Mutagenetix > Incidental Mutation

Incidental Mutation 'R8837:Uck2'

674197

Institutional Source

Beutler Lab

Gene Symbol

Uck2

Ensembl Gene

ENSMUSG00000026558

Gene Name

uridine-cytidine kinase 2

Synonyms

TSA903, Umpk

MMRRC Submission

068665-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.209) question?

Stock #

R8837 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

167050464-167112657 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 167070715 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 5 (F5L)

Ref Sequence

ENSEMBL: ENSMUSP00000027839 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000027839] [ENSMUST00000053686] [ENSMUST00000191745] [ENSMUST00000192702]

AlphaFold

Q99PM9

Predicted Effect

probably benign
Transcript: ENSMUST00000027839
AA Change: F5L

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000027839
Gene: ENSMUSG00000026558
AA Change: F5L

Domain	Start	End	E-Value	Type
Pfam:CoaE	21	195	3.5e-9	PFAM
Pfam:PRK	22	217	5.4e-56	PFAM
Pfam:AAA_18	23	187	8.8e-9	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000053686

SMART Domains

Protein: ENSMUSP00000060202
Gene: ENSMUSG00000026558

Domain	Start	End	E-Value	Type
Pfam:CoaE	21	195	3.5e-9	PFAM
Pfam:PRK	22	217	5.4e-56	PFAM
Pfam:AAA_18	23	187	8.8e-9	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000191745

SMART Domains

Protein: ENSMUSP00000141787
Gene: ENSMUSG00000026558

Domain	Start	End	E-Value	Type
PDB:1UJ2\|B	1	33	1e-17	PDB
SCOP:d1esma_	12	33	6e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000192269

Predicted Effect

probably benign
Transcript: ENSMUST00000192702

SMART Domains

Protein: ENSMUSP00000141216
Gene: ENSMUSG00000026558

Domain	Start	End	E-Value	Type
Pfam:PRK	22	129	6.7e-19	PFAM

Meta Mutation Damage Score

0.0846

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.9%

Validation Efficiency

100% (59/59)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a pyrimidine ribonucleoside kinase. The encoded protein (EC 2.7.1.48) catalyzes phosphorylation of uridine and cytidine to uridine monophosphate (UMP) and cytidine monophosphate (CMP), respectively.[provided by RefSeq, Oct 2010]

Allele List at MGI

Other mutations in this stock

Total: 59 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb4	T	G	5: 8,986,873 (GRCm39)	F764C	probably damaging	Het
Aff1	A	G	5: 103,982,078 (GRCm39)	D739G	possibly damaging	Het
Atosb	A	G	4: 43,034,531 (GRCm39)	S355P	probably damaging	Het
Atp1a3	T	C	7: 24,677,980 (GRCm39)	Y1012C	probably damaging	Het
Btbd10	T	C	7: 112,929,133 (GRCm39)	T206A	probably benign	Het
Capn8	G	T	1: 182,456,199 (GRCm39)	A650S	possibly damaging	Het
Catsper1	A	C	19: 5,386,070 (GRCm39)	N101T	probably damaging	Het
Cdh23	A	C	10: 60,160,755 (GRCm39)	S2070R	probably benign	Het
Cep350	A	G	1: 155,737,518 (GRCm39)	V2775A	probably benign	Het
Clybl	G	A	14: 122,419,194 (GRCm39)		probably null	Het
Cog4	T	A	8: 111,579,004 (GRCm39)	N148K	probably benign	Het
Dbnl	G	A	11: 5,741,839 (GRCm39)	G44D	possibly damaging	Het
Dgcr2	A	T	16: 17,667,630 (GRCm39)	N276K	possibly damaging	Het
Dnah9	T	A	11: 65,746,060 (GRCm39)	T4018S	possibly damaging	Het
Dock3	A	G	9: 106,774,539 (GRCm39)	L72P	probably benign	Het
Dync2i2	T	C	2: 29,928,374 (GRCm39)	D84G	probably benign	Het
Fabp4	T	C	3: 10,271,105 (GRCm39)	T51A	probably benign	Het
Fars2	T	A	13: 36,430,409 (GRCm39)	I279N	probably damaging	Het
Fas	A	T	19: 34,296,049 (GRCm39)	Q164L	probably benign	Het
Focad	A	G	4: 88,072,905 (GRCm39)	K107E	probably damaging	Het
Gga3	G	A	11: 115,479,305 (GRCm39)	S338L	probably benign	Het
Grip1	A	G	10: 119,765,940 (GRCm39)	R91G	probably damaging	Het
Igkv3-7	A	G	6: 70,584,942 (GRCm39)	D94G	possibly damaging	Het
Kank3	G	C	17: 34,036,627 (GRCm39)	R165P	probably damaging	Het
Kmt2d	A	T	15: 98,762,048 (GRCm39)	L434Q	unknown	Het
Krt18	A	G	15: 101,938,265 (GRCm39)	T163A	possibly damaging	Het
Lcn10	T	A	2: 25,575,298 (GRCm39)		probably benign	Het
Lrrc37a	G	T	11: 103,394,795 (GRCm39)	P210Q	probably benign	Het
Lyst	T	A	13: 13,852,548 (GRCm39)	S2183T	probably benign	Het
Mga	G	A	2: 119,769,272 (GRCm39)		probably benign	Het
Myh9	G	A	15: 77,661,137 (GRCm39)	A818V	possibly damaging	Het
Or1j15	T	C	2: 36,458,703 (GRCm39)	I31T	probably benign	Het
Or1o3	G	T	17: 37,573,807 (GRCm39)	Y249*	probably null	Het
Or8b1	A	T	9: 38,399,597 (GRCm39)	I91F	probably benign	Het
Pde7b	A	G	10: 20,314,469 (GRCm39)		probably null	Het
Pik3cb	A	T	9: 98,936,117 (GRCm39)	Y772N	possibly damaging	Het
Ppl	C	G	16: 4,906,854 (GRCm39)	R1147P	probably damaging	Het
Prl3d2	A	T	13: 27,307,926 (GRCm39)	D69V	probably benign	Het
Psd3	A	G	8: 68,172,596 (GRCm39)	F871L	probably damaging	Het
Rlf	G	A	4: 121,045,432 (GRCm39)	P152S	probably benign	Het
Rpa1	T	C	11: 75,204,167 (GRCm39)	E270G	possibly damaging	Het
Scfd2	T	C	5: 74,691,656 (GRCm39)	T209A	probably benign	Het
Scn11a	A	G	9: 119,621,410 (GRCm39)	L669P	probably damaging	Het
Sec31b	A	T	19: 44,506,106 (GRCm39)	C933*	probably null	Het
Serpina3k	G	T	12: 104,309,292 (GRCm39)	M245I	probably benign	Het
Slc9a3	T	A	13: 74,305,823 (GRCm39)	I280N	probably damaging	Het
Soat1	A	G	1: 156,261,772 (GRCm39)	V412A	probably damaging	Het
Spata31d1a	A	T	13: 59,850,596 (GRCm39)	S511T	possibly damaging	Het
Sphkap	A	T	1: 83,253,384 (GRCm39)	V1455E	possibly damaging	Het
Spns1	G	A	7: 125,971,593 (GRCm39)	S319F	possibly damaging	Het
Tbxas1	G	T	6: 39,048,364 (GRCm39)	M403I		Het
Tln2	A	T	9: 67,157,866 (GRCm39)	C1158S	probably damaging	Het
Tnrc18	T	C	5: 142,778,811 (GRCm39)	T98A	possibly damaging	Het
Ttc23	T	C	7: 67,319,494 (GRCm39)	L118P	probably damaging	Het
Tyr	T	A	7: 87,087,223 (GRCm39)	I430L	probably damaging	Het
Ush2a	G	A	1: 188,485,847 (GRCm39)	V2986I	probably benign	Het
Vmn2r96	A	G	17: 18,802,888 (GRCm39)	D266G	probably benign	Het
Yrdc	A	G	4: 124,747,677 (GRCm39)	D213G	probably benign	Het
Zfp612	C	A	8: 110,815,603 (GRCm39)	T270K	probably damaging	Het

Other mutations in Uck2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0112:Uck2	UTSW	1	167,055,340 (GRCm39)	missense	probably damaging	0.98
R0682:Uck2	UTSW	1	167,064,259 (GRCm39)	missense	probably damaging	1.00
R1517:Uck2	UTSW	1	167,062,293 (GRCm39)	missense	probably damaging	1.00
R7202:Uck2	UTSW	1	167,054,084 (GRCm39)	missense	probably damaging	1.00
R7362:Uck2	UTSW	1	167,065,211 (GRCm39)	missense	possibly damaging	0.93
R8985:Uck2	UTSW	1	167,070,681 (GRCm39)	missense	probably benign
R9224:Uck2	UTSW	1	167,065,171 (GRCm39)	missense	probably damaging	0.98
T0722:Uck2	UTSW	1	167,062,280 (GRCm39)	missense	probably benign	0.24

Predicted Primers

PCR Primer
(F):5'- TAAGAATGGCAGCGTTCCTAC -3'
(R):5'- CGATTCTGTATTCAGGCGGAG -3'

Sequencing Primer
(F):5'- CCTGAGTTAGTCATTAGCTAGGCAAG -3'
(R):5'- CTGTATTCAGGCGGAGGGTGAG -3'

Posted On

2021-07-15