Mutagenetix > Incidental Mutation

Incidental Mutation 'R5119:Kcnt1'

392778

Institutional Source

Beutler Lab

Gene Symbol

Kcnt1

Ensembl Gene

ENSMUSG00000058740

Gene Name

potassium channel, subfamily T, member 1

Synonyms

C030030G16Rik, Slack, slo2

MMRRC Submission

042707-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.194) question?

Stock #

R5119 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

25753807-25808285 bp(+) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

G to T at 25799334 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000143482 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000037580] [ENSMUST00000114172] [ENSMUST00000114176] [ENSMUST00000153001] [ENSMUST00000200434] [ENSMUST00000171268] [ENSMUST00000197917] [ENSMUST00000198204]

AlphaFold

Q6ZPR4

Predicted Effect

probably benign
Transcript: ENSMUST00000037580

SMART Domains

Protein: ENSMUSP00000039058
Gene: ENSMUSG00000058740

Domain	Start	End	E-Value	Type
low complexity region	13	32	N/A	INTRINSIC
transmembrane domain	98	117	N/A	INTRINSIC
transmembrane domain	157	179	N/A	INTRINSIC
transmembrane domain	188	210	N/A	INTRINSIC
Pfam:Ion_trans_2	252	335	1.3e-12	PFAM
transmembrane domain	355	377	N/A	INTRINSIC
Pfam:BK_channel_a	477	579	5.8e-32	PFAM
PDB:3U6N\|H	794	983	6e-6	PDB
low complexity region	1059	1076	N/A	INTRINSIC
low complexity region	1212	1229	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000114172

SMART Domains

Protein: ENSMUSP00000109809
Gene: ENSMUSG00000058740

Domain	Start	End	E-Value	Type
low complexity region	13	32	N/A	INTRINSIC
transmembrane domain	98	117	N/A	INTRINSIC
transmembrane domain	157	179	N/A	INTRINSIC
transmembrane domain	188	210	N/A	INTRINSIC
Pfam:Ion_trans_2	255	335	5.2e-13	PFAM
transmembrane domain	355	377	N/A	INTRINSIC
Pfam:BK_channel_a	475	580	3.3e-38	PFAM
PDB:3U6N\|H	792	981	7e-6	PDB
low complexity region	1057	1074	N/A	INTRINSIC
low complexity region	1210	1227	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000114176

SMART Domains

Protein: ENSMUSP00000109813
Gene: ENSMUSG00000058740

Domain	Start	End	E-Value	Type
low complexity region	13	32	N/A	INTRINSIC
transmembrane domain	98	117	N/A	INTRINSIC
transmembrane domain	157	179	N/A	INTRINSIC
transmembrane domain	188	210	N/A	INTRINSIC
Pfam:Ion_trans_2	255	335	5.1e-13	PFAM
transmembrane domain	355	377	N/A	INTRINSIC
Pfam:BK_channel_a	475	580	3.2e-38	PFAM
PDB:3U6N\|H	794	983	6e-6	PDB
low complexity region	1059	1076	N/A	INTRINSIC
low complexity region	1191	1208	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000131529

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000138568

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000145544

Predicted Effect

probably benign
Transcript: ENSMUST00000153001

SMART Domains

Protein: ENSMUSP00000142532
Gene: ENSMUSG00000058740

Domain	Start	End	E-Value	Type
PDB:4HPF\|B	79	285	6e-9	PDB

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000199269

Predicted Effect

probably benign
Transcript: ENSMUST00000200434

SMART Domains

Protein: ENSMUSP00000143482
Gene: ENSMUSG00000058740

Domain	Start	End	E-Value	Type
transmembrane domain	64	83	N/A	INTRINSIC
transmembrane domain	123	145	N/A	INTRINSIC
transmembrane domain	154	176	N/A	INTRINSIC
Pfam:Ion_trans_2	221	301	5.1e-11	PFAM
transmembrane domain	321	343	N/A	INTRINSIC
Pfam:BK_channel_a	441	546	1.3e-35	PFAM
PDB:3U6N\|H	758	947	6e-6	PDB
low complexity region	1023	1040	N/A	INTRINSIC
low complexity region	1176	1193	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000171268

SMART Domains

Protein: ENSMUSP00000132212
Gene: ENSMUSG00000058740

Domain	Start	End	E-Value	Type
transmembrane domain	78	97	N/A	INTRINSIC
transmembrane domain	137	159	N/A	INTRINSIC
transmembrane domain	168	190	N/A	INTRINSIC
Pfam:Ion_trans_2	235	315	5.1e-13	PFAM
transmembrane domain	335	357	N/A	INTRINSIC
Pfam:BK_channel_a	455	560	3.2e-38	PFAM
PDB:3U6N\|H	774	963	7e-6	PDB
low complexity region	1039	1056	N/A	INTRINSIC
low complexity region	1192	1209	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000197917

SMART Domains

Protein: ENSMUSP00000143106
Gene: ENSMUSG00000058740

Domain	Start	End	E-Value	Type
low complexity region	13	32	N/A	INTRINSIC
transmembrane domain	98	117	N/A	INTRINSIC
transmembrane domain	157	179	N/A	INTRINSIC
transmembrane domain	188	210	N/A	INTRINSIC
Pfam:Ion_trans_2	255	335	5.2e-13	PFAM
transmembrane domain	355	377	N/A	INTRINSIC
Pfam:BK_channel_a	475	580	3.3e-38	PFAM
PDB:3U6N\|H	792	981	7e-6	PDB
low complexity region	1057	1074	N/A	INTRINSIC
low complexity region	1210	1227	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000198204

SMART Domains

Protein: ENSMUSP00000142870
Gene: ENSMUSG00000058740

Domain	Start	End	E-Value	Type
transmembrane domain	64	83	N/A	INTRINSIC
transmembrane domain	123	145	N/A	INTRINSIC
transmembrane domain	154	176	N/A	INTRINSIC
Pfam:Ion_trans_2	221	301	5e-11	PFAM
transmembrane domain	321	343	N/A	INTRINSIC
Pfam:BK_channel_a	441	546	1.2e-35	PFAM
PDB:3U6N\|H	760	949	6e-6	PDB
low complexity region	1025	1042	N/A	INTRINSIC
low complexity region	1157	1174	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 94.1%

Validation Efficiency

100% (127/127)

MGI Phenotype

FUNCTION: This gene encodes a member of the Slo potassium channel family that has shown to be activated by both sodium and chloride ions. This channel represents the largest potassium channel subunit yet identified. This channel may be important in development and pain signaling. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2014]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit impaired action potential firing in sensory neurons and increased mechanical hypersensitivity in neuropathic pain models. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 120 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930470P17Rik	C	A	2: 170,421,505 (GRCm39)	G125V	unknown	Het
Actr6	A	T	10: 89,561,717 (GRCm39)	L143Q	probably damaging	Het
Adamts18	A	G	8: 114,425,642 (GRCm39)	Y1207H	probably benign	Het
Adamts5	T	A	16: 85,696,466 (GRCm39)	R230S	probably benign	Het
Adat2	A	T	10: 13,432,650 (GRCm39)	N51Y	probably damaging	Het
Adgrv1	T	C	13: 81,567,546 (GRCm39)	Y5209C	possibly damaging	Het
Ahnak	G	T	19: 8,991,008 (GRCm39)	M4097I	probably benign	Het
Akap13	A	G	7: 75,337,000 (GRCm39)	T820A	probably damaging	Het
Als2cl	C	T	9: 110,719,887 (GRCm39)	R492C	probably damaging	Het
Aox3	G	A	1: 58,227,683 (GRCm39)		probably null	Het
Arid4b	G	A	13: 14,338,866 (GRCm39)	V446M	probably benign	Het
Armc2	A	G	10: 41,798,144 (GRCm39)	L794P	probably damaging	Het
Atp6v0a1	T	A	11: 100,911,341 (GRCm39)	M80K	probably benign	Het
Aup1	T	C	6: 83,032,115 (GRCm39)	V94A	probably damaging	Het
Bank1	A	T	3: 135,940,443 (GRCm39)	I180K	possibly damaging	Het
Becn1	A	G	11: 101,182,221 (GRCm39)	L116P	probably damaging	Het
Bsg	A	G	10: 79,546,057 (GRCm39)		probably benign	Het
Camk2a	A	T	18: 61,076,208 (GRCm39)		probably benign	Het
Ccdc180	A	G	4: 45,914,603 (GRCm39)	E706G	possibly damaging	Het
Cdk8	A	T	5: 146,220,437 (GRCm39)		probably null	Het
Cpne4	A	G	9: 104,778,720 (GRCm39)		probably null	Het
Cspp1	T	A	1: 10,196,688 (GRCm39)	N900K	probably damaging	Het
Cyp2c38	C	A	19: 39,449,065 (GRCm39)	G96V	probably damaging	Het
Dhx40	A	G	11: 86,667,462 (GRCm39)	I261T	probably damaging	Het
Dnah10	T	C	5: 124,856,322 (GRCm39)	F2038L	probably damaging	Het
Dnah7a	A	T	1: 53,737,851 (GRCm39)	D27E	probably benign	Het
Dock10	A	T	1: 80,545,711 (GRCm39)		probably null	Het
Dst	A	T	1: 34,235,050 (GRCm39)	K3710*	probably null	Het
Dtl	G	T	1: 191,273,618 (GRCm39)	A430D	probably damaging	Het
Ece2	T	C	16: 20,437,381 (GRCm39)	L241P	probably damaging	Het
Ecel1	T	A	1: 87,078,861 (GRCm39)	Y526F	probably benign	Het
Enpp2	T	A	15: 54,733,701 (GRCm39)	R420*	probably null	Het
Epb41	A	C	4: 131,664,747 (GRCm39)		probably benign	Het
Eppin	T	C	2: 164,431,371 (GRCm39)	Y85C	probably damaging	Het
Fam171a2	G	A	11: 102,329,559 (GRCm39)	A400V	probably damaging	Het
Fem1c	A	C	18: 46,639,436 (GRCm39)	C189G	probably damaging	Het
Frmd4b	A	G	6: 97,277,275 (GRCm39)	V560A	probably benign	Het
Fsip2	A	T	2: 82,818,535 (GRCm39)	D4756V	probably damaging	Het
Gabbr1	T	C	17: 37,359,330 (GRCm39)	S102P	probably damaging	Het
Garin3	G	A	11: 46,297,863 (GRCm39)	G389D	probably damaging	Het
Gm28042	G	A	2: 119,865,124 (GRCm39)	A250T	probably damaging	Het
Gm30275	T	C	14: 54,312,978 (GRCm39)		probably benign	Het
Gm9762	A	T	3: 78,873,707 (GRCm39)		noncoding transcript	Het
Gpr183	G	T	14: 122,192,275 (GRCm39)	T82N	possibly damaging	Het
Gps2	A	G	11: 69,805,617 (GRCm39)	K45R	probably benign	Het
Gramd2a	A	G	9: 59,621,603 (GRCm39)		probably benign	Het
Grap2	G	A	15: 80,530,345 (GRCm39)	R155Q	possibly damaging	Het
Hsdl1	T	A	8: 120,292,606 (GRCm39)	Y203F	possibly damaging	Het
Ifi204	A	T	1: 173,583,234 (GRCm39)	I328N	probably damaging	Het
Igsf3	T	A	3: 101,346,677 (GRCm39)		probably null	Het
Il1rap	T	C	16: 26,442,949 (GRCm39)	I15T	probably benign	Het
Il23r	A	T	6: 67,443,300 (GRCm39)	C268S	probably damaging	Het
Irx4	A	G	13: 73,417,040 (GRCm39)	T479A	probably benign	Het
Kcnk7	G	A	19: 5,756,352 (GRCm39)	V193I	probably benign	Het
Kif13b	T	G	14: 64,994,902 (GRCm39)	C885G	probably benign	Het
Kif21b	C	A	1: 136,090,838 (GRCm39)	D1215E	probably benign	Het
Klhdc2	A	G	12: 69,343,736 (GRCm39)		probably benign	Het
Kmt2d	G	A	15: 98,745,075 (GRCm39)		probably benign	Het
Lama4	A	G	10: 38,924,050 (GRCm39)	N486S	probably benign	Het
Ldah	G	A	12: 8,277,237 (GRCm39)	A58T	probably benign	Het
Lrrc24	T	C	15: 76,600,200 (GRCm39)	Q313R	probably benign	Het
Luzp1	A	G	4: 136,270,708 (GRCm39)	D977G	possibly damaging	Het
Meak7	A	C	8: 120,494,882 (GRCm39)	L292R	probably damaging	Het
Mrgpra4	A	G	7: 47,631,466 (GRCm39)	L45P	probably damaging	Het
Mrps28	C	T	3: 8,988,756 (GRCm39)	G34D	possibly damaging	Het
Myh8	A	G	11: 67,189,184 (GRCm39)	E1120G	probably damaging	Het
Myt1l	A	G	12: 29,882,302 (GRCm39)	E499G	unknown	Het
Ncan	C	T	8: 70,567,675 (GRCm39)	E146K	probably damaging	Het
Nlgn1	A	T	3: 25,487,958 (GRCm39)	D763E	probably damaging	Het
Or11g26	T	C	14: 50,752,966 (GRCm39)	F102L	probably benign	Het
Or13c7c	G	T	4: 43,836,433 (GRCm39)	A19D	probably benign	Het
Or1e17	A	T	11: 73,831,378 (GRCm39)	Y102F	possibly damaging	Het
Or4c12	A	T	2: 89,774,147 (GRCm39)	I104N	possibly damaging	Het
Or5b118	C	T	19: 13,448,910 (GRCm39)	T192I	probably benign	Het
Or6c8b	T	A	10: 128,882,711 (GRCm39)	I74F	possibly damaging	Het
Pak6	A	T	2: 118,525,029 (GRCm39)	I552F	probably damaging	Het
Pcbp1	G	A	6: 86,501,897 (GRCm39)	A334V	probably damaging	Het
Pclaf	T	C	9: 65,798,062 (GRCm39)	V32A	probably benign	Het
Pga5	T	A	19: 10,654,053 (GRCm39)	H50L	probably benign	Het
Phyhipl	A	T	10: 70,404,904 (GRCm39)	D56E	probably damaging	Het
Pik3ap1	C	T	19: 41,270,415 (GRCm39)	R758H	probably benign	Het
Plekha1	A	G	7: 130,507,094 (GRCm39)		probably benign	Het
Plekhm1	A	T	11: 103,278,141 (GRCm39)	N318K	possibly damaging	Het
Ppargc1b	G	A	18: 61,440,725 (GRCm39)	A731V	probably benign	Het
Pptc7	T	C	5: 122,451,844 (GRCm39)	V100A	possibly damaging	Het
Prl7a1	A	T	13: 27,817,564 (GRCm39)	H233Q	possibly damaging	Het
Prpf40a	A	G	2: 53,034,861 (GRCm39)	F776L	probably damaging	Het
Prrc2c	T	C	1: 162,533,009 (GRCm39)		probably benign	Het
Psmb1	T	C	17: 15,718,524 (GRCm39)	M1V	probably null	Het
Ptpn3	A	G	4: 57,218,513 (GRCm39)	F650S	possibly damaging	Het
Ranbp17	A	T	11: 33,354,181 (GRCm39)	*577R	probably null	Het
Reln	T	A	5: 22,176,868 (GRCm39)	N1933Y	probably benign	Het
Rgl2	T	A	17: 34,156,094 (GRCm39)	H727Q	probably benign	Het
Rhpn2	A	G	7: 35,070,549 (GRCm39)	T160A	probably damaging	Het
Rlf	G	A	4: 121,004,652 (GRCm39)	H1443Y	probably damaging	Het
Rpgrip1l	T	C	8: 92,007,444 (GRCm39)	E382G	probably damaging	Het
Rxrb	T	C	17: 34,252,562 (GRCm39)	S50P	probably benign	Het
Scn4b	A	T	9: 45,059,056 (GRCm39)	E109V	probably damaging	Het
Scrib	C	T	15: 75,923,602 (GRCm39)		probably null	Het
Slc22a29	A	T	19: 8,195,194 (GRCm39)	V147D	probably damaging	Het
Slc4a4	A	T	5: 89,102,721 (GRCm39)	E53V	probably null	Het
Slx4	A	G	16: 3,819,063 (GRCm39)	S37P	possibly damaging	Het
Spag9	G	A	11: 94,013,548 (GRCm39)	G1127D	probably damaging	Het
Srek1	T	A	13: 103,889,064 (GRCm39)		probably benign	Het
Supt5	G	T	7: 28,015,795 (GRCm39)	P849Q	probably damaging	Het
Tex14	T	C	11: 87,324,639 (GRCm39)	S2P	probably damaging	Het
Them7	A	G	2: 105,209,153 (GRCm39)	T158A	probably benign	Het
Tll2	A	G	19: 41,118,948 (GRCm39)	V260A	possibly damaging	Het
Tlr6	A	G	5: 65,111,644 (GRCm39)	V421A	probably benign	Het
Tmc3	T	G	7: 83,264,218 (GRCm39)	C649G	probably damaging	Het
Tnn	A	G	1: 159,948,122 (GRCm39)	W864R	probably damaging	Het
Tsc2	A	C	17: 24,822,254 (GRCm39)	V1095G	probably benign	Het
Vmn1r124	C	T	7: 20,994,172 (GRCm39)	G124D	probably damaging	Het
Vmn2r116	T	C	17: 23,606,138 (GRCm39)	V350A	probably benign	Het
Vps13d	A	G	4: 144,832,468 (GRCm39)	S2813P	possibly damaging	Het
Wrap53	T	A	11: 69,454,758 (GRCm39)	M204L	possibly damaging	Het
Zfp277	A	G	12: 40,378,687 (GRCm39)	V390A	possibly damaging	Het
Zfp687	A	T	3: 94,918,987 (GRCm39)	S262T	probably benign	Het
Zfp831	T	A	2: 174,547,103 (GRCm39)	S1429T	probably benign	Het
Znfx1	G	A	2: 166,907,307 (GRCm39)		probably benign	Het

Other mutations in Kcnt1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00718:Kcnt1	APN	2	25,782,419 (GRCm39)	missense	probably damaging	0.98
IGL01358:Kcnt1	APN	2	25,806,017 (GRCm39)	missense	probably damaging	1.00
IGL01593:Kcnt1	APN	2	25,788,766 (GRCm39)	missense	probably damaging	1.00
IGL01779:Kcnt1	APN	2	25,790,979 (GRCm39)	missense	probably damaging	1.00
IGL01800:Kcnt1	APN	2	25,778,137 (GRCm39)	missense	probably damaging	1.00
IGL01834:Kcnt1	APN	2	25,802,731 (GRCm39)	critical splice donor site	probably null
IGL02001:Kcnt1	APN	2	25,798,164 (GRCm39)	missense	probably damaging	1.00
IGL02061:Kcnt1	APN	2	25,790,494 (GRCm39)	critical splice donor site	probably null
IGL02121:Kcnt1	APN	2	25,791,877 (GRCm39)	missense	probably damaging	1.00
IGL02646:Kcnt1	APN	2	25,790,892 (GRCm39)	splice site	probably benign
IGL02683:Kcnt1	APN	2	25,790,937 (GRCm39)	missense	possibly damaging	0.85
IGL03028:Kcnt1	APN	2	25,799,215 (GRCm39)	critical splice acceptor site	probably null
IGL03139:Kcnt1	APN	2	25,784,480 (GRCm39)	splice site	probably benign
R0070:Kcnt1	UTSW	2	25,782,374 (GRCm39)	missense	probably benign	0.00
R0070:Kcnt1	UTSW	2	25,782,374 (GRCm39)	missense	probably benign	0.00
R0149:Kcnt1	UTSW	2	25,788,276 (GRCm39)	splice site	probably benign
R0294:Kcnt1	UTSW	2	25,778,122 (GRCm39)	missense	probably damaging	0.99
R0367:Kcnt1	UTSW	2	25,797,640 (GRCm39)	missense	probably damaging	1.00
R0481:Kcnt1	UTSW	2	25,782,508 (GRCm39)	missense	probably damaging	0.98
R0666:Kcnt1	UTSW	2	25,781,255 (GRCm39)	splice site	probably benign
R1364:Kcnt1	UTSW	2	25,798,106 (GRCm39)	missense	probably damaging	0.99
R1553:Kcnt1	UTSW	2	25,790,397 (GRCm39)	missense	probably damaging	1.00
R1916:Kcnt1	UTSW	2	25,790,481 (GRCm39)	missense	probably damaging	1.00
R1999:Kcnt1	UTSW	2	25,782,372 (GRCm39)	missense	probably benign
R2079:Kcnt1	UTSW	2	25,790,260 (GRCm39)	missense	possibly damaging	0.48
R2166:Kcnt1	UTSW	2	25,781,195 (GRCm39)	splice site	probably benign
R2295:Kcnt1	UTSW	2	25,790,933 (GRCm39)	missense	probably damaging	1.00
R3688:Kcnt1	UTSW	2	25,784,371 (GRCm39)	missense	probably damaging	1.00
R3820:Kcnt1	UTSW	2	25,790,904 (GRCm39)	missense	probably damaging	1.00
R3826:Kcnt1	UTSW	2	25,805,880 (GRCm39)	critical splice donor site	probably null
R3980:Kcnt1	UTSW	2	25,783,226 (GRCm39)	missense	possibly damaging	0.91
R4031:Kcnt1	UTSW	2	25,806,060 (GRCm39)	missense	possibly damaging	0.77
R4093:Kcnt1	UTSW	2	25,767,927 (GRCm39)	missense	probably damaging	0.99
R4361:Kcnt1	UTSW	2	25,768,044 (GRCm39)	missense	probably benign	0.03
R4367:Kcnt1	UTSW	2	25,797,638 (GRCm39)	missense	probably damaging	1.00
R4850:Kcnt1	UTSW	2	25,798,112 (GRCm39)	missense	probably damaging	1.00
R5005:Kcnt1	UTSW	2	25,791,358 (GRCm39)	missense	probably damaging	1.00
R5223:Kcnt1	UTSW	2	25,793,434 (GRCm39)	missense	probably benign
R5243:Kcnt1	UTSW	2	25,798,086 (GRCm39)	missense	probably damaging	1.00
R5323:Kcnt1	UTSW	2	25,799,289 (GRCm39)	missense	possibly damaging	0.59
R5665:Kcnt1	UTSW	2	25,791,921 (GRCm39)	nonsense	probably null
R5888:Kcnt1	UTSW	2	25,798,122 (GRCm39)	missense	probably damaging	1.00
R5906:Kcnt1	UTSW	2	25,788,413 (GRCm39)	missense	probably damaging	1.00
R5906:Kcnt1	UTSW	2	25,784,536 (GRCm39)	intron	probably benign
R5927:Kcnt1	UTSW	2	25,799,388 (GRCm39)	intron	probably benign
R6160:Kcnt1	UTSW	2	25,782,395 (GRCm39)	missense	probably damaging	0.96
R6161:Kcnt1	UTSW	2	25,793,397 (GRCm39)	missense	probably benign	0.00
R6179:Kcnt1	UTSW	2	25,783,192 (GRCm39)	missense	probably damaging	1.00
R6222:Kcnt1	UTSW	2	25,782,522 (GRCm39)	missense	probably damaging	1.00
R6268:Kcnt1	UTSW	2	25,793,609 (GRCm39)	splice site	probably null
R6336:Kcnt1	UTSW	2	25,778,767 (GRCm39)	splice site	probably null
R6395:Kcnt1	UTSW	2	25,799,251 (GRCm39)	missense	possibly damaging	0.81
R6564:Kcnt1	UTSW	2	25,801,063 (GRCm39)	missense	probably benign	0.09
R6944:Kcnt1	UTSW	2	25,767,840 (GRCm39)	intron	probably benign
R7236:Kcnt1	UTSW	2	25,799,951 (GRCm39)	splice site	probably null
R7308:Kcnt1	UTSW	2	25,790,475 (GRCm39)	missense	possibly damaging	0.74
R7346:Kcnt1	UTSW	2	25,753,855 (GRCm39)	unclassified	probably benign
R7419:Kcnt1	UTSW	2	25,806,011 (GRCm39)	missense	probably benign	0.11
R7461:Kcnt1	UTSW	2	25,791,358 (GRCm39)	missense	probably benign	0.01
R7470:Kcnt1	UTSW	2	25,799,845 (GRCm39)	missense	probably damaging	0.96
R7566:Kcnt1	UTSW	2	25,806,048 (GRCm39)	missense	probably benign	0.31
R7613:Kcnt1	UTSW	2	25,791,358 (GRCm39)	missense	probably benign	0.01
R7778:Kcnt1	UTSW	2	25,791,901 (GRCm39)	missense	probably benign	0.10
R8031:Kcnt1	UTSW	2	25,798,054 (GRCm39)	splice site	probably benign
R8088:Kcnt1	UTSW	2	25,784,326 (GRCm39)	missense	possibly damaging	0.63
R8113:Kcnt1	UTSW	2	25,791,223 (GRCm39)	missense	possibly damaging	0.67
R8378:Kcnt1	UTSW	2	25,797,283 (GRCm39)	missense	probably benign	0.03
R8954:Kcnt1	UTSW	2	25,784,338 (GRCm39)	missense	probably benign
R9231:Kcnt1	UTSW	2	25,801,074 (GRCm39)	missense	probably benign	0.00
R9445:Kcnt1	UTSW	2	25,767,959 (GRCm39)	missense	probably damaging	1.00
R9733:Kcnt1	UTSW	2	25,797,351 (GRCm39)	missense	probably benign	0.00
Z1176:Kcnt1	UTSW	2	25,796,808 (GRCm39)	missense	probably benign	0.07
Z1177:Kcnt1	UTSW	2	25,799,277 (GRCm39)	nonsense	probably null
Z1177:Kcnt1	UTSW	2	25,791,240 (GRCm39)	nonsense	probably null

Predicted Primers

PCR Primer
(F):5'- ATCCTATGAACACTCTGATGGCC -3'
(R):5'- ATGTGAGGCAGACACTCCAG -3'

Sequencing Primer
(F):5'- GATGGCCACCCACAATCCTTTG -3'
(R):5'- ACTCAGAACCTGCCTGCCG -3'

Posted On

2016-06-15