Mutagenetix > Incidental Mutation

Incidental Mutation 'R5109:H2-T22'

459847

Institutional Source

Beutler Lab

Gene Symbol

H2-T22

Ensembl Gene

ENSMUSG00000056116

Gene Name

histocompatibility 2, T region locus 22

Synonyms

H2-T17, H-2T17, H-2T22

MMRRC Submission

042697-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.086) question?

Stock #

R5109 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

36348020-36353634 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

T to A at 36350113 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Stop codon at position 334 (R334*)

Ref Sequence

ENSEMBL: ENSMUSP00000078927 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000058801] [ENSMUST00000077960] [ENSMUST00000080015] [ENSMUST00000097331] [ENSMUST00000173280]

AlphaFold

Q31615

Predicted Effect

probably null
Transcript: ENSMUST00000058801
AA Change: R299*

SMART Domains

Protein: ENSMUSP00000056041
Gene: ENSMUSG00000056116
AA Change: R299*

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
Pfam:MHC_I	29	191	5.8e-47	PFAM
IGc1	210	281	2.06e-23	SMART

Predicted Effect

probably null
Transcript: ENSMUST00000077960
AA Change: R334*

SMART Domains

Protein: ENSMUSP00000077111
Gene: ENSMUSG00000056116
AA Change: R334*

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
Pfam:MHC_I	29	191	4e-47	PFAM
IGc1	210	281	2.06e-23	SMART
transmembrane domain	295	317	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000080015
AA Change: R334*

SMART Domains

Protein: ENSMUSP00000078927
Gene: ENSMUSG00000056116
AA Change: R334*

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
Pfam:MHC_I	29	191	7.3e-47	PFAM
IGc1	210	281	2.06e-23	SMART
transmembrane domain	295	317	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000097331

SMART Domains

Protein: ENSMUSP00000094943
Gene: ENSMUSG00000073407

Domain	Start	End	E-Value	Type
transmembrane domain	15	37	N/A	INTRINSIC
low complexity region	103	115	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000172633

Predicted Effect

probably benign
Transcript: ENSMUST00000173280

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000173900

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.1%
3x: 98.2%
10x: 95.9%
20x: 91.2%

Validation Efficiency

95% (78/82)

Allele List at MGI

Other mutations in this stock

Total: 72 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ankrd17	T	C	5: 90,391,395 (GRCm39)	S1841G	possibly damaging	Het
Anxa10	T	C	8: 62,516,093 (GRCm39)	E193G	possibly damaging	Het
Ap3d1	T	C	10: 80,545,284 (GRCm39)	S1056G	probably benign	Het
Apbb1	T	C	7: 105,214,242 (GRCm39)	N62D	probably damaging	Het
Apobec2	A	T	17: 48,730,022 (GRCm39)	Y215N	probably damaging	Het
Apobec2	T	A	17: 48,730,024 (GRCm39)	Y214F	probably damaging	Het
Appl2	A	T	10: 83,436,871 (GRCm39)	V630E	probably benign	Het
Bud23	T	C	5: 135,089,877 (GRCm39)		probably benign	Het
Cacna1b	A	T	2: 24,580,797 (GRCm39)	M683K	possibly damaging	Het
Cbfa2t2	T	A	2: 154,373,293 (GRCm39)	D187E	probably damaging	Het
Cfap54	G	T	10: 92,773,753 (GRCm39)	F96L	probably benign	Het
Cimap1a	A	T	7: 140,429,461 (GRCm39)	S197C	probably benign	Het
Crebbp	A	G	16: 3,906,295 (GRCm39)		probably benign	Het
Crocc	C	T	4: 140,755,722 (GRCm39)	R1102Q	probably damaging	Het
Dcaf12	T	C	4: 41,298,329 (GRCm39)	D273G	possibly damaging	Het
Dchs1	T	C	7: 105,414,221 (GRCm39)	T865A	probably benign	Het
Dhfr	A	T	13: 92,491,788 (GRCm39)	I8F	probably damaging	Het
Dnaja2	A	T	8: 86,279,887 (GRCm39)	F97L	possibly damaging	Het
Dnase1l1	C	T	X: 73,320,644 (GRCm39)		probably null	Het
Doc2b	T	C	11: 75,667,967 (GRCm39)	D261G	probably benign	Het
Ear1	A	G	14: 44,056,485 (GRCm39)	Y128H	probably benign	Het
Elac2	T	A	11: 64,883,142 (GRCm39)	I171N	probably damaging	Het
Entpd3	C	A	9: 120,395,380 (GRCm39)	N454K	possibly damaging	Het
Flrt3	A	G	2: 140,502,663 (GRCm39)	S322P	possibly damaging	Het
Fn1	C	T	1: 71,688,394 (GRCm39)	C170Y	probably damaging	Het
Gabbr1	T	A	17: 37,382,920 (GRCm39)		probably benign	Het
Gm7247	T	G	14: 51,602,774 (GRCm39)	S37A	probably damaging	Het
Gm8775	T	A	3: 4,277,008 (GRCm39)		noncoding transcript	Het
Gprc5c	G	T	11: 114,755,093 (GRCm39)	V257L	possibly damaging	Het
Gria4	A	C	9: 4,472,168 (GRCm39)	N440K	probably damaging	Het
Ift172	T	C	5: 31,423,330 (GRCm39)	D817G	probably benign	Het
Igkv9-124	T	A	6: 67,919,348 (GRCm39)	R21S	possibly damaging	Het
Itgam	G	A	7: 127,712,390 (GRCm39)	V846I	probably benign	Het
Kif11	T	A	19: 37,373,063 (GRCm39)	M94K	possibly damaging	Het
Krtcap2	T	C	3: 89,154,085 (GRCm39)	V2A	probably benign	Het
Lrrc47	A	G	4: 154,101,933 (GRCm39)	D400G	probably damaging	Het
Man2a1	T	A	17: 65,059,443 (GRCm39)	V1110E	probably benign	Het
Mfsd9	T	A	1: 40,813,365 (GRCm39)	I317F	probably damaging	Het
Mindy4	A	T	6: 55,193,730 (GRCm39)		probably null	Het
Mrpl53	A	G	6: 83,086,541 (GRCm39)	T82A	probably damaging	Het
Myo3b	A	G	2: 69,925,637 (GRCm39)	K35E	possibly damaging	Het
Nalcn	A	G	14: 123,515,650 (GRCm39)	V1717A	possibly damaging	Het
Ncoa2	A	G	1: 13,257,070 (GRCm39)	V143A	probably damaging	Het
Ndufa9	A	C	6: 126,809,520 (GRCm39)		probably null	Het
Or10ag60	G	A	2: 87,438,319 (GRCm39)	G196R	possibly damaging	Het
Or10ag60	G	A	2: 87,437,755 (GRCm39)	A8T	possibly damaging	Het
Or12e9	A	G	2: 87,201,878 (GRCm39)	M1V	probably null	Het
Or5k17	A	G	16: 58,746,422 (GRCm39)	S171P	probably benign	Het
Or5p55	T	C	7: 107,567,104 (GRCm39)	S167P	probably benign	Het
Or6c202	T	C	10: 128,996,106 (GRCm39)	Y249C	probably damaging	Het
Or7g28	A	T	9: 19,272,438 (GRCm39)	I71N	probably damaging	Het
Or9g8	G	A	2: 85,607,668 (GRCm39)	V247M	probably damaging	Het
Pde4b	G	T	4: 102,458,741 (GRCm39)	A466S	probably damaging	Het
Pfkfb3	A	T	2: 11,491,162 (GRCm39)		probably benign	Het
Ppp1r21	A	G	17: 88,866,268 (GRCm39)	K355E	probably damaging	Het
Psme4	T	A	11: 30,741,095 (GRCm39)	Y90*	probably null	Het
Rbms1	G	A	2: 60,612,284 (GRCm39)	L161F	probably damaging	Het
Rdh16f2	A	G	10: 127,702,672 (GRCm39)	D83G	probably damaging	Het
Sec16b	C	T	1: 157,392,361 (GRCm39)	R910*	probably null	Het
Sema4c	CTGGGCTT	C	1: 36,591,381 (GRCm39)		probably null	Het
Spata31e5	T	C	1: 28,816,636 (GRCm39)	I465M	possibly damaging	Het
Stambp	A	G	6: 83,540,803 (GRCm39)		probably null	Het
Tcf21	T	C	10: 22,695,558 (GRCm39)	N82S	probably damaging	Het
Tlr2	A	T	3: 83,745,030 (GRCm39)	V351D	probably damaging	Het
Tmem39a	G	A	16: 38,411,326 (GRCm39)	G359D	probably damaging	Het
Ttc23l	G	T	15: 10,551,636 (GRCm39)	T30K	possibly damaging	Het
Vmn2r17	C	A	5: 109,577,342 (GRCm39)	F464L	probably benign	Het
Vmn2r49	T	A	7: 9,710,204 (GRCm39)	T843S	probably benign	Het
Vmn2r7	T	C	3: 64,598,088 (GRCm39)	D823G	probably null	Het
Wrnip1	T	A	13: 33,000,319 (GRCm39)	L442Q	probably damaging	Het
Zbtb38	G	T	9: 96,569,062 (GRCm39)	S674Y	probably damaging	Het
Zfp639	T	G	3: 32,574,585 (GRCm39)		probably null	Het

Other mutations in H2-T22

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01088:H2-T22	APN	17	36,352,811 (GRCm39)	missense	probably damaging	0.99
IGL02978:H2-T22	APN	17	36,352,517 (GRCm39)	missense	probably benign	0.00
R0078:H2-T22	UTSW	17	36,351,501 (GRCm39)	missense	probably damaging	0.99
R0448:H2-T22	UTSW	17	36,353,278 (GRCm39)	missense	possibly damaging	0.96
R1402:H2-T22	UTSW	17	36,351,161 (GRCm39)	missense	possibly damaging	0.95
R1402:H2-T22	UTSW	17	36,351,161 (GRCm39)	missense	possibly damaging	0.95
R1592:H2-T22	UTSW	17	36,352,469 (GRCm39)	missense	probably damaging	0.99
R1830:H2-T22	UTSW	17	36,352,434 (GRCm39)	missense	probably benign	0.00
R2105:H2-T22	UTSW	17	36,351,409 (GRCm39)	missense	probably benign	0.23
R2116:H2-T22	UTSW	17	36,349,949 (GRCm39)	splice site	probably null
R2964:H2-T22	UTSW	17	36,351,537 (GRCm39)	missense	probably damaging	1.00
R2965:H2-T22	UTSW	17	36,351,537 (GRCm39)	missense	probably damaging	1.00
R3425:H2-T22	UTSW	17	36,352,472 (GRCm39)	missense	probably damaging	1.00
R3875:H2-T22	UTSW	17	36,351,195 (GRCm39)	missense	probably benign	0.03
R4614:H2-T22	UTSW	17	36,351,429 (GRCm39)	missense	probably benign	0.28
R4691:H2-T22	UTSW	17	36,352,462 (GRCm39)	frame shift	probably null
R4870:H2-T22	UTSW	17	36,349,924 (GRCm39)	missense	probably benign	0.00
R4954:H2-T22	UTSW	17	36,352,851 (GRCm39)	missense	probably damaging	1.00
R5995:H2-T22	UTSW	17	36,352,377 (GRCm39)	missense	probably benign	0.18
R7379:H2-T22	UTSW	17	36,353,232 (GRCm39)	critical splice donor site	probably null
R7597:H2-T22	UTSW	17	36,351,408 (GRCm39)	missense	probably damaging	1.00
R8719:H2-T22	UTSW	17	36,352,835 (GRCm39)	missense	probably benign	0.04
R8861:H2-T22	UTSW	17	36,353,290 (GRCm39)	missense	possibly damaging	0.86
R9661:H2-T22	UTSW	17	36,353,371 (GRCm39)	start gained	probably benign
Z1088:H2-T22	UTSW	17	36,352,530 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- GTGGCCTAGACAAGTTTTACAGGAC -3'
(R):5'- TCCCATGCCACCCATATGTG -3'

Sequencing Primer
(F):5'- TTACAGGACTTAATCTTCCAAAAGC -3'
(R):5'- CATATGTGGTTTTTCTTTCCTCAGG -3'

Posted On

2017-02-27