Mutagenetix > Incidental Mutation

Incidental Mutation 'R2105:H2-T22'

230919

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

040109-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.092) question?

Stock #

R2105 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

36348020-36353634 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 36351409 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Asparagine at position 274 (Y274N)

Ref Sequence

ENSEMBL: ENSMUSP00000078927 (fasta)

Gene Model

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

AlphaFold

Q31615

Predicted Effect

probably benign
Transcript: ENSMUST00000058801
AA Change: Y274N

PolyPhen 2 Score 0.232 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000056041
Gene: ENSMUSG00000056116
AA Change: Y274N

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 benign
Transcript: ENSMUST00000077960
AA Change: Y274N

PolyPhen 2 Score 0.232 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000077111
Gene: ENSMUSG00000056116
AA Change: Y274N

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 benign
Transcript: ENSMUST00000080015
AA Change: Y274N

PolyPhen 2 Score 0.232 (Sensitivity: 0.91; Specificity: 0.88)

SMART Domains

Protein: ENSMUSP00000078927
Gene: ENSMUSG00000056116
AA Change: Y274N

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

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.4%
20x: 95.5%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 86 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2m	C	T	6: 121,650,459 (GRCm39)	P1189L	probably benign	Het
Acbd4	G	A	11: 102,995,265 (GRCm39)	D57N	probably damaging	Het
Acot4	A	T	12: 84,085,516 (GRCm39)	M78L	probably damaging	Het
Ago1	A	T	4: 126,355,581 (GRCm39)	M76K	probably benign	Het
Agrn	G	T	4: 156,261,756 (GRCm39)	Y511*	probably null	Het
Arhgef15	A	T	11: 68,838,507 (GRCm39)		probably null	Het
Atp1a3	A	T	7: 24,689,278 (GRCm39)	M594K	probably damaging	Het
Atp4a	G	A	7: 30,419,793 (GRCm39)		probably null	Het
Bckdk	T	A	7: 127,506,489 (GRCm39)	I272N	probably damaging	Het
Bod1l	A	G	5: 41,989,622 (GRCm39)	V367A	probably benign	Het
C1galt1c1	T	C	X: 37,720,145 (GRCm39)	M284V	possibly damaging	Het
Cenpk	T	A	13: 104,366,105 (GRCm39)	C4*	probably null	Het
Cfap53	T	C	18: 74,416,294 (GRCm39)	V9A	possibly damaging	Het
Chil3	T	C	3: 106,067,794 (GRCm39)	I124V	possibly damaging	Het
Creld2	G	A	15: 88,704,834 (GRCm39)	W103*	probably null	Het
Cyp2c67	T	C	19: 39,614,681 (GRCm39)	Y282C	probably benign	Het
D5Ertd579e	C	T	5: 36,770,793 (GRCm39)	A1201T	probably benign	Het
Dock4	A	G	12: 40,742,988 (GRCm39)	H381R	probably benign	Het
Drc1	C	T	5: 30,513,785 (GRCm39)	S447F	probably benign	Het
Fam83g	G	T	11: 61,594,284 (GRCm39)	R606L	probably benign	Het
Fmnl1	A	C	11: 103,085,518 (GRCm39)	S688R	probably benign	Het
Fryl	C	T	5: 73,279,642 (GRCm39)	V219I	probably benign	Het
Golgb1	T	A	16: 36,735,026 (GRCm39)	N1424K	probably benign	Het
Gpr39	T	C	1: 125,605,621 (GRCm39)	V183A	possibly damaging	Het
Hif1a	T	A	12: 73,984,519 (GRCm39)	Y313N	probably damaging	Het
Hip1r	T	A	5: 124,138,267 (GRCm39)	M787K	probably damaging	Het
Hipk3	T	C	2: 104,269,737 (GRCm39)	E484G	probably damaging	Het
Hsh2d	T	A	8: 72,954,490 (GRCm39)	F291I	probably benign	Het
Ino80	T	C	2: 119,262,410 (GRCm39)	E692G	probably null	Het
Itgam	T	A	7: 127,680,884 (GRCm39)	V271D	probably damaging	Het
Kansl1	A	C	11: 104,226,385 (GRCm39)	I924S	probably damaging	Het
Kcnq2	A	G	2: 180,723,145 (GRCm39)	C628R	probably benign	Het
Krt78	A	C	15: 101,855,849 (GRCm39)	V654G	possibly damaging	Het
Lrit2	A	G	14: 36,793,913 (GRCm39)	T326A	probably damaging	Het
Ltk	T	C	2: 119,582,569 (GRCm39)	E710G	probably damaging	Het
Lysmd1	T	C	3: 95,042,285 (GRCm39)	L53S	probably damaging	Het
Mc4r	T	C	18: 66,992,669 (GRCm39)	Y148C	probably damaging	Het
Mfn2	G	A	4: 147,973,162 (GRCm39)	Q172*	probably null	Het
Mknk2	A	G	10: 80,504,435 (GRCm39)	L242P	possibly damaging	Het
Mrpl45	A	T	11: 97,216,573 (GRCm39)	H167L	probably benign	Het
Myc	T	C	15: 61,859,951 (GRCm39)	V208A	probably damaging	Het
Myh7b	A	G	2: 155,471,377 (GRCm39)	E1175G	probably benign	Het
Myo18a	A	T	11: 77,741,060 (GRCm39)	M1456L	probably benign	Het
Myocd	G	A	11: 65,109,484 (GRCm39)	Q96*	probably null	Het
Nckap5	T	A	1: 125,954,255 (GRCm39)	I766F	probably damaging	Het
Ndst1	T	C	18: 60,824,325 (GRCm39)	E784G	probably benign	Het
Nf1	A	T	11: 79,360,652 (GRCm39)	R1443S	possibly damaging	Het
Nhlrc3	A	G	3: 53,361,072 (GRCm39)	W228R	probably damaging	Het
Nup107	G	A	10: 117,609,225 (GRCm39)	T378I	probably damaging	Het
Or14c40	A	T	7: 86,313,591 (GRCm39)	K240N	probably damaging	Het
Or1o3	A	T	17: 37,573,964 (GRCm39)	M197K	probably benign	Het
Or52d13	T	A	7: 103,109,480 (GRCm39)		probably null	Het
Or5m3b	C	T	2: 85,871,674 (GRCm39)	T5I	probably damaging	Het
Or5w11	A	G	2: 87,459,283 (GRCm39)	T159A	probably benign	Het
Or6b13	T	A	7: 139,782,656 (GRCm39)	D9V	probably benign	Het
Otop1	A	G	5: 38,457,801 (GRCm39)	D520G	probably benign	Het
Papln	C	T	12: 83,827,010 (GRCm39)	P712S	probably benign	Het
Pcbd2	T	A	13: 55,880,846 (GRCm39)	I34N	probably damaging	Het
Pkd1l3	T	A	8: 110,374,205 (GRCm39)	C29*	probably null	Het
Pou5f1	G	A	17: 35,820,899 (GRCm39)	V114M	probably benign	Het
Pramel28	A	T	4: 143,692,390 (GRCm39)	Y204N	probably benign	Het
Prpf4b	C	A	13: 35,068,214 (GRCm39)		probably benign	Het
Prr23a1	C	T	9: 98,724,709 (GRCm39)	P24S	probably damaging	Het
Ptch1	T	A	13: 63,693,059 (GRCm39)	M65L	probably benign	Het
Rc3h2	A	T	2: 37,289,636 (GRCm39)	I392K	possibly damaging	Het
Reck	G	T	4: 43,943,195 (GRCm39)	D916Y	probably damaging	Het
Rtf2	A	G	2: 172,287,285 (GRCm39)	D68G	probably damaging	Het
Ryr1	G	T	7: 28,789,575 (GRCm39)	T1513K	probably damaging	Het
Sacs	A	G	14: 61,410,890 (GRCm39)	D55G	possibly damaging	Het
Scn9a	A	G	2: 66,398,527 (GRCm39)	S28P	probably benign	Het
Scrn3	A	G	2: 73,160,196 (GRCm39)	M280V	probably damaging	Het
Snx29	C	T	16: 11,328,898 (GRCm39)	T559I	possibly damaging	Het
Spn	C	T	7: 126,735,413 (GRCm39)	E109K	probably damaging	Het
Sra1	C	T	18: 36,808,121 (GRCm39)	R369H	probably benign	Het
Srsf11	C	T	3: 157,724,982 (GRCm39)	A64T	probably damaging	Het
Stk17b	A	G	1: 53,815,764 (GRCm39)	S12P	probably benign	Het
Sult1d1	C	A	5: 87,707,661 (GRCm39)	G153V	probably damaging	Het
Sycp2	A	T	2: 177,991,931 (GRCm39)		probably null	Het
Tgfb3	T	C	12: 86,116,543 (GRCm39)	E165G	possibly damaging	Het
Tns2	C	A	15: 102,015,941 (GRCm39)	H160N	probably benign	Het
Ubn1	T	A	16: 4,895,088 (GRCm39)	C711*	probably null	Het
Usp13	A	T	3: 32,956,135 (GRCm39)	D469V	probably damaging	Het
Vmn1r231	A	T	17: 21,110,380 (GRCm39)	H178Q	possibly damaging	Het
Vwa1	A	G	4: 155,857,250 (GRCm39)	S183P	probably damaging	Het
Xpo7	A	G	14: 70,928,431 (GRCm39)	I424T	probably benign	Het
Zfp109	A	G	7: 23,936,041 (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
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
R5109:H2-T22	UTSW	17	36,350,113 (GRCm39)	nonsense	probably null
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'- TTTTGGTACCATGCAGGCTCTG -3'
(R):5'- AAAGGCACATGTGACCCGTC -3'

Sequencing Primer
(F):5'- TACCATGCAGGCTCTGGGAAG -3'
(R):5'- GTCACCCCAGACCTGAAGG -3'

Posted On

2014-09-18