Mutagenetix > Incidental Mutation

Incidental Mutation 'R5151:H2-T23'

395405

Institutional Source

Beutler Lab

Gene Symbol

H2-T23

Ensembl Gene

ENSMUSG00000067212

Gene Name

histocompatibility 2, T region locus 23

Synonyms

Qed-1, H-2T23, 37c, Qa-1, T23b, T23d, Qa1, T18c, T18c(37), 37b

MMRRC Submission

042733-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.051) question?

Stock #

R5151 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

36340869-36343593 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 36343230 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 49 (D49G)

Ref Sequence

ENSEMBL: ENSMUSP00000099739 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000102678]

AlphaFold

P06339

PDB Structure

Structure of the MHC class Ib molecule Qa-1b [X-RAY DIFFRACTION]

Predicted Effect

probably damaging
Transcript: ENSMUST00000102678
AA Change: D49G

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000099739
Gene: ENSMUSG00000067212
AA Change: D49G

Domain	Start	End	E-Value	Type
signal peptide	1	20	N/A	INTRINSIC
Pfam:MHC_I	21	199	1.9e-93	PFAM
IGc1	218	289	1.89e-22	SMART
transmembrane domain	304	326	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000172633

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000173900

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000174161

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000174471

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000174839

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.0%
20x: 94.6%

Validation Efficiency

MGI Phenotype

PHENOTYPE: CD4⁺ T cells from mice with a homozygous null mutation have enhanced responses after infection or immunization, are resistant to suppressor activity mediated by a subset of CD8⁺ T cells, but are more susceptible to NK cell lysis. [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
Acvr1b	T	A	15: 101,108,651 (GRCm39)	C476S	probably damaging	Het
Agpat2	A	G	2: 26,487,218 (GRCm39)	M120T	probably damaging	Het
Ahnak	A	G	19: 8,994,933 (GRCm39)	T5406A	probably benign	Het
Ano4	A	G	10: 88,948,775 (GRCm39)	F112L	probably damaging	Het
Arhgef11	T	A	3: 87,642,667 (GRCm39)	V1371D	probably damaging	Het
Ascc3	A	G	10: 50,514,059 (GRCm39)	N286S	probably damaging	Het
Ate1	T	C	7: 130,109,394 (GRCm39)	K202E	possibly damaging	Het
Cacna1d	T	C	14: 29,845,280 (GRCm39)	T630A	probably damaging	Het
Ccdc187	G	T	2: 26,183,451 (GRCm39)	T183N	probably damaging	Het
Cdk12	C	T	11: 98,140,749 (GRCm39)		probably benign	Het
Ciita	A	G	16: 10,341,594 (GRCm39)	N978S	probably damaging	Het
Cit	A	T	5: 116,117,894 (GRCm39)	Q1268L	probably damaging	Het
Csf2rb	C	T	15: 78,224,781 (GRCm39)	R180W	probably damaging	Het
Dnah17	T	C	11: 117,918,293 (GRCm39)	I4079V	probably damaging	Het
Dnah7a	A	G	1: 53,659,929 (GRCm39)	V693A	probably benign	Het
Dnah8	T	A	17: 30,931,269 (GRCm39)	V1428E	probably benign	Het
Dnhd1	C	A	7: 105,362,647 (GRCm39)	Q3777K	probably benign	Het
Dock9	A	G	14: 121,815,582 (GRCm39)	Y1666H	probably damaging	Het
Dpysl3	C	T	18: 43,571,145 (GRCm39)	G43D	probably benign	Het
Eftud2	A	G	11: 102,758,670 (GRCm39)		probably null	Het
Erich4	T	C	7: 25,315,292 (GRCm39)		probably benign	Het
Fah	T	A	7: 84,250,259 (GRCm39)	D99V	possibly damaging	Het
Fat1	T	C	8: 45,404,851 (GRCm39)	V534A	possibly damaging	Het
Fgf21	G	C	7: 45,263,456 (GRCm39)	S207R	probably damaging	Het
Fras1	C	T	5: 96,792,969 (GRCm39)	P967S	probably damaging	Het
Hmcn2	A	G	2: 31,279,455 (GRCm39)	N1819S	probably null	Het
Hoxc12	A	G	15: 102,846,881 (GRCm39)	I258V	probably damaging	Het
Ighv1-22	T	A	12: 114,709,928 (GRCm39)	T106S	probably damaging	Het
Inpp5j	T	C	11: 3,452,270 (GRCm39)	T327A	probably damaging	Het
Iqgap3	G	T	3: 88,025,067 (GRCm39)	M689I	possibly damaging	Het
Itga7	G	A	10: 128,780,380 (GRCm39)	G559S	possibly damaging	Het
Kcnq1	G	T	7: 142,979,749 (GRCm39)	V632L	probably benign	Het
Lsamp	T	C	16: 41,954,792 (GRCm39)	V230A	probably damaging	Het
Mfn2	A	T	4: 147,970,785 (GRCm39)	S305T	probably benign	Het
Myom3	A	G	4: 135,516,883 (GRCm39)	T818A	probably benign	Het
Nacc2	G	A	2: 25,980,365 (GRCm39)	R24C	probably damaging	Het
Ntrk3	A	C	7: 77,897,048 (GRCm39)	I663R	probably damaging	Het
Nyap1	A	G	5: 137,734,376 (GRCm39)	V219A	probably damaging	Het
Obox3	A	T	7: 15,360,173 (GRCm39)	N165K	probably damaging	Het
Or13a1	T	A	6: 116,470,765 (GRCm39)	L65*	probably null	Het
Or13j1	A	T	4: 43,706,518 (GRCm39)	F17I	probably damaging	Het
Or2y12	A	G	11: 49,426,242 (GRCm39)	T77A	possibly damaging	Het
Or52e2	C	A	7: 102,804,593 (GRCm39)	M120I	probably damaging	Het
Or55b4	G	A	7: 102,134,192 (GRCm39)	T45I	probably benign	Het
Pask	A	T	1: 93,262,350 (GRCm39)	L170H	probably damaging	Het
Piezo2	A	T	18: 63,163,480 (GRCm39)	I2146N	possibly damaging	Het
Pitpnm2	A	T	5: 124,274,449 (GRCm39)	M220K	probably damaging	Het
Pkhd1l1	A	G	15: 44,368,705 (GRCm39)	D841G	probably benign	Het
Pla2g3	C	T	11: 3,440,827 (GRCm39)	T264M	probably benign	Het
Plcb1	A	T	2: 135,104,165 (GRCm39)	Y278F	probably benign	Het
Prkdc	T	C	16: 15,533,899 (GRCm39)	L1579P	probably damaging	Het
Rad51ap2	T	A	12: 11,507,516 (GRCm39)	N479K	probably benign	Het
Rasgrf2	T	C	13: 92,044,155 (GRCm39)	H966R	probably damaging	Het
Rbm27	A	G	18: 42,471,509 (GRCm39)	D996G	probably damaging	Het
Rif1	A	C	2: 52,010,321 (GRCm39)	K2337T	probably damaging	Het
Rpl13a	G	T	7: 44,775,385 (GRCm39)	N442K	probably benign	Het
Serpini2	T	A	3: 75,153,820 (GRCm39)	T380S	possibly damaging	Het
Setbp1	A	T	18: 78,901,214 (GRCm39)	W818R	probably damaging	Het
Siae	T	A	9: 37,542,869 (GRCm39)	C185S	probably benign	Het
Slc15a2	A	G	16: 36,572,659 (GRCm39)	V674A	probably damaging	Het
Slc40a1	A	T	1: 45,950,516 (GRCm39)	M312K	possibly damaging	Het
Slc46a3	A	G	5: 147,823,566 (GRCm39)	L92S	probably damaging	Het
Son	T	C	16: 91,452,587 (GRCm39)	S445P	probably damaging	Het
Syne2	T	C	12: 76,090,484 (GRCm39)	F351L	probably benign	Het
Tmed3	G	A	9: 89,581,825 (GRCm39)	R213*	probably null	Het
Tmem248	T	A	5: 130,269,238 (GRCm39)	L277H	probably damaging	Het
Unc13c	T	A	9: 73,838,757 (GRCm39)	H698L	probably benign	Het
Ushbp1	A	G	8: 71,847,799 (GRCm39)	V24A	possibly damaging	Het
Usp24	G	T	4: 106,256,309 (GRCm39)		probably null	Het
Vmn2r50	T	G	7: 9,786,970 (GRCm39)	I46L	probably benign	Het
Zfp106	T	C	2: 120,365,208 (GRCm39)	T423A	probably benign	Het
Zfp663	T	A	2: 165,195,113 (GRCm39)	T369S	probably benign	Het
Zmynd11	T	C	13: 9,740,953 (GRCm39)	T382A	probably damaging	Het

Other mutations in H2-T23

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00435:H2-T23	APN	17	36,342,673 (GRCm39)	missense	probably damaging	1.00
IGL01685:H2-T23	APN	17	36,343,536 (GRCm39)	missense	probably benign	0.29
IGL02756:H2-T23	APN	17	36,342,580 (GRCm39)	missense	probably damaging	1.00
IGL03036:H2-T23	APN	17	36,343,249 (GRCm39)	missense	possibly damaging	0.73
LCD18:H2-T23	UTSW	17	36,342,108 (GRCm39)	intron	probably benign
R0539:H2-T23	UTSW	17	36,343,033 (GRCm39)	splice site	probably benign
R0845:H2-T23	UTSW	17	36,341,475 (GRCm39)	missense	probably benign	0.00
R1727:H2-T23	UTSW	17	36,342,545 (GRCm39)	missense	possibly damaging	0.52
R2044:H2-T23	UTSW	17	36,343,083 (GRCm39)	missense	probably damaging	1.00
R3121:H2-T23	UTSW	17	36,341,855 (GRCm39)	missense	probably benign	0.13
R3122:H2-T23	UTSW	17	36,341,855 (GRCm39)	missense	probably benign	0.13
R3943:H2-T23	UTSW	17	36,341,535 (GRCm39)	missense	probably benign	0.01
R3944:H2-T23	UTSW	17	36,341,535 (GRCm39)	missense	probably benign	0.01
R4492:H2-T23	UTSW	17	36,343,058 (GRCm39)	missense	probably damaging	0.97
R4660:H2-T23	UTSW	17	36,341,108 (GRCm39)	missense	probably damaging	0.99
R4669:H2-T23	UTSW	17	36,342,690 (GRCm39)	missense	probably damaging	1.00
R4740:H2-T23	UTSW	17	36,343,016 (GRCm39)	intron	probably benign
R5196:H2-T23	UTSW	17	36,343,499 (GRCm39)	critical splice donor site	probably null
R5237:H2-T23	UTSW	17	36,341,258 (GRCm39)	splice site	probably null
R5307:H2-T23	UTSW	17	36,343,108 (GRCm39)	missense	probably benign	0.00
R5336:H2-T23	UTSW	17	36,342,550 (GRCm39)	missense	possibly damaging	0.85
R5646:H2-T23	UTSW	17	36,342,695 (GRCm39)	missense	possibly damaging	0.49
R5800:H2-T23	UTSW	17	36,342,496 (GRCm39)	intron	probably benign
R6013:H2-T23	UTSW	17	36,341,474 (GRCm39)	missense	probably benign	0.00
R6081:H2-T23	UTSW	17	36,342,707 (GRCm39)	missense	possibly damaging	0.90
R6382:H2-T23	UTSW	17	36,342,724 (GRCm39)	missense	probably damaging	1.00
R7043:H2-T23	UTSW	17	36,342,803 (GRCm39)	missense	probably damaging	1.00
R7134:H2-T23	UTSW	17	36,342,709 (GRCm39)	missense	probably damaging	1.00
R9383:H2-T23	UTSW	17	36,343,227 (GRCm39)	missense	possibly damaging	0.64
R9550:H2-T23	UTSW	17	36,342,712 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ATTGTAGTAGCCGAGCAGGG -3'
(R):5'- TCCCGACCCAGAGTAGTAAG -3'

Sequencing Primer
(F):5'- AGCAGGGTCCTCAGGTTTACTC -3'
(R):5'- GTGCAGCACCCCAAGTTC -3'

Posted On

2016-06-21