Mutagenetix > Incidental Mutation

Incidental Mutation 'R9313:Crlf1'

705721

Institutional Source

Beutler Lab

Gene Symbol

Crlf1

Ensembl Gene

ENSMUSG00000007888

Gene Name

cytokine receptor-like factor 1

Synonyms

cytokine receptor like molecule 3, CRLM3, CLF-1

MMRRC Submission

Accession Numbers

Essential gene?

Probably essential (E-score: 0.791) question?

Stock #

R9313 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

70945808-70956731 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 70951466 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 115 (D115G)

Ref Sequence

ENSEMBL: ENSMUSP00000008032 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000008032] [ENSMUST00000132648]

AlphaFold

Q9JM58

Predicted Effect

probably damaging
Transcript: ENSMUST00000008032
AA Change: D115G

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

SMART Domains

Protein: ENSMUSP00000008032
Gene: ENSMUSG00000007888
AA Change: D115G

Domain	Start	End	E-Value	Type
signal peptide	1	40	N/A	INTRINSIC
Pfam:Lep_receptor_Ig	41	127	5.7e-8	PFAM
FN3	138	223	2.11e0	SMART
FN3	238	323	1.5e-5	SMART
low complexity region	345	361	N/A	INTRINSIC
low complexity region	415	425	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000127983

SMART Domains

Protein: ENSMUSP00000115614
Gene: ENSMUSG00000007888

Domain	Start	End	E-Value	Type
Blast:FN3	2	28	2e-12	BLAST
SCOP:d1eerb2	2	46	1e-8	SMART
low complexity region	50	66	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000132648

SMART Domains

Protein: ENSMUSP00000119545
Gene: ENSMUSG00000007888

Domain	Start	End	E-Value	Type
FN3	16	101	2.11e0	SMART
low complexity region	104	122	N/A	INTRINSIC

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

MGI Phenotype

FUNCTION: This gene encodes a member of the cytokine type I receptor family. The encoded protein functions as a cytokine receptor subunit and may be involved in immune system regulation and fetal development. [provided by RefSeq, Dec 2015]
PHENOTYPE: Mice homozygous for a targeted mutation fail to suckle effectively and do not survive beyond 24 hrs after birth. Newborns exhibit reduced numbers of hematopoietic progenitor cells as well as a significant reduction in the number of motoneurons in the lumbar spinal cord and facial nucleus. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700006A11Rik	T	C	3: 124,207,220 (GRCm39)	T324A	probably benign	Het
Aadat	G	A	8: 60,979,635 (GRCm39)	V166I	probably benign	Het
Abca17	C	T	17: 24,565,207 (GRCm39)	S75N	probably benign	Het
Adgrb1	A	G	15: 74,411,624 (GRCm39)	T376A	probably damaging	Het
Atp5po	CTTTGACG	C	16: 91,723,804 (GRCm39)		probably null	Het
Atp5po	TTTGACGGT	TT	16: 91,723,805 (GRCm39)		probably null	Het
Car9	A	G	4: 43,507,180 (GRCm39)	E42G	probably benign	Het
Ccdc168	A	G	1: 44,096,520 (GRCm39)	V1526A	probably benign	Het
Cep41	T	C	6: 30,680,345 (GRCm39)	K9R	probably null	Het
Cfap20dc	T	A	14: 8,518,635 (GRCm38)	T274S	probably benign	Het
Ckm	A	G	7: 19,149,398 (GRCm39)	T141A	probably benign	Het
Clcc1	G	T	3: 108,581,976 (GRCm39)	R360S	probably benign	Het
Clcn3	A	C	8: 61,390,503 (GRCm39)	I146R	probably damaging	Het
Dnah1	T	A	14: 30,987,970 (GRCm39)	I3483F	probably damaging	Het
Dop1a	T	C	9: 86,406,641 (GRCm39)	*386Q	probably null	Het
Eftud2	A	G	11: 102,730,262 (GRCm39)	V899A	probably benign	Het
Ephx3	C	G	17: 32,408,290 (GRCm39)	D45H	probably benign	Het
Faap100	A	G	11: 120,267,688 (GRCm39)	S362P	probably damaging	Het
Fdps	A	T	3: 89,006,655 (GRCm39)	D78E	probably benign	Het
Fsd1l	T	G	4: 53,694,760 (GRCm39)	W405G	probably damaging	Het
Fsd1l	T	C	4: 53,701,093 (GRCm39)	V485A	possibly damaging	Het
Gm12887	C	T	4: 121,473,701 (GRCm39)	V50M	probably benign	Het
Gm45785	T	C	7: 140,398,616 (GRCm39)	I94V	unknown	Het
Hcls1	C	T	16: 36,777,000 (GRCm39)	A230V	probably benign	Het
Hmcn1	A	C	1: 150,522,343 (GRCm39)	V3519G	probably benign	Het
Hmgcs1	A	G	13: 120,165,963 (GRCm39)	Y360C	probably benign	Het
Hsd17b13	A	G	5: 104,113,639 (GRCm39)		probably null	Het
Ift57	T	A	16: 49,557,085 (GRCm39)	D235E	possibly damaging	Het
Il22b	A	G	10: 118,130,138 (GRCm39)	C89R	probably damaging	Het
Iqcn	G	A	8: 71,161,353 (GRCm39)	G182D	probably damaging	Het
Krt9	T	A	11: 100,079,547 (GRCm39)	Y615F	unknown	Het
Ltbp2	G	A	12: 84,837,864 (GRCm39)	P1192L	probably benign	Het
Marco	T	C	1: 120,421,814 (GRCm39)	E130G	probably damaging	Het
Ms4a18	A	T	19: 10,988,804 (GRCm39)	L184Q	probably damaging	Het
Mtus1	A	T	8: 41,535,923 (GRCm39)	S598T	probably damaging	Het
Nbeal2	C	A	9: 110,463,436 (GRCm39)	R1265L	probably damaging	Het
Odf2	G	T	2: 29,816,815 (GRCm39)	G754C	probably benign	Het
Or2m12	T	G	16: 19,105,100 (GRCm39)	Y131S	probably benign	Het
Or4x13	C	A	2: 90,231,917 (GRCm39)	T304K	probably benign	Het
Or5w11	T	C	2: 87,459,076 (GRCm39)	S90P	probably benign	Het
Or6c69b	A	T	10: 129,626,789 (GRCm39)	I223N	probably damaging	Het
Paqr8	G	A	1: 21,005,128 (GRCm39)	W94*	probably null	Het
Pkd1	G	A	17: 24,813,932 (GRCm39)	G4132D	probably damaging	Het
Pom121l2	A	G	13: 22,168,506 (GRCm39)	M926V	probably benign	Het
Postn	A	T	3: 54,273,336 (GRCm39)	Y79F	probably damaging	Het
Prl7d1	T	C	13: 27,893,182 (GRCm39)	E242G	probably benign	Het
Rcor3	G	T	1: 191,810,181 (GRCm39)	H165Q	possibly damaging	Het
Rnf157	A	G	11: 116,250,718 (GRCm39)	V161A	probably damaging	Het
Rnf38	G	A	4: 44,143,584 (GRCm39)	T150M	probably damaging	Het
Scn4b	T	A	9: 45,058,013 (GRCm39)	V35E	probably damaging	Het
Serpina3i	T	C	12: 104,231,672 (GRCm39)	I103T	probably damaging	Het
Shcbp1	T	A	8: 4,794,518 (GRCm39)	D425V	probably damaging	Het
Sidt2	T	C	9: 45,852,658 (GRCm39)	T776A	possibly damaging	Het
Siglecg	A	G	7: 43,061,856 (GRCm39)	D534G	probably benign	Het
Sipa1l3	T	A	7: 29,077,439 (GRCm39)	T778S	probably benign	Het
Slc13a1	A	G	6: 24,108,203 (GRCm39)	V291A	probably benign	Het
Stra6l	A	G	4: 45,881,454 (GRCm39)	I439V	probably benign	Het
Tdrd7	G	A	4: 46,005,319 (GRCm39)	S375N	probably benign	Het
Tut7	A	T	13: 59,947,798 (GRCm39)	M841K	probably benign	Het
Vmn1r192	T	A	13: 22,372,191 (GRCm39)	I10L	probably benign	Het
Vmn2r34	T	G	7: 7,686,817 (GRCm39)	L293F	possibly damaging	Het
Xirp2	G	T	2: 67,347,322 (GRCm39)	A3188S	probably damaging	Het
Zfp219	A	G	14: 52,246,200 (GRCm39)	V309A	probably damaging	Het
Zfp341	C	A	2: 154,469,907 (GRCm39)	P197T	probably damaging	Het
Zfp628	G	A	7: 4,922,549 (GRCm39)	R257H	probably benign	Het
Zfp644	T	G	5: 106,784,324 (GRCm39)	Y741S	probably benign	Het

Other mutations in Crlf1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02878:Crlf1	APN	8	70,956,290 (GRCm39)	critical splice donor site	probably null
R0317:Crlf1	UTSW	8	70,951,249 (GRCm39)	missense	probably benign
R0398:Crlf1	UTSW	8	70,951,739 (GRCm39)	splice site	probably benign
R0437:Crlf1	UTSW	8	70,952,164 (GRCm39)	splice site	probably null
R1191:Crlf1	UTSW	8	70,951,478 (GRCm39)	missense	probably damaging	1.00
R1741:Crlf1	UTSW	8	70,953,556 (GRCm39)	missense	probably damaging	0.99
R3730:Crlf1	UTSW	8	70,952,092 (GRCm39)	missense	probably benign	0.03
R3731:Crlf1	UTSW	8	70,952,092 (GRCm39)	missense	probably benign	0.03
R4467:Crlf1	UTSW	8	70,953,606 (GRCm39)	nonsense	probably null
R5557:Crlf1	UTSW	8	70,951,317 (GRCm39)	missense	probably benign	0.12
R6009:Crlf1	UTSW	8	70,956,129 (GRCm39)	missense	probably damaging	1.00
R6348:Crlf1	UTSW	8	70,945,990 (GRCm39)	missense	probably benign
R6606:Crlf1	UTSW	8	70,953,824 (GRCm39)	missense	probably damaging	1.00
R7947:Crlf1	UTSW	8	70,951,862 (GRCm39)	missense	probably damaging	1.00
R9348:Crlf1	UTSW	8	70,951,316 (GRCm39)	missense	probably benign	0.21
X0062:Crlf1	UTSW	8	70,951,487 (GRCm39)	splice site	probably null

Predicted Primers

PCR Primer
(F):5'- AAGTGTCGTCTTTGACCCCAG -3'
(R):5'- ATGCAAGTGAGAGCCCATG -3'

Sequencing Primer
(F):5'- TCGTCTTTGACCCCAGACACAG -3'
(R):5'- GGCTCTGCCCCAGGACAG -3'

Posted On

2022-03-25