ZMP
wu:fc90d11
Ensembl ID:
ZFIN ID:
Human Orthologue:
TMEM63B
Human Description:
transmembrane protein 63B [Source:HGNC Symbol;Acc:17735]
Mouse Orthologue:
Tmem63b
Mouse Description:
transmembrane protein 63b Gene [Source:MGI Symbol;Acc:MGI:2387609]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24946 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15075 | Nonsense | Available for shipment | Available now |
sa42297 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11587 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24946
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 |
---|---|---|---|---|---|
ENSDART00000004666 | Nonsense | 264 | 816 | 11 | 24 |
Genomic Location (Zv9):
Chromosome 13 (position 47276887)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 46488149 |
GRCz11 | 13 | 46777984 |
KASP Assay ID:
554-7342.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTCTGTCTAACCTTTTTTCTCGTTTGTGTTGTTATTCAGGAAAGCATA[T/A]GAAAACTGTGTGGTTCTGGATGCTCGCATTTGTTACAATGTCGCCAAACT
Long Flanking Sequence:
AGCAGTCTCAAAGTATGTTTGCCACAGAGTTTGATCAACCTTGTAGGCTTCCTTAGACCTATTACTATAATTCAGATGGAACTTGTGATTTCACACTGTAAATATTTTCCTGTAATGTCATCAGTGTTCATCAGTGTTAAGACTGCTGTGTCATTATTTGAAAAGCTTATCAGATTGTTGCATTAGTTTTCTACTATTGATTAGATTTACTCGCCCCTATGCATCACATAAAATAAAACAACAGTGGCCGGTCATTTTACATGCTGGTCAGTCTCTTCCCGTCTAAGTGAGTCATTTCTGGTCGACATAAACTATAGTGTGCGCCAGACAATGCTGAAGTCTGGCTCCTGCAAGACTATCAACACTGTGTTCCAGTGCCAGGATAAAGAAGAAAGTGGGAATTAGTAGTAGGACTTCTTCCTTCTCCTCTCATGGGAGTGTTATGCCTTTAACTCTGTCTAACCTTTTTTCTCGTTTGTGTTGTTATTCAGGAAAGCATA[T/A]GAAAACTGTGTGGTTCTGGATGCTCGCATTTGTTACAATGTCGCCAAACTAATGTCTTTGGAGTCTGAAAGGTACACTTTTTAGAACTTGTTTGTTTGTTTATTTGTTTGACTTTATTAATCCCAAAGGGAAATTCAAAAGTCACAGCAGAGCTCTACATTACTAAAAATAGATACAGGGTTCCTACGGTCATTTAAAAACCTAAAGTTATGGTATTTTGACATGGCATTTTCCAGGCCTGGAAAAGTTTTGGAAAACCTAAAAACCCCACAAAGTTTTGGAAAAGTCATAGAAATTTACTCTAAAGTCCTGGAAAAAAAATTGTAGAATATATATATATATATATATATATATATATATATATATATATATATATACGTGGCTGAGTGCCTTAGTGCCCCCACCAGTGCCGATAAACAGCCATATCGCACTGCTATGAATGTGATATTCTGTTTATACAACTGTTTGACGACATAATTTTGTATATAAAAACAAAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15075
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004666 | Nonsense | 485 | 816 | 16 | 24 |
Genomic Location (Zv9):
Chromosome 13 (position 47264681)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 46500355 |
GRCz11 | 13 | 46790190 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCCTCCAGAACCCCATCGTCACTCAGTTCTTCCCTACCCTGCTGTTGTG[G/A]TGCTTTTCGGCCCTCCTCCCTACCATCGTCTACTACTCCGCCTTTTTTGA
Long Flanking Sequence:
GCCTAGAGCGCCATCTGCTGTTGAAAACTAGCCTAGAGCGCTGAACTAGCCTAGAGCGCCGTCTGCTGTTAAAAACTAGCCTAGAGCGTTGCTGCTGTTAAAAACTAACCTAGAGCGCCGTCTGCTGTTGAAAACTAGCCTAGAGCGCTGAACTAGCCTAGAGCACCATCTGCTGTTGAAAACTAGCCTAGAGCACCGTCTGCTGTTAAAAACTAGCCTTGAGCGCCGTCTGCTGTTGAAAACTAGCCTACAGCGCCGTCTGCTGTTAAAAACTAATGTCAGAATCCATTAAAAATACAAAATAGGGATGCACTTTGAAAATCTCAGCATCGTTGCAGAATTGATTTCTCAAATAATTGTTCGCCAGTCGCCATGGCTCTAATAAACACAATGCTCTTGAGTCATGATTCTGTCAGTCATCTCAAACCTCCCTCCGTTTCCCTGTGTCTGTTCCTCCAGAACCCCATCGTCACTCAGTTCTTCCCTACCCTGCTGTTGTG[G/A]TGCTTTTCGGCCCTCCTCCCTACCATCGTCTACTACTCCGCCTTTTTTGAGGCCCACTGGACACGGTACAATCCCAATCCCTGTATATCAGTTAACCTAATTGACCCGGAGATGGTCTCCATTTATAGCAACTAAACTAGGGCTGCACAATAGATTGCTTTTAAGTTCTGTGACTCAGCATTTCATTCGTTTCAAACATTTGAGCACAAAAAAATTATGATGTTTTGAGGTGTAACAGAAATTAATTGTACAGTATTTAAGTATTTATACATTTATATACACTCACCGGCCACTTTATTAGGTACACCTGTCCCACTGCTTGTTAATGAAAATTTGTCACATGTGATGGTGGTCACATGGGAGCAACTCAATGCATTTAGGCATGTAAACATGGTCAAGACGATCTGCTGCAGTTCAAAGCGAGCATCAAAATGGAGAAGAAAGGTAATTTAAGTGACTTTGAATGTGGCATGGATGTTGGTGGCAGACTGGCTCAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42297
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004666 | Essential Splice Site | 704 | 816 | 22 | 24 |
Genomic Location (Zv9):
Chromosome 13 (position 47259424)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 46505612 |
GRCz11 | 13 | 46795447 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCTGTAATATGATTTTTCAATCTTGCTTGTCTTTTTTTCAATCTGACA[G/T]GATTTGGTGCTCCGACATCCATGTTTACTTTTGTGGTTCTGATCATCACC
Long Flanking Sequence:
AGGTAGTGTATTCACTAACATATACACAATGAACAATACATTTATTACATTGTTTGTTTAAATAAAGTTGTTCATTGTTAGTTCGTGTTCACTTGTAATAAATGCTGTACGAGTATCGTTTATAATTAGTTAGTAAATACATTAACTAATAAAACCCCATTGTAAAGTGTGACCTGTATCTTTGCCTCAGTTGCATTTATCGAATGTAATTAATTATATTTTATGCAGATGCAGTGCTCTACATATCATTCCAATCAATCTAAAACAATTATTCCTTTTCAAAAATGATGAATGCTTTTTAAAAATAGATGTTCAAGTCACCTGGTGAATATGTAATAATATTAAAGTTTTTTCCAATACTGTGCAGCCCTATTCAAGATGCAGTTACAGTATGTTTCTAAAAATACAGCAGTGCTAAAAGTAGCAAAAAGTACAGGCAGATTTTTGGCGTATCTGTAATATGATTTTTCAATCTTGCTTGTCTTTTTTTCAATCTGACA[G/T]GATTTGGTGCTCCGACATCCATGTTTACTTTTGTGGTTCTGATCATCACCATCATTATTTGCCTCTCGCATATAGTCTTCGGTCATTTCAAATACCTCAGCGCGCACAATTACAAGGTCAGAAACAGGTTGATTATGATTTTAAGAAATCATAAAGGCCAGAATTATAAACCCAAATGTGATTGAATTCTCTGCAGATTGACATGGATGGTGTGGACAATGGACGACTGCGAGGTTCATCCCCACCGGTCAAGTCTATGGTAAGTTTTAACCCTCAGGGATGTTTATATATTCTCAGGGGAGCTAATAATTCTTCAACTGTTTTGTGCAGCCCTAATTGACGCACTACTATGTTGTCCTGTCTGATGTTTTCTATCTGCTTTACACATTCTGCACTGTTTTTTTTTTTTTAAATCAACAGCAGACGTACATTGCTCAAGTGCTACAGGACCCAAACTCAGACGAGACCGGAAGTGACCAGGGTCAAGGGTCATCGCAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11587
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004666 | Nonsense | 783 | 816 | 24 | 24 |
Genomic Location (Zv9):
Chromosome 13 (position 47258955)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 46506081 |
GRCz11 | 13 | 46795916 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCAGACGTACATTGCTCAAGTGCTACAGGACCCAAACTCAGAYGAGACC[G/T]GAAGTGACCAGGGTCAAGGGTCATCGCAGGACRAGGAAGGSGTGACCGAG
Long Flanking Sequence:
CAATCTTGCTTGTCTTTTTTTCAATCTGACAGGATTTGGTGCTCCGACATCCATGTTTACTTTTGTGGTTCTGATCATCACCATCATTATTTGCCTCTCGCATATAGTCTTCGGTCATTTCAAATACCTCAGCGCGCACAATTACAAGGTCAGAAACAGGTTGATTATGATTTTAAGAAATCATAAAGGCCAGAATTATAAACCCAAATGTGATTGAATTCTCTGCAGATTGACATGGATGGTGTGGACAATGGACGACTGCGAGGTTCATCCCCACCGGTCAAGTCTATGGTAAGTTTTAACCCTCAGGGATGTTTATATATTCTCAGGGGAGCTAATAATTCTTCAACTGTTTTGTGCAGCCCTAATTGACGCACTACTATGTTGTCCTGTCTGATGTTTTCTATCTGCTTTACACATTCTGCACTGTTTTTTTTTTTTTAAATCAACAGCAGACGTACATTGCTCAAGTGCTACAGGACCCAAACTCAGACGAGACC[G/T]GAAGTGACCAGGGTCAAGGGTCATCGCAGGACGAGGAAGGGGTGACCGAGGGTGACTTCCAGTCAGGAGAGGACAGTCTAATTGAAAACGAAGTGCACCAGTGACCCAGGCCGGGCCACGGCATGTGCTGAACTGAGAGAAACTAGCAGGACTCCCCACATAACCAAACGGAGATACACTACACTAACTGTGTGTGAGTCCATCCCAGCTGACAGCTCAAACACTCCTTTATCTTTAATGTTTGGAGACAGGATGGCCAATTGTCAAGAACCTGGAGAGTGGCTTGTGATTGTACTCCAATATTGTTCATCATAGTTTCATAATTCATCCTCACATTGTTTGTCCTGGATTTGGTAGGTACAGAGTTTCCTGCCGTTACAATGCATGTTTAGTCAGTAAGACCAAAAATATAAATGATTAGCAAAAAAATGAATTATGACAGCTGTAGTGCTGTATCAGTTGGCCAGTAATGTTTTATAATAATATATTTGCTTACAGAT
Associated Phenotype:
Not determined