Mutagenetix > Incidental Mutation

Incidental Mutation 'R6226:H2-T10'

504372

Institutional Source

Beutler Lab

Gene Symbol

H2-T10

Ensembl Gene

ENSMUSG00000079491

Gene Name

histocompatibility 2, T region locus 10

Synonyms

H-2T10

MMRRC Submission

044397-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.064) question?

Stock #

R6226 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

36426763-36432336 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 36431975 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tryptophan to Arginine at position 23 (W23R)

Ref Sequence

ENSEMBL: ENSMUSP00000133893 (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 damaging
Transcript: ENSMUST00000166442
AA Change: W23R

PolyPhen 2 Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000127602
Gene: ENSMUSG00000079491
AA Change: W23R

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 benign
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 damaging
Transcript: ENSMUST00000174382
AA Change: W23R

PolyPhen 2 Score 0.986 (Sensitivity: 0.74; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000133893
Gene: ENSMUSG00000079491
AA Change: W23R

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

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 98.3%
20x: 95.3%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 70 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Actn2	T	C	13: 12,293,853 (GRCm39)	T62A	probably benign	Het
Adam33	G	A	2: 130,897,530 (GRCm39)	T265I	probably damaging	Het
Afap1l2	T	C	19: 56,904,560 (GRCm39)	T654A	probably benign	Het
Agrn	A	G	4: 156,258,066 (GRCm39)	S992P	probably damaging	Het
Anapc1	A	G	2: 128,492,292 (GRCm39)	F939L	probably damaging	Het
Anks1	G	A	17: 28,276,304 (GRCm39)	V1016I	probably benign	Het
Ankzf1	A	G	1: 75,173,238 (GRCm39)	T401A	probably benign	Het
Atad1	G	T	19: 32,678,987 (GRCm39)	D105E	probably benign	Het
Carmil2	A	G	8: 106,415,664 (GRCm39)	T313A	possibly damaging	Het
Cdk15	T	C	1: 59,304,792 (GRCm39)	V131A	probably damaging	Het
Cldnd1	A	T	16: 58,551,663 (GRCm39)		probably null	Het
Col16a1	A	T	4: 129,948,882 (GRCm39)		probably benign	Het
Cts3	T	A	13: 61,716,535 (GRCm39)	I34L	probably benign	Het
Dnah7b	A	C	1: 46,165,828 (GRCm39)	K498Q	probably benign	Het
Dnase2b	A	G	3: 146,290,318 (GRCm39)	Y218H	probably benign	Het
Dsg2	T	A	18: 20,712,506 (GRCm39)	V170D	probably damaging	Het
Dst	T	C	1: 34,309,955 (GRCm39)	V1543A	probably damaging	Het
Ell3	A	T	2: 121,272,258 (GRCm39)	I72K	probably damaging	Het
Fank1	A	G	7: 133,463,927 (GRCm39)	Y41C	probably benign	Het
Foxd3	T	C	4: 99,545,261 (GRCm39)	Y134H	probably damaging	Het
Frmd6	A	G	12: 70,910,685 (GRCm39)		probably benign	Het
Gale	A	G	4: 135,692,916 (GRCm39)	E53G	possibly damaging	Het
Glis3	A	G	19: 28,294,702 (GRCm39)	S699P	probably damaging	Het
Gm12830	T	A	4: 114,702,246 (GRCm39)	M136K	unknown	Het
Grik3	T	C	4: 125,553,582 (GRCm39)	V438A	probably benign	Het
Gsap	A	G	5: 21,422,429 (GRCm39)	N133D	probably damaging	Het
Gsg1	T	A	6: 135,217,110 (GRCm39)	D239V	probably damaging	Het
Itgae	A	G	11: 73,031,583 (GRCm39)	T1100A	probably benign	Het
Kcnh7	A	T	2: 62,607,903 (GRCm39)	F559L	probably damaging	Het
Kdm5b	G	T	1: 134,536,616 (GRCm39)	R612L	probably damaging	Het
Lrrc74a	T	A	12: 86,795,231 (GRCm39)	N253K	possibly damaging	Het
Mcm3ap	A	G	10: 76,351,540 (GRCm39)	H1961R	possibly damaging	Het
Ncam1	C	T	9: 49,476,304 (GRCm39)	E262K	probably benign	Het
Nckap1	A	G	2: 80,339,125 (GRCm39)	S968P	possibly damaging	Het
Nkapd1	T	C	9: 50,519,070 (GRCm39)	T181A	possibly damaging	Het
Nr2f2	T	G	7: 70,009,744 (GRCm39)	S112R	probably benign	Het
Nup93	T	C	8: 95,013,165 (GRCm39)	W137R	probably damaging	Het
Or10ag53	A	G	2: 87,082,736 (GRCm39)	S152G	probably benign	Het
Or2t26	A	G	11: 49,039,660 (GRCm39)	D192G	possibly damaging	Het
Or4a78	A	T	2: 89,497,333 (GRCm39)	L299H	probably damaging	Het
Or52n1	A	T	7: 104,383,243 (GRCm39)	F109L	probably damaging	Het
Or8b12	T	A	9: 37,657,433 (GRCm39)	M1K	probably null	Het
Or8b55	T	C	9: 38,727,666 (GRCm39)	I289T	probably damaging	Het
Otogl	A	T	10: 107,607,067 (GRCm39)	Y2105*	probably null	Het
Pibf1	A	G	14: 99,338,555 (GRCm39)	S24G	probably damaging	Het
Pitx2	C	T	3: 129,009,491 (GRCm39)	R130W	probably damaging	Het
Pkd1l1	T	C	11: 8,851,287 (GRCm39)	N715S	probably benign	Het
Pou6f2	A	T	13: 18,303,739 (GRCm39)	I123N	possibly damaging	Het
Prss29	T	A	17: 25,539,513 (GRCm39)	H35Q	possibly damaging	Het
Ptpn21	A	G	12: 98,646,375 (GRCm39)	F1028L	probably benign	Het
Ptpn21	A	T	12: 98,681,431 (GRCm39)	Y68N	probably damaging	Het
Ptprk	A	G	10: 28,440,099 (GRCm39)	T856A	probably benign	Het
Rnd2	C	T	11: 101,359,825 (GRCm39)	L57F	probably damaging	Het
Rpl22l1	A	G	3: 28,860,676 (GRCm39)	T13A	possibly damaging	Het
Rptn	C	G	3: 93,305,437 (GRCm39)	H923Q	possibly damaging	Het
Sec14l5	G	A	16: 4,994,429 (GRCm39)	V408I	probably damaging	Het
Serpina5	T	C	12: 104,068,037 (GRCm39)	S33P	possibly damaging	Het
Sgip1	A	G	4: 102,823,392 (GRCm39)	N524S	probably damaging	Het
Shkbp1	C	A	7: 27,051,405 (GRCm39)	R218M	probably null	Het
Sorcs1	T	A	19: 50,169,852 (GRCm39)	I970F	probably damaging	Het
Spg11	A	G	2: 121,918,743 (GRCm39)	V962A	possibly damaging	Het
Sptbn1	A	G	11: 30,086,054 (GRCm39)	M1205T	probably damaging	Het
Sufu	G	A	19: 46,462,093 (GRCm39)	V369M	probably damaging	Het
Tmem98	T	C	11: 80,712,220 (GRCm39)	F219S	probably benign	Het
Trim27	T	C	13: 21,365,086 (GRCm39)		probably benign	Het
Trim43b	T	C	9: 88,973,328 (GRCm39)	E135G	possibly damaging	Het
Ube2m	A	G	7: 12,769,815 (GRCm39)	V110A	probably damaging	Het
Ugt2b36	A	G	5: 87,239,989 (GRCm39)	V132A	probably damaging	Het
Usp36	A	T	11: 118,168,100 (GRCm39)	S86T	probably damaging	Het
Zfp941	A	T	7: 140,392,398 (GRCm39)	D320E	probably benign	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
R5162:H2-T10	UTSW	17	36,429,843 (GRCm39)	splice site	probably null
R5568:H2-T10	UTSW	17	36,430,079 (GRCm39)	critical splice donor site	probably null
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'- CTAAGCGAGTGTGAACCTGG -3'
(R):5'- ATGACTTGGCACTAGTTCTCAC -3'

Sequencing Primer
(F):5'- GATGAGACCCCGACCTCCTC -3'
(R):5'- CTTGATTGGCTAATGACGACGAC -3'

Posted On

2018-02-28