Mutagenetix > Incidental Mutation

Incidental Mutation 'R3976:Kcnma1'

475195

Institutional Source

Beutler Lab

Gene Symbol

Kcnma1

Ensembl Gene

ENSMUSG00000063142

Gene Name

potassium large conductance calcium-activated channel, subfamily M, alpha member 1

Synonyms

MaxiK, BKCa, 5730414M22Rik, BK channel alpha subunit, Slo, Slo1, mSlo1

MMRRC Submission

040842-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.856) question?

Stock #

R3976 (G1)

Quality Score

147

Status

Not validated

Chromosome

Chromosomal Location

23342356-24055173 bp(-) (GRCm39)

Type of Mutation

critical splice donor site (1 bp from exon)

DNA Base Change (assembly)

C to T at 24053815 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000152959 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000145596] [ENSMUST00000188210] [ENSMUST00000188285] [ENSMUST00000188991] [ENSMUST00000190044] [ENSMUST00000190339] [ENSMUST00000190339] [ENSMUST00000190985] [ENSMUST00000224232] [ENSMUST00000224812] [ENSMUST00000225315] [ENSMUST00000223655] [ENSMUST00000224468] [ENSMUST00000224077] [ENSMUST00000223727] [ENSMUST00000225431] [ENSMUST00000224285] [ENSMUST00000223749] [ENSMUST00000224787] [ENSMUST00000225556] [ENSMUST00000225794] [ENSMUST00000225471] [ENSMUST00000226051]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000145596

Predicted Effect

probably null
Transcript: ENSMUST00000188210

SMART Domains

Protein: ENSMUSP00000141069
Gene: ENSMUSG00000063142

Domain	Start	End	E-Value	Type
low complexity region	4	23	N/A	INTRINSIC
transmembrane domain	86	108	N/A	INTRINSIC
low complexity region	145	156	N/A	INTRINSIC
transmembrane domain	179	198	N/A	INTRINSIC
Pfam:Ion_trans	216	387	1.3e-18	PFAM
Pfam:Ion_trans_2	305	393	5.2e-16	PFAM
Pfam:TrkA_N	439	538	7.8e-7	PFAM
Pfam:BK_channel_a	536	634	5e-31	PFAM
low complexity region	988	996	N/A	INTRINSIC
low complexity region	1044	1055	N/A	INTRINSIC
low complexity region	1158	1184	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000188285

SMART Domains

Protein: ENSMUSP00000140275
Gene: ENSMUSG00000063142

Domain	Start	End	E-Value	Type
low complexity region	4	23	N/A	INTRINSIC
transmembrane domain	86	108	N/A	INTRINSIC
low complexity region	145	156	N/A	INTRINSIC
transmembrane domain	179	198	N/A	INTRINSIC
Pfam:Ion_trans	216	387	1.3e-18	PFAM
Pfam:Ion_trans_2	305	393	5.4e-16	PFAM
Pfam:TrkA_N	439	538	8e-7	PFAM
Pfam:BK_channel_a	536	634	5.2e-31	PFAM
low complexity region	1019	1027	N/A	INTRINSIC
low complexity region	1075	1086	N/A	INTRINSIC
low complexity region	1189	1215	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000188991

SMART Domains

Protein: ENSMUSP00000140751
Gene: ENSMUSG00000063142

Domain	Start	End	E-Value	Type
low complexity region	4	23	N/A	INTRINSIC
transmembrane domain	86	108	N/A	INTRINSIC
low complexity region	145	156	N/A	INTRINSIC
transmembrane domain	179	198	N/A	INTRINSIC
Pfam:Ion_trans	216	387	3.3e-18	PFAM
Pfam:Ion_trans_2	305	393	1.1e-15	PFAM
Pfam:TrkA_N	439	538	3.7e-7	PFAM
Pfam:BK_channel_a	536	634	3.4e-31	PFAM
low complexity region	1015	1023	N/A	INTRINSIC
low complexity region	1071	1082	N/A	INTRINSIC
low complexity region	1185	1211	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000190044

SMART Domains

Protein: ENSMUSP00000140033
Gene: ENSMUSG00000063142

Domain	Start	End	E-Value	Type
low complexity region	4	23	N/A	INTRINSIC
transmembrane domain	86	108	N/A	INTRINSIC
low complexity region	145	156	N/A	INTRINSIC
transmembrane domain	179	198	N/A	INTRINSIC
Pfam:Ion_trans	216	387	1.3e-18	PFAM
Pfam:Ion_trans_2	305	393	5.1e-16	PFAM
Pfam:TrkA_N	439	538	7.5e-7	PFAM
Pfam:BK_channel_a	536	634	4.9e-31	PFAM
low complexity region	957	965	N/A	INTRINSIC
low complexity region	1013	1024	N/A	INTRINSIC
low complexity region	1127	1153	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000190339

SMART Domains

Protein: ENSMUSP00000141143
Gene: ENSMUSG00000063142

Domain	Start	End	E-Value	Type
low complexity region	4	23	N/A	INTRINSIC
transmembrane domain	86	108	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000190339

SMART Domains

Protein: ENSMUSP00000141143
Gene: ENSMUSG00000063142

Domain	Start	End	E-Value	Type
low complexity region	4	23	N/A	INTRINSIC
transmembrane domain	86	108	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000190985

Predicted Effect

probably null
Transcript: ENSMUST00000224232

Predicted Effect

probably null
Transcript: ENSMUST00000224812

Predicted Effect

probably null
Transcript: ENSMUST00000225315

Predicted Effect

probably null
Transcript: ENSMUST00000223655

Predicted Effect

probably null
Transcript: ENSMUST00000224468

Predicted Effect

probably null
Transcript: ENSMUST00000224077

Predicted Effect

probably null
Transcript: ENSMUST00000223727

Predicted Effect

probably null
Transcript: ENSMUST00000225431

Predicted Effect

probably null
Transcript: ENSMUST00000224285

Predicted Effect

probably null
Transcript: ENSMUST00000224025

Predicted Effect

probably null
Transcript: ENSMUST00000223749

Predicted Effect

probably null
Transcript: ENSMUST00000224787

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000223609

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000223837

Predicted Effect

probably null
Transcript: ENSMUST00000225556

Predicted Effect

probably benign
Transcript: ENSMUST00000225794

Predicted Effect

probably null
Transcript: ENSMUST00000225471

Predicted Effect

probably benign
Transcript: ENSMUST00000226051

Coding Region Coverage

1x: 99.1%
3x: 98.4%
10x: 96.8%
20x: 93.3%

Validation Efficiency

98% (49/50)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] MaxiK channels are large conductance, voltage and calcium-sensitive potassium channels which are fundamental to the control of smooth muscle tone and neuronal excitability. MaxiK channels can be formed by 2 subunits: the pore-forming alpha subunit, which is the product of this gene, and the modulatory beta subunit. Intracellular calcium regulates the physical association between the alpha and beta subunits. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous inactivation of this gene leads to cerebellar ataxia, Purkinje cell dysfunction, uneven gait patterns, bladder hyperactivity, urinary incontinence, abnormal colonic K+ secretion, and hearing impairment. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca9	T	C	11: 110,039,615 (GRCm39)	D466G	probably benign	Het
Asb4	A	T	6: 5,390,771 (GRCm39)	M55L	probably benign	Het
Atxn7l1	T	C	12: 33,375,954 (GRCm39)	S10P	probably damaging	Het
Bola3	T	C	6: 83,328,249 (GRCm39)	L45P	probably benign	Het
Cacna2d4	A	G	6: 119,255,134 (GRCm39)		probably null	Het
Cfap54	A	G	10: 92,675,333 (GRCm39)	S2863P	possibly damaging	Het
Cyb5r3	A	G	15: 83,044,330 (GRCm39)	V180A	possibly damaging	Het
Dglucy	A	T	12: 100,807,648 (GRCm39)	T186S	probably benign	Het
Eml5	A	T	12: 98,768,724 (GRCm39)		probably benign	Het
Fam90a1a	G	A	8: 22,451,432 (GRCm39)	D98N	probably damaging	Het
Fbxo16	T	A	14: 65,524,606 (GRCm39)	L42Q	probably damaging	Het
Fbxw16	A	G	9: 109,268,697 (GRCm39)	V231A	probably benign	Het
Fermt3	G	A	19: 6,979,792 (GRCm39)	A447V	possibly damaging	Het
Fignl2	A	G	15: 100,950,467 (GRCm39)	L605P	unknown	Het
Gcsam	T	G	16: 45,440,192 (GRCm39)	N78K	probably damaging	Het
Gdf2	T	A	14: 33,666,791 (GRCm39)	V171D	probably damaging	Het
Gm28042	C	T	2: 119,867,237 (GRCm39)	H218Y	probably benign	Het
Herpud2	A	G	9: 25,021,734 (GRCm39)	V304A	probably damaging	Het
Lrp3	T	C	7: 34,903,530 (GRCm39)	D251G	probably benign	Het
Mapkbp1	T	C	2: 119,852,339 (GRCm39)	V957A	possibly damaging	Het
Mepe	C	T	5: 104,484,944 (GRCm39)	P28L	probably benign	Het
Muc2	T	A	7: 141,300,541 (GRCm39)		probably benign	Het
Nt5dc2	T	C	14: 30,860,832 (GRCm39)	S439P	probably damaging	Het
Opn4	C	T	14: 34,319,066 (GRCm39)	R173H	probably benign	Het
Or2k2	A	G	4: 58,785,164 (GRCm39)	L186P	probably damaging	Het
Or4f14	C	T	2: 111,742,951 (GRCm39)	G108D	possibly damaging	Het
Phf8-ps	A	T	17: 33,285,405 (GRCm39)	S466T	probably benign	Het
Ppp1r12a	T	C	10: 108,089,341 (GRCm39)	V660A	probably benign	Het
Prdm6	T	C	18: 53,673,278 (GRCm39)	I186T	possibly damaging	Het
Rab18	T	A	18: 6,778,529 (GRCm39)	D53E	probably benign	Het
Rel	A	G	11: 23,692,939 (GRCm39)	S365P	probably benign	Het
Rhbg	C	A	3: 88,151,843 (GRCm39)	G383V	probably damaging	Het
Rnps1-ps	A	T	6: 7,983,149 (GRCm39)		noncoding transcript	Het
Rp1l1	T	A	14: 64,267,758 (GRCm39)	Y1115N	probably damaging	Het
Runx2	T	C	17: 44,920,966 (GRCm39)	T339A	possibly damaging	Het
Ryr3	T	C	2: 112,506,182 (GRCm39)	E3455G	possibly damaging	Het
Serpina1d	A	T	12: 103,734,107 (GRCm39)	S66T	probably benign	Het
Setd3	T	C	12: 108,131,417 (GRCm39)	K3R	possibly damaging	Het
Spg7	A	G	8: 123,806,187 (GRCm39)	D299G	probably damaging	Het
Sptbn5	C	T	2: 119,878,742 (GRCm39)		noncoding transcript	Het
Srcap	A	G	7: 127,148,411 (GRCm39)	T1859A	probably benign	Het
Suox	A	G	10: 128,506,906 (GRCm39)	V374A	probably damaging	Het
Tesk1	C	T	4: 43,445,786 (GRCm39)	P280S	possibly damaging	Het
Tsc22d1	T	C	14: 76,656,049 (GRCm39)	S761P	probably damaging	Het
Tubal3	C	T	13: 3,982,946 (GRCm39)	S242L	probably benign	Het
Ugt2b1	C	A	5: 87,065,534 (GRCm39)	V502L	probably benign	Het

Other mutations in Kcnma1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01318:Kcnma1	APN	14	23,364,390 (GRCm39)	splice site	probably benign
IGL01520:Kcnma1	APN	14	23,551,211 (GRCm39)	missense	possibly damaging	0.94
IGL01977:Kcnma1	APN	14	23,580,367 (GRCm39)	splice site	probably benign
IGL02140:Kcnma1	APN	14	23,359,113 (GRCm39)	missense	probably damaging	1.00
IGL02165:Kcnma1	APN	14	23,387,035 (GRCm39)	missense	possibly damaging	0.93
IGL02186:Kcnma1	APN	14	23,576,881 (GRCm39)	missense	probably benign	0.28
IGL02268:Kcnma1	APN	14	23,593,144 (GRCm39)	missense	probably damaging	1.00
IGL02353:Kcnma1	APN	14	23,641,681 (GRCm39)	missense	probably damaging	1.00
IGL02360:Kcnma1	APN	14	23,641,681 (GRCm39)	missense	probably damaging	1.00
IGL02491:Kcnma1	APN	14	23,361,757 (GRCm39)	missense	probably damaging	1.00
IGL02552:Kcnma1	APN	14	23,436,327 (GRCm39)	critical splice donor site	probably null
IGL02625:Kcnma1	APN	14	23,413,900 (GRCm39)	missense	probably damaging	1.00
IGL02677:Kcnma1	APN	14	23,513,224 (GRCm39)	missense	probably damaging	1.00
IGL02706:Kcnma1	APN	14	23,359,222 (GRCm39)	missense	probably damaging	1.00
G1citation:Kcnma1	UTSW	14	24,053,812 (GRCm39)	splice site	probably null
PIT4495001:Kcnma1	UTSW	14	23,475,665 (GRCm39)	missense	probably benign	0.00
PIT4514001:Kcnma1	UTSW	14	23,359,103 (GRCm39)	splice site	probably null
PIT4576001:Kcnma1	UTSW	14	23,359,103 (GRCm39)	splice site	probably null
R0071:Kcnma1	UTSW	14	23,576,835 (GRCm39)	missense	probably damaging	1.00
R0071:Kcnma1	UTSW	14	23,576,835 (GRCm39)	missense	probably damaging	1.00
R0115:Kcnma1	UTSW	14	23,364,243 (GRCm39)	missense	probably damaging	1.00
R0172:Kcnma1	UTSW	14	23,853,234 (GRCm39)	missense	probably damaging	1.00
R0178:Kcnma1	UTSW	14	23,576,835 (GRCm39)	missense	probably damaging	1.00
R0183:Kcnma1	UTSW	14	23,558,120 (GRCm39)	missense	probably damaging	1.00
R0240:Kcnma1	UTSW	14	23,544,647 (GRCm39)	missense	probably damaging	1.00
R0240:Kcnma1	UTSW	14	23,544,647 (GRCm39)	missense	probably damaging	1.00
R0328:Kcnma1	UTSW	14	23,423,265 (GRCm39)	missense	probably damaging	1.00
R0501:Kcnma1	UTSW	14	23,361,784 (GRCm39)	missense	possibly damaging	0.80
R0631:Kcnma1	UTSW	14	23,559,852 (GRCm39)	splice site	probably benign
R0668:Kcnma1	UTSW	14	23,417,563 (GRCm39)	missense	probably damaging	1.00
R0811:Kcnma1	UTSW	14	23,350,086 (GRCm39)	missense	probably damaging	0.96
R0812:Kcnma1	UTSW	14	23,350,086 (GRCm39)	missense	probably damaging	0.96
R1080:Kcnma1	UTSW	14	23,544,675 (GRCm39)	missense	probably damaging	1.00
R1419:Kcnma1	UTSW	14	23,417,710 (GRCm39)	missense	probably damaging	0.99
R1446:Kcnma1	UTSW	14	23,361,792 (GRCm39)	missense	probably damaging	1.00
R1454:Kcnma1	UTSW	14	23,513,268 (GRCm39)	missense	probably damaging	1.00
R1651:Kcnma1	UTSW	14	23,364,262 (GRCm39)	missense	probably damaging	1.00
R1826:Kcnma1	UTSW	14	23,380,997 (GRCm39)	missense	probably damaging	1.00
R1827:Kcnma1	UTSW	14	23,380,997 (GRCm39)	missense	probably damaging	1.00
R1828:Kcnma1	UTSW	14	23,380,997 (GRCm39)	missense	probably damaging	1.00
R1864:Kcnma1	UTSW	14	23,853,230 (GRCm39)	missense	probably damaging	1.00
R2002:Kcnma1	UTSW	14	23,387,097 (GRCm39)	missense	probably damaging	0.99
R2140:Kcnma1	UTSW	14	23,364,288 (GRCm39)	missense	probably damaging	1.00
R2278:Kcnma1	UTSW	14	23,593,151 (GRCm39)	nonsense	probably null
R2866:Kcnma1	UTSW	14	23,423,275 (GRCm39)	missense	probably benign	0.16
R2867:Kcnma1	UTSW	14	23,423,275 (GRCm39)	missense	probably benign	0.16
R2867:Kcnma1	UTSW	14	23,423,275 (GRCm39)	missense	probably benign	0.16
R2900:Kcnma1	UTSW	14	23,853,228 (GRCm39)	missense	probably damaging	1.00
R3820:Kcnma1	UTSW	14	23,350,006 (GRCm39)	missense	possibly damaging	0.66
R3821:Kcnma1	UTSW	14	23,417,679 (GRCm39)	missense	probably damaging	1.00
R3901:Kcnma1	UTSW	14	23,555,323 (GRCm39)	missense	probably damaging	0.98
R3975:Kcnma1	UTSW	14	24,053,815 (GRCm39)	critical splice donor site	probably null
R4352:Kcnma1	UTSW	14	23,361,720 (GRCm39)	missense	probably damaging	1.00
R4517:Kcnma1	UTSW	14	23,387,097 (GRCm39)	missense	probably damaging	1.00
R4598:Kcnma1	UTSW	14	23,853,228 (GRCm39)	missense	probably damaging	1.00
R4604:Kcnma1	UTSW	14	23,359,106 (GRCm39)	critical splice donor site	probably null
R4743:Kcnma1	UTSW	14	23,853,270 (GRCm39)	missense	probably damaging	1.00
R4754:Kcnma1	UTSW	14	23,413,904 (GRCm39)	missense	probably damaging	0.96
R4908:Kcnma1	UTSW	14	23,359,220 (GRCm39)	missense	probably damaging	0.99
R4960:Kcnma1	UTSW	14	24,054,186 (GRCm39)	intron	probably benign
R5175:Kcnma1	UTSW	14	23,386,106 (GRCm39)	critical splice donor site	probably null
R5218:Kcnma1	UTSW	14	23,513,253 (GRCm39)	missense	probably damaging	0.96
R5435:Kcnma1	UTSW	14	23,578,472 (GRCm39)	nonsense	probably null
R5705:Kcnma1	UTSW	14	24,053,839 (GRCm39)	missense	possibly damaging	0.73
R5746:Kcnma1	UTSW	14	23,544,635 (GRCm39)	missense	probably damaging	1.00
R5780:Kcnma1	UTSW	14	23,436,419 (GRCm39)	nonsense	probably null
R5793:Kcnma1	UTSW	14	23,359,103 (GRCm39)	splice site	probably null
R6039:Kcnma1	UTSW	14	23,359,105 (GRCm39)	missense	probably benign	0.42
R6039:Kcnma1	UTSW	14	23,359,105 (GRCm39)	missense	probably benign	0.42
R6133:Kcnma1	UTSW	14	24,053,936 (GRCm39)	missense	probably damaging	0.98
R6271:Kcnma1	UTSW	14	23,559,957 (GRCm39)	missense	probably damaging	1.00
R6490:Kcnma1	UTSW	14	23,386,165 (GRCm39)	missense	possibly damaging	0.46
R6704:Kcnma1	UTSW	14	24,052,882 (GRCm39)	nonsense	probably null
R6822:Kcnma1	UTSW	14	24,053,812 (GRCm39)	splice site	probably null
R6855:Kcnma1	UTSW	14	23,417,679 (GRCm39)	missense	probably damaging	1.00
R6920:Kcnma1	UTSW	14	23,576,602 (GRCm39)	critical splice donor site	probably null
R7017:Kcnma1	UTSW	14	23,544,711 (GRCm39)	missense	possibly damaging	0.79
R7081:Kcnma1	UTSW	14	23,350,086 (GRCm39)	missense	probably damaging	0.96
R7113:Kcnma1	UTSW	14	23,513,224 (GRCm39)	missense	probably damaging	1.00
R7131:Kcnma1	UTSW	14	23,417,562 (GRCm39)	missense	probably damaging	1.00
R7172:Kcnma1	UTSW	14	23,576,691 (GRCm39)	missense	probably damaging	1.00
R7207:Kcnma1	UTSW	14	23,359,083 (GRCm39)	makesense	probably null
R7308:Kcnma1	UTSW	14	23,381,003 (GRCm39)	missense	probably damaging	0.99
R7371:Kcnma1	UTSW	14	23,544,638 (GRCm39)	missense	possibly damaging	0.94
R7404:Kcnma1	UTSW	14	24,052,902 (GRCm39)	missense	unknown
R7560:Kcnma1	UTSW	14	23,580,310 (GRCm39)	missense	probably benign	0.15
R7693:Kcnma1	UTSW	14	23,417,680 (GRCm39)	missense	probably damaging	1.00
R7763:Kcnma1	UTSW	14	23,350,074 (GRCm39)	missense	possibly damaging	0.66
R7809:Kcnma1	UTSW	14	23,423,324 (GRCm39)	missense	probably benign	0.16
R7832:Kcnma1	UTSW	14	23,440,991 (GRCm39)	missense	probably benign
R7884:Kcnma1	UTSW	14	23,387,057 (GRCm39)	missense	probably benign	0.01
R8013:Kcnma1	UTSW	14	23,423,211 (GRCm39)	missense	probably benign	0.31
R8014:Kcnma1	UTSW	14	23,423,211 (GRCm39)	missense	probably benign	0.31
R8066:Kcnma1	UTSW	14	23,361,744 (GRCm39)	missense	probably benign	0.00
R8097:Kcnma1	UTSW	14	23,381,032 (GRCm39)	missense	probably damaging	1.00
R8154:Kcnma1	UTSW	14	23,361,822 (GRCm39)	missense	possibly damaging	0.62
R8507:Kcnma1	UTSW	14	23,641,706 (GRCm39)	missense	probably benign	0.00
R8672:Kcnma1	UTSW	14	23,551,230 (GRCm39)	missense	probably damaging	1.00
R8677:Kcnma1	UTSW	14	23,436,418 (GRCm39)	missense	probably benign	0.36
R8725:Kcnma1	UTSW	14	23,436,332 (GRCm39)	missense	probably benign	0.00
R8727:Kcnma1	UTSW	14	23,436,332 (GRCm39)	missense	probably benign	0.00
R8827:Kcnma1	UTSW	14	23,417,548 (GRCm39)	missense	probably damaging	1.00
R8880:Kcnma1	UTSW	14	23,417,718 (GRCm39)	missense	probably damaging	1.00
R8997:Kcnma1	UTSW	14	23,513,037 (GRCm39)	intron	probably benign
R9056:Kcnma1	UTSW	14	23,700,214 (GRCm39)	missense	possibly damaging	0.80
R9346:Kcnma1	UTSW	14	23,700,233 (GRCm39)	missense	possibly damaging	0.94
R9403:Kcnma1	UTSW	14	23,593,145 (GRCm39)	missense	probably benign	0.05
R9438:Kcnma1	UTSW	14	23,417,653 (GRCm39)	missense	probably benign	0.00
R9482:Kcnma1	UTSW	14	23,441,033 (GRCm39)	missense	probably benign
R9511:Kcnma1	UTSW	14	23,361,793 (GRCm39)	missense	possibly damaging	0.90
R9649:Kcnma1	UTSW	14	23,501,666 (GRCm39)	critical splice donor site	probably null
R9663:Kcnma1	UTSW	14	24,053,897 (GRCm39)	missense	probably benign	0.15
R9673:Kcnma1	UTSW	14	23,558,123 (GRCm39)	missense	probably benign	0.01
RF001:Kcnma1	UTSW	14	23,361,765 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

Posted On

2017-04-14