het
Ppp3ca	A	G	3: 136,583,531 (GRCm39)	R213G	possibly damaging	Het
Pramel18	G	A	4: 101,767,189 (GRCm39)	R146H	probably benign	Het
Prrc1	C	T	18: 57,495,619 (GRCm39)	S32L	probably null	Het
Prss47	C	T	13: 65,197,116 (GRCm39)	V207I	probably benign	Het
Prtg	G	A	9: 72,819,414 (GRCm39)	V1136I	possibly damaging	Het
Psmb8	T	A	17: 34,418,265 (GRCm39)	M69K	possibly damaging	Het
Rb1	A	T	14: 73,436,636 (GRCm39)	D876E	probably damaging	Het
Rnasel	T	C	1: 153,637,867 (GRCm39)	M680T	probably damaging	Het
Rnf111	G	T	9: 70,383,692 (GRCm39)	N80K	possibly damaging	Het
Senp1	C	T	15: 97,946,074 (GRCm39)	C557Y	probably damaging	Het
Serpina3a	A	T	12: 104,082,710 (GRCm39)	Y161F	probably damaging	Het
Serpinb11	A	T	1: 107,299,781 (GRCm39)		probably null	Het
Sgpl1	C	A	10: 60,947,936 (GRCm39)		probably null	Het
Slc37a4	A	G	9: 44,310,576 (GRCm39)	Y60C	probably damaging	Het
Slc5a7	C	T	17: 54,585,849 (GRCm39)	V323I	probably damaging	Het
Slco1a7	T	A	6: 141,668,818 (GRCm39)		probably null	Het
Smarcal1	A	T	1: 72,655,716 (GRCm39)	E665V	possibly damaging	Het
Specc1	C	A	11: 62,023,164 (GRCm39)	N736K	probably damaging	Het
Tas2r121	T	C	6: 132,677,495 (GRCm39)	Y159C	probably benign	Het
Tex54	A	G	19: 8,718,462 (GRCm39)	D68G	probably benign	Het
Trank1	A	G	9: 111,196,268 (GRCm39)	I1431V	probably damaging	Het
Ttll6	T	C	11: 96,047,414 (GRCm39)	V671A	probably benign	Het
Ttn	A	T	2: 76,748,931 (GRCm39)		probably benign	Het
Uimc1	T	C	13: 55,188,389 (GRCm39)	T557A	possibly damaging	Het
Uri1	C	A	7: 37,661,974 (GRCm39)	V446L	probably benign	Het
Vpreb1b	C	T	16: 17,798,771 (GRCm39)	R86C	probably damaging	Het
Vwa8	A	G	14: 79,331,184 (GRCm39)	K1231E	probably benign	Het
Xcr1	G	A	9: 123,684,854 (GRCm39)	R303C	probably damaging	Het
Zfp619	C	A	7: 39,186,454 (GRCm39)	A828E	possibly damaging	Het
Zfp687	T	C	3: 94,915,049 (GRCm39)	S1151G	possibly 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
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
R9230: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'- CCGCACACCAGAGTATTAGC -3'
(R):5'- GGGCCTAAAGTCACAAACTGG -3'

Sequencing Primer
(F):5'- GAACAGAGACGTTCGTTTATCGCTC -3'
(R):5'- CCTGCCTTTCAGTGTGAGGC -3'

Posted On

2018-05-04