ZMP
NP_001153308.1
Ensembl ID:
Description:
transmembrane protein 63C [Source:RefSeq peptide;Acc:NP_001153308]
Human Orthologue:
TMEM63C
Human Description:
transmembrane protein 63C [Source:HGNC Symbol;Acc:23787]
Mouse Orthologue:
Tmem63c
Mouse Description:
transmembrane protein 63c Gene [Source:MGI Symbol;Acc:MGI:2444386]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36506 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36507 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36508 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23169 | Splice Site, Nonsense | Available for shipment | Available now |
sa15405 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36506
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074802 | Nonsense | 122 | 825 | 4 | 22 |
Genomic Location (Zv9):
Chromosome 17 (position 45017478)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44737351 |
GRCz11 | 17 | 44851116 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTTTTATGACACCGTTGTCTTCCCTCCCTCTCTTTATAGGGCTTCTG[T/A]TCCTGGCTCACATCTTTGTACCACATGAAGTAAGTGTGCAGAAGTGGTGA
Long Flanking Sequence:
CTTGAGTGAACCAAATCCGACAATACAAAATCCCAAACCATTGCATAAAAACAAATAAAAGCATCAGTACAACTAATAGAAATTGTTTCTAGCATCCCAGTCACCTCTATGATGATCCATATTCACAACTGCTAAAACCTAAAGACACATAGAGGCACAAACAAAGTTCAATCTGTCGACGTGCATTAGTCAACTGCATCACCCCGGAGCTGATGTCATCTCAAAAGACGCTATTTTCTTTTATGCACAGTATCTGTCCGTTTATATCCTAACCTCACTCTGTCTCCTTGTGTTTTATGTGTGATGACAGTTCACGTCCTCACAGCCATGTTAAAGATATGCATGGCTTTTTTCCGCTTGTTACGCTGCGCATGTTCACTTAAAGAACAAATGAGTCCGACAGATGCTAAGCTAGCCAGACGTGCTCTTTTTTTATTATTATTATCCAGGCCTTTTTTATGACACCGTTGTCTTCCCTCCCTCTCTTTATAGGGCTTCTG[T/A]TCCTGGCTCACATCTTTGTACCACATGAAGTAAGTGTGCAGAAGTGGTGATGTCATCAAGCGGCGTCCTGTTTGCTCATGTTATATCTCATTAAGAAGGGAAAACACTGGGGTAAAAGTGGACCGGGCAGTTTCCTAGCACATCTAATGTCTCAAAAACAGCCTTTCAGAACCGCTAGTCTGTCTCCAGGGTTGCTGAGATGTTATTTGGACGACTCGGGTAGCGTGTCCGTGCCATATTTAGCTGGTTCCTTTTAAAAATCTTCTTGAGAGTCTCCTCACTCTGTGTGAGGCGAAGCCAGAGGCGTGTGTGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTATCTTGTAATCATAATAGCCCTCAATGCTCTTATGTATTTGTGTGGTCTTTTAAAGAAGCTGCCACACATATATTGTTGACTGAAGCCAATAATTCTCTGGGAACAGAGTGAACATGGTCACAGAGGCTTCCTGGGCACTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36507
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074802 | Essential Splice Site | 180 | 825 | 5 | 22 |
Genomic Location (Zv9):
Chromosome 17 (position 45024114)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44743987 |
GRCz11 | 17 | 44857752 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTCCCTCACCATCATCTTGCCCGTGAATCTCTCTGGAAACCTCCTCGG[T/C]ACCTTCACTACACACATCCTGCACTGGTTACTGTTTTCTCCAGCATGTGC
Long Flanking Sequence:
TATTTAAAACACAAACCTGTGTTTCAATGACGGATGTGGGTGTCAAAAAATACTTTTTAAATCAATGTTTTTGTCTTAATATTATTTAATGTGAACAACACTTAATAAAAATTTTAATGTATTTATTTCACCACCTTATTGGAAAAAACTGTATCAATTACAGTGCTTCCCGCGCTTGGGTGGTAGCCGGATTGAAACACACCATTTACCCACATCACATAAATAGCCGGTAGATCGTGCGACAGTAAGGGTCACATTGAACTCTCACCTACTGTAGCTTGTTTTCCATGTGTCTGCCAAATGAAGCAATACCAATGTAAAGATCATAATAAGCCTTTCTTTTCTTTGCCCTGCAGGGATGAAGAGATCCGCAGTAAATGTGGCATTGATGCGGTCACATACTTGTCTTTCCAGCGCCACATAATTCTGCTGATGATGGTGGTGTGTTTGCTGTCCCTCACCATCATCTTGCCCGTGAATCTCTCTGGAAACCTCCTCGG[T/C]ACCTTCACTACACACATCCTGCACTGGTTACTGTTTTCTCCAGCATGTGCTCAGCCATAAAGAGTTCATGACAACAGACACAACACATTCAGTCTCCAGGAAAAGGCAGTATATTTATAAAACAACATTACATCAACTGCTTAATTCATCAGCGTGCTTAAACCTAAAAAAGGCTGGTTAGAATAATCTCATAAATTAGTTTTGACAGGCTGTTTGAATAATTGGGCTTGTTTCACTGATTTTGAAGTCGTAGTCTAGAAGAATGTTCTATAAAGATATATACAGAAGTCAGAATTATGAGCCCTCCTAAATTACTATTTCCGCCCCAATTTCTGTTGAACGGAAAGAAGATTTTTCAACCACATAATAGTTTATTAACTCATTTCTAATAACTGATGTCTTTTATATCTGCCATAATGACAACACATACTATTTTAATATTTATCATAATATTTTTCAAGATACTAGTGTTCAGCTTTAAGTGACACTTAAATGCTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36508
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074802 | Essential Splice Site | 604 | 825 | 18 | 22 |
Genomic Location (Zv9):
Chromosome 17 (position 45061215)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44781088 |
GRCz11 | 17 | 44894853 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAAGAGCCAATAAATACTTTAGCCACCTCTTTCTCCTTTCTCCCCTC[A/T]GAGTCAGGCCTATGAGTTTCAGTTTGGTCTGGAATACGCCTGGACCATGT
Long Flanking Sequence:
TTTCAACACATTTCTAAACAAAATAGTTTTAATAACTCATTTCTAATAACTGATTTATTTTATCTTTGTCATGATGACAGTAAACAATATTTGACTAGATATTTTTCAAGACACTTCTACACAGCTTAAAGTGACATTTAAAGGCTTAACTATGTTAATTAGATTAACTAGGCAGGTTAGGGTAATTAGGCAAGTTATTGTATATTGATGGTTCGTTCTGTAGACTTCGGTAGATCGAAAAAATATATAGCTTAAAGGGGCTAATAATTTTGAAATTAAAGGTTGTCTTTTTTGTCAGACACTGCAATTTATTTATTTTTTAATGATTTTTTATTCAAATCATTCTAAATTGCATTCACTGTTATTTTAAACACTAAAAATATGTAAAGCTTCTGCATTTTGCTCTTTTTCCATATAATCACGGCTGAAAATGATTATCAGGCACTCCCAAAAAAAGAGCCAATAAATACTTTAGCCACCTCTTTCTCCTTTCTCCCCTC[A/T]GAGTCAGGCCTATGAGTTTCAGTTTGGTCTGGAATACGCCTGGACCATGTGTATATTTTCAGTCAGCATGACCTACAGCATCACCTGCCCCGTCATCGTACCTTTTGGTGAGTCTGAGTATGCTTTTTACTTCACCACAAACCGACCTTTTCTTTTAGCACTCCTTGTTCCATGCCCCAATTCTTCTTTCCTCCTAATTTGTGCTCAAACCCATTTGTCTCCTCTGCACCATTTGTGTGGTGTGTTTCTTTTGCTCTCATATCCTCTGTTGCCTGCAGCTCTCTCTTTGTCTGCCTTTATTTCTTCTTTCCGTCAGCCTTCATTTCTACCTCTGTGAGTGTTCTGATACCTCAGTCAGTGTGTGGGAGTCAGAGCCGTATCTCCAACAACATCTCAGTATCGCGGTGTGACATGGCCGCTAGGTGTGAACCCGCTGTAGTCTTCCAGACGCTGCGACCCGTCTAGCCAAGATCCAGACGCCCACTCCACGCCTGTTCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23169
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074802 | Splice Site, Nonsense | 733 | 825 | 20 | 22 |
Genomic Location (Zv9):
Chromosome 17 (position 45078187)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44798060 |
GRCz11 | 17 | 44911825 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTTGGATTCTGTATGAAAAAACTACGAGCTGACAGATCAACAAGCTAT[C/T]AGGTCAGCCACAGAAGCCTTTATCTTGAAACTTAAAAACTGTAATACTAG
Long Flanking Sequence:
AAAACCCAACTGTCAATTTTCATGAAGTGATGGTGATAAAATGTGGAATTTATTGCAGCATTAATTCCAAATGCTGAGCCACTTTGATGGCTAATTAGAGCCACAGAATCCTTCCTTATTCTAATTATGAAGATATTTCGCTGACTCAAGCTGCCTGAGGTAATTTCAGTTTTTTTGGGGGAAATTTTAGTCTAGACTGTGGTCTTCTCTAAGGATATAATAAATGTATGTTTCCAGAAGCAGACCTAAACTGAGAGACTAGTAATGAGACCCAGATCAAGGAAATGTTTGTGTGGTCTTCAGAGATCTTTAGACAAAGACCACAAGATCAGGACTCCAACTTTGTCACATATTAAAACATACACTGGTGGTTTATCTCCTTTGCAGGTCCAGTGCAGCCCATTACTCTGTTCACCTTCATTACTCTCCTGTGCTCCATTGCCTTCTCCTGCTTTGGATTCTGTATGAAAAAACTACGAGCTGACAGATCAACAAGCTAT[C/T]AGGTCAGCCACAGAAGCCTTTATCTTGAAACTTAAAAACTGTAATACTAGGGTGTGTTTCACCAAAATGATCAGAGAAACATATGCTGTTATATTTTTTTCTCAAGTAAAATAACAAATATTATATATATATATATATATATATATATATTTGCATAGTCACATATTTTTATTAGTTTATAAATAAACAATACATTTACAGCATTTATTATTTATAGTTTCCACTCTGACGTGTGTCTGGAAAACACTTTGGGGAGATCACTAGACCACTGACCGATCACTTTTGAAGAGTAAGAAAACAGGCCACAGTGGTTGTGTCGGTTCATCCCCCGAGATGCCCACGCCTCCGATTTATGACACTGGAGATCAGACACCCATTGCAATATCGGAGGGCAAGCTGTCATGTTCAGATGACAGACCGAGCTCGCTACATCCTATTGGGTGCAATGCATCTTCATGGGAATTCTGACGTGTGTCTGGAAAACACTTTGGGGAGCTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15405
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074802 | Essential Splice Site | 733 | 825 | 20 | 22 |
Genomic Location (Zv9):
Chromosome 17 (position 45078190)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 44798063 |
GRCz11 | 17 | 44911828 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGGATTCTGTMTGAAAAAACTACGRGCTGAMAGATCAACAAGCTATCAG[G/A]TCAGCCACAGAAGCCTTTATCTTSAAACTTAAAAACTGTAATACTAGRGT
Long Flanking Sequence:
ACCCAACTGTCAATTTTCATGAAGTGATGGTGATAAAATGTGGAATTTATTGCAGCATTAATTCCAAATGCTGAGCCACTTTGATGGCTAATTAGAGCCACAGAATCCTTCCTTATTCTAATTATGAAGATATTTCGCTGACTCAAGCTGCCTGAGGTAATTTCAGTTTTTTTGGGGGAAATTTTAGTCTAGACTGTGGTCTTCTCTAAGGATATAATAAATGTATGTTTCCAGAAGCAGACCTAAACTGAGAGACTAGTAATGAGACCCAGATCAAGGAAATGTTTGTGTGGTCTTCAGAGATCTTTAGACAAAGACCACAAGATCAGGACTCCAACTTTGTCACATATTAAAACATACACTGGTGGTTTATCTCCTTTGCAGGTCCAGTGCAGCCCATTACTCTGTTCACCTTCATTACTCTCCTGTGCTCCATTGCCTTCTCCTGCTTTGGATTCTGTATGAAAAAACTACGAGCTGACAGATCAACAAGCTATCAG[G/A]TCAGCCACAGAAGCCTTTATCTTGAAACTTAAAAACTGTAATACTAGGGTGTGTTTCACCAAAATGATCAGAGAAACATATGCTGTTATATTTTTTTCTCAAGTAAAATAACAAATATTATATATATATATATATATATATATATATTTGCATAGTCACATATTTTTATTAGTTTATAAATAAACAATACATTTACAGCATTTATTATTTATAGTTTCCACTCTGACGTGTGTCTGGAAAACACTTTGGGGAGATCACTAGACCACTGACCGATCACTTTTGAAGAGTAAGAAAACAGGCCACAGTGGTTGTGTCGGTTCATCCCCCGAGATGCCCACGCCTCCGATTTATGACACTGGAGATCAGACACCCATTGCAATATCGGAGGGCAAGCTGTCATGTTCAGATGACAGACCGAGCTCGCTACATCCTATTGGGTGCAATGCATCTTCATGGGAATTCTGACGTGTGTCTGGAAAACACTTTGGGGAGCTCACTAG
Associated Phenotype:
Not determined