Mutagenetix > Incidental Mutation

Incidental Mutation 'R7058:Kcng1'

548035

Institutional Source

Beutler Lab

Gene Symbol

Kcng1

Ensembl Gene

ENSMUSG00000074575

Gene Name

potassium voltage-gated channel, subfamily G, member 1

Synonyms

OTTMUSG00000016048

MMRRC Submission

045155-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.132) question?

Stock #

R7058 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

168102037-168123453 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 168104529 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 439 (V439A)

Ref Sequence

ENSEMBL: ENSMUSP00000104815 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000099069] [ENSMUST00000109191]

AlphaFold

A2BDX4

Predicted Effect

probably damaging
Transcript: ENSMUST00000099069
AA Change: V439A

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000096668
Gene: ENSMUSG00000074575
AA Change: V439A

Domain	Start	End	E-Value	Type
BTB	63	172	4.22e-5	SMART
low complexity region	174	197	N/A	INTRINSIC
Pfam:Ion_trans	226	470	8.6e-41	PFAM
Pfam:Ion_trans_2	379	465	7.6e-16	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000109191
AA Change: V439A

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000104815
Gene: ENSMUSG00000074575
AA Change: V439A

Domain	Start	End	E-Value	Type
BTB	63	172	4.22e-5	SMART
low complexity region	174	197	N/A	INTRINSIC
Pfam:Ion_trans	270	459	1.9e-31	PFAM
Pfam:Ion_trans_2	379	465	1e-15	PFAM

Meta Mutation Damage Score

0.8398

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.0%

Validation Efficiency

100% (87/87)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Voltage-gated potassium (Kv) channels represent the most complex class of voltage-gated ion channels from both functional and structural standpoints. Their diverse functions include regulating neurotransmitter release, heart rate, insulin secretion, neuronal excitability, epithelial electrolyte transport, smooth muscle contraction, and cell volume. This gene encodes a member of the potassium channel, voltage-gated, subfamily G. This gene is abundantly expressed in skeletal muscle. Multiple alternatively spliced transcript variants have been found in normal and cancerous tissues. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 87 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610021A01Rik	T	C	7: 41,275,554 (GRCm39)	I419T	possibly damaging	Het
Afap1	T	C	5: 36,119,604 (GRCm39)	V294A	probably benign	Het
Amotl1	T	A	9: 14,486,532 (GRCm39)	Q454L	possibly damaging	Het
Ap2a1	T	C	7: 44,550,215 (GRCm39)	S961G	probably damaging	Het
Asxl3	A	G	18: 22,650,731 (GRCm39)	K907E	probably damaging	Het
BC028528	A	T	3: 95,792,323 (GRCm39)	L137I	possibly damaging	Het
Cand1	A	T	10: 119,047,659 (GRCm39)	N610K	probably benign	Het
Cat	A	G	2: 103,304,698 (GRCm39)	I109T	probably benign	Het
Ccdc18	T	C	5: 108,341,664 (GRCm39)	V853A	probably benign	Het
Chd4	C	A	6: 125,085,405 (GRCm39)	D805E	possibly damaging	Het
Cnih1	A	C	14: 47,017,652 (GRCm39)	F77V	probably damaging	Het
Cntd1	A	T	11: 101,178,252 (GRCm39)	I284F	probably damaging	Het
Col6a3	C	A	1: 90,755,759 (GRCm39)	E177*	probably null	Het
Cpxm2	T	A	7: 131,745,408 (GRCm39)	D139V	probably benign	Het
Cyp1a2	G	T	9: 57,584,525 (GRCm39)	R510S	probably damaging	Het
D2hgdh	T	C	1: 93,763,096 (GRCm39)	S294P	probably damaging	Het
Dchs1	A	G	7: 105,406,228 (GRCm39)	C2335R	probably benign	Het
Disc1	G	T	8: 125,977,724 (GRCm39)	C719F	probably damaging	Het
Dnah14	A	C	1: 181,525,614 (GRCm39)	D2180A	probably benign	Het
Dop1b	G	A	16: 93,573,878 (GRCm39)	R1582Q	probably benign	Het
Dsg2	A	T	18: 20,725,332 (GRCm39)	H481L	probably benign	Het
Epha6	A	G	16: 59,503,013 (GRCm39)	S965P	probably damaging	Het
Esrrg	G	T	1: 187,882,503 (GRCm39)	L253F	probably damaging	Het
Exoc6b	T	C	6: 84,831,704 (GRCm39)	K438R	probably damaging	Het
Fam98a	C	A	17: 75,845,384 (GRCm39)	R454L	unknown	Het
Fam98c	A	T	7: 28,855,308 (GRCm39)		probably null	Het
Fhad1	CGG	CG	4: 141,645,602 (GRCm39)		probably null	Het
Galnt13	A	G	2: 54,988,587 (GRCm39)	T470A	probably damaging	Het
Ggt7	A	T	2: 155,345,015 (GRCm39)		probably null	Het
Golim4	T	C	3: 75,785,957 (GRCm39)	E606G	probably damaging	Het
Gpd2	G	A	2: 57,197,112 (GRCm39)		probably null	Het
Grin2b	T	C	6: 135,757,304 (GRCm39)	M386V	probably damaging	Het
Hfm1	A	T	5: 107,059,306 (GRCm39)	S239T	probably benign	Het
Hmcn1	G	A	1: 150,649,641 (GRCm39)	T615I	probably benign	Het
Hook2	G	A	8: 85,724,040 (GRCm39)	E446K	possibly damaging	Het
Hsd3b1	C	T	3: 98,765,131 (GRCm39)		probably null	Het
Igsf9b	A	G	9: 27,234,150 (GRCm39)	Y421C	probably damaging	Het
Il21	A	G	3: 37,286,629 (GRCm39)	L29P	probably damaging	Het
Ildr1	A	G	16: 36,542,730 (GRCm39)	S421G	probably benign	Het
Kat2b	C	A	17: 53,972,894 (GRCm39)	T736K	probably benign	Het
Kif21a	A	T	15: 90,833,106 (GRCm39)		probably null	Het
Lat	A	G	7: 125,968,318 (GRCm39)		probably null	Het
Mastl	T	A	2: 23,023,425 (GRCm39)	K433*	probably null	Het
Mettl2	A	G	11: 105,019,719 (GRCm39)	R119G	probably benign	Het
Mia2	C	T	12: 59,231,021 (GRCm39)	P1223L	possibly damaging	Het
Mkrn2os	G	T	6: 115,563,635 (GRCm39)	D133E	probably benign	Het
Mslnl	A	G	17: 25,962,186 (GRCm39)	T195A	probably benign	Het
Muc16	T	G	9: 18,551,051 (GRCm39)	T5081P	probably benign	Het
Mylpf	G	C	7: 126,813,139 (GRCm39)	R110P	probably damaging	Het
Myo19	G	T	11: 84,798,194 (GRCm39)	C738F	possibly damaging	Het
Nat8f4	T	A	6: 85,878,271 (GRCm39)	N84I	possibly damaging	Het
Nol8	C	T	13: 49,829,862 (GRCm39)	R1104C	probably damaging	Het
Notch1	A	T	2: 26,353,830 (GRCm39)	D1932E	probably benign	Het
Nsun3	A	T	16: 62,596,663 (GRCm39)	C152S	possibly damaging	Het
Opcml	G	A	9: 28,586,507 (GRCm39)	W75*	probably null	Het
Or14j10	A	G	17: 37,934,597 (GRCm39)	F310L	probably benign	Het
Pcdh7	G	A	5: 57,879,582 (GRCm39)	E1046K	probably damaging	Het
Pcdhb9	T	A	18: 37,536,334 (GRCm39)	V776D	probably benign	Het
Pla2g4a	A	G	1: 149,727,103 (GRCm39)	L551S	probably damaging	Het
Plaa	G	A	4: 94,458,060 (GRCm39)	Q637*	probably null	Het
Plekhh1	A	T	12: 79,122,204 (GRCm39)	E1099V	probably damaging	Het
Ppp4r1	A	T	17: 66,136,495 (GRCm39)	N551Y	probably benign	Het
R3hdm2	T	C	10: 127,320,382 (GRCm39)	V554A	probably damaging	Het
Rab44	A	G	17: 29,357,150 (GRCm39)		probably null	Het
Rab5c	G	A	11: 100,610,789 (GRCm39)	R40C	probably damaging	Het
Rasgrf2	T	C	13: 92,034,521 (GRCm39)	T1119A	probably damaging	Het
Rims2	A	G	15: 39,449,044 (GRCm39)	D1194G	probably damaging	Het
Scarb1	A	T	5: 125,374,294 (GRCm39)	C280S	probably damaging	Het
Sde2	T	C	1: 180,693,827 (GRCm39)	F439S	probably damaging	Het
Setd5	T	C	6: 113,092,532 (GRCm39)	I304T	probably benign	Het
Sipa1l1	A	G	12: 82,449,896 (GRCm39)	E1106G	probably benign	Het
Sis	T	G	3: 72,810,940 (GRCm39)	S1694R	probably damaging	Het
Smad9	T	A	3: 54,693,614 (GRCm39)	F181Y	probably benign	Het
Smg1	A	G	7: 117,797,502 (GRCm39)		probably benign	Het
Sspo	T	C	6: 48,425,516 (GRCm39)	Y46H	probably damaging	Het
Tdrd12	A	G	7: 35,177,534 (GRCm39)	M940T	unknown	Het
Tmem44	G	T	16: 30,366,213 (GRCm39)	T71K	possibly damaging	Het
Tmf1	T	A	6: 97,133,911 (GRCm39)	E1009V	probably damaging	Het
Ttc39a	C	T	4: 109,288,763 (GRCm39)	R288W	probably damaging	Het
Ttc9c	G	A	19: 8,796,191 (GRCm39)		probably benign	Het
Usp28	T	A	9: 48,950,456 (GRCm39)	Y634N	probably damaging	Het
Vmn1r211	C	T	13: 23,036,063 (GRCm39)	M201I	probably benign	Het
Vmn2r54	T	A	7: 12,349,722 (GRCm39)	Q620L	possibly damaging	Het
Vps13c	T	C	9: 67,831,110 (GRCm39)	L1580P	probably benign	Het
Vrk3	C	A	7: 44,417,890 (GRCm39)	F308L	probably damaging	Het
Zdbf2	T	A	1: 63,346,563 (GRCm39)	H1647Q	possibly damaging	Het
Zfp984	A	T	4: 147,840,002 (GRCm39)	M283K	probably benign	Het

Other mutations in Kcng1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00091:Kcng1	APN	2	168,110,684 (GRCm39)	missense	probably benign
IGL01316:Kcng1	APN	2	168,110,960 (GRCm39)	missense	probably damaging	1.00
PIT4378001:Kcng1	UTSW	2	168,104,604 (GRCm39)	missense	probably damaging	0.98
R0104:Kcng1	UTSW	2	168,110,966 (GRCm39)	missense	probably damaging	1.00
R0692:Kcng1	UTSW	2	168,104,683 (GRCm39)	missense	probably damaging	0.99
R1574:Kcng1	UTSW	2	168,110,961 (GRCm39)	missense	probably damaging	1.00
R1574:Kcng1	UTSW	2	168,110,961 (GRCm39)	missense	probably damaging	1.00
R1591:Kcng1	UTSW	2	168,110,630 (GRCm39)	missense	possibly damaging	0.76
R1731:Kcng1	UTSW	2	168,110,609 (GRCm39)	missense	probably benign	0.00
R1937:Kcng1	UTSW	2	168,104,941 (GRCm39)	missense	probably benign	0.02
R1960:Kcng1	UTSW	2	168,104,904 (GRCm39)	missense	probably benign	0.03
R2145:Kcng1	UTSW	2	168,110,952 (GRCm39)	missense	probably damaging	1.00
R4167:Kcng1	UTSW	2	168,104,617 (GRCm39)	missense	probably damaging	1.00
R5215:Kcng1	UTSW	2	168,105,053 (GRCm39)	missense	probably benign	0.20
R5816:Kcng1	UTSW	2	168,110,643 (GRCm39)	missense	possibly damaging	0.90
R6367:Kcng1	UTSW	2	168,104,572 (GRCm39)	missense	probably damaging	1.00
R7920:Kcng1	UTSW	2	168,104,904 (GRCm39)	missense	probably benign	0.03
R7984:Kcng1	UTSW	2	168,104,406 (GRCm39)	missense	possibly damaging	0.93
R8494:Kcng1	UTSW	2	168,105,018 (GRCm39)	missense	probably damaging	1.00
R8994:Kcng1	UTSW	2	168,110,768 (GRCm39)	missense	probably benign	0.10
R9111:Kcng1	UTSW	2	168,104,535 (GRCm39)	missense	probably damaging	1.00
R9178:Kcng1	UTSW	2	168,111,105 (GRCm39)	missense	possibly damaging	0.93
R9507:Kcng1	UTSW	2	168,111,152 (GRCm39)	missense	probably damaging	0.96
R9562:Kcng1	UTSW	2	168,104,797 (GRCm39)	missense	probably damaging	1.00
X0063:Kcng1	UTSW	2	168,110,993 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TTGTCCCTAGTGTCTGAAGAGG -3'
(R):5'- TGAATTCGGGCTTCTGCTGC -3'

Sequencing Primer
(F):5'- ACAAGATGTCACTGTCCTGG -3'
(R):5'- CTTTTCCTGTGTGTGGCCATCG -3'

Posted On

2019-05-13