Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02678:Ktn1'

303268

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Ktn1

Ensembl Gene

ENSMUSG00000021843

Gene Name

kinectin 1

Synonyms

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

IGL02678

Quality Score

Status

Chromosome

Chromosomal Location

47886551-47974021 bp(+) (GRCm39)

Type of Mutation

critical splice acceptor site

DNA Base Change (assembly)

A to T at 47971610 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000139946 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000022391] [ENSMUST00000185343] [ENSMUST00000185940] [ENSMUST00000186627] [ENSMUST00000186761] [ENSMUST00000187039] [ENSMUST00000187262] [ENSMUST00000187839] [ENSMUST00000190535] [ENSMUST00000190999] [ENSMUST00000190252] [ENSMUST00000191446] [ENSMUST00000191511] [ENSMUST00000191018] [ENSMUST00000189533] [ENSMUST00000188330] [ENSMUST00000189101] [ENSMUST00000190182] [ENSMUST00000188553] [ENSMUST00000189986]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000022391

SMART Domains

Protein: ENSMUSP00000022391
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
transmembrane domain	7	29	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	1028	N/A	INTRINSIC
coiled coil region	1089	1267	N/A	INTRINSIC
coiled coil region	1302	1326	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000185343

SMART Domains

Protein: ENSMUSP00000140186
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	792	N/A	INTRINSIC
low complexity region	816	825	N/A	INTRINSIC
coiled coil region	836	1005	N/A	INTRINSIC
coiled coil region	1066	1192	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000185940

SMART Domains

Protein: ENSMUSP00000139625
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	792	N/A	INTRINSIC
low complexity region	816	825	N/A	INTRINSIC
coiled coil region	836	993	N/A	INTRINSIC
coiled coil region	1037	1163	N/A	INTRINSIC
coiled coil region	1198	1222	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000186627

SMART Domains

Protein: ENSMUSP00000140873
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	792	N/A	INTRINSIC
low complexity region	816	825	N/A	INTRINSIC
coiled coil region	836	993	N/A	INTRINSIC
coiled coil region	1037	1191	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000186761

SMART Domains

Protein: ENSMUSP00000139521
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	1016	N/A	INTRINSIC
coiled coil region	1060	1210	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000187039

SMART Domains

Protein: ENSMUSP00000140202
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	792	N/A	INTRINSIC
low complexity region	816	825	N/A	INTRINSIC
coiled coil region	836	993	N/A	INTRINSIC
coiled coil region	1037	1163	N/A	INTRINSIC
coiled coil region	1198	1222	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000187262

SMART Domains

Protein: ENSMUSP00000140206
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	1028	N/A	INTRINSIC
coiled coil region	1089	1215	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000187839

SMART Domains

Protein: ENSMUSP00000140324
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
transmembrane domain	7	29	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	1028	N/A	INTRINSIC
coiled coil region	1089	1267	N/A	INTRINSIC
coiled coil region	1302	1326	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000190535

SMART Domains

Protein: ENSMUSP00000139952
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	792	N/A	INTRINSIC
low complexity region	816	825	N/A	INTRINSIC
coiled coil region	836	1005	N/A	INTRINSIC
coiled coil region	1066	1244	N/A	INTRINSIC
coiled coil region	1279	1303	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000190999

SMART Domains

Protein: ENSMUSP00000139673
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	792	N/A	INTRINSIC
low complexity region	816	825	N/A	INTRINSIC
coiled coil region	836	993	N/A	INTRINSIC
coiled coil region	1037	1215	N/A	INTRINSIC
coiled coil region	1250	1274	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000190252

SMART Domains

Protein: ENSMUSP00000140011
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	1016	N/A	INTRINSIC
coiled coil region	1060	1210	N/A	INTRINSIC
coiled coil region	1245	1269	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000191446

SMART Domains

Protein: ENSMUSP00000140748
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	1028	N/A	INTRINSIC
coiled coil region	1089	1215	N/A	INTRINSIC
coiled coil region	1250	1274	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000191511

SMART Domains

Protein: ENSMUSP00000139946
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	792	N/A	INTRINSIC
low complexity region	816	825	N/A	INTRINSIC
coiled coil region	836	1005	N/A	INTRINSIC
coiled coil region	1066	1192	N/A	INTRINSIC
coiled coil region	1227	1251	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000191018

SMART Domains

Protein: ENSMUSP00000139585
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	792	N/A	INTRINSIC
low complexity region	816	825	N/A	INTRINSIC
coiled coil region	836	1005	N/A	INTRINSIC
coiled coil region	1066	1220	N/A	INTRINSIC
coiled coil region	1255	1279	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000189533

SMART Domains

Protein: ENSMUSP00000140142
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	792	N/A	INTRINSIC
low complexity region	816	825	N/A	INTRINSIC
coiled coil region	836	993	N/A	INTRINSIC
coiled coil region	1037	1187	N/A	INTRINSIC
coiled coil region	1222	1246	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000190857

Predicted Effect

probably benign
Transcript: ENSMUST00000188330

SMART Domains

Protein: ENSMUSP00000140845
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	792	N/A	INTRINSIC
low complexity region	816	825	N/A	INTRINSIC
coiled coil region	836	993	N/A	INTRINSIC
coiled coil region	1037	1187	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000189101

SMART Domains

Protein: ENSMUSP00000140178
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	792	N/A	INTRINSIC
low complexity region	816	825	N/A	INTRINSIC
coiled coil region	836	993	N/A	INTRINSIC
coiled coil region	1037	1163	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000190182

SMART Domains

Protein: ENSMUSP00000140301
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	1016	N/A	INTRINSIC
coiled coil region	1060	1238	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000188553

SMART Domains

Protein: ENSMUSP00000140865
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
signal peptide	1	39	N/A	INTRINSIC
coiled coil region	40	66	N/A	INTRINSIC
low complexity region	108	127	N/A	INTRINSIC
low complexity region	150	173	N/A	INTRINSIC
low complexity region	203	221	N/A	INTRINSIC
coiled coil region	329	372	N/A	INTRINSIC
coiled coil region	402	727	N/A	INTRINSIC
coiled coil region	764	792	N/A	INTRINSIC
low complexity region	816	825	N/A	INTRINSIC
coiled coil region	836	1005	N/A	INTRINSIC
coiled coil region	1066	1216	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000189986

SMART Domains

Protein: ENSMUSP00000139970
Gene: ENSMUSG00000021843

Domain	Start	End	E-Value	Type
Pfam:Rib_recp_KP_reg	29	172	2.1e-7	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000192676

Coding Region Coverage

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a targeted null mutation or a floxed allele exhibit no discernable phenotype; mice are viable and fertile up to one year of age. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 57 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aasdh	A	G	5: 77,035,867 (GRCm39)		probably benign	Het
Adgrb1	A	G	15: 74,410,177 (GRCm39)	E272G	probably damaging	Het
Alcam	G	A	16: 52,094,401 (GRCm39)	P416S	probably damaging	Het
B3galt1	A	G	2: 67,949,254 (GRCm39)	H323R	probably benign	Het
Bahcc1	G	A	11: 120,163,697 (GRCm39)	S665N	probably damaging	Het
Birc6	T	C	17: 74,956,898 (GRCm39)	S3631P	probably damaging	Het
Capn3	A	C	2: 120,333,479 (GRCm39)	N621T	probably damaging	Het
Cblif	T	C	19: 11,725,839 (GRCm39)	M43T	probably damaging	Het
Ccdc162	G	A	10: 41,437,151 (GRCm39)	H480Y	probably damaging	Het
Ccr2	T	A	9: 123,906,783 (GRCm39)	D354E	probably benign	Het
Cdc42bpb	T	G	12: 111,292,530 (GRCm39)	D335A	probably damaging	Het
Cdcp3	A	G	7: 130,830,646 (GRCm39)	Y360C	probably damaging	Het
Chrd	G	T	16: 20,552,770 (GRCm39)	R89L	probably damaging	Het
Cops2	T	C	2: 125,686,831 (GRCm39)	R91G	probably benign	Het
Ddi1	T	C	9: 6,266,106 (GRCm39)	T88A	probably benign	Het
Dnai1	A	C	4: 41,602,917 (GRCm39)	E140A	probably benign	Het
Eif1ad17	C	A	12: 87,978,946 (GRCm39)	P110Q	possibly damaging	Het
Gcn1	A	G	5: 115,751,814 (GRCm39)	D2063G	probably damaging	Het
Gdpd4	A	T	7: 97,623,584 (GRCm39)		probably benign	Het
Gng7	C	A	10: 80,787,518 (GRCm39)	L48F	probably damaging	Het
Htt	G	T	5: 35,057,246 (GRCm39)	C2725F	probably damaging	Het
Inpp4b	A	G	8: 82,583,373 (GRCm39)	K159R	probably damaging	Het
Insr	G	T	8: 3,223,570 (GRCm39)	N854K	probably benign	Het
Lcat	A	G	8: 106,668,572 (GRCm39)		probably null	Het
Mb21d2	T	C	16: 28,646,801 (GRCm39)	E391G	probably benign	Het
Mms19	A	G	19: 41,942,915 (GRCm39)	S354P	possibly damaging	Het
Mx2	G	A	16: 97,357,320 (GRCm39)		probably null	Het
Mycl	G	A	4: 122,893,776 (GRCm39)	R192Q	probably damaging	Het
Mzf1	A	G	7: 12,786,836 (GRCm39)	V78A	probably benign	Het
Nipbl	G	T	15: 8,380,594 (GRCm39)	P733T	possibly damaging	Het
Nploc4	A	G	11: 120,280,198 (GRCm39)	I450T	probably benign	Het
Omd	A	T	13: 49,745,757 (GRCm39)	E389V	probably benign	Het
Or8g30	C	T	9: 39,230,217 (GRCm39)	S231N	probably benign	Het
Oxgr1	A	G	14: 120,259,580 (GRCm39)	L209P	probably damaging	Het
Pak1	A	C	7: 97,543,209 (GRCm39)	T291P	probably damaging	Het
Pcmtd1	T	A	1: 7,240,045 (GRCm39)	I338K	probably damaging	Het
Phrf1	A	G	7: 140,840,195 (GRCm39)	D364G	probably damaging	Het
Pomk	G	A	8: 26,473,135 (GRCm39)	P273S	probably damaging	Het
Psg22	A	T	7: 18,453,418 (GRCm39)	I38F	probably damaging	Het
Rbks	G	T	5: 31,830,757 (GRCm39)	T42N	probably damaging	Het
Rrbp1	A	G	2: 143,832,107 (GRCm39)	V20A	probably damaging	Het
Six4	T	C	12: 73,159,408 (GRCm39)	Y176C	probably damaging	Het
Slc11a2	T	A	15: 100,310,081 (GRCm39)	M9L	possibly damaging	Het
Slc16a11	T	C	11: 70,106,242 (GRCm39)	L112S	probably damaging	Het
Slc25a28	A	T	19: 43,655,586 (GRCm39)		probably benign	Het
Slc30a3	G	A	5: 31,245,676 (GRCm39)	R237*	probably null	Het
Slco1a8	A	T	6: 141,954,444 (GRCm39)	Y10N	probably damaging	Het
Smc1b	G	A	15: 84,949,201 (GRCm39)	R1237*	probably null	Het
Smtn	T	C	11: 3,476,353 (GRCm39)	E585G	possibly damaging	Het
Spatc1	A	T	15: 76,176,572 (GRCm39)	D441V	probably damaging	Het
Tenm4	A	G	7: 96,545,426 (GRCm39)	N2481D	probably damaging	Het
Tnks2	A	T	19: 36,823,143 (GRCm39)	I137F	possibly damaging	Het
Trip11	T	C	12: 101,849,649 (GRCm39)	K1472E	probably damaging	Het
Ttn	C	A	2: 76,708,660 (GRCm39)	E1846*	probably null	Het
Vwa8	A	G	14: 79,221,640 (GRCm39)	D532G	probably damaging	Het
Zfp268	A	T	4: 145,349,067 (GRCm39)	H168L	probably damaging	Het
Zfp977	G	A	7: 42,232,419 (GRCm39)	T14I	probably damaging	Het

Other mutations in Ktn1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01017:Ktn1	APN	14	47,946,335 (GRCm39)	missense	probably benign	0.30
IGL01109:Ktn1	APN	14	47,952,178 (GRCm39)	missense	probably damaging	1.00
IGL02300:Ktn1	APN	14	47,927,517 (GRCm39)	missense	probably damaging	1.00
IGL02339:Ktn1	APN	14	47,920,835 (GRCm39)	splice site	probably benign
IGL02525:Ktn1	APN	14	47,962,200 (GRCm39)	critical splice donor site	probably null
IGL02565:Ktn1	APN	14	47,910,391 (GRCm39)	splice site	probably benign
IGL03181:Ktn1	APN	14	47,970,741 (GRCm39)	missense	probably benign	0.19
IGL03393:Ktn1	APN	14	47,928,391 (GRCm39)	missense	probably damaging	1.00
PIT4520001:Ktn1	UTSW	14	47,923,774 (GRCm39)	missense	probably damaging	0.96
R0035:Ktn1	UTSW	14	47,967,836 (GRCm39)	missense	probably benign	0.07
R0035:Ktn1	UTSW	14	47,967,836 (GRCm39)	missense	probably benign	0.07
R0270:Ktn1	UTSW	14	47,952,119 (GRCm39)	missense	probably benign	0.00
R0370:Ktn1	UTSW	14	47,901,532 (GRCm39)	missense	probably benign	0.00
R0371:Ktn1	UTSW	14	47,961,460 (GRCm39)	nonsense	probably null
R0530:Ktn1	UTSW	14	47,970,700 (GRCm39)	missense	probably benign	0.14
R0531:Ktn1	UTSW	14	47,901,398 (GRCm39)	missense	probably damaging	0.98
R0611:Ktn1	UTSW	14	47,932,073 (GRCm39)	missense	probably benign
R0836:Ktn1	UTSW	14	47,938,519 (GRCm39)	splice site	probably null
R1076:Ktn1	UTSW	14	47,932,095 (GRCm39)	missense	probably damaging	0.99
R1522:Ktn1	UTSW	14	47,904,873 (GRCm39)	missense	probably damaging	1.00
R1554:Ktn1	UTSW	14	47,932,964 (GRCm39)	missense	probably damaging	1.00
R1992:Ktn1	UTSW	14	47,932,978 (GRCm39)	missense	probably damaging	1.00
R2040:Ktn1	UTSW	14	47,938,069 (GRCm39)	splice site	probably benign
R2080:Ktn1	UTSW	14	47,963,417 (GRCm39)	missense	probably damaging	1.00
R2110:Ktn1	UTSW	14	47,931,345 (GRCm39)	missense	possibly damaging	0.47
R2144:Ktn1	UTSW	14	47,952,109 (GRCm39)	missense	probably damaging	1.00
R3730:Ktn1	UTSW	14	47,938,606 (GRCm39)	missense	probably damaging	1.00
R3780:Ktn1	UTSW	14	47,943,860 (GRCm39)	splice site	probably benign
R3782:Ktn1	UTSW	14	47,943,860 (GRCm39)	splice site	probably benign
R4414:Ktn1	UTSW	14	47,962,387 (GRCm39)	nonsense	probably null
R4610:Ktn1	UTSW	14	47,963,636 (GRCm39)	intron	probably benign
R4784:Ktn1	UTSW	14	47,930,953 (GRCm39)	critical splice donor site	probably null
R4838:Ktn1	UTSW	14	47,963,413 (GRCm39)	nonsense	probably null
R4909:Ktn1	UTSW	14	47,943,917 (GRCm39)	missense	probably damaging	0.99
R4976:Ktn1	UTSW	14	47,907,756 (GRCm39)	critical splice donor site	probably null
R5110:Ktn1	UTSW	14	47,941,744 (GRCm39)	splice site	probably benign
R5257:Ktn1	UTSW	14	47,904,820 (GRCm39)	missense	probably benign	0.05
R5469:Ktn1	UTSW	14	47,928,377 (GRCm39)	missense	probably damaging	1.00
R5600:Ktn1	UTSW	14	47,927,490 (GRCm39)	missense	probably damaging	1.00
R5607:Ktn1	UTSW	14	47,971,554 (GRCm39)	intron	probably benign
R5608:Ktn1	UTSW	14	47,971,554 (GRCm39)	intron	probably benign
R5920:Ktn1	UTSW	14	47,961,481 (GRCm39)	nonsense	probably null
R6045:Ktn1	UTSW	14	47,914,253 (GRCm39)	missense	probably damaging	1.00
R6139:Ktn1	UTSW	14	47,963,672 (GRCm39)	splice site	probably null
R6282:Ktn1	UTSW	14	47,901,428 (GRCm39)	missense	probably damaging	1.00
R6654:Ktn1	UTSW	14	47,927,457 (GRCm39)	missense	probably damaging	1.00
R6957:Ktn1	UTSW	14	47,904,810 (GRCm39)	nonsense	probably null
R6959:Ktn1	UTSW	14	47,957,713 (GRCm39)	missense	probably damaging	1.00
R7170:Ktn1	UTSW	14	47,943,867 (GRCm39)	missense	probably damaging	1.00
R7206:Ktn1	UTSW	14	47,932,985 (GRCm39)	missense	probably damaging	0.97
R7442:Ktn1	UTSW	14	47,952,097 (GRCm39)	missense	probably benign	0.01
R7462:Ktn1	UTSW	14	47,932,089 (GRCm39)	missense	probably null	1.00
R7513:Ktn1	UTSW	14	47,901,541 (GRCm39)	missense	possibly damaging	0.77
R7743:Ktn1	UTSW	14	47,907,750 (GRCm39)	missense	probably damaging	1.00
R8010:Ktn1	UTSW	14	47,943,230 (GRCm39)	missense	possibly damaging	0.60
R8062:Ktn1	UTSW	14	47,962,429 (GRCm39)	critical splice donor site	probably null
R8244:Ktn1	UTSW	14	47,912,280 (GRCm39)	missense	probably null	1.00
R8387:Ktn1	UTSW	14	47,944,744 (GRCm39)	splice site	probably null
R8724:Ktn1	UTSW	14	47,931,335 (GRCm39)	missense	probably benign	0.00
R8725:Ktn1	UTSW	14	47,907,757 (GRCm39)	critical splice donor site	probably benign
R8962:Ktn1	UTSW	14	47,901,248 (GRCm39)	missense	probably damaging	1.00
R9001:Ktn1	UTSW	14	47,910,409 (GRCm39)	missense	probably damaging	0.99
R9072:Ktn1	UTSW	14	47,941,694 (GRCm39)	missense	probably benign	0.25
R9324:Ktn1	UTSW	14	47,948,353 (GRCm39)	missense	probably benign	0.02
R9423:Ktn1	UTSW	14	47,912,318 (GRCm39)	missense	probably benign	0.00
R9479:Ktn1	UTSW	14	47,962,174 (GRCm39)	missense	probably damaging	0.98
R9674:Ktn1	UTSW	14	47,922,213 (GRCm39)	missense	possibly damaging	0.77
R9718:Ktn1	UTSW	14	47,910,508 (GRCm39)	missense	probably damaging	0.98
Z1177:Ktn1	UTSW	14	47,929,895 (GRCm39)	critical splice acceptor site	probably null

Posted On

2015-04-16