Mutagenetix > Incidental Mutation

Incidental Mutation 'R5724:Klhl26'

452386

Institutional Source

Beutler Lab

Gene Symbol

Klhl26

Ensembl Gene

ENSMUSG00000055707

Gene Name

kelch-like 26

Synonyms

C630013N10Rik

MMRRC Submission

043342-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R5724 (G1)

Quality Score

135

Status

Validated

Chromosome

Chromosomal Location

70902869-70929618 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 70904404 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Phenylalanine at position 468 (Y468F)

Ref Sequence

ENSEMBL: ENSMUSP00000147385 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000066597] [ENSMUST00000166976] [ENSMUST00000209415] [ENSMUST00000209567] [ENSMUST00000210250]

AlphaFold

Q8BGY4

Predicted Effect

probably damaging
Transcript: ENSMUST00000066597
AA Change: Y502F

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

SMART Domains

Protein: ENSMUSP00000069077
Gene: ENSMUSG00000055707
AA Change: Y502F

Domain	Start	End	E-Value	Type
low complexity region	3	19	N/A	INTRINSIC
BTB	54	151	1.56e-26	SMART
BACK	156	257	1.62e-28	SMART
Blast:Kelch	301	352	4e-27	BLAST
Kelch	353	404	1.44e0	SMART
Kelch	405	451	2.86e-4	SMART
Kelch	452	499	1.21e-2	SMART
Kelch	500	550	4.27e-3	SMART
Kelch	551	597	4.93e0	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000166976
AA Change: Y441F

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

SMART Domains

Protein: ENSMUSP00000129607
Gene: ENSMUSG00000055707
AA Change: Y441F

Domain	Start	End	E-Value	Type
Pfam:BTB	19	89	1.7e-13	PFAM
BACK	95	196	1.62e-28	SMART
Blast:Kelch	240	291	4e-27	BLAST
Kelch	292	343	1.44e0	SMART
Kelch	344	390	2.86e-4	SMART
Kelch	391	438	1.21e-2	SMART
Kelch	439	489	4.27e-3	SMART
Kelch	490	536	4.93e0	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000209415

Predicted Effect

probably damaging
Transcript: ENSMUST00000209567
AA Change: Y421F

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

Predicted Effect

probably damaging
Transcript: ENSMUST00000210250
AA Change: Y468F

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

Meta Mutation Damage Score

0.2952

Coding Region Coverage

1x: 99.1%
3x: 98.3%
10x: 96.5%
20x: 93.1%

Validation Efficiency

100% (62/62)

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3830408C21Rik	A	T	13: 107,168,905 (GRCm39)		noncoding transcript	Het
Adam5	T	A	8: 25,294,511 (GRCm39)	K363*	probably null	Het
Adamts12	T	C	15: 11,286,836 (GRCm39)	Y814H	probably benign	Het
Adar	G	T	3: 89,642,476 (GRCm39)	G119V	probably benign	Het
Adprs	G	T	4: 126,211,869 (GRCm39)	Q148K	probably damaging	Het
Atr	G	T	9: 95,748,641 (GRCm39)	L395F	probably damaging	Het
Bahcc1	A	G	11: 120,176,192 (GRCm39)	I1946V	possibly damaging	Het
Bend4	T	A	5: 67,575,284 (GRCm39)	D199V	probably damaging	Het
Bpifb1	C	A	2: 154,046,712 (GRCm39)	H77Q	probably benign	Het
Clca3a1	T	C	3: 144,714,833 (GRCm39)	T595A	probably benign	Het
Crebbp	A	T	16: 3,905,499 (GRCm39)		probably benign	Het
Cxcl16	T	C	11: 70,349,990 (GRCm39)	D12G	probably damaging	Het
Dnah10	T	C	5: 124,819,090 (GRCm39)	W459R	probably benign	Het
Dock8	T	C	19: 25,099,785 (GRCm39)	L636P	probably damaging	Het
Eif2ak3	A	G	6: 70,853,824 (GRCm39)	T197A	probably benign	Het
Fbxo40	T	A	16: 36,790,692 (GRCm39)	R139S	probably benign	Het
Fer	C	A	17: 64,231,152 (GRCm39)	T301K	probably damaging	Het
Fgf21	A	T	7: 45,264,729 (GRCm39)	M1K	probably null	Het
Gm11677	C	T	11: 111,615,537 (GRCm39)		noncoding transcript	Het
Gm38706	A	T	6: 130,459,963 (GRCm39)		noncoding transcript	Het
H2-Q6	A	C	17: 35,644,628 (GRCm39)	Y139S	probably damaging	Het
Ift70a2	T	C	2: 75,808,074 (GRCm39)	D146G	probably benign	Het
Igkv4-53	A	T	6: 69,625,991 (GRCm39)	Y59N	probably damaging	Het
Jrkl	T	C	9: 13,244,891 (GRCm39)	M257V	possibly damaging	Het
Kat8	G	A	7: 127,523,988 (GRCm39)	E343K	probably damaging	Het
Lamb2	T	A	9: 108,357,950 (GRCm39)		probably null	Het
Lcp1	A	G	14: 75,464,422 (GRCm39)	T548A	probably benign	Het
Lct	T	A	1: 128,228,073 (GRCm39)	Q1140L	probably benign	Het
Lrp2	T	G	2: 69,281,726 (GRCm39)	N3882H	probably damaging	Het
Magi1	A	G	6: 93,657,852 (GRCm39)	I1126T	probably benign	Het
Magi1	A	G	6: 93,722,682 (GRCm39)	S399P	probably damaging	Het
Med16	A	G	10: 79,731,243 (GRCm39)	C825R	probably damaging	Het
Mtx3	C	T	13: 92,984,095 (GRCm39)	P124L	probably damaging	Het
Nabp2	C	T	10: 128,245,555 (GRCm39)		probably benign	Het
Or5b113	T	A	19: 13,342,515 (GRCm39)	H174Q	possibly damaging	Het
Pak4	A	T	7: 28,264,005 (GRCm39)	S244T	possibly damaging	Het
Pccb	C	T	9: 100,869,900 (GRCm39)	V307I	probably benign	Het
Plekhh2	A	G	17: 84,874,233 (GRCm39)	D506G	probably benign	Het
Plk4	T	C	3: 40,755,481 (GRCm39)	V26A	probably damaging	Het
Ppp2r3c	A	T	12: 55,344,617 (GRCm39)	M117K	probably benign	Het
Pramel21	A	G	4: 143,344,026 (GRCm39)	D442G	probably benign	Het
Pspc1	C	T	14: 57,015,529 (GRCm39)	E30K	probably benign	Het
Reps1	A	G	10: 17,990,231 (GRCm39)	S448G	possibly damaging	Het
Rnf34	C	T	5: 123,004,952 (GRCm39)	Q241*	probably null	Het
Sgta	A	T	10: 80,883,522 (GRCm39)		probably null	Het
Sh3bp5	C	A	14: 31,099,452 (GRCm39)	R265L	probably benign	Het
Siglech	A	G	7: 55,418,293 (GRCm39)	N87S	probably damaging	Het
Sptbn1	A	G	11: 30,094,113 (GRCm39)	I392T	possibly damaging	Het
St18	T	A	1: 6,841,174 (GRCm39)	M21K	probably benign	Het
Sugp1	C	T	8: 70,522,799 (GRCm39)	R500C	probably damaging	Het
Tasp1	T	C	2: 139,899,339 (GRCm39)	K5E	probably damaging	Het
Tbx3	G	A	5: 119,813,668 (GRCm39)	V235I	possibly damaging	Het
Toporsl	A	T	4: 52,611,346 (GRCm39)	N413I	probably damaging	Het
Ubqln3	G	A	7: 103,790,674 (GRCm39)	P472L	probably benign	Het
Zfp60	A	G	7: 27,447,758 (GRCm39)	Y142C	probably benign	Het

Other mutations in Klhl26

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01655:Klhl26	APN	8	70,904,533 (GRCm39)	missense	probably damaging	1.00
IGL02508:Klhl26	APN	8	70,905,381 (GRCm39)	missense	probably damaging	1.00
IGL03089:Klhl26	APN	8	70,908,283 (GRCm39)	missense	probably benign	0.05
IGL03144:Klhl26	APN	8	70,905,214 (GRCm39)	missense	probably damaging	1.00
R0365:Klhl26	UTSW	8	70,904,479 (GRCm39)	missense	probably damaging	1.00
R0408:Klhl26	UTSW	8	70,905,130 (GRCm39)	missense	probably damaging	1.00
R0494:Klhl26	UTSW	8	70,904,251 (GRCm39)	missense	probably damaging	1.00
R1889:Klhl26	UTSW	8	70,904,383 (GRCm39)	missense	probably damaging	0.99
R1940:Klhl26	UTSW	8	70,904,911 (GRCm39)	missense	probably damaging	1.00
R3902:Klhl26	UTSW	8	70,905,016 (GRCm39)	missense	probably damaging	0.98
R4458:Klhl26	UTSW	8	70,905,342 (GRCm39)	missense	possibly damaging	0.89
R4459:Klhl26	UTSW	8	70,904,194 (GRCm39)	missense	probably damaging	1.00
R4460:Klhl26	UTSW	8	70,904,194 (GRCm39)	missense	probably damaging	1.00
R4461:Klhl26	UTSW	8	70,904,194 (GRCm39)	missense	probably damaging	1.00
R5135:Klhl26	UTSW	8	70,905,368 (GRCm39)	missense	probably benign	0.19
R5334:Klhl26	UTSW	8	70,904,968 (GRCm39)	missense	probably damaging	1.00
R5342:Klhl26	UTSW	8	70,908,215 (GRCm39)	missense	probably damaging	1.00
R5711:Klhl26	UTSW	8	70,904,974 (GRCm39)	missense	probably damaging	0.98
R5965:Klhl26	UTSW	8	70,905,381 (GRCm39)	missense	probably damaging	1.00
R7319:Klhl26	UTSW	8	70,905,592 (GRCm39)	missense	probably damaging	0.99
R7390:Klhl26	UTSW	8	70,905,499 (GRCm39)	missense	probably damaging	0.98
R8917:Klhl26	UTSW	8	70,905,455 (GRCm39)	missense	possibly damaging	0.90
R9115:Klhl26	UTSW	8	70,904,896 (GRCm39)	missense	possibly damaging	0.80
R9386:Klhl26	UTSW	8	70,904,156 (GRCm39)	missense	probably benign	0.32
R9471:Klhl26	UTSW	8	70,904,803 (GRCm39)	missense	probably damaging	1.00
R9545:Klhl26	UTSW	8	70,904,164 (GRCm39)	missense	probably damaging	1.00
Z1088:Klhl26	UTSW	8	70,904,449 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- GTTCAGCCTCCAGTTGTAGC -3'
(R):5'- ACAGCTGGGATTTTGCCTGC -3'

Sequencing Primer
(F):5'- AGTTGTAGCCACCCACGATGTAG -3'
(R):5'- GGATTTTGCCTGCCCACTCAAG -3'

Posted On

2017-01-03