Mutagenetix > Incidental Mutation

Incidental Mutation 'R7060:Il10ra'

548197

Institutional Source

Beutler Lab

Gene Symbol

Il10ra

Ensembl Gene

ENSMUSG00000032089

Gene Name

interleukin 10 receptor, alpha

Synonyms

Il10r, mIL-10R, CDw210

MMRRC Submission

045157-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7060 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

45165135-45180447 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 45167522 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Threonine at position 343 (I343T)

Ref Sequence

ENSEMBL: ENSMUSP00000135461 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000034594] [ENSMUST00000176222] [ENSMUST00000176808]

AlphaFold

Q61727

Predicted Effect

probably benign
Transcript: ENSMUST00000034594
AA Change: I345T

PolyPhen 2 Score 0.003 (Sensitivity: 0.98; Specificity: 0.44)

SMART Domains

Protein: ENSMUSP00000034594
Gene: ENSMUSG00000032089
AA Change: I345T

Domain	Start	End	E-Value	Type
Pfam:Tissue_fac	5	114	3.3e-29	PFAM
SCOP:d1lqsr2	125	231	5e-59	SMART
transmembrane domain	239	261	N/A	INTRINSIC
low complexity region	482	491	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000176222
AA Change: I343T

PolyPhen 2 Score 0.005 (Sensitivity: 0.97; Specificity: 0.74)

SMART Domains

Protein: ENSMUSP00000135461
Gene: ENSMUSG00000032089
AA Change: I343T

Domain	Start	End	E-Value	Type
Pfam:Tissue_fac	2	112	3.5e-26	PFAM
SCOP:d1lqsr2	123	229	5e-59	SMART
transmembrane domain	237	259	N/A	INTRINSIC
low complexity region	480	489	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000176808

SMART Domains

Protein: ENSMUSP00000135361
Gene: ENSMUSG00000032089

Domain	Start	End	E-Value	Type
signal peptide	1	23	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.0%

Validation Efficiency

96% (78/81)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a receptor for interleukin 10. This protein is structurally related to interferon receptors. It has been shown to mediate the immunosuppressive signal of interleukin 10, and thus inhibits the synthesis of proinflammatory cytokines. This receptor is reported to promote survival of progenitor myeloid cells through the insulin receptor substrate-2/PI 3-kinase/AKT pathway. Activation of this receptor leads to tyrosine phosphorylation of JAK1 and TYK2 kinases. Two transcript variants, one protein-coding and the other not protein-coding, have been found for this gene. [provided by RefSeq, Jan 2009]
PHENOTYPE: Mice homozygous for an ENU-generated null allele suffer from a severe inflammatory bowel syndrome. Mice heterozygote for an NZW variant allele have high sera levels of anti-chromatin antibodies. Mice homozygous for a knock-out allele exhibit increased susceptibility to induced colitis. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcg4	T	A	9: 44,186,425 (GRCm39)	T535S	probably benign	Het
Adamts19	A	T	18: 58,970,712 (GRCm39)	R99*	probably null	Het
Alg6	C	T	4: 99,650,198 (GRCm39)	L473F	possibly damaging	Het
Ankar	A	T	1: 72,695,272 (GRCm39)	N893K	probably benign	Het
Ankrd54	G	A	15: 78,939,739 (GRCm39)	A183V	possibly damaging	Het
Anpep	G	T	7: 79,491,542 (GRCm39)	T153K	probably benign	Het
Arap1	A	G	7: 101,058,564 (GRCm39)		probably null	Het
Aspg	A	T	12: 112,089,387 (GRCm39)	T392S	probably benign	Het
B230307C23Rik	A	C	16: 97,811,331 (GRCm39)	R68S	probably benign	Het
Bdp1	G	C	13: 100,196,002 (GRCm39)	N1253K	probably damaging	Het
Ccrl2	G	A	9: 110,884,682 (GRCm39)	S272F	probably damaging	Het
Cdon	T	C	9: 35,398,205 (GRCm39)	L974P	probably damaging	Het
Celsr1	C	A	15: 85,916,856 (GRCm39)	E372D	probably benign	Het
Cers1	A	T	8: 70,768,555 (GRCm39)	M16L	possibly damaging	Het
Col2a1	G	T	15: 97,874,022 (GRCm39)	Q1387K	unknown	Het
Ddx39b	G	A	17: 35,471,726 (GRCm39)	V291M	probably damaging	Het
Dppa2	T	A	16: 48,136,076 (GRCm39)	S143T	probably benign	Het
Dpy19l1	A	T	9: 24,334,419 (GRCm39)	M583K	possibly damaging	Het
Eno3	A	T	11: 70,552,245 (GRCm39)	D299V	possibly damaging	Het
Epha8	C	T	4: 136,658,469 (GRCm39)	V969M	probably damaging	Het
Fcgbp	A	T	7: 27,791,358 (GRCm39)	H873L	probably benign	Het
Fhad1	CGG	CG	4: 141,645,602 (GRCm39)		probably null	Het
Fntb	A	C	12: 76,934,649 (GRCm39)	N173T	possibly damaging	Het
Gins2	T	A	8: 121,308,880 (GRCm39)	M125L	probably benign	Het
Gys1	G	A	7: 45,089,437 (GRCm39)	A199T	probably damaging	Het
Herpud1	C	A	8: 95,117,391 (GRCm39)	H116N	probably benign	Het
Hoga1	C	A	19: 42,048,685 (GRCm39)	Y134*	probably null	Het
Inava	T	C	1: 136,147,935 (GRCm39)	K339R	possibly damaging	Het
Inpp5j	C	T	11: 3,450,133 (GRCm39)		probably null	Het
Itpkb	T	C	1: 180,160,695 (GRCm39)	S274P	probably damaging	Het
Kalrn	C	T	16: 34,177,418 (GRCm39)	C249Y	probably damaging	Het
Klhl35	G	C	7: 99,117,665 (GRCm39)	A70P	possibly damaging	Het
Lhx1	A	G	11: 84,411,108 (GRCm39)		probably null	Het
Lmbrd1	T	C	1: 24,732,047 (GRCm39)	V88A	probably benign	Het
Macc1	T	G	12: 119,411,190 (GRCm39)	L653V	probably damaging	Het
Madd	T	C	2: 91,007,452 (GRCm39)	D220G	probably damaging	Het
Mllt10	T	A	2: 18,164,371 (GRCm39)	H300Q	possibly damaging	Het
Mlxipl	G	A	5: 135,161,169 (GRCm39)	A363T	possibly damaging	Het
Mus81	G	T	19: 5,537,821 (GRCm39)	D78E	probably benign	Het
Mxd1	A	T	6: 86,630,141 (GRCm39)	L26M	probably damaging	Het
Nhsl1	C	T	10: 18,402,251 (GRCm39)	T1159M	probably damaging	Het
Nos1ap	A	G	1: 170,165,694 (GRCm39)	S190P	possibly damaging	Het
Nwd1	A	C	8: 73,393,322 (GRCm39)	D195A	probably damaging	Het
Or12d13	G	T	17: 37,647,352 (GRCm39)	T257N	probably benign	Het
Or6k4	A	T	1: 173,964,376 (GRCm39)	D22V	probably benign	Het
Or8c14-ps1	G	A	9: 38,101,392 (GRCm39)	V124I	probably damaging	Het
Or8k24	T	A	2: 86,216,569 (GRCm39)	R64S	possibly damaging	Het
Otof	T	C	5: 30,545,700 (GRCm39)	D500G	possibly damaging	Het
Pcgf5	T	A	19: 36,420,339 (GRCm39)	Y190*	probably null	Het
Pdcd11	C	T	19: 47,099,418 (GRCm39)	T839I	probably benign	Het
Ppard	G	C	17: 28,517,886 (GRCm39)	S318T	probably benign	Het
Ppfia2	A	G	10: 106,597,970 (GRCm39)	K178E	probably damaging	Het
Ppm1n	G	T	7: 19,013,187 (GRCm39)	R255S	probably damaging	Het
Ppp1r21	A	G	17: 88,887,972 (GRCm39)	Y693C	probably damaging	Het
Ppp2r5d	A	T	17: 46,998,279 (GRCm39)	V169E	possibly damaging	Het
Prc1	A	T	7: 79,954,121 (GRCm39)	T53S	probably benign	Het
Pwp2	A	C	10: 78,009,084 (GRCm39)		probably null	Het
Rab5c	G	A	11: 100,610,789 (GRCm39)	R40C	probably damaging	Het
Ring1	A	G	17: 34,242,364 (GRCm39)	C48R	probably damaging	Het
Rpap1	T	C	2: 119,604,043 (GRCm39)	D496G	probably damaging	Het
Rspo4	C	A	2: 151,714,998 (GRCm39)	Q212K	unknown	Het
Samd9l	T	A	6: 3,372,716 (GRCm39)	D1515V	probably damaging	Het
Serinc3	T	C	2: 163,478,879 (GRCm39)	T83A	probably benign	Het
Setd5	A	C	6: 113,094,343 (GRCm39)	D420A	probably damaging	Het
Sidt2	T	C	9: 45,864,544 (GRCm39)	T62A	possibly damaging	Het
Smarcal1	T	C	1: 72,652,101 (GRCm39)	V621A	probably damaging	Het
Srcin1	A	G	11: 97,464,711 (GRCm39)	L12P	probably damaging	Het
Stx18	G	A	5: 38,278,599 (GRCm39)	D165N	possibly damaging	Het
Sumf2	A	G	5: 129,883,341 (GRCm39)	K139E	possibly damaging	Het
Tdo2	A	T	3: 81,876,866 (GRCm39)	I102N	probably damaging	Het
Tdp1	T	A	12: 99,877,947 (GRCm39)	S410T	probably benign	Het
Tmem94	A	T	11: 115,683,764 (GRCm39)	I726F	probably damaging	Het
Ttc21a	A	G	9: 119,795,742 (GRCm39)	E1192G	probably damaging	Het
Ttc8	T	C	12: 98,909,726 (GRCm39)	I52T	probably benign	Het
Vmn2r99	A	T	17: 19,614,826 (GRCm39)	R849*	probably null	Het
Wwc1	T	C	11: 35,806,003 (GRCm39)	K77E	possibly damaging	Het
Xirp2	A	T	2: 67,345,952 (GRCm39)	E2731V	probably damaging	Het
Zfp1006	A	C	8: 129,945,613 (GRCm39)	I404R	probably benign	Het
Zfp423	G	A	8: 88,509,507 (GRCm39)	T258I	probably damaging	Het

Other mutations in Il10ra

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01874:Il10ra	APN	9	45,178,458 (GRCm39)	missense	probably damaging	1.00
IGL01916:Il10ra	APN	9	45,167,444 (GRCm39)	missense	probably damaging	1.00
IGL03067:Il10ra	APN	9	45,167,157 (GRCm39)	missense	probably benign	0.01
R0081:Il10ra	UTSW	9	45,167,247 (GRCm39)	missense	probably benign	0.04
R0266:Il10ra	UTSW	9	45,176,950 (GRCm39)	missense	probably benign	0.11
R1734:Il10ra	UTSW	9	45,167,241 (GRCm39)	missense	probably benign	0.02
R1901:Il10ra	UTSW	9	45,167,654 (GRCm39)	missense	probably benign	0.39
R1991:Il10ra	UTSW	9	45,167,109 (GRCm39)	missense	probably benign	0.28
R2103:Il10ra	UTSW	9	45,167,109 (GRCm39)	missense	probably benign	0.28
R2218:Il10ra	UTSW	9	45,176,914 (GRCm39)	missense	probably benign
R4686:Il10ra	UTSW	9	45,180,357 (GRCm39)	missense	probably damaging	1.00
R4908:Il10ra	UTSW	9	45,166,919 (GRCm39)	missense	probably benign	0.21
R4982:Il10ra	UTSW	9	45,180,357 (GRCm39)	missense	probably damaging	1.00
R5590:Il10ra	UTSW	9	45,176,924 (GRCm39)	nonsense	probably null
R5739:Il10ra	UTSW	9	45,167,368 (GRCm39)	missense	possibly damaging	0.65
R5872:Il10ra	UTSW	9	45,166,951 (GRCm39)	missense	possibly damaging	0.92
R6053:Il10ra	UTSW	9	45,167,601 (GRCm39)	missense	probably damaging	0.99
R6282:Il10ra	UTSW	9	45,171,703 (GRCm39)	missense	probably damaging	0.98
R6798:Il10ra	UTSW	9	45,167,730 (GRCm39)	missense	probably damaging	0.99
R7561:Il10ra	UTSW	9	45,167,117 (GRCm39)	missense	probably benign	0.00
R7630:Il10ra	UTSW	9	45,167,369 (GRCm39)	missense	probably damaging	1.00
R7709:Il10ra	UTSW	9	45,171,697 (GRCm39)	missense	probably benign	0.01
R8880:Il10ra	UTSW	9	45,175,631 (GRCm39)	missense	probably damaging	1.00
R8939:Il10ra	UTSW	9	45,177,802 (GRCm39)	missense	unknown
R9069:Il10ra	UTSW	9	45,167,396 (GRCm39)	missense	probably damaging	0.98
R9511:Il10ra	UTSW	9	45,167,690 (GRCm39)	missense	probably benign	0.06
Z1176:Il10ra	UTSW	9	45,177,930 (GRCm39)	missense	possibly damaging	0.66

Predicted Primers

PCR Primer
(F):5'- GAGTTCTGGACTAGGTTAACGTC -3'
(R):5'- TCCCAGGTCTTCAAGAAGCC -3'

Sequencing Primer
(F):5'- GGACTAGGTTAACGTCACTGTCATC -3'
(R):5'- GGTCTTCAAGAAGCCTCACG -3'

Posted On

2019-05-13