Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01464:Rnf123'

88059

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Rnf123

Ensembl Gene

ENSMUSG00000041528

Gene Name

ring finger protein 123

Synonyms

KPC1

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.163) question?

Stock #

IGL01464

Quality Score

Status

Chromosome

Chromosomal Location

108051534-108083346 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 108052302 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Glycine at position 1217 (D1217G)

Ref Sequence

ENSEMBL: ENSMUSP00000125495 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000035214] [ENSMUST00000047746] [ENSMUST00000047947] [ENSMUST00000085060] [ENSMUST00000112295] [ENSMUST00000160249] [ENSMUST00000178267] [ENSMUST00000160649] [ENSMUST00000162355] [ENSMUST00000162753]

AlphaFold

Q5XPI3

Predicted Effect

probably benign
Transcript: ENSMUST00000035214

SMART Domains

Protein: ENSMUSP00000035214
Gene: ENSMUSG00000032594

Domain	Start	End	E-Value	Type
low complexity region	114	129	N/A	INTRINSIC
Pfam:IPK	207	426	2.2e-67	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000047746
AA Change: D1223G

PolyPhen 2 Score 0.870 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000040803
Gene: ENSMUSG00000041528
AA Change: D1223G

Domain	Start	End	E-Value	Type
low complexity region	104	115	N/A	INTRINSIC
SPRY	132	253	1.52e-28	SMART
low complexity region	471	488	N/A	INTRINSIC
low complexity region	508	518	N/A	INTRINSIC
coiled coil region	1047	1067	N/A	INTRINSIC
low complexity region	1242	1251	N/A	INTRINSIC
RING	1260	1297	5.27e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000047947

SMART Domains

Protein: ENSMUSP00000036898
Gene: ENSMUSG00000070284

Domain	Start	End	E-Value	Type
Pfam:NTP_transferase	2	234	8e-48	PFAM
Pfam:NTP_transf_3	3	202	6.6e-12	PFAM
Pfam:Hexapep	259	294	1.8e-9	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000085060

SMART Domains

Protein: ENSMUSP00000082137
Gene: ENSMUSG00000032593

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
LRRNT	33	65	2.55e-2	SMART
LRR	65	83	6.97e1	SMART
LRR_TYP	84	107	1.56e-2	SMART
LRR	109	131	2.84e1	SMART
LRR	132	155	7.05e-1	SMART
LRR	156	176	3.98e1	SMART
LRR	182	206	5.56e0	SMART
Blast:LRRCT	219	274	8e-23	BLAST
IG	285	372	1.59e-6	SMART
transmembrane domain	383	405	N/A	INTRINSIC
low complexity region	407	422	N/A	INTRINSIC
low complexity region	492	504	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000112295

SMART Domains

Protein: ENSMUSP00000107914
Gene: ENSMUSG00000070284

Domain	Start	End	E-Value	Type
Pfam:NTP_transferase	2	235	2.1e-51	PFAM
Pfam:NTP_transf_3	3	199	1.1e-11	PFAM
Pfam:Hexapep	259	294	9.4e-11	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000137284

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000145330

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000150700

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159136

Predicted Effect

probably benign
Transcript: ENSMUST00000159306

SMART Domains

Protein: ENSMUSP00000125695
Gene: ENSMUSG00000041528

Domain	Start	End	E-Value	Type
coiled coil region	172	192	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159523

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159526

Predicted Effect

possibly damaging
Transcript: ENSMUST00000160249
AA Change: D1217G

PolyPhen 2 Score 0.936 (Sensitivity: 0.80; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000124548
Gene: ENSMUSG00000041528
AA Change: D1217G

Domain	Start	End	E-Value	Type
low complexity region	104	115	N/A	INTRINSIC
SPRY	132	253	1.52e-28	SMART
low complexity region	471	488	N/A	INTRINSIC
low complexity region	508	518	N/A	INTRINSIC
coiled coil region	1041	1061	N/A	INTRINSIC
low complexity region	1236	1245	N/A	INTRINSIC
RING	1254	1291	5.27e-4	SMART

Predicted Effect

possibly damaging
Transcript: ENSMUST00000178267
AA Change: D1217G

PolyPhen 2 Score 0.936 (Sensitivity: 0.80; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000136953
Gene: ENSMUSG00000041528
AA Change: D1217G

Domain	Start	End	E-Value	Type
low complexity region	104	115	N/A	INTRINSIC
SPRY	132	253	1.52e-28	SMART
low complexity region	471	488	N/A	INTRINSIC
low complexity region	508	518	N/A	INTRINSIC
coiled coil region	1041	1061	N/A	INTRINSIC
low complexity region	1236	1245	N/A	INTRINSIC
RING	1254	1291	5.27e-4	SMART

Predicted Effect

probably damaging
Transcript: ENSMUST00000160649
AA Change: D1217G

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000125495
Gene: ENSMUSG00000041528
AA Change: D1217G

Domain	Start	End	E-Value	Type
low complexity region	104	115	N/A	INTRINSIC
SPRY	132	253	1.52e-28	SMART
low complexity region	471	488	N/A	INTRINSIC
low complexity region	508	518	N/A	INTRINSIC
coiled coil region	1041	1061	N/A	INTRINSIC

Predicted Effect

possibly damaging
Transcript: ENSMUST00000162355
AA Change: D1223G

PolyPhen 2 Score 0.870 (Sensitivity: 0.83; Specificity: 0.93)

SMART Domains

Protein: ENSMUSP00000125745
Gene: ENSMUSG00000041528
AA Change: D1223G

Domain	Start	End	E-Value	Type
low complexity region	104	115	N/A	INTRINSIC
SPRY	132	253	1.52e-28	SMART
low complexity region	471	488	N/A	INTRINSIC
low complexity region	508	518	N/A	INTRINSIC
coiled coil region	1047	1067	N/A	INTRINSIC
low complexity region	1242	1251	N/A	INTRINSIC
RING	1260	1297	5.27e-4	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000162123

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000161673

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000173683

Predicted Effect

probably benign
Transcript: ENSMUST00000162753

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains a C-terminal RING finger domain, a motif present in a variety of functionally distinct proteins and known to be involved in protein-protein and protein-DNA interactions, and an N-terminal SPRY domain. This protein displays E3 ubiquitin ligase activity toward the cyclin-dependent kinase inhibitor 1B which is also known as p27 or KIP1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2016]

Allele List at MGI

Other mutations in this stock

Total: 28 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adcy10	C	A	1: 165,546,587 (GRCm38)	H748Q	probably damaging	Het
Aebp1	T	C	11: 5,869,822 (GRCm38)	V329A	possibly damaging	Het
Ankk1	T	C	9: 49,415,972 (GRCm38)	T636A	probably benign	Het
Apoh	A	T	11: 108,395,890 (GRCm38)	I47F	probably damaging	Het
Atg9a	A	G	1: 75,190,366 (GRCm38)	S14P	probably damaging	Het
Calb1	T	A	4: 15,881,485 (GRCm38)		probably benign	Het
Ccdc121rt3	A	G	5: 112,355,533 (GRCm38)	S102P	possibly damaging	Het
Cd86	T	C	16: 36,620,953 (GRCm38)	S51G	probably benign	Het
Ctsll3	C	T	13: 60,800,320 (GRCm38)	G181D	probably damaging	Het
Elmod2	G	A	8: 83,316,792 (GRCm38)		probably benign	Het
Ephx3	A	G	17: 32,188,245 (GRCm38)	S240P	probably damaging	Het
Greb1	T	C	12: 16,714,826 (GRCm38)	I435M	probably damaging	Het
Itpr1	A	G	6: 108,386,727 (GRCm38)	D770G	possibly damaging	Het
Kmt2c	G	A	5: 25,352,244 (GRCm38)	T1155I	possibly damaging	Het
Lrp2	T	C	2: 69,472,439 (GRCm38)	D2982G	probably damaging	Het
Map1b	C	T	13: 99,432,743 (GRCm38)	V1157I	unknown	Het
Nlrp4c	T	C	7: 6,100,784 (GRCm38)	C906R	possibly damaging	Het
Nlrp9b	T	A	7: 20,062,655 (GRCm38)	N976K	probably benign	Het
Nos1	T	C	5: 117,943,192 (GRCm38)	F1153S	probably damaging	Het
Pnrc1	T	C	4: 33,246,395 (GRCm38)	Y188C	probably benign	Het
Polr3a	A	C	14: 24,470,681 (GRCm38)		probably benign	Het
Rgs22	T	C	15: 36,083,641 (GRCm38)	T512A	possibly damaging	Het
Rhbdf2	C	T	11: 116,600,908 (GRCm38)	G574S	probably benign	Het
Slc19a2	T	C	1: 164,260,861 (GRCm38)	S92P	probably damaging	Het
Sycp2	A	T	2: 178,401,632 (GRCm38)	I139N	probably damaging	Het
Vmn2r91	A	G	17: 18,107,602 (GRCm38)	N486S	probably null	Het
Xpo1	T	A	11: 23,267,703 (GRCm38)	H56Q	probably damaging	Het
Zbtb44	T	A	9: 31,054,284 (GRCm38)	L330H	probably damaging	Het

Other mutations in Rnf123

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00950:Rnf123	APN	9	108,067,395 (GRCm38)	critical splice donor site	probably null
IGL01358:Rnf123	APN	9	108,069,182 (GRCm38)	missense	probably damaging	1.00
IGL01637:Rnf123	APN	9	108,058,238 (GRCm38)	missense	probably damaging	1.00
IGL01669:Rnf123	APN	9	108,058,356 (GRCm38)	missense	probably damaging	0.98
IGL01905:Rnf123	APN	9	108,071,370 (GRCm38)	splice site	probably benign
IGL02070:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02072:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02073:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02074:Rnf123	APN	9	108,066,889 (GRCm38)	missense	probably damaging	1.00
IGL02079:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02080:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02231:Rnf123	APN	9	108,066,399 (GRCm38)	missense	probably benign	0.17
IGL02281:Rnf123	APN	9	108,071,452 (GRCm38)	missense	probably benign	0.01
IGL02336:Rnf123	APN	9	108,061,842 (GRCm38)	missense	probably damaging	1.00
IGL02543:Rnf123	APN	9	108,066,348 (GRCm38)	missense	probably damaging	1.00
IGL02565:Rnf123	APN	9	108,052,212 (GRCm38)	critical splice donor site	probably null
IGL02571:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02572:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02574:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02586:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02589:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02600:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02601:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02602:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02603:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02609:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02628:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02629:Rnf123	APN	9	108,070,789 (GRCm38)	splice site	probably benign
IGL02629:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02630:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02631:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02632:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02650:Rnf123	APN	9	108,069,748 (GRCm38)	missense	probably benign	0.29
IGL02690:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02691:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02692:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02693:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02713:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02736:Rnf123	APN	9	108,068,302 (GRCm38)	nonsense	probably null
IGL02929:Rnf123	APN	9	108,069,076 (GRCm38)	missense	probably benign
R1175:Rnf123	UTSW	9	108,077,373 (GRCm38)	missense	probably benign
R1465:Rnf123	UTSW	9	108,071,466 (GRCm38)	splice site	probably benign
R1502:Rnf123	UTSW	9	108,068,510 (GRCm38)	splice site	probably null
R1682:Rnf123	UTSW	9	108,077,398 (GRCm38)	missense	probably benign	0.16
R1817:Rnf123	UTSW	9	108,062,926 (GRCm38)	missense	probably benign	0.41
R1855:Rnf123	UTSW	9	108,061,791 (GRCm38)	missense	probably damaging	1.00
R2394:Rnf123	UTSW	9	108,063,536 (GRCm38)	missense	probably benign	0.00
R2483:Rnf123	UTSW	9	108,063,521 (GRCm38)	missense	probably benign	0.16
R3896:Rnf123	UTSW	9	108,069,103 (GRCm38)	splice site	probably benign
R3940:Rnf123	UTSW	9	108,064,035 (GRCm38)	splice site	probably benign
R4206:Rnf123	UTSW	9	108,063,963 (GRCm38)	missense	probably benign	0.01
R4641:Rnf123	UTSW	9	108,058,587 (GRCm38)	missense	probably damaging	1.00
R4714:Rnf123	UTSW	9	108,052,439 (GRCm38)	splice site	probably null
R4767:Rnf123	UTSW	9	108,052,089 (GRCm38)	missense	probably damaging	1.00
R4849:Rnf123	UTSW	9	108,056,091 (GRCm38)	missense	probably damaging	1.00
R4899:Rnf123	UTSW	9	108,063,680 (GRCm38)	missense	probably damaging	1.00
R5274:Rnf123	UTSW	9	108,064,003 (GRCm38)	frame shift	probably null
R5275:Rnf123	UTSW	9	108,064,003 (GRCm38)	frame shift	probably null
R5276:Rnf123	UTSW	9	108,064,003 (GRCm38)	frame shift	probably null
R5294:Rnf123	UTSW	9	108,064,003 (GRCm38)	frame shift	probably null
R5295:Rnf123	UTSW	9	108,064,003 (GRCm38)	frame shift	probably null
R5394:Rnf123	UTSW	9	108,070,731 (GRCm38)	missense	probably damaging	1.00
R5717:Rnf123	UTSW	9	108,067,424 (GRCm38)	missense	probably damaging	1.00
R6186:Rnf123	UTSW	9	108,069,958 (GRCm38)	missense	possibly damaging	0.55
R6449:Rnf123	UTSW	9	108,056,053 (GRCm38)	missense	probably benign	0.17
R6502:Rnf123	UTSW	9	108,068,332 (GRCm38)	missense	possibly damaging	0.46
R6944:Rnf123	UTSW	9	108,063,623 (GRCm38)	missense	probably benign	0.02
R7003:Rnf123	UTSW	9	108,063,683 (GRCm38)	critical splice acceptor site	probably null
R7088:Rnf123	UTSW	9	108,058,536 (GRCm38)	missense	probably null	1.00
R7092:Rnf123	UTSW	9	108,068,600 (GRCm38)	missense	probably benign	0.07
R7100:Rnf123	UTSW	9	108,056,639 (GRCm38)	missense	probably damaging	1.00
R7257:Rnf123	UTSW	9	108,069,029 (GRCm38)	missense	probably damaging	1.00
R7453:Rnf123	UTSW	9	108,070,408 (GRCm38)	splice site	probably null
R7468:Rnf123	UTSW	9	108,069,009 (GRCm38)	missense	probably benign	0.00
R7517:Rnf123	UTSW	9	108,070,274 (GRCm38)	nonsense	probably null
R7577:Rnf123	UTSW	9	108,070,619 (GRCm38)	missense	probably damaging	1.00
R8296:Rnf123	UTSW	9	108,062,890 (GRCm38)	missense	probably damaging	1.00
R8322:Rnf123	UTSW	9	108,068,507 (GRCm38)	missense	probably benign	0.26
R8754:Rnf123	UTSW	9	108,071,164 (GRCm38)	missense	probably damaging	1.00
R8783:Rnf123	UTSW	9	108,069,073 (GRCm38)	missense	probably benign
R9052:Rnf123	UTSW	9	108,059,731 (GRCm38)	missense	probably damaging	1.00
R9156:Rnf123	UTSW	9	108,063,028 (GRCm38)	splice site	probably benign
R9170:Rnf123	UTSW	9	108,071,176 (GRCm38)	missense	probably damaging	1.00
R9332:Rnf123	UTSW	9	108,067,505 (GRCm38)	missense	probably benign	0.00
R9385:Rnf123	UTSW	9	108,052,268 (GRCm38)	missense	probably benign	0.02
R9394:Rnf123	UTSW	9	108,065,706 (GRCm38)	missense	probably damaging	1.00
R9432:Rnf123	UTSW	9	108,059,809 (GRCm38)	missense	probably damaging	0.96
R9717:Rnf123	UTSW	9	108,077,764 (GRCm38)	missense	probably benign	0.43
Z1176:Rnf123	UTSW	9	108,062,981 (GRCm38)	missense	probably damaging	1.00
Z1176:Rnf123	UTSW	9	108,058,395 (GRCm38)	missense	probably damaging	1.00

Posted On

2013-11-18