Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03123:Kctd4'

410054

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Kctd4

Ensembl Gene

ENSMUSG00000046523

Gene Name

potassium channel tetramerisation domain containing 4

Synonyms

2210017A09Rik

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.153) question?

Stock #

IGL03123

Quality Score

Status

Chromosome

Chromosomal Location

76192443-76202657 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 76200418 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tryptophan to Arginine at position 130 (W130R)

Ref Sequence

ENSEMBL: ENSMUSP00000061734 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000050120] [ENSMUST00000088922]

AlphaFold

Q9D7X1

Predicted Effect

possibly damaging
Transcript: ENSMUST00000050120
AA Change: W130R

PolyPhen 2 Score 0.799 (Sensitivity: 0.84; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000061734
Gene: ENSMUSG00000046523
AA Change: W130R

Domain	Start	End	E-Value	Type
low complexity region	2	13	N/A	INTRINSIC
BTB	33	134	2.3e-6	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000088922

SMART Domains

Protein: ENSMUSP00000086312
Gene: ENSMUSG00000067995

Domain	Start	End	E-Value	Type
Pfam:TFIIF_beta	7	105	6.7e-19	PFAM
Pfam:TFIIF_beta	99	240	1e-44	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ap5m1	T	C	14: 49,311,218 (GRCm39)	V96A	probably damaging	Het
Atp10b	T	C	11: 43,044,110 (GRCm39)	V112A	probably benign	Het
Caprin2	G	T	6: 148,796,505 (GRCm39)	A36E	probably damaging	Het
Castor1	A	T	11: 4,170,278 (GRCm39)	T119S	probably damaging	Het
Dnase1l2	T	C	17: 24,661,226 (GRCm39)	M28V	possibly damaging	Het
Eci1	T	A	17: 24,655,300 (GRCm39)		probably null	Het
Edil3	T	A	13: 89,279,855 (GRCm39)	S178T	probably damaging	Het
Epha5	A	G	5: 84,479,085 (GRCm39)		probably null	Het
Exoc3l4	A	G	12: 111,388,547 (GRCm39)	E12G	probably damaging	Het
Frmd7	G	A	X: 49,984,835 (GRCm39)	T445I	probably benign	Het
Golga4	A	G	9: 118,365,953 (GRCm39)	E344G	probably damaging	Het
H2-M10.4	A	G	17: 36,772,812 (GRCm39)	Y57H	probably damaging	Het
Hnmt	T	C	2: 23,909,171 (GRCm39)	I81V	probably benign	Het
Hsd17b7	C	T	1: 169,780,649 (GRCm39)	E320K	probably damaging	Het
Htra3	C	T	5: 35,823,477 (GRCm39)	V280I	probably damaging	Het
Impg2	G	T	16: 56,087,485 (GRCm39)	E992D	probably damaging	Het
Kdm3b	T	A	18: 34,942,544 (GRCm39)		probably null	Het
Kmt2d	G	A	15: 98,759,652 (GRCm39)	T1202M	unknown	Het
Lrp11	A	T	10: 7,478,689 (GRCm39)	D326V	probably damaging	Het
Lrrcc1	A	T	3: 14,601,144 (GRCm39)	I59F	probably damaging	Het
Lyg2	G	A	1: 37,954,845 (GRCm39)		probably benign	Het
Med16	A	G	10: 79,732,667 (GRCm39)	V699A	probably damaging	Het
Myo18b	G	T	5: 113,022,804 (GRCm39)		probably benign	Het
Nrxn2	A	G	19: 6,531,767 (GRCm39)	T744A	probably damaging	Het
Or1e1f	T	A	11: 73,855,812 (GRCm39)	I126N	probably damaging	Het
Oser1	A	T	2: 163,253,309 (GRCm39)		probably benign	Het
Pcdhgc5	T	C	18: 37,952,966 (GRCm39)	V80A	probably benign	Het
Pi4ka	C	T	16: 17,100,539 (GRCm39)	G1857D	possibly damaging	Het
Pitpnc1	C	T	11: 107,228,237 (GRCm39)		probably null	Het
Pofut2	A	G	10: 77,102,844 (GRCm39)	E137G	probably benign	Het
Rgsl1	A	T	1: 153,701,687 (GRCm39)	W291R	probably damaging	Het
Rnf113a2	T	C	12: 84,465,050 (GRCm39)	I314T	probably benign	Het
Rps2	C	T	17: 24,939,263 (GRCm39)		probably benign	Het
Setbp1	T	C	18: 78,900,224 (GRCm39)	K1148E	probably damaging	Het
Slc45a2	A	G	15: 11,012,741 (GRCm39)	D248G	probably benign	Het
Slit2	G	T	5: 48,368,681 (GRCm39)	R352L	probably damaging	Het
Smg1	A	G	7: 117,756,404 (GRCm39)		probably benign	Het
Sycp2	A	T	2: 177,994,272 (GRCm39)	C1217*	probably null	Het
Tbcb	A	G	7: 29,926,261 (GRCm39)		probably benign	Het
Tinf2	T	C	14: 55,918,346 (GRCm39)	D128G	probably damaging	Het
Traf3ip2	A	G	10: 39,515,218 (GRCm39)	D332G	possibly damaging	Het
Tram1	A	G	1: 13,659,829 (GRCm39)	F40L	probably benign	Het
Trank1	A	T	9: 111,196,475 (GRCm39)	I1500L	probably damaging	Het
Wdfy4	G	A	14: 32,884,827 (GRCm39)	P25L	probably benign	Het
Wnt5a	G	T	14: 28,244,882 (GRCm39)	Q376H	probably damaging	Het
Zfp526	A	C	7: 24,924,049 (GRCm39)	T103P	probably benign	Het

Other mutations in Kctd4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00806:Kctd4	APN	14	76,200,448 (GRCm39)	missense	probably benign	0.17
IGL00955:Kctd4	APN	14	76,200,668 (GRCm39)	missense	probably damaging	1.00
wellwater	UTSW	14	76,200,037 (GRCm39)	intron	probably benign
R1526:Kctd4	UTSW	14	76,200,523 (GRCm39)	missense	probably benign	0.00
R3780:Kctd4	UTSW	14	76,200,251 (GRCm39)	missense	probably benign	0.10
R3803:Kctd4	UTSW	14	76,200,726 (GRCm39)	missense	probably benign	0.01
R4821:Kctd4	UTSW	14	76,200,217 (GRCm39)	missense	probably benign	0.00
R5192:Kctd4	UTSW	14	76,200,127 (GRCm39)	missense	probably benign	0.01
R5196:Kctd4	UTSW	14	76,200,127 (GRCm39)	missense	probably benign	0.01
R5366:Kctd4	UTSW	14	76,200,259 (GRCm39)	missense	probably damaging	1.00
R6328:Kctd4	UTSW	14	76,200,037 (GRCm39)	intron	probably benign
R6818:Kctd4	UTSW	14	76,200,748 (GRCm39)	missense	probably damaging	0.99
R8713:Kctd4	UTSW	14	76,200,366 (GRCm39)	missense	probably benign	0.00
R8866:Kctd4	UTSW	14	76,200,465 (GRCm39)	missense	probably benign	0.09
X0063:Kctd4	UTSW	14	76,200,443 (GRCm39)	missense	possibly damaging	0.49

Posted On

2016-08-02