Incidental Mutation 'PIT4305001:Cutc'
ID554590
Institutional Source Beutler Lab
Gene Symbol Cutc
Ensembl Gene ENSMUSG00000025193
Gene NamecutC copper transporter
Synonyms2310039I18Rik, CGI-32
Accession Numbers
Is this an essential gene? Possibly non essential (E-score: 0.309) question?
Stock #PIT4305001 (G1)
Quality Score225.009
Status Not validated
Chromosome19
Chromosomal Location43752996-43768638 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 43768269 bp
ZygosityHeterozygous
Amino Acid Change Alanine to Serine at position 267 (A267S)
Ref Sequence ENSEMBL: ENSMUSP00000107678 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026199] [ENSMUST00000112047] [ENSMUST00000153295]
Predicted Effect probably benign
Transcript: ENSMUST00000026199
AA Change: A257S

PolyPhen 2 Score 0.108 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000026199
Gene: ENSMUSG00000025193
AA Change: A257S

DomainStartEndE-ValueType
Pfam:CutC 25 216 1.1e-71 PFAM
Predicted Effect probably damaging
Transcript: ENSMUST00000112047
AA Change: A267S

PolyPhen 2 Score 0.992 (Sensitivity: 0.70; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000107678
Gene: ENSMUSG00000025193
AA Change: A267S

DomainStartEndE-ValueType
Pfam:CutC 25 226 7.8e-81 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000153295
SMART Domains Protein: ENSMUSP00000118906
Gene: ENSMUSG00000025193

DomainStartEndE-ValueType
Pfam:CutC 23 224 7.7e-82 PFAM
Coding Region Coverage
  • 1x: 93.4%
  • 3x: 91.3%
  • 10x: 86.8%
  • 20x: 76.6%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Members of the CUT family of copper transporters are associated with copper homeostasis and are involved in the uptake, storage, delivery, and efflux of copper (Gupta et al., 1995 [PubMed 7635807]; Li et al., 2005 [PubMed 16182249]).[supplied by OMIM, Mar 2008]
Allele List at MGI
Other mutations in this stock
Total: 63 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts4 A G 1: 171,259,041 N801D probably benign Het
Adcy2 T C 13: 68,678,602 K661R probably benign Het
Akap1 A T 11: 88,844,378 M486K probably benign Het
Arhgap40 T A 2: 158,531,905 I202N probably benign Het
C1qtnf2 T A 11: 43,491,195 L248Q probably damaging Het
Casp1 A T 9: 5,306,135 H340L probably benign Het
Cd5 A G 19: 10,726,386 V104A possibly damaging Het
Celsr1 T A 15: 85,900,937 E3032V possibly damaging Het
Cts7 A G 13: 61,356,572 I59T probably damaging Het
Dmwd A G 7: 19,080,718 Q431R probably damaging Het
Dnah6 T C 6: 73,065,755 N3280S probably benign Het
Dnah7b A T 1: 46,373,348 N4039I probably damaging Het
Dnaja4 T C 9: 54,710,634 I260T probably benign Het
Drd5 T C 5: 38,320,584 F307L probably damaging Het
Dsc2 C T 18: 20,046,243 S256N probably damaging Het
Dstyk G T 1: 132,455,896 E617* probably null Het
Dusp15 G A 2: 152,945,476 H72Y probably benign Het
Dysf C T 6: 84,100,234 R660* probably null Het
Fbxl13 T A 5: 21,522,148 I584L probably benign Het
Gm10354 T C 5: 14,978,790 D29G probably benign Het
Gsap T C 5: 21,186,409 L16P probably damaging Het
Hgsnat C T 8: 25,945,199 A636T possibly damaging Het
Hivep1 A G 13: 42,181,671 T161A Het
Hspg2 T C 4: 137,550,373 S2928P possibly damaging Het
Ifi214 G A 1: 173,527,919 P108S probably benign Het
Il17ra A T 6: 120,481,406 Y506F probably damaging Het
Il9r T A 11: 32,194,734 Q53L probably benign Het
Irf2bp2 C T 8: 126,592,659 G260R probably damaging Het
Jdp2 T A 12: 85,638,852 I129N probably damaging Het
Kif1b T C 4: 149,220,792 probably null Het
Klrd1 A G 6: 129,596,707 T120A unknown Het
Lfng A G 5: 140,612,528 N202D probably damaging Het
Ltbp3 A G 19: 5,752,067 E757G probably damaging Het
Ltn1 G A 16: 87,420,323 P342L probably damaging Het
Lum A C 10: 97,568,876 Y211S probably damaging Het
Ncapd2 G A 6: 125,184,027 R292* probably null Het
Nlrc4 T C 17: 74,446,309 T360A probably damaging Het
Olfr1231 T C 2: 89,303,383 I70V probably benign Het
Olfr850 T C 9: 19,478,061 Y63C probably damaging Het
Palm2 C A 4: 57,638,029 T22K possibly damaging Het
Pde3a A G 6: 141,492,310 D1035G probably benign Het
Phf20l1 A T 15: 66,613,052 K322I possibly damaging Het
Pik3r3 A C 4: 116,292,126 N349T probably benign Het
Poc1a A G 9: 106,349,829 Q420R Het
Prl7d1 A T 13: 27,714,337 M63K possibly damaging Het
Rap1gds1 C A 3: 138,956,300 M398I probably benign Het
Rapgef6 T A 11: 54,679,377 V1192D probably damaging Het
Rif1 T C 2: 52,111,958 V166A Het
Robo4 T C 9: 37,411,391 Y847H probably damaging Het
Sardh T C 2: 27,228,314 N468S probably damaging Het
Sema5a A G 15: 32,628,199 T553A probably benign Het
Serpina12 A G 12: 104,035,717 Y247H probably damaging Het
Ston2 G T 12: 91,648,502 D377E possibly damaging Het
Syne1 A G 10: 5,333,023 S1557P probably damaging Het
Syt6 C T 3: 103,575,453 R26W possibly damaging Het
Tep1 C T 14: 50,829,227 G2305R possibly damaging Het
Ticrr A G 7: 79,679,023 T637A possibly damaging Het
Tnn A T 1: 160,086,077 F1546Y possibly damaging Het
Tpr A G 1: 150,440,137 D2055G possibly damaging Het
Trim39 A G 17: 36,268,970 V31A possibly damaging Het
Trpc7 G T 13: 56,887,508 T204K probably benign Het
Urgcp T C 11: 5,717,996 Y157C probably damaging Het
Vmn1r81 A T 7: 12,260,663 I6K probably benign Het
Other mutations in Cutc
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL03245:Cutc APN 19 43768182 missense possibly damaging 0.83
P0028:Cutc UTSW 19 43764969 missense possibly damaging 0.84
R0095:Cutc UTSW 19 43753199 missense probably benign
R0479:Cutc UTSW 19 43768216 missense probably damaging 1.00
R5635:Cutc UTSW 19 43755630 missense probably benign 0.09
R5898:Cutc UTSW 19 43760029 missense probably benign 0.00
R6150:Cutc UTSW 19 43759889 missense probably damaging 1.00
R6217:Cutc UTSW 19 43759997 missense probably damaging 0.99
R6392:Cutc UTSW 19 43760050 missense possibly damaging 0.58
Predicted Primers PCR Primer
(F):5'- GTAGTGCAGCATCCTTGACC -3'
(R):5'- TATCCATGATGACAGACACCAATG -3'

Sequencing Primer
(F):5'- CCCTTACTCTGAGCCATGAATTAATG -3'
(R):5'- TGATGACAGACACCAATGACTAC -3'
Posted On2019-06-07