Mutagenetix > Incidental Mutation

Incidental Mutation 'R5162:H2-T10'

397077

Institutional Source

Beutler Lab

Gene Symbol

H2-T10

Ensembl Gene

ENSMUSG00000079491

Gene Name

histocompatibility 2, T region locus 10

Synonyms

H-2T10

MMRRC Submission

042744-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.069) question?

Stock #

R5162 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

36426763-36432336 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to A at 36429843 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000134339 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000046131] [ENSMUST00000166442] [ENSMUST00000173128] [ENSMUST00000174382]

AlphaFold

F6T1I5

Predicted Effect

probably benign
Transcript: ENSMUST00000046131

SMART Domains

Protein: ENSMUSP00000040558
Gene: ENSMUSG00000092243

Domain	Start	End	E-Value	Type
signal peptide	1	23	N/A	INTRINSIC
Pfam:MHC_I	26	204	2.3e-81	PFAM
IGc1	220	285	8.12e-13	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000166442
AA Change: M317L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000127602
Gene: ENSMUSG00000079491
AA Change: M317L

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
Pfam:MHC_I	29	191	6.2e-49	PFAM
IGc1	210	281	4.18e-24	SMART
transmembrane domain	294	313	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000173128

SMART Domains

Protein: ENSMUSP00000134339
Gene: ENSMUSG00000092277

Domain	Start	End	E-Value	Type
low complexity region	103	115	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000174382

SMART Domains

Protein: ENSMUSP00000133893
Gene: ENSMUSG00000079491

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
Pfam:MHC_I	29	205	9.5e-47	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000174625

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000174728

Meta Mutation Damage Score

0.4797

Coding Region Coverage

1x: 99.3%
3x: 98.6%
10x: 97.2%
20x: 94.8%

Validation Efficiency

98% (61/62)

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2010315B03Rik	T	A	9: 124,056,301 (GRCm39)	T229S	probably benign	Het
Adrb3	T	C	8: 27,717,348 (GRCm39)	E367G	probably benign	Het
Ak9	T	A	10: 41,233,653 (GRCm39)	N630K	probably damaging	Het
Atp8b1	T	C	18: 64,694,733 (GRCm39)	I516M	possibly damaging	Het
Bcor	C	T	X: 11,906,725 (GRCm39)	R1551Q	probably damaging	Het
Cry1	T	A	10: 84,969,150 (GRCm39)	H558L	probably benign	Het
Cstdc3	A	T	16: 36,132,918 (GRCm39)	H65L	probably damaging	Het
Cyp3a57	T	A	5: 145,305,893 (GRCm39)	W126R	probably damaging	Het
Dhx36	A	T	3: 62,401,201 (GRCm39)	V355E	probably damaging	Het
Dpp6	A	G	5: 27,604,013 (GRCm39)		probably benign	Het
Ehmt1	G	T	2: 24,767,509 (GRCm39)	P135T	probably damaging	Het
Enpp2	T	C	15: 54,710,692 (GRCm39)	D694G	probably benign	Het
Esrp2	T	C	8: 106,859,930 (GRCm39)	E336G	probably damaging	Het
Faah	A	T	4: 115,857,938 (GRCm39)		probably benign	Het
Fat1	G	A	8: 45,478,846 (GRCm39)	G2608R	probably benign	Het
Fbxo8	A	T	8: 57,022,354 (GRCm39)	Y122F	probably damaging	Het
Fgd5	A	G	6: 92,051,215 (GRCm39)	D1497G	probably damaging	Het
Fn3krp	T	C	11: 121,320,410 (GRCm39)	F252L	probably damaging	Het
Fnip2	T	C	3: 79,389,084 (GRCm39)	Y549C	probably damaging	Het
Gcm2	T	C	13: 41,257,131 (GRCm39)	N206S	probably benign	Het
Grn	C	A	11: 102,321,380 (GRCm39)		probably benign	Het
Henmt1	T	C	3: 108,847,366 (GRCm39)		probably null	Het
Man1b1	T	A	2: 25,233,365 (GRCm39)	L246Q	probably damaging	Het
Mdh2	T	C	5: 135,812,329 (GRCm39)		probably null	Het
Mocos	T	C	18: 24,787,109 (GRCm39)	F43L	probably damaging	Het
Msh2	C	A	17: 88,030,841 (GRCm39)	A906E	probably benign	Het
Naip5	T	A	13: 100,359,914 (GRCm39)	I441F	possibly damaging	Het
Naip6	C	T	13: 100,437,108 (GRCm39)	A472T	probably benign	Het
Nars2	T	C	7: 96,709,027 (GRCm39)		probably benign	Het
Ncoa2	A	T	1: 13,245,396 (GRCm39)	M434K	possibly damaging	Het
Nlrp4g	T	A	9: 124,350,394 (GRCm38)		noncoding transcript	Het
Or14j8	T	A	17: 38,263,255 (GRCm39)	Q220L	probably benign	Het
Or9a2	G	T	6: 41,748,706 (GRCm39)	H176N	possibly damaging	Het
Pals2	T	A	6: 50,155,495 (GRCm39)	W259R	probably damaging	Het
Pars2	A	G	4: 106,511,735 (GRCm39)	T506A	probably benign	Het
Pkp2	T	C	16: 16,078,200 (GRCm39)	S481P	probably damaging	Het
Plod3	T	C	5: 137,020,161 (GRCm39)	W459R	probably damaging	Het
Pramel13	A	T	4: 144,121,482 (GRCm39)	L181M	probably damaging	Het
Prdm10	A	T	9: 31,251,714 (GRCm39)	I361F	possibly damaging	Het
Ptpro	T	A	6: 137,420,592 (GRCm39)	V1007D	probably damaging	Het
Raver2	T	C	4: 100,959,921 (GRCm39)	C134R	probably damaging	Het
Rnf130	G	C	11: 49,943,722 (GRCm39)	A123P	probably damaging	Het
Slc29a4	G	A	5: 142,707,207 (GRCm39)	A517T	possibly damaging	Het
Slc38a6	T	A	12: 73,376,759 (GRCm39)	S138T	possibly damaging	Het
Spred1	T	C	2: 117,008,102 (GRCm39)	V336A	possibly damaging	Het
Sptlc3	T	A	2: 139,473,263 (GRCm39)	M504K	probably benign	Het
Syt11	T	C	3: 88,655,149 (GRCm39)	D78G	probably damaging	Het
Trim23	C	T	13: 104,317,682 (GRCm39)	T61I	probably damaging	Het
Tsg101	T	C	7: 46,542,174 (GRCm39)	T260A	probably damaging	Het
Tyw5	T	C	1: 57,440,618 (GRCm39)	Y48C	probably damaging	Het
Utp25	G	T	1: 192,796,089 (GRCm39)	T192K	probably damaging	Het
Vmn1r17	A	G	6: 57,337,828 (GRCm39)	V130A	probably benign	Het
Vmn2r89	C	A	14: 51,693,620 (GRCm39)	H323Q	possibly damaging	Het
Vps18	A	G	2: 119,123,423 (GRCm39)	S117G	probably benign	Het
Zfp93	C	G	7: 23,975,757 (GRCm39)	Q581E	probably damaging	Het

Other mutations in H2-T10

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01296:H2-T10	APN	17	36,431,602 (GRCm39)	missense	probably benign	0.08
IGL01946:H2-T10	APN	17	36,431,608 (GRCm39)	missense	possibly damaging	0.45
IGL03367:H2-T10	APN	17	36,431,285 (GRCm39)	missense	possibly damaging	0.81
IGL03381:H2-T10	APN	17	36,430,249 (GRCm39)	nonsense	probably null
IGL03381:H2-T10	APN	17	36,430,246 (GRCm39)	missense	probably benign
FR4304:H2-T10	UTSW	17	36,431,173 (GRCm39)	frame shift	probably null
R0305:H2-T10	UTSW	17	36,430,260 (GRCm39)	missense	probably damaging	1.00
R1446:H2-T10	UTSW	17	36,430,266 (GRCm39)	missense	possibly damaging	0.87
R1483:H2-T10	UTSW	17	36,432,038 (GRCm39)	missense	probably benign	0.44
R2038:H2-T10	UTSW	17	36,430,317 (GRCm39)	missense	probably benign	0.00
R2402:H2-T10	UTSW	17	36,428,631 (GRCm39)	splice site	probably null
R4755:H2-T10	UTSW	17	36,429,837 (GRCm39)	nonsense	probably null
R4957:H2-T10	UTSW	17	36,428,308 (GRCm39)	utr 3 prime	probably benign
R5568:H2-T10	UTSW	17	36,430,079 (GRCm39)	critical splice donor site	probably null
R6226:H2-T10	UTSW	17	36,431,975 (GRCm39)	missense	probably damaging	0.99
R6850:H2-T10	UTSW	17	36,430,152 (GRCm39)	missense	probably damaging	1.00
R7249:H2-T10	UTSW	17	36,430,269 (GRCm39)	missense	probably damaging	0.99
R7324:H2-T10	UTSW	17	36,430,189 (GRCm39)	missense	probably damaging	1.00
R7466:H2-T10	UTSW	17	36,431,741 (GRCm39)	missense	probably benign	0.10
R7679:H2-T10	UTSW	17	36,430,216 (GRCm39)	missense	not run
R7767:H2-T10	UTSW	17	36,428,622 (GRCm39)	missense	probably benign	0.02
R7901:H2-T10	UTSW	17	36,431,143 (GRCm39)	missense	probably benign
R8278:H2-T10	UTSW	17	36,429,832 (GRCm39)	missense	probably benign	0.00
R8315:H2-T10	UTSW	17	36,429,905 (GRCm39)	missense	probably benign	0.41
R9646:H2-T10	UTSW	17	36,431,157 (GRCm39)	missense	probably damaging	0.96
RF032:H2-T10	UTSW	17	36,431,186 (GRCm39)	frame shift	probably null
RF046:H2-T10	UTSW	17	36,431,186 (GRCm39)	frame shift	probably null

Predicted Primers

PCR Primer
(F):5'- AGAAACTGCTGTTTAGTCCCC -3'
(R):5'- AGTTACACGTGCCATGTGGAC -3'

Sequencing Primer
(F):5'- GAAACTGCTGTTTAGTCCCCTTCAC -3'
(R):5'- AAAGCTGGAGCCTTCTGC -3'

Posted On

2016-06-21