Mutagenetix > Incidental Mutation

Incidental Mutation 'R9025:Il17rb'

716025

Institutional Source

Beutler Lab

Gene Symbol

Il17rb

Ensembl Gene

ENSMUSG00000015966

Gene Name

interleukin 17 receptor B

Synonyms

IL-17Rh1, Il17br, IL17RH1, IL-17ER, Evi27

MMRRC Submission

068854-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.068) question?

Stock #

R9025 (G1)

Quality Score

197.009

Status

Validated

Chromosome

Chromosomal Location

29718125-29730853 bp(-) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

C to A at 29724857 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000153076 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000016110] [ENSMUST00000122205] [ENSMUST00000135888] [ENSMUST00000136726] [ENSMUST00000224797]

AlphaFold

Q9JIP3

Predicted Effect

probably benign
Transcript: ENSMUST00000016110

SMART Domains

Protein: ENSMUSP00000016110
Gene: ENSMUSG00000015966

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
Pfam:IL17R_fnIII_D1	22	175	4.3e-26	PFAM
Pfam:IL17R_fnIII_D2	176	268	1.3e-11	PFAM
transmembrane domain	287	309	N/A	INTRINSIC
Pfam:SEFIR	329	476	3.5e-49	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000122205

SMART Domains

Protein: ENSMUSP00000113686
Gene: ENSMUSG00000015966

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
PDB:4HSA\|F	34	276	2e-23	PDB
transmembrane domain	287	309	N/A	INTRINSIC
Pfam:SEFIR	329	476	1.7e-49	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000135888

SMART Domains

Protein: ENSMUSP00000121407
Gene: ENSMUSG00000015966

Domain	Start	End	E-Value	Type
signal peptide	1	17	N/A	INTRINSIC
Pfam:IL17R_fnIII_D1	22	123	1.1e-13	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000136726
AA Change: A210S

SMART Domains

Protein: ENSMUSP00000117802
Gene: ENSMUSG00000015966
AA Change: A210S

Domain	Start	End	E-Value	Type
PDB:3JVF\|C	13	171	5e-12	PDB

Predicted Effect

probably benign
Transcript: ENSMUST00000224797

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

99% (80/81)

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 cytokine receptor. This receptor specifically binds to IL17B and IL17E, but does not bind to IL17 and IL17C. This receptor has been shown to mediate the activation of NF-kappaB and the production of IL8 induced by IL17E. The expression of the rat counterpart of this gene was found to be significantly up-regulated during intestinal inflammation, which suggested the immunoregulatory activity of this receptor. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice that are homozygous for a null allele have defects in their response to IL17A or IL17F. In addition this locus is a common site of retoviral integration in BXH2 murine myeloid leukemias and occurred at a CpG island 6 kb upstream of the Il17rb gene. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2ml1	G	T	6: 128,534,545 (GRCm39)	N837K	possibly damaging	Het
Adam29	A	T	8: 56,325,196 (GRCm39)	C419*	probably null	Het
Adamts7	C	A	9: 90,067,848 (GRCm39)	S446*	probably null	Het
Ager	A	G	17: 34,819,594 (GRCm39)	R371G	probably damaging	Het
Apobr	T	A	7: 126,185,629 (GRCm39)	V380E	possibly damaging	Het
Arhgap26	T	C	18: 39,379,898 (GRCm39)	S105P		Het
Atrip	A	G	9: 108,902,906 (GRCm39)	F56S	probably damaging	Het
Bag2	T	C	1: 33,785,905 (GRCm39)	Y139C		Het
Bccip	C	T	7: 133,319,346 (GRCm39)	Q146*	probably null	Het
Btbd10	G	A	7: 112,951,031 (GRCm39)	R20W	possibly damaging	Het
Catsperd	T	A	17: 56,962,156 (GRCm39)	N443K	probably damaging	Het
Cdh26	G	A	2: 178,104,409 (GRCm39)	E265K	probably benign	Het
Cep76	T	C	18: 67,767,885 (GRCm39)	R216G	probably damaging	Het
Cgas	C	A	9: 78,349,787 (GRCm39)	V192L	probably benign	Het
Cnot1	T	A	8: 96,475,660 (GRCm39)	M1000L	probably benign	Het
Cyp1a1	A	G	9: 57,610,070 (GRCm39)	T495A	possibly damaging	Het
Cyp2w1	T	A	5: 139,342,470 (GRCm39)	M421K	probably benign	Het
Dlg5	T	C	14: 24,199,546 (GRCm39)	T1453A	probably benign	Het
Dnah5	G	T	15: 28,409,412 (GRCm39)	W3610L	probably damaging	Het
Dnah9	T	C	11: 65,896,651 (GRCm39)	D2391G	probably damaging	Het
Dnajc10	G	A	2: 80,179,637 (GRCm39)	G724R	probably damaging	Het
Dst	T	A	1: 34,227,585 (GRCm39)	I1726N	possibly damaging	Het
Dync2h1	A	T	9: 7,139,462 (GRCm39)	L1391*	probably null	Het
Dzank1	T	C	2: 144,318,012 (GRCm39)	S718G	probably benign	Het
E230025N22Rik	T	C	18: 36,819,890 (GRCm39)	D300G	probably damaging	Het
Ebf3	T	C	7: 136,914,098 (GRCm39)	I131V	possibly damaging	Het
Eif3g	T	C	9: 20,807,426 (GRCm39)	I131V	probably benign	Het
Eppk1	T	A	15: 75,990,503 (GRCm39)	Q2126L	possibly damaging	Het
Fam83h	T	C	15: 75,874,182 (GRCm39)	R1052G	probably benign	Het
Fry	A	T	5: 150,219,273 (GRCm39)		probably benign	Het
Ggt6	C	T	11: 72,328,123 (GRCm39)	H208Y	possibly damaging	Het
Gm15821	T	A	17: 34,433,235 (GRCm39)	E28V	unknown	Het
Gprin2	T	C	14: 33,916,957 (GRCm39)	Q271R	probably damaging	Het
Gsdmd	T	C	15: 75,739,053 (GRCm39)	F477L	probably benign	Het
Hes7	T	C	11: 69,013,782 (GRCm39)	S214P	probably benign	Het
Hmcn2	A	G	2: 31,347,967 (GRCm39)	H4871R	possibly damaging	Het
Il15ra	G	A	2: 11,723,233 (GRCm39)	V86I	possibly damaging	Het
Itpr3	G	A	17: 27,337,651 (GRCm39)		probably benign	Het
Kcnab2	T	C	4: 152,491,635 (GRCm39)	Y63C	probably damaging	Het
Kctd17	A	T	15: 78,314,282 (GRCm39)	Y84F	probably damaging	Het
Lama1	T	A	17: 68,119,491 (GRCm39)	V2656E		Het
Lama2	T	C	10: 26,860,367 (GRCm39)	N3040S	probably benign	Het
Ldha	C	T	7: 46,500,433 (GRCm39)	R173C	unknown	Het
Lig1	A	G	7: 13,037,746 (GRCm39)	I665M	probably damaging	Het
Lipe	G	A	7: 25,083,923 (GRCm39)	A412V	probably damaging	Het
Lrrc63	T	C	14: 75,322,284 (GRCm39)	T607A	probably benign	Het
Majin	G	A	19: 6,263,427 (GRCm39)		probably null	Het
Map3k19	A	G	1: 127,758,175 (GRCm39)	L335P	probably benign	Het
Map3k9	A	G	12: 81,819,507 (GRCm39)	L249P	probably damaging	Het
Muc5b	G	T	7: 141,426,209 (GRCm39)	D4769Y	probably damaging	Het
Myh9	T	C	15: 77,653,192 (GRCm39)	T1382A	probably benign	Het
Nedd4l	T	A	18: 65,311,995 (GRCm39)	D407E	probably damaging	Het
Ngp	A	G	9: 110,251,451 (GRCm39)	I160V	possibly damaging	Het
Nmrk1	A	G	19: 18,617,156 (GRCm39)		probably benign	Het
Nnmt	C	A	9: 48,503,461 (GRCm39)	K188N	probably damaging	Het
Nup153	T	A	13: 46,837,709 (GRCm39)	Q1171L	probably benign	Het
Oplah	T	A	15: 76,187,417 (GRCm39)	E556V	probably benign	Het
Or9g3	T	G	2: 85,589,879 (GRCm39)	L280F	possibly damaging	Het
Otog	A	G	7: 45,937,520 (GRCm39)	D1743G	probably benign	Het
Otogl	T	C	10: 107,613,432 (GRCm39)	Y2011C	probably damaging	Het
Pbx4	C	T	8: 70,317,097 (GRCm39)	P118L	probably benign	Het
Plekha6	T	A	1: 133,212,999 (GRCm39)	S757T	probably benign	Het
Plk5	C	G	10: 80,193,830 (GRCm39)	R40G	probably damaging	Het
Polr3a	C	T	14: 24,519,479 (GRCm39)	S643N	probably damaging	Het
Pwp1	T	A	10: 85,718,745 (GRCm39)	L304Q	probably damaging	Het
Qrich2	GCTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTG	GCTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTGCAACACACCAGGCTGAACTGCACCTGGTTG	11: 116,348,367 (GRCm39)		probably benign	Het
Rab11fip1	A	G	8: 27,644,736 (GRCm39)	F350L	probably benign	Het
Safb2	T	C	17: 56,873,614 (GRCm39)	E683G	probably damaging	Het
Scarb1	A	T	5: 125,381,414 (GRCm39)	N43K	probably damaging	Het
Serpina3k	A	G	12: 104,307,230 (GRCm39)	E154G	probably damaging	Het
Sgsm3	T	A	15: 80,892,182 (GRCm39)	V250D	probably damaging	Het
Slit1	T	A	19: 41,612,968 (GRCm39)	I851F	probably benign	Het
Spag4	G	A	2: 155,910,424 (GRCm39)	G350E	probably damaging	Het
Sult2a7	A	T	7: 14,225,755 (GRCm39)	L77Q	probably damaging	Het
Tbc1d2	T	A	4: 46,607,062 (GRCm39)	T783S	probably damaging	Het
Thoc6	T	C	17: 23,888,862 (GRCm39)	E182G		Het
Tmem132a	A	T	19: 10,837,525 (GRCm39)	I595N	probably damaging	Het
Trim69	A	G	2: 122,003,771 (GRCm39)	N240S	probably benign	Het
Ush1c	A	T	7: 45,846,614 (GRCm39)		probably benign	Het
Wnk4	T	G	11: 101,153,641 (GRCm39)	Y234*	probably null	Het
Zfp943	A	G	17: 22,211,321 (GRCm39)	N136D	possibly damaging	Het
Znhit2	G	A	19: 6,111,669 (GRCm39)	R138H	possibly damaging	Het

Other mutations in Il17rb

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01584:Il17rb	APN	14	29,725,637 (GRCm39)	missense	probably damaging	1.00
IGL03151:Il17rb	APN	14	29,728,810 (GRCm39)	missense	probably benign	0.05
R0276:Il17rb	UTSW	14	29,726,337 (GRCm39)	missense	probably damaging	1.00
R0391:Il17rb	UTSW	14	29,728,112 (GRCm39)	splice site	probably null
R0391:Il17rb	UTSW	14	29,726,304 (GRCm39)	missense	probably benign	0.00
R0408:Il17rb	UTSW	14	29,718,637 (GRCm39)	missense	probably benign	0.02
R2011:Il17rb	UTSW	14	29,718,797 (GRCm39)	nonsense	probably null
R2012:Il17rb	UTSW	14	29,718,797 (GRCm39)	nonsense	probably null
R2057:Il17rb	UTSW	14	29,719,111 (GRCm39)	missense	probably benign	0.01
R2227:Il17rb	UTSW	14	29,728,038 (GRCm39)	missense	probably benign	0.02
R3548:Il17rb	UTSW	14	29,730,729 (GRCm39)	splice site	probably null
R4199:Il17rb	UTSW	14	29,718,601 (GRCm39)	missense	probably benign
R4578:Il17rb	UTSW	14	29,724,356 (GRCm39)	missense	probably damaging	0.97
R5092:Il17rb	UTSW	14	29,724,333 (GRCm39)	missense	probably benign	0.00
R5928:Il17rb	UTSW	14	29,726,232 (GRCm39)	critical splice donor site	probably null
R6280:Il17rb	UTSW	14	29,724,928 (GRCm39)	missense	probably benign	0.00
R6378:Il17rb	UTSW	14	29,722,320 (GRCm39)	missense	probably damaging	0.97
R6470:Il17rb	UTSW	14	29,724,866 (GRCm39)	missense	probably benign	0.10
R6741:Il17rb	UTSW	14	29,722,293 (GRCm39)	missense	possibly damaging	0.82
R6919:Il17rb	UTSW	14	29,726,228 (GRCm39)	splice site	probably null
R7133:Il17rb	UTSW	14	29,718,828 (GRCm39)	missense	probably damaging	1.00
R7423:Il17rb	UTSW	14	29,719,072 (GRCm39)	missense	probably damaging	0.97
R7470:Il17rb	UTSW	14	29,719,990 (GRCm39)	missense	probably damaging	1.00
R7559:Il17rb	UTSW	14	29,719,000 (GRCm39)	missense	probably damaging	1.00
R7847:Il17rb	UTSW	14	29,718,763 (GRCm39)	missense	probably damaging	1.00
R8685:Il17rb	UTSW	14	29,726,297 (GRCm39)	missense	probably benign	0.32
R8835:Il17rb	UTSW	14	29,722,308 (GRCm39)	missense	possibly damaging	0.95
R9434:Il17rb	UTSW	14	29,728,054 (GRCm39)	missense	probably damaging	0.98

Predicted Primers

PCR Primer
(F):5'- CTGCCTCTTCCAGACATGAAG -3'
(R):5'- CGCTGGTCATTGGCATCTTG -3'

Sequencing Primer
(F):5'- TTCCAGACATGAAGCTCCAGGTG -3'
(R):5'- CATCTTGTTTTCAGGGTGCAC -3'

Posted On

2022-06-27