Mutagenetix > Incidental Mutation

Incidental Mutation 'R6848:Casp16'

534889

Institutional Source

Beutler Lab

Gene Symbol

Casp16

Ensembl Gene

ENSMUSG00000067882

Gene Name

caspase 16, apoptosis-related cysteine peptidase

Synonyms

Casp16-ps, Gm5146, Casp16

MMRRC Submission

045022-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.058) question?

Stock #

R6848 (G1)

Quality Score

132.008

Status

Validated

Chromosome

Chromosomal Location

23770054-23774304 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

A to T at 23770053 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Stop codon at position 175 (C175*)

Ref Sequence

ENSEMBL: ENSMUSP00000086048 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000088673] [ENSMUST00000182769]

AlphaFold

I6L890

Predicted Effect

probably null
Transcript: ENSMUST00000088673
AA Change: C175*

SMART Domains

Protein: ENSMUSP00000086048
Gene: ENSMUSG00000067882
AA Change: C175*

Domain	Start	End	E-Value	Type
Pfam:Peptidase_C14	3	162	4.5e-9	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000182769
AA Change: F455I

SMART Domains

Protein: ENSMUSP00000138283
Gene: ENSMUSG00000067882
AA Change: F455I

Domain	Start	End	E-Value	Type
Pfam:Peptidase_C14	18	175	1.7e-7	PFAM

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.5%
20x: 98.2%

Validation Efficiency

98% (54/55)

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acap1	T	C	11: 69,775,487 (GRCm39)	N290S	probably damaging	Het
Acox3	G	T	5: 35,749,528 (GRCm39)	G218C	probably damaging	Het
Acsf3	G	A	8: 123,517,329 (GRCm39)	G375D	probably damaging	Het
Adamts9	G	T	6: 92,840,335 (GRCm39)	N568K	possibly damaging	Het
Akr1cl	G	A	1: 65,063,928 (GRCm39)	T87I	probably damaging	Het
Brcc3dc	A	T	10: 108,535,451 (GRCm39)	V168E	probably damaging	Het
Cacna1s	G	A	1: 136,020,432 (GRCm39)	R823Q	probably benign	Het
Cast	T	C	13: 74,844,052 (GRCm39)	K694R	possibly damaging	Het
Cep70	G	A	9: 99,144,954 (GRCm39)	R100H	probably benign	Het
Cep72	C	T	13: 74,186,395 (GRCm39)	A259T	possibly damaging	Het
Chsy1	T	A	7: 65,820,785 (GRCm39)	M340K	probably damaging	Het
Col27a1	T	C	4: 63,220,608 (GRCm39)	S182P	probably benign	Het
Crlf2	A	C	5: 109,704,897 (GRCm39)	F103V	possibly damaging	Het
Dync2h1	T	C	9: 7,159,632 (GRCm39)	N652S	probably benign	Het
Ephx4	G	A	5: 107,574,784 (GRCm39)	G274D	probably damaging	Het
Fer	T	A	17: 64,298,601 (GRCm39)	F517I	probably damaging	Het
Fsip2	A	T	2: 82,813,131 (GRCm39)	H3150L	probably benign	Het
Gata3	T	A	2: 9,863,339 (GRCm39)	N392Y	possibly damaging	Het
Gria4	C	T	9: 4,793,822 (GRCm39)	V79M	probably damaging	Het
Grk3	A	C	5: 113,133,641 (GRCm39)	N60K	probably damaging	Het
Idh2	TCCCAGG	T	7: 79,748,079 (GRCm39)		probably benign	Het
Igf1r	T	G	7: 67,653,927 (GRCm39)	I155R	probably damaging	Het
Igsf9	T	C	1: 172,323,329 (GRCm39)	L681P	probably damaging	Het
Intu	T	C	3: 40,648,685 (GRCm39)	M789T	probably benign	Het
Kit	A	T	5: 75,767,872 (GRCm39)	Q85L	probably benign	Het
Klhdc2	T	A	12: 69,355,750 (GRCm39)	C325*	probably null	Het
Mcidas	A	G	13: 113,130,419 (GRCm39)	E5G	probably benign	Het
Mcm5	G	T	8: 75,853,918 (GRCm39)	R724L	possibly damaging	Het
Nrbp2	G	A	15: 75,963,332 (GRCm39)		probably benign	Het
Nrg1	A	G	8: 32,308,084 (GRCm39)	I655T	probably damaging	Het
Nsun4	T	C	4: 115,910,131 (GRCm39)	D143G	possibly damaging	Het
Opn3	C	T	1: 175,490,615 (GRCm39)	V349M	probably damaging	Het
Or51ag1	A	G	7: 103,155,664 (GRCm39)	V163A	possibly damaging	Het
Or5d47	A	T	2: 87,804,514 (GRCm39)	V165E	possibly damaging	Het
Or6d14	T	C	6: 116,533,736 (GRCm39)	S117P	probably damaging	Het
Pank2	C	A	2: 131,124,546 (GRCm39)	L297I	probably damaging	Het
Pcdh20	T	A	14: 88,704,690 (GRCm39)	E870V	probably benign	Het
Pdcd6	T	A	13: 74,457,959 (GRCm39)	M71L	possibly damaging	Het
Phkb	A	T	8: 86,756,246 (GRCm39)	I847F	probably damaging	Het
Psmb1	A	G	17: 15,697,509 (GRCm39)	F202S	probably benign	Het
Pwp2	C	G	10: 78,020,127 (GRCm39)		probably null	Het
Rbms3	A	G	9: 117,080,809 (GRCm39)	Y21H	probably damaging	Het
Rhbdl1	T	A	17: 26,055,158 (GRCm39)	K17*	probably null	Het
Rp1l1	C	A	14: 64,265,667 (GRCm39)	Q418K	possibly damaging	Het
Scpppq1	A	G	5: 104,222,603 (GRCm39)		probably benign	Het
Slc22a4	A	T	11: 53,898,615 (GRCm39)	V159E	possibly damaging	Het
Spata31d1a	T	C	13: 59,849,777 (GRCm39)	T784A	possibly damaging	Het
Tll1	A	G	8: 64,551,544 (GRCm39)	M279T	probably damaging	Het
Tmem163	A	T	1: 127,479,117 (GRCm39)	V134D	probably damaging	Het
Top2b	A	G	14: 16,409,958 (GRCm38)	N875S	possibly damaging	Het
Tpd52l1	T	C	10: 31,208,853 (GRCm39)	E205G	probably benign	Het
Tpsb2	T	A	17: 25,586,802 (GRCm39)	Y271*	probably null	Het
Ugt3a1	G	A	15: 9,280,138 (GRCm39)		probably null	Het
Vmn2r67	T	C	7: 84,801,840 (GRCm39)	M154V	probably benign	Het
Zfp740	T	G	15: 102,117,243 (GRCm39)	I89S	probably benign	Het

Other mutations in Casp16

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01767:Casp16	APN	17	23,771,027 (GRCm39)	missense	probably damaging	1.00
R0316:Casp16	UTSW	17	23,771,066 (GRCm39)	missense	probably damaging	1.00
R1717:Casp16	UTSW	17	23,771,024 (GRCm39)	missense	possibly damaging	0.93
R3901:Casp16	UTSW	17	23,771,922 (GRCm39)	missense	probably damaging	1.00
R8358:Casp16	UTSW	17	23,772,348 (GRCm39)	missense	probably damaging	0.98
R9133:Casp16	UTSW	17	23,771,003 (GRCm39)	missense	probably damaging	1.00
R9158:Casp16	UTSW	17	23,769,948 (GRCm39)	unclassified	probably benign
RF008:Casp16	UTSW	17	23,774,201 (GRCm39)	unclassified	probably benign

Predicted Primers

PCR Primer
(F):5'- TTCAACCTCTGGTTCCCGAGAG -3'
(R):5'- CCTCCAGCAGACAATGACTG -3'

Sequencing Primer
(F):5'- TTCCCGAGAGCACAGTCGATC -3'
(R):5'- ACAATGACTGCAGTGGGTGTG -3'

Posted On

2018-09-12