Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02884:H2-M10.2'

362899

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

H2-M10.2

Ensembl Gene

ENSMUSG00000023083

Gene Name

histocompatibility 2, M region locus 10.2

Synonyms

4.7H

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.049) question?

Stock #

IGL02884

Quality Score

Status

Chromosome

Chromosomal Location

36595173-36597313 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 36595568 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glycine at position 241 (R241G)

Ref Sequence

ENSEMBL: ENSMUSP00000023845 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000023845]

AlphaFold

Q85ZW9

Predicted Effect

probably damaging
Transcript: ENSMUST00000023845
AA Change: R241G

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000023845
Gene: ENSMUSG00000023083
AA Change: R241G

Domain	Start	End	E-Value	Type
Pfam:MHC_I	23	201	6.5e-50	PFAM
IGc1	220	291	1.32e-21	SMART
transmembrane domain	304	326	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 53 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930438A08Rik	A	G	11: 58,178,302 (GRCm39)	I121V	probably benign	Het
Adprh	C	T	16: 38,266,396 (GRCm39)	V249I	probably benign	Het
Akap11	A	T	14: 78,736,402 (GRCm39)	M1797K	probably benign	Het
Akap6	T	A	12: 52,933,405 (GRCm39)	I299N	probably benign	Het
Akr1c12	A	T	13: 4,322,211 (GRCm39)	M277K	possibly damaging	Het
Ankrd17	A	T	5: 90,412,616 (GRCm39)	M1236K	probably damaging	Het
Arhgef11	A	G	3: 87,635,313 (GRCm39)	D874G	probably damaging	Het
Atg4b	T	C	1: 93,715,437 (GRCm39)		probably benign	Het
Bcl9	G	A	3: 97,117,368 (GRCm39)	P442L	probably damaging	Het
Ccdc107	A	T	4: 43,495,228 (GRCm39)	K98*	probably null	Het
Cenpl	A	G	1: 160,913,619 (GRCm39)	Q343R	probably benign	Het
Cep104	T	C	4: 154,074,319 (GRCm39)	C524R	probably damaging	Het
Clec3b	C	T	9: 122,985,827 (GRCm39)	T75I	probably benign	Het
Col13a1	A	T	10: 61,741,064 (GRCm39)		probably benign	Het
Crot	C	T	5: 9,028,197 (GRCm39)		probably null	Het
Ddo	G	A	10: 40,513,360 (GRCm39)	V101I	probably benign	Het
Disp2	T	C	2: 118,618,032 (GRCm39)		probably benign	Het
Dnmt3b	A	C	2: 153,516,297 (GRCm39)	Y474S	probably damaging	Het
Dpp6	T	A	5: 27,839,554 (GRCm39)	N298K	possibly damaging	Het
Fbf1	C	T	11: 116,037,339 (GRCm39)	E940K	probably damaging	Het
Fgd6	A	G	10: 93,881,501 (GRCm39)		probably benign	Het
Haghl	A	T	17: 26,002,072 (GRCm39)	F207Y	possibly damaging	Het
Helt	G	A	8: 46,745,620 (GRCm39)	R88C	probably damaging	Het
Igf2bp2	T	C	16: 21,981,635 (GRCm39)	K27E	probably benign	Het
Il1b	T	C	2: 129,207,022 (GRCm39)	H246R	probably benign	Het
Itprid1	T	C	6: 55,851,339 (GRCm39)		probably null	Het
Kcnu1	C	T	8: 26,411,556 (GRCm39)	S167L	probably damaging	Het
Kif16b	A	T	2: 142,544,534 (GRCm39)		probably benign	Het
Myh7	A	T	14: 55,230,276 (GRCm39)	S19T	probably benign	Het
Ncaph2	T	C	15: 89,248,447 (GRCm39)		probably null	Het
Nlrp4c	T	C	7: 6,101,951 (GRCm39)	L879P	probably damaging	Het
Nqo2	T	A	13: 34,156,344 (GRCm39)	N19K	probably damaging	Het
Or2r2	C	T	6: 42,463,540 (GRCm39)	V196M	probably damaging	Het
Osbpl1a	C	A	18: 12,952,635 (GRCm39)	G93*	probably null	Het
Pdxdc1	A	G	16: 13,661,659 (GRCm39)	F459L	possibly damaging	Het
Phc2	A	T	4: 128,601,809 (GRCm39)	H88L	probably damaging	Het
Pkd1l2	G	A	8: 117,792,484 (GRCm39)	T436I	probably benign	Het
Ptchd4	A	T	17: 42,813,340 (GRCm39)	T414S	possibly damaging	Het
Rab7b	A	G	1: 131,626,280 (GRCm39)	R103G	probably damaging	Het
Retnla	A	G	16: 48,662,943 (GRCm39)	Y3C	probably benign	Het
Samd7	G	A	3: 30,810,322 (GRCm39)	R113H	probably damaging	Het
Shisa9	G	A	16: 11,814,907 (GRCm39)		probably benign	Het
Soat1	A	T	1: 156,268,926 (GRCm39)	I208N	possibly damaging	Het
Stab1	C	A	14: 30,872,100 (GRCm39)		probably null	Het
Tti2	C	T	8: 31,641,505 (GRCm39)	L210F	possibly damaging	Het
Ube2v2	A	G	16: 15,374,349 (GRCm39)	V77A	probably benign	Het
Ubr5	T	C	15: 37,998,620 (GRCm39)	E1617G	probably damaging	Het
Vmn2r16	T	A	5: 109,508,757 (GRCm39)	I495K	possibly damaging	Het
Vwce	G	T	19: 10,623,943 (GRCm39)	R278L	possibly damaging	Het
Wdr26	C	T	1: 181,010,349 (GRCm39)	A551T	probably damaging	Het
Wee1	A	G	7: 109,725,269 (GRCm39)	I304V	probably benign	Het
Xrcc5	C	T	1: 72,385,396 (GRCm39)	H496Y	possibly damaging	Het
Zfp142	G	T	1: 74,611,142 (GRCm39)	S884R	probably damaging	Het

Other mutations in H2-M10.2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00771:H2-M10.2	APN	17	36,597,288 (GRCm39)	missense	probably damaging	0.99
IGL01490:H2-M10.2	APN	17	36,596,377 (GRCm39)	missense	probably damaging	0.96
IGL02347:H2-M10.2	APN	17	36,596,505 (GRCm39)	missense	probably benign	0.00
IGL03244:H2-M10.2	APN	17	36,596,463 (GRCm39)	missense	probably benign	0.33
R0383:H2-M10.2	UTSW	17	36,595,253 (GRCm39)	missense	probably benign	0.04
R1756:H2-M10.2	UTSW	17	36,597,015 (GRCm39)	splice site	probably benign
R1803:H2-M10.2	UTSW	17	36,596,763 (GRCm39)	missense	probably benign
R2496:H2-M10.2	UTSW	17	36,596,771 (GRCm39)	missense	possibly damaging	0.93
R3816:H2-M10.2	UTSW	17	36,597,254 (GRCm39)	nonsense	probably null
R4597:H2-M10.2	UTSW	17	36,596,285 (GRCm39)	missense	probably benign	0.07
R4832:H2-M10.2	UTSW	17	36,595,219 (GRCm39)	missense	probably damaging	0.99
R5200:H2-M10.2	UTSW	17	36,595,641 (GRCm39)	missense	probably benign	0.17
R5325:H2-M10.2	UTSW	17	36,596,471 (GRCm39)	missense	probably benign	0.00
R7443:H2-M10.2	UTSW	17	36,596,945 (GRCm39)	missense	probably benign
R8064:H2-M10.2	UTSW	17	36,595,442 (GRCm39)	missense	probably damaging	1.00
R8894:H2-M10.2	UTSW	17	36,595,555 (GRCm39)	missense	possibly damaging	0.65
R9420:H2-M10.2	UTSW	17	36,595,643 (GRCm39)	missense	probably benign	0.01
R9489:H2-M10.2	UTSW	17	36,596,936 (GRCm39)	missense	probably benign	0.04

Posted On

2015-12-18