Mutagenetix > Incidental Mutation

Incidental Mutation 'R1491:Kctd19'

163748

Institutional Source

Beutler Lab

Gene Symbol

Kctd19

Ensembl Gene

ENSMUSG00000051648

Gene Name

potassium channel tetramerisation domain containing 19

Synonyms

4922504H04Rik

MMRRC Submission

039543-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.054) question?

Stock #

R1491 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

106109439-106140134 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 106113694 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Leucine at position 660 (I660L)

Ref Sequence

ENSEMBL: ENSMUSP00000050687 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000014927] [ENSMUST00000063071] [ENSMUST00000159286] [ENSMUST00000160191] [ENSMUST00000167294] [ENSMUST00000168196] [ENSMUST00000214056]

AlphaFold

Q562E2

Predicted Effect

probably benign
Transcript: ENSMUST00000014927

SMART Domains

Protein: ENSMUSP00000014927
Gene: ENSMUSG00000014782

Domain	Start	End	E-Value	Type
low complexity region	364	377	N/A	INTRINSIC
low complexity region	440	451	N/A	INTRINSIC
low complexity region	463	475	N/A	INTRINSIC
low complexity region	535	547	N/A	INTRINSIC
low complexity region	559	577	N/A	INTRINSIC
low complexity region	653	664	N/A	INTRINSIC
low complexity region	701	718	N/A	INTRINSIC
RhoGEF	729	900	3.15e-29	SMART
PH	914	1022	1.44e-5	SMART
low complexity region	1148	1169	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000063071
AA Change: I660L

PolyPhen 2 Score 0.595 (Sensitivity: 0.87; Specificity: 0.91)

SMART Domains

Protein: ENSMUSP00000050687
Gene: ENSMUSG00000051648
AA Change: I660L

Domain	Start	End	E-Value	Type
Pfam:BTB_2	15	92	1.3e-9	PFAM
internal_repeat_1	173	251	8.34e-9	PROSPERO
internal_repeat_1	429	509	8.34e-9	PROSPERO

Predicted Effect

probably benign
Transcript: ENSMUST00000159286

SMART Domains

Protein: ENSMUSP00000125556
Gene: ENSMUSG00000014782

Domain	Start	End	E-Value	Type
SCOP:d1aua_2	136	275	5e-9	SMART
Blast:SEC14	137	271	9e-8	BLAST

Predicted Effect

probably benign
Transcript: ENSMUST00000160191

SMART Domains

Protein: ENSMUSP00000125249
Gene: ENSMUSG00000014782

Domain	Start	End	E-Value	Type
low complexity region	295	308	N/A	INTRINSIC
low complexity region	371	382	N/A	INTRINSIC
low complexity region	394	406	N/A	INTRINSIC
low complexity region	466	478	N/A	INTRINSIC
low complexity region	490	508	N/A	INTRINSIC
low complexity region	584	595	N/A	INTRINSIC
low complexity region	632	649	N/A	INTRINSIC
RhoGEF	660	831	3.15e-29	SMART
PH	845	953	1.44e-5	SMART
low complexity region	1079	1100	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000161672

Predicted Effect

possibly damaging
Transcript: ENSMUST00000167294
AA Change: I637L

PolyPhen 2 Score 0.460 (Sensitivity: 0.89; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000130831
Gene: ENSMUSG00000051648
AA Change: I637L

Domain	Start	End	E-Value	Type
Pfam:BTB_2	15	93	3.9e-10	PFAM
internal_repeat_1	173	251	6.24e-9	PROSPERO
internal_repeat_1	406	486	6.24e-9	PROSPERO

Predicted Effect

probably benign
Transcript: ENSMUST00000168196

Predicted Effect

probably benign
Transcript: ENSMUST00000214056

Coding Region Coverage

1x: 99.0%
3x: 98.1%
10x: 95.5%
20x: 90.2%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 81 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A730018C14Rik	T	A	12: 112,381,489 (GRCm39)		noncoding transcript	Het
Acss3	A	G	10: 106,773,169 (GRCm39)	S606P	probably benign	Het
Adamts13	C	T	2: 26,868,327 (GRCm39)	T146M	probably damaging	Het
Adora2b	G	A	11: 62,156,363 (GRCm39)	V271M	probably benign	Het
Agpat5	A	G	8: 18,896,739 (GRCm39)	Y55C	probably damaging	Het
AI987944	A	C	7: 41,023,772 (GRCm39)	Y402*	probably null	Het
Angptl4	C	T	17: 34,000,165 (GRCm39)	A68T	possibly damaging	Het
Ankmy1	T	C	1: 92,814,531 (GRCm39)	I325M	probably benign	Het
Arfgap2	A	G	2: 91,105,204 (GRCm39)	K423E	probably damaging	Het
Arfgef3	A	T	10: 18,522,302 (GRCm39)	S575T	probably damaging	Het
Arhgap24	A	G	5: 103,008,198 (GRCm39)	I40V	possibly damaging	Het
Arhgef7	T	C	8: 11,869,733 (GRCm39)		probably null	Het
Arid1a	C	A	4: 133,448,237 (GRCm39)	S477I	unknown	Het
Armc7	T	C	11: 115,367,029 (GRCm39)	V58A	probably damaging	Het
Arrdc5	A	T	17: 56,601,222 (GRCm39)	I301N	probably damaging	Het
Capn15	G	A	17: 26,183,453 (GRCm39)	P343S	probably damaging	Het
Catspere2	C	T	1: 177,843,495 (GRCm39)	T69I	possibly damaging	Het
Ccdc39	T	C	3: 33,880,629 (GRCm39)	K446R	probably damaging	Het
Cgn	C	T	3: 94,670,535 (GRCm39)	R1002Q	probably damaging	Het
Clstn3	A	T	6: 124,414,449 (GRCm39)	I759N	possibly damaging	Het
Cops5	A	G	1: 10,104,243 (GRCm39)	V166A	possibly damaging	Het
Cramp1	G	T	17: 25,191,323 (GRCm39)	T1046K	probably benign	Het
Cthrc1	T	G	15: 38,950,072 (GRCm39)	V143G	probably damaging	Het
Cul9	G	A	17: 46,849,490 (GRCm39)	Q552*	probably null	Het
Cyp27b1	A	T	10: 126,886,957 (GRCm39)	D391V	probably damaging	Het
Dcun1d2	A	G	8: 13,331,040 (GRCm39)	L30S	probably damaging	Het
Dsc3	T	C	18: 20,120,091 (GRCm39)	E189G	probably damaging	Het
Dst	T	G	1: 34,193,675 (GRCm39)	S295A	probably damaging	Het
Dusp22	A	G	13: 30,892,798 (GRCm39)	T192A	probably benign	Het
Esp24	A	T	17: 39,349,176 (GRCm39)	M1L	probably null	Het
Evc2	G	A	5: 37,550,541 (GRCm39)		probably null	Het
Fgd6	A	G	10: 93,880,694 (GRCm39)	N516S	probably benign	Het
Fmn1	T	C	2: 113,426,714 (GRCm39)	Y1144H	probably damaging	Het
Fut8	T	A	12: 77,495,448 (GRCm39)	I346K	possibly damaging	Het
Gata3	A	C	2: 9,882,201 (GRCm39)	V32G	probably damaging	Het
Glrb	A	T	3: 80,819,282 (GRCm39)	C39S	possibly damaging	Het
Gpr171	A	G	3: 59,005,016 (GRCm39)	V253A	probably benign	Het
Hdac5	A	G	11: 102,092,079 (GRCm39)	V670A	probably benign	Het
Hmgxb3	T	C	18: 61,266,980 (GRCm39)	S1085G	probably benign	Het
Hspa4l	A	G	3: 40,741,226 (GRCm39)	N746S	probably benign	Het
Hyal5	A	G	6: 24,877,902 (GRCm39)	T333A	probably benign	Het
Ippk	T	C	13: 49,615,069 (GRCm39)	V484A	probably benign	Het
Jmjd8	A	T	17: 26,048,266 (GRCm39)	T33S	possibly damaging	Het
Lrat	A	G	3: 82,810,649 (GRCm39)	V124A	probably benign	Het
Madcam1	A	G	10: 79,502,358 (GRCm39)	I281V	probably benign	Het
Mast2	T	A	4: 116,173,688 (GRCm39)	I455F	possibly damaging	Het
Mroh7	A	G	4: 106,560,255 (GRCm39)	L683P	probably benign	Het
Myo15b	C	A	11: 115,777,683 (GRCm39)		probably null	Het
Ncam1	T	C	9: 49,416,849 (GRCm39)	E814G	probably benign	Het
Ncoa3	A	G	2: 165,897,182 (GRCm39)	T658A	probably benign	Het
Or13a20	T	G	7: 140,232,650 (GRCm39)	Y253D	probably damaging	Het
Or9a2	T	C	6: 41,748,456 (GRCm39)	Y259C	possibly damaging	Het
P2ry13	T	C	3: 59,116,939 (GRCm39)	K280E	probably damaging	Het
Paqr8	C	A	1: 21,005,048 (GRCm39)	F67L	probably benign	Het
Pfkfb3	G	T	2: 11,498,747 (GRCm39)	R37S	probably damaging	Het
Phf14	A	G	6: 11,941,478 (GRCm39)	D310G	possibly damaging	Het
Phkb	A	G	8: 86,602,286 (GRCm39)	S26G	possibly damaging	Het
Pkd1l2	T	A	8: 117,755,147 (GRCm39)	I1684F	probably damaging	Het
Plod2	T	C	9: 92,488,637 (GRCm39)	V621A	probably benign	Het
Plvap	T	C	8: 71,964,116 (GRCm39)	N82S	probably damaging	Het
Pomgnt2	A	G	9: 121,811,326 (GRCm39)	V485A	probably damaging	Het
Psmd9	A	G	5: 123,366,410 (GRCm39)	E14G	probably benign	Het
Pwwp2b	A	G	7: 138,835,879 (GRCm39)	E440G	probably damaging	Het
Rasgrp1	G	A	2: 117,113,100 (GRCm39)	Q771*	probably null	Het
Rft1	C	T	14: 30,388,744 (GRCm39)	Q223*	probably null	Het
Rgs22	C	A	15: 36,093,047 (GRCm39)	V409F	probably damaging	Het
Rgsl1	G	A	1: 153,701,672 (GRCm39)	P261S	possibly damaging	Het
Rpl7a	A	G	2: 26,801,127 (GRCm39)	N38S	probably damaging	Het
Sh3rf2	T	A	18: 42,187,004 (GRCm39)	F41Y	probably damaging	Het
Spata6	T	A	4: 111,603,388 (GRCm39)	S34R	probably damaging	Het
Sult2a3	A	T	7: 13,856,867 (GRCm39)	Y18N	probably benign	Het
Tapt1	A	G	5: 44,375,444 (GRCm39)		probably null	Het
Tex2	A	T	11: 106,394,466 (GRCm39)	C615S	possibly damaging	Het
Trim43b	T	C	9: 88,969,665 (GRCm39)	K261R	possibly damaging	Het
Unc5c	T	A	3: 141,495,583 (GRCm39)	M484K	probably damaging	Het
Vezf1	T	A	11: 87,964,573 (GRCm39)	S242T	probably damaging	Het
Vmn2r1	A	G	3: 63,997,034 (GRCm39)	Y230C	probably damaging	Het
Vmn2r94	A	G	17: 18,477,965 (GRCm39)	S149P	probably damaging	Het
Wfdc1	T	A	8: 120,393,405 (GRCm39)		probably null	Het
Zfp975	T	C	7: 42,312,236 (GRCm39)	T126A	probably benign	Het
Zmym4	T	C	4: 126,776,105 (GRCm39)		probably null	Het

Other mutations in Kctd19

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00418:Kctd19	APN	8	106,115,095 (GRCm39)	critical splice donor site	probably null
IGL01546:Kctd19	APN	8	106,113,594 (GRCm39)	missense	probably benign
IGL01786:Kctd19	APN	8	106,116,936 (GRCm39)	missense	probably benign	0.03
IGL01964:Kctd19	APN	8	106,115,157 (GRCm39)	missense	probably damaging	0.99
IGL02275:Kctd19	APN	8	106,123,006 (GRCm39)	missense	probably damaging	0.99
IGL02479:Kctd19	APN	8	106,111,400 (GRCm39)	missense	probably damaging	1.00
IGL03124:Kctd19	APN	8	106,113,702 (GRCm39)	missense	possibly damaging	0.48
R0003:Kctd19	UTSW	8	106,121,993 (GRCm39)	missense	probably damaging	0.99
R1183:Kctd19	UTSW	8	106,109,598 (GRCm39)	missense	probably benign
R1388:Kctd19	UTSW	8	106,118,683 (GRCm39)	missense	probably null	0.93
R1517:Kctd19	UTSW	8	106,122,008 (GRCm39)	missense	probably damaging	1.00
R1540:Kctd19	UTSW	8	106,114,511 (GRCm39)	missense	probably damaging	0.96
R1582:Kctd19	UTSW	8	106,122,092 (GRCm39)	missense	probably damaging	1.00
R1964:Kctd19	UTSW	8	106,115,102 (GRCm39)	missense	probably damaging	0.98
R1996:Kctd19	UTSW	8	106,121,932 (GRCm39)	missense	probably null	1.00
R2129:Kctd19	UTSW	8	106,111,804 (GRCm39)	missense	probably damaging	0.98
R2281:Kctd19	UTSW	8	106,113,898 (GRCm39)	missense	probably benign	0.00
R3767:Kctd19	UTSW	8	106,123,112 (GRCm39)	missense	probably benign	0.04
R3768:Kctd19	UTSW	8	106,123,112 (GRCm39)	missense	probably benign	0.04
R4285:Kctd19	UTSW	8	106,109,581 (GRCm39)	unclassified	probably benign
R4621:Kctd19	UTSW	8	106,123,103 (GRCm39)	missense	probably damaging	1.00
R4701:Kctd19	UTSW	8	106,117,061 (GRCm39)	missense	possibly damaging	0.76
R4969:Kctd19	UTSW	8	106,122,959 (GRCm39)	splice site	probably null
R5070:Kctd19	UTSW	8	106,118,631 (GRCm39)	missense	probably damaging	1.00
R5401:Kctd19	UTSW	8	106,109,617 (GRCm39)	missense	probably benign	0.00
R5582:Kctd19	UTSW	8	106,135,075 (GRCm39)	missense	probably damaging	1.00
R5783:Kctd19	UTSW	8	106,113,612 (GRCm39)	missense	probably benign
R6056:Kctd19	UTSW	8	106,123,082 (GRCm39)	missense	probably damaging	0.99
R6057:Kctd19	UTSW	8	106,123,082 (GRCm39)	missense	probably damaging	0.99
R6269:Kctd19	UTSW	8	106,121,992 (GRCm39)	missense	possibly damaging	0.96
R6273:Kctd19	UTSW	8	106,112,117 (GRCm39)	missense	probably benign
R6631:Kctd19	UTSW	8	106,111,960 (GRCm39)	critical splice donor site	probably null
R7298:Kctd19	UTSW	8	106,109,616 (GRCm39)	missense	probably benign	0.01
R7474:Kctd19	UTSW	8	106,118,664 (GRCm39)	missense	probably benign	0.25
R7540:Kctd19	UTSW	8	106,113,567 (GRCm39)	missense	probably benign	0.00
R7923:Kctd19	UTSW	8	106,111,690 (GRCm39)	missense	probably damaging	1.00
R8059:Kctd19	UTSW	8	106,122,983 (GRCm39)	missense	probably benign	0.02
R8117:Kctd19	UTSW	8	106,122,069 (GRCm39)	missense	unknown
R8836:Kctd19	UTSW	8	106,112,028 (GRCm39)	missense	probably damaging	0.98
R9155:Kctd19	UTSW	8	106,120,571 (GRCm39)	missense	probably benign	0.01
R9429:Kctd19	UTSW	8	106,109,652 (GRCm39)	missense	probably damaging	0.98
R9481:Kctd19	UTSW	8	106,120,249 (GRCm39)	missense	probably benign	0.00
R9627:Kctd19	UTSW	8	106,113,997 (GRCm39)	missense	probably benign	0.01
Z1088:Kctd19	UTSW	8	106,111,967 (GRCm39)	missense	probably benign	0.02
Z1176:Kctd19	UTSW	8	106,111,768 (GRCm39)	missense	probably damaging	1.00
Z1177:Kctd19	UTSW	8	106,115,149 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- ATGGCTTAAAGGTTGGCTCTGGAC -3'
(R):5'- TCCAGGAATGCAGTGACAGGACTC -3'

Sequencing Primer
(F):5'- CAGCATCCTTCTCAGAGGTTATGG -3'
(R):5'- TGAGCAGTATACCCGGACTATTC -3'

Posted On

2014-03-28