Incidental Mutation 'R6161:Zfp623'
ID 489892
Institutional Source Beutler Lab
Gene Symbol Zfp623
Ensembl Gene ENSMUSG00000050846
Gene Name zinc finger protein 623
Synonyms 2610029D06Rik
MMRRC Submission 044308-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.368) question?
Stock # R6161 (G1)
Quality Score 225.009
Status Validated
Chromosome 15
Chromosomal Location 75812801-75821249 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 75820470 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glutamic Acid at position 475 (D475E)
Ref Sequence ENSEMBL: ENSMUSP00000036049 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000037260]
AlphaFold Q9CY99
Predicted Effect probably benign
Transcript: ENSMUST00000037260
AA Change: D475E

PolyPhen 2 Score 0.218 (Sensitivity: 0.91; Specificity: 0.88)
SMART Domains Protein: ENSMUSP00000036049
Gene: ENSMUSG00000050846
AA Change: D475E

DomainStartEndE-ValueType
ZnF_C2H2 119 141 5.59e-4 SMART
ZnF_C2H2 147 169 9.96e-1 SMART
ZnF_C2H2 175 197 2.4e-3 SMART
ZnF_C2H2 203 225 6.42e-4 SMART
ZnF_C2H2 231 253 1.3e-4 SMART
ZnF_C2H2 259 281 1.3e-4 SMART
ZnF_C2H2 287 309 1.28e-3 SMART
ZnF_C2H2 315 337 3.21e-4 SMART
ZnF_C2H2 343 365 3.39e-3 SMART
ZnF_C2H2 371 393 4.87e-4 SMART
ZnF_C2H2 399 421 2.53e-2 SMART
ZnF_C2H2 427 449 3.95e-4 SMART
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 97.9%
  • 20x: 93.9%
Validation Efficiency 100% (54/54)
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca16 A T 7: 120,139,934 (GRCm39) K1533M probably damaging Het
Aldh1l2 C T 10: 83,356,202 (GRCm39) V63I probably benign Het
Atr A G 9: 95,747,372 (GRCm39) H218R probably benign Het
Atxn7l1 T A 12: 33,408,662 (GRCm39) S275T possibly damaging Het
Cacna1c T C 6: 119,034,263 (GRCm39) K88R probably damaging Het
Ccl7 T C 11: 81,937,412 (GRCm39) Y49H probably damaging Het
Cers5 A G 15: 99,636,544 (GRCm39) probably null Het
Chuk T C 19: 44,071,076 (GRCm39) E543G probably damaging Het
Dip2c T C 13: 9,697,043 (GRCm39) V1318A probably damaging Het
Ercc5 A G 1: 44,206,512 (GRCm39) H475R probably benign Het
Fat3 A G 9: 16,288,818 (GRCm39) L235P probably damaging Het
Fbn1 A T 2: 125,211,721 (GRCm39) C892* probably null Het
Fbxw8 T C 5: 118,230,740 (GRCm39) T354A possibly damaging Het
Fsip2 A C 2: 82,817,601 (GRCm39) T4445P possibly damaging Het
Gpld1 A T 13: 25,155,397 (GRCm39) Q344L probably benign Het
Hao1 A T 2: 134,347,545 (GRCm39) D253E probably benign Het
Hmcn2 A G 2: 31,246,266 (GRCm39) D745G probably benign Het
Kcnt1 A G 2: 25,793,397 (GRCm39) T658A probably benign Het
Klhl35 A G 7: 99,122,544 (GRCm39) probably benign Het
Lnx2 C T 5: 146,978,836 (GRCm39) probably null Het
Map3k5 T C 10: 19,876,321 (GRCm39) V160A probably damaging Het
Masp2 A T 4: 148,698,469 (GRCm39) I517F possibly damaging Het
Mc4r A T 18: 66,992,251 (GRCm39) Y287* probably null Het
Mthfr A G 4: 148,126,211 (GRCm39) D94G probably benign Het
Muc16 A G 9: 18,559,114 (GRCm39) I2393T unknown Het
Mybbp1a G T 11: 72,336,838 (GRCm39) V557L probably damaging Het
Mycbp2 A T 14: 103,536,183 (GRCm39) W256R probably damaging Het
Nacad G A 11: 6,550,902 (GRCm39) S763L probably benign Het
Nebl A G 2: 17,735,641 (GRCm39) V11A probably benign Het
Notch1 A T 2: 26,358,743 (GRCm39) C1363S probably damaging Het
Nphp3 A G 9: 103,909,105 (GRCm39) N772D probably benign Het
Nqo2 G A 13: 34,163,634 (GRCm39) V98M probably damaging Het
Pak4 A G 7: 28,264,692 (GRCm39) I70T possibly damaging Het
Pbx2 A G 17: 34,812,574 (GRCm39) K2E probably damaging Het
Pikfyve A G 1: 65,255,202 (GRCm39) T352A probably benign Het
Polr1g G A 7: 19,091,558 (GRCm39) T183I possibly damaging Het
Pop1 T C 15: 34,526,456 (GRCm39) Y684H probably damaging Het
Rpa1 A G 11: 75,205,721 (GRCm39) V212A probably damaging Het
Rpap2 A G 5: 107,768,536 (GRCm39) E458G probably damaging Het
Sin3a T C 9: 57,002,708 (GRCm39) V200A possibly damaging Het
Sla T C 15: 66,654,447 (GRCm39) T280A probably null Het
Slc22a26 A T 19: 7,763,812 (GRCm39) I406K possibly damaging Het
Slc24a1 T C 9: 64,844,545 (GRCm39) N606S unknown Het
Slc39a10 G A 1: 46,866,567 (GRCm39) T443M probably damaging Het
Smg1 A T 7: 117,762,553 (GRCm39) probably benign Het
Sra1 G A 18: 36,803,336 (GRCm39) A9V probably damaging Het
Stard4 A G 18: 33,342,109 (GRCm39) V47A probably damaging Het
Stat4 A T 1: 52,113,836 (GRCm39) D182V possibly damaging Het
Syt1 A G 10: 108,467,668 (GRCm39) F210L probably damaging Het
Ube2q1 T A 3: 89,688,667 (GRCm39) probably null Het
Vmn1r159 C T 7: 22,542,612 (GRCm39) C140Y possibly damaging Het
Wnt8a T C 18: 34,678,599 (GRCm39) F138L possibly damaging Het
Zfp646 C T 7: 127,477,897 (GRCm39) R25W probably damaging Het
Other mutations in Zfp623
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00226:Zfp623 APN 15 75,820,052 (GRCm39) missense probably damaging 1.00
IGL01524:Zfp623 APN 15 75,819,528 (GRCm39) missense probably benign
IGL01927:Zfp623 APN 15 75,819,354 (GRCm39) missense possibly damaging 0.57
IGL03199:Zfp623 APN 15 75,819,119 (GRCm39) missense probably benign 0.40
R0076:Zfp623 UTSW 15 75,819,058 (GRCm39) missense probably benign
R0352:Zfp623 UTSW 15 75,820,433 (GRCm39) missense probably benign 0.00
R0360:Zfp623 UTSW 15 75,820,510 (GRCm39) missense probably benign
R0364:Zfp623 UTSW 15 75,820,510 (GRCm39) missense probably benign
R1783:Zfp623 UTSW 15 75,819,760 (GRCm39) missense probably damaging 0.99
R2219:Zfp623 UTSW 15 75,819,379 (GRCm39) missense possibly damaging 0.90
R5975:Zfp623 UTSW 15 75,820,012 (GRCm39) missense probably benign 0.43
R6342:Zfp623 UTSW 15 75,819,837 (GRCm39) nonsense probably null
R6490:Zfp623 UTSW 15 75,820,308 (GRCm39) missense probably damaging 1.00
R6513:Zfp623 UTSW 15 75,819,317 (GRCm39) missense probably benign
R7028:Zfp623 UTSW 15 75,820,154 (GRCm39) missense probably damaging 0.99
R7399:Zfp623 UTSW 15 75,819,247 (GRCm39) missense probably damaging 0.98
R7716:Zfp623 UTSW 15 75,820,271 (GRCm39) missense probably damaging 1.00
R8362:Zfp623 UTSW 15 75,819,488 (GRCm39) missense probably damaging 1.00
R8445:Zfp623 UTSW 15 75,819,402 (GRCm39) nonsense probably null
R9028:Zfp623 UTSW 15 75,819,349 (GRCm39) missense probably damaging 0.97
R9035:Zfp623 UTSW 15 75,820,162 (GRCm39) missense possibly damaging 0.93
R9310:Zfp623 UTSW 15 75,819,949 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GTGGGAAAGCCTTCATCCAGAG -3'
(R):5'- CTGCCTTGGTGACAGACAAC -3'

Sequencing Primer
(F):5'- GGAAAGCCTTCATCCAGAGTTCTAAG -3'
(R):5'- CAGTAACAGCCTATCAATGACTTG -3'
Posted On 2017-10-10