Incidental Mutation 'IGL02579:Calhm6'
ID 299290
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Calhm6
Ensembl Gene ENSMUSG00000046031
Gene Name calcium homeostasis modulator family member 6
Synonyms Fam26f, A630077B13Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # IGL02579
Quality Score
Status
Chromosome 10
Chromosomal Location 34002063-34003968 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 34003423 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Isoleucine at position 161 (M161I)
Ref Sequence ENSEMBL: ENSMUSP00000051575 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000062784]
AlphaFold Q8C9E8
Predicted Effect probably benign
Transcript: ENSMUST00000062784
AA Change: M161I

PolyPhen 2 Score 0.012 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000051575
Gene: ENSMUSG00000046031
AA Change: M161I

DomainStartEndE-ValueType
Pfam:Ca_hom_mod 1 244 1.4e-94 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 23 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb4 A G 5: 9,005,537 (GRCm39) E1140G probably damaging Het
Alcam T C 16: 52,091,135 (GRCm39) E461G probably damaging Het
Bahcc1 A G 11: 120,176,175 (GRCm39) probably benign Het
Dnmt1 A G 9: 20,829,416 (GRCm39) M729T possibly damaging Het
Enpep G A 3: 129,077,739 (GRCm39) T626M probably benign Het
Gje1 A T 10: 14,592,492 (GRCm39) C97S probably benign Het
Igkv4-58 T A 6: 69,477,385 (GRCm39) I71F probably damaging Het
Itfg1 G A 8: 86,507,194 (GRCm39) T222M possibly damaging Het
Mon1b G T 8: 114,365,455 (GRCm39) R261L possibly damaging Het
Mtmr6 T A 14: 60,519,378 (GRCm39) probably benign Het
Nwd1 A T 8: 73,434,155 (GRCm39) I1251F probably damaging Het
Or5b101 T C 19: 13,004,892 (GRCm39) D267G probably damaging Het
Pip5k1c C A 10: 81,153,155 (GRCm39) probably null Het
Pold1 T C 7: 44,192,703 (GRCm39) E53G probably damaging Het
Prkdc A T 16: 15,488,465 (GRCm39) D529V possibly damaging Het
Rgl2 A G 17: 34,156,134 (GRCm39) T741A probably benign Het
Tex44 A G 1: 86,354,169 (GRCm39) N26S probably benign Het
Traf5 G T 1: 191,731,848 (GRCm39) P28Q probably damaging Het
Ttn A G 2: 76,589,433 (GRCm39) Y21274H probably damaging Het
Vmn2r76 T A 7: 85,877,961 (GRCm39) K479* probably null Het
Zfp322a A T 13: 23,541,613 (GRCm39) V43E probably damaging Het
Zfp385c C A 11: 100,521,605 (GRCm39) G152C probably damaging Het
Zfpm2 A T 15: 40,962,868 (GRCm39) N177Y possibly damaging Het
Other mutations in Calhm6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01103:Calhm6 APN 10 34,002,361 (GRCm39) missense probably benign 0.00
IGL01860:Calhm6 APN 10 34,002,561 (GRCm39) missense probably damaging 1.00
IGL01992:Calhm6 APN 10 34,003,533 (GRCm39) missense probably damaging 1.00
IGL02484:Calhm6 APN 10 34,002,400 (GRCm39) missense probably benign 0.03
R0492:Calhm6 UTSW 10 34,003,647 (GRCm39) nonsense probably null
R1681:Calhm6 UTSW 10 34,003,896 (GRCm39) missense probably benign 0.22
R2090:Calhm6 UTSW 10 34,002,358 (GRCm39) missense probably damaging 0.99
R2141:Calhm6 UTSW 10 34,003,691 (GRCm39) missense probably damaging 0.97
R4433:Calhm6 UTSW 10 34,003,827 (GRCm39) missense probably damaging 1.00
R4455:Calhm6 UTSW 10 34,002,531 (GRCm39) missense probably damaging 0.97
R7620:Calhm6 UTSW 10 34,003,614 (GRCm39) missense probably damaging 0.98
R8514:Calhm6 UTSW 10 34,002,399 (GRCm39) missense possibly damaging 0.94
R9155:Calhm6 UTSW 10 34,002,363 (GRCm39) missense probably damaging 0.99
R9786:Calhm6 UTSW 10 34,003,643 (GRCm39) missense probably benign 0.00
R9792:Calhm6 UTSW 10 34,002,544 (GRCm39) missense probably damaging 0.99
R9795:Calhm6 UTSW 10 34,002,544 (GRCm39) missense probably damaging 0.99
Posted On 2015-04-16