Incidental Mutation 'R0583:Ikzf5'
ID56512
Institutional Source Beutler Lab
Gene Symbol Ikzf5
Ensembl Gene ENSMUSG00000040167
Gene NameIKAROS family zinc finger 5
SynonymsZfpn1a5, 2610034F18Rik
MMRRC Submission 038773-MU
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.291) question?
Stock #R0583 (G1)
Quality Score143
Status Not validated
Chromosome7
Chromosomal Location131388652-131410521 bp(-) (GRCm38)
Type of Mutationunclassified (3953 bp from exon)
DNA Base Change (assembly) A to G at 131391785 bp
ZygosityHeterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000046306] [ENSMUST00000075610] [ENSMUST00000121033] [ENSMUST00000124096] [ENSMUST00000128432] [ENSMUST00000142349] [ENSMUST00000145114] [ENSMUST00000154602] [ENSMUST00000207243]
Predicted Effect probably benign
Transcript: ENSMUST00000046306
AA Change: V371A

PolyPhen 2 Score 0.044 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000035583
Gene: ENSMUSG00000040167
AA Change: V371A

DomainStartEndE-ValueType
ZnF_C2H2 82 104 3.58e-2 SMART
ZnF_C2H2 110 132 1.53e-1 SMART
ZnF_C2H2 138 161 1.79e-2 SMART
low complexity region 289 320 N/A INTRINSIC
ZnF_C2H2 364 386 8.09e0 SMART
ZnF_C2H2 392 416 9.22e0 SMART
Predicted Effect probably null
Transcript: ENSMUST00000075610
SMART Domains Protein: ENSMUSP00000075037
Gene: ENSMUSG00000063179

DomainStartEndE-ValueType
low complexity region 3 12 N/A INTRINSIC
Pfam:AAA_33 20 213 2.7e-11 PFAM
Pfam:KTI12 136 345 3.7e-19 PFAM
Predicted Effect possibly damaging
Transcript: ENSMUST00000121033
AA Change: V218A

PolyPhen 2 Score 0.657 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000113714
Gene: ENSMUSG00000040167
AA Change: V218A

DomainStartEndE-ValueType
ZnF_C2H2 82 104 3.58e-2 SMART
low complexity region 136 167 N/A INTRINSIC
ZnF_C2H2 211 233 8.09e0 SMART
ZnF_C2H2 239 263 9.22e0 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000124096
SMART Domains Protein: ENSMUSP00000130971
Gene: ENSMUSG00000030849

DomainStartEndE-ValueType
Pfam:Pkinase 1 118 4.8e-19 PFAM
Pfam:Pkinase_Tyr 1 118 1.7e-50 PFAM
low complexity region 146 160 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000124672
Predicted Effect probably null
Transcript: ENSMUST00000128092
Predicted Effect probably benign
Transcript: ENSMUST00000128432
SMART Domains Protein: ENSMUSP00000139528
Gene: ENSMUSG00000040167

DomainStartEndE-ValueType
ZnF_C2H2 82 104 1.5e-4 SMART
Predicted Effect probably null
Transcript: ENSMUST00000133284
Predicted Effect probably benign
Transcript: ENSMUST00000142349
Predicted Effect probably benign
Transcript: ENSMUST00000145114
SMART Domains Protein: ENSMUSP00000118636
Gene: ENSMUSG00000063179

DomainStartEndE-ValueType
low complexity region 3 12 N/A INTRINSIC
Pfam:KTI12 18 88 5.6e-8 PFAM
Pfam:AAA_17 20 212 3.2e-8 PFAM
Pfam:AAA_33 20 213 2.2e-13 PFAM
Pfam:KTI12 136 265 1.6e-16 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000148533
Predicted Effect probably benign
Transcript: ENSMUST00000154602
SMART Domains Protein: ENSMUSP00000123530
Gene: ENSMUSG00000040167

DomainStartEndE-ValueType
ZnF_C2H2 82 104 3.58e-2 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000207243
Predicted Effect probably benign
Transcript: ENSMUST00000207489
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208084
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208700
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208966
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.1%
  • 20x: 93.2%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Members of the Ikaros (ZNFN1A1; MIM 603023) family of transcription factors, which includes Pegasus, are expressed in lymphocytes and are implicated in the control of lymphoid development.[supplied by OMIM, Jul 2002]
Allele List at MGI
Other mutations in this stock
Total: 52 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700017B05Rik A G 9: 57,257,643 S483P probably benign Het
2700081O15Rik A G 19: 7,420,274 D62G probably damaging Het
5730480H06Rik A G 5: 48,380,128 H169R probably damaging Het
Actn1 T A 12: 80,199,029 I127F probably damaging Het
AW822073 G A 10: 58,223,388 L515F probably damaging Het
Cadm3 T G 1: 173,341,171 T277P probably benign Het
Cast T C 13: 74,713,678 T629A probably damaging Het
Cblc C A 7: 19,792,561 C201F probably benign Het
Ccdc154 T A 17: 25,168,424 D375E possibly damaging Het
Cdk6 A G 5: 3,473,183 D201G probably damaging Het
Cep95 T C 11: 106,814,623 V478A probably benign Het
Ciita T C 16: 10,523,804 probably null Het
Clec4e A G 6: 123,283,694 F135S probably damaging Het
Cntn6 A G 6: 104,776,314 D337G possibly damaging Het
Crlf3 A T 11: 80,059,281 H174Q probably damaging Het
Cyb5r1 T A 1: 134,407,601 F93I probably damaging Het
Dopey2 T C 16: 93,755,486 I271T probably benign Het
Fcho1 T C 8: 71,715,725 Y218C probably damaging Het
Fhad1 C T 4: 141,903,990 M1297I probably benign Het
Igdcc4 T C 9: 65,121,813 V244A possibly damaging Het
Ilvbl T A 10: 78,583,267 V450E probably damaging Het
Kcns3 T G 12: 11,091,478 N407H probably damaging Het
Klhl11 T C 11: 100,464,324 K224E possibly damaging Het
Klra17 T A 6: 129,868,693 D186V probably damaging Het
Lrrc37a T C 11: 103,498,437 D2054G probably benign Het
Mef2a G T 7: 67,235,148 S406* probably null Het
Mrgbp A G 2: 180,584,446 N104S probably benign Het
Mroh2a GT GTT 1: 88,256,166 probably null Het
Muc5ac C A 7: 141,807,608 T1552N probably damaging Het
Muc5b T A 7: 141,856,698 Y1269* probably null Het
Myef2 T C 2: 125,097,981 probably null Het
Myg1 C T 15: 102,337,790 Q367* probably null Het
Nalcn T C 14: 123,294,343 N1365S possibly damaging Het
Nfu1 T C 6: 87,009,952 C18R probably benign Het
Nkx2-6 A T 14: 69,174,779 Q132L probably damaging Het
Olfr1085 T A 2: 86,658,360 I33F probably benign Het
Olfr516 C T 7: 108,845,414 A199T possibly damaging Het
Pak3 TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC TTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTC X: 143,743,893 probably benign Het
Prh1 A T 6: 132,571,833 Q101L unknown Het
Ribc2 A T 15: 85,132,914 probably null Het
Rnf19a C A 15: 36,253,005 R396L probably damaging Het
Sdad1 A G 5: 92,305,064 I105T probably damaging Het
Sec24b G T 3: 130,041,311 Y79* probably null Het
Tatdn2 A G 6: 113,702,525 E277G possibly damaging Het
Tex10 A C 4: 48,451,952 F725V probably damaging Het
Themis3 T C 17: 66,559,753 D164G probably benign Het
Ubxn7 T C 16: 32,375,914 W220R probably damaging Het
Usp33 C A 3: 152,368,254 R246S probably damaging Het
Vmn2r102 T A 17: 19,676,781 V130E probably benign Het
Vmn2r112 C T 17: 22,618,949 P797L probably damaging Het
Vmn2r114 ATTT ATT 17: 23,290,932 probably null Het
Yme1l1 T C 2: 23,186,250 V340A probably damaging Het
Other mutations in Ikzf5
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03149:Ikzf5 APN 7 131396765 missense probably damaging 1.00
R0545:Ikzf5 UTSW 7 131392500 missense possibly damaging 0.87
R1471:Ikzf5 UTSW 7 131391767 missense probably damaging 1.00
R2680:Ikzf5 UTSW 7 131396761 missense probably damaging 1.00
R4496:Ikzf5 UTSW 7 131396664 unclassified probably null
R4625:Ikzf5 UTSW 7 131393753 critical splice donor site probably null
R6307:Ikzf5 UTSW 7 131391648 missense probably damaging 1.00
R6828:Ikzf5 UTSW 7 131391672 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ACCCTGGGAATCCTTATGGACAAGTG -3'
(R):5'- GCCATCGCATAGTCAGAGGAACTAC -3'

Sequencing Primer
(F):5'- TCCTTATGGACAAGTGTAGGAAACTG -3'
(R):5'- ACTACAGTCCAGTGGCAGG -3'
Posted On2013-07-11