Mutagenetix > Incidental Mutation

Incidental Mutation 'R9610:Hypk'

724131

Institutional Source

Beutler Lab

Gene Symbol

Hypk

Ensembl Gene

ENSMUSG00000027245

Gene Name

huntingtin interacting protein K

Synonyms

2310003F16Rik

MMRRC Submission

Accession Numbers

Essential gene?

Probably essential (E-score: 0.951) question?

Stock #

R9610 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

121287569-121288921 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 121288154 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 72 (S72P)

Ref Sequence

ENSEMBL: ENSMUSP00000117946 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000056312] [ENSMUST00000056732] [ENSMUST00000110612] [ENSMUST00000110613] [ENSMUST00000126764] [ENSMUST00000139253] [ENSMUST00000148575] [ENSMUST00000154418]

AlphaFold

Q9CR41

Predicted Effect

probably benign
Transcript: ENSMUST00000056312

SMART Domains

Protein: ENSMUSP00000051261
Gene: ENSMUSG00000046110

Domain	Start	End	E-Value	Type
Pfam:Serinc	33	488	3e-125	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000056732

SMART Domains

Protein: ENSMUSP00000049548
Gene: ENSMUSG00000048222

Domain	Start	End	E-Value	Type
low complexity region	51	59	N/A	INTRINSIC
low complexity region	64	84	N/A	INTRINSIC
low complexity region	108	123	N/A	INTRINSIC
coiled coil region	134	150	N/A	INTRINSIC
Pfam:MFAP1	190	399	1.6e-81	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000110612
AA Change: S72P

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000106242
Gene: ENSMUSG00000027245
AA Change: S72P

Domain	Start	End	E-Value	Type
coiled coil region	69	111	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000110613

SMART Domains

Protein: ENSMUSP00000106243
Gene: ENSMUSG00000046110

Domain	Start	End	E-Value	Type
Pfam:Serinc	34	280	5.6e-67	PFAM
low complexity region	342	364	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000126764
AA Change: S72P

PolyPhen 2 Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)

SMART Domains

Protein: ENSMUSP00000117946
Gene: ENSMUSG00000027245
AA Change: S72P

Domain	Start	End	E-Value	Type
coiled coil region	69	111	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000127435

SMART Domains

Protein: ENSMUSP00000119373
Gene: ENSMUSG00000046110

Domain	Start	End	E-Value	Type
Pfam:Serinc	2	192	7.7e-61	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000139253

SMART Domains

Protein: ENSMUSP00000123181
Gene: ENSMUSG00000074884

Domain	Start	End	E-Value	Type
Pfam:4F5	1	38	1e-14	PFAM
low complexity region	45	59	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000140135

SMART Domains

Protein: ENSMUSP00000117054
Gene: ENSMUSG00000046110

Domain	Start	End	E-Value	Type
Pfam:Serinc	1	75	8.2e-14	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000140752

SMART Domains

Protein: ENSMUSP00000116676
Gene: ENSMUSG00000046110

Domain	Start	End	E-Value	Type
Pfam:Serinc	2	78	7.3e-14	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000148575

SMART Domains

Protein: ENSMUSP00000121895
Gene: ENSMUSG00000074884

Domain	Start	End	E-Value	Type
Pfam:4F5	1	38	2.9e-14	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000154418

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 99.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 65 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts19	A	T	18: 59,023,399 (GRCm39)	T265S	probably benign	Het
Arhgef5	A	G	6: 43,257,890 (GRCm39)	I1311M	probably damaging	Het
Bcr	T	A	10: 74,990,743 (GRCm39)	Y750N	probably damaging	Het
Bcr	T	A	10: 74,990,745 (GRCm39)	Y750*	probably null	Het
Btbd16	T	A	7: 130,407,595 (GRCm39)	M295K	probably benign	Het
Ccdc88a	T	C	11: 29,427,316 (GRCm39)	L1007P	possibly damaging	Het
Cnep1r1	A	G	8: 88,860,457 (GRCm39)	*126W	probably null	Het
Cstf1	T	A	2: 172,214,984 (GRCm39)	I35N	probably benign	Het
Cstpp1	T	C	2: 91,135,127 (GRCm39)	D111G	probably damaging	Het
Cul9	A	G	17: 46,830,823 (GRCm39)	L1690P	possibly damaging	Het
Dnm2	A	T	9: 21,414,973 (GRCm39)	K677*	probably null	Het
Dscaml1	C	A	9: 45,579,522 (GRCm39)	N356K	possibly damaging	Het
Dvl3	A	G	16: 20,346,008 (GRCm39)	D446G	probably damaging	Het
Ecm2	A	G	13: 49,668,518 (GRCm39)	N74D	probably benign	Het
Ecm2	A	G	13: 49,681,216 (GRCm39)	I450M	probably damaging	Het
Emc1	T	A	4: 139,091,035 (GRCm39)	D460E	probably benign	Het
Fhip2b	T	C	14: 70,824,258 (GRCm39)	Y493C	probably benign	Het
Fuom	T	A	7: 139,679,828 (GRCm39)	E121V	possibly damaging	Het
Fyco1	T	C	9: 123,657,585 (GRCm39)	T864A	possibly damaging	Het
Galk2	T	C	2: 125,817,218 (GRCm39)	Y336H	probably damaging	Het
Gcsh	T	A	8: 117,720,125 (GRCm39)	Y14F	probably benign	Het
Grip1	G	A	10: 119,874,569 (GRCm39)	E778K	possibly damaging	Het
Gucy2g	T	C	19: 55,194,605 (GRCm39)	I937M	probably damaging	Het
Hsp90ab1	T	C	17: 45,880,600 (GRCm39)	I370M	possibly damaging	Het
Izumo1r	T	G	9: 14,811,840 (GRCm39)	I183L	possibly damaging	Het
Kctd13	G	T	7: 126,544,180 (GRCm39)	G293C	probably damaging	Het
Kmt2d	CTGTTG	CTG	15: 98,743,057 (GRCm39)		probably benign	Het
Krt13	T	C	11: 100,012,318 (GRCm39)	S2G	probably benign	Het
Mark4	C	A	7: 19,167,338 (GRCm39)	R467L	possibly damaging	Het
Mrps33	T	A	6: 39,779,422 (GRCm39)	K91M	probably damaging	Het
Muc5ac	T	A	7: 141,350,078 (GRCm39)	V608D	possibly damaging	Het
Myb	G	A	10: 21,030,627 (GRCm39)	Q57*	probably null	Het
Or51f1	T	G	7: 102,506,147 (GRCm39)	H114P	probably damaging	Het
Peg10	GCAC	GCACCAC	6: 4,756,452 (GRCm39)		probably benign	Het
Phldb3	G	A	7: 24,328,372 (GRCm39)	V639M	probably damaging	Het
Pip4k2c	A	C	10: 127,036,069 (GRCm39)	L266R	probably damaging	Het
Plg	T	C	17: 12,609,213 (GRCm39)	Y173H	probably benign	Het
Pmp22	G	T	11: 63,024,065 (GRCm39)	V25F	probably benign	Het
Ppp1r16b	T	A	2: 158,537,998 (GRCm39)	Y40N	probably damaging	Het
Prl5a1	A	G	13: 28,329,492 (GRCm39)	E57G	possibly damaging	Het
Psmb10	A	G	8: 106,664,144 (GRCm39)	F75S	probably benign	Het
Ptprm	C	A	17: 67,000,483 (GRCm39)	R1167M	probably damaging	Het
Rbm46	T	C	3: 82,771,541 (GRCm39)	H358R	probably benign	Het
Rgl1	A	G	1: 152,397,115 (GRCm39)	S684P	probably benign	Het
Rmnd5b	T	C	11: 51,517,869 (GRCm39)	I162V	probably damaging	Het
Sh3d19	T	C	3: 86,014,529 (GRCm39)	V440A	possibly damaging	Het
Sik1	T	A	17: 32,073,246 (GRCm39)	K70M	probably damaging	Het
Slc44a4	C	T	17: 35,147,793 (GRCm39)	S611F	probably benign	Het
Stk32a	A	G	18: 43,430,620 (GRCm39)	I177V	probably benign	Het
Syt7	G	A	19: 10,421,459 (GRCm39)	D548N	probably benign	Het
Tcf7l2	A	G	19: 55,899,038 (GRCm39)	D215G	probably null	Het
Tex14	T	A	11: 87,377,084 (GRCm39)	F143I	probably damaging	Het
Tjp3	A	G	10: 81,119,411 (GRCm39)	V26A	possibly damaging	Het
Tpx2	T	A	2: 152,715,124 (GRCm39)	V115D	probably benign	Het
Tubb2b	C	A	13: 34,311,742 (GRCm39)	K350N	probably damaging	Het
Usf3	T	C	16: 44,036,936 (GRCm39)	V472A	probably benign	Het
Vps13b	G	T	15: 35,642,555 (GRCm39)	G1389V	possibly damaging	Het
Vps39	T	C	2: 120,172,485 (GRCm39)	R183G	probably damaging	Het
Wnk4	G	T	11: 101,159,250 (GRCm39)	E556*	probably null	Het
Xpo7	T	A	14: 70,925,617 (GRCm39)	E474V	probably benign	Het
Zbtb18	A	G	1: 177,275,341 (GRCm39)	R234G	probably null	Het
Zc3h14	T	A	12: 98,737,663 (GRCm39)	I50N	possibly damaging	Het
Zfat	A	G	15: 68,051,655 (GRCm39)	V713A	possibly damaging	Het
Zfp462	T	C	4: 55,009,545 (GRCm39)	S504P	possibly damaging	Het
Zmiz1	T	C	14: 25,651,022 (GRCm39)	V502A	probably benign	Het

Other mutations in Hypk

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01543:Hypk	APN	2	121,287,776 (GRCm39)	splice site	probably null
IGL03309:Hypk	APN	2	121,288,674 (GRCm39)	missense	probably damaging	1.00
IGL03309:Hypk	APN	2	121,288,673 (GRCm39)	nonsense	probably null
R2230:Hypk	UTSW	2	121,287,773 (GRCm39)	critical splice donor site	probably null
R3923:Hypk	UTSW	2	121,288,683 (GRCm39)	missense	possibly damaging	0.65
R4060:Hypk	UTSW	2	121,284,160 (GRCm39)	intron	probably benign
R4438:Hypk	UTSW	2	121,288,475 (GRCm39)	missense	probably damaging	0.98
R4551:Hypk	UTSW	2	121,283,961 (GRCm39)	critical splice donor site	probably null
R4791:Hypk	UTSW	2	121,288,136 (GRCm39)	splice site	probably null
R5075:Hypk	UTSW	2	121,286,111 (GRCm39)	utr 3 prime	probably benign
R7133:Hypk	UTSW	2	121,283,961 (GRCm39)	critical splice donor site	probably null
R7274:Hypk	UTSW	2	121,284,805 (GRCm39)	intron	probably benign
R8130:Hypk	UTSW	2	121,286,859 (GRCm39)	utr 3 prime	probably benign
R9136:Hypk	UTSW	2	121,287,636 (GRCm39)	nonsense	probably null
R9203:Hypk	UTSW	2	121,288,163 (GRCm39)	nonsense	probably null
R9611:Hypk	UTSW	2	121,288,154 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- GCCTAAATAGATCTCATGTGCACG -3'
(R):5'- ATAAACGCGCCAACTCTTTC -3'

Sequencing Primer
(F):5'- TCTCATGTGCACGAAATTAGGCG -3'
(R):5'- CCCCTGGAGGTTTTACAGTAAG -3'

Posted On

2022-09-12