ZMP
clptm1
Ensembl ID:
ZFIN ID:
Description:
Cleft lip and palate transmembrane protein 1 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q6DEL2]
Human Orthologue:
CLPTM1
Human Description:
cleft lip and palate associated transmembrane protein 1 [Source:HGNC Symbol;Acc:2087]
Mouse Orthologue:
Clptm1
Mouse Description:
cleft lip and palate associated transmembrane protein 1 Gene [Source:MGI Symbol;Acc:MGI:1927155]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13817 | Nonsense | Available for shipment | Available now |
sa45533 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14801 | Essential Splice Site | Available for shipment | Available now |
sa17636 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13817
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046648 | Nonsense | 46 | 631 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 16098622)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17143585 |
GRCz11 | 15 | 17079607 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGTAGCTCAGACAGGTGCAACTGCACAGGACCCCCAACAACAGCAACAA[C/T]AACAGCCCAGTGCCTGGCAGGTGATTAAAGGTGTCCTCTTTAGGTGAGTT
Long Flanking Sequence:
CTGTGTAGCTTCTCTGTAAACTATGGCTTTGTTGCTGCTACATCTAAAAGCATGTGAAAATGCCACATTTCAGACATTTTTACTTCACGCTCGCTTCATAACTTAAGTCAAGTGTTTAAGTCTTTCTGTGAGAATATTCCATATTTATGTGTTTATTAATCAGTGTAAGCAGTTAAATCTAGCAACCACCATAGGGATTTCATGTAGTCTTCATGAGTATTTGGAGTTTCATGTGAGAGCTTTCTGGGCTTTGAAGGAGATTTACTACTGATCTTCCGTGAAAAGATGTTCATAAAAACCACAGCATTTGCTTAATTGCAGTTGCAATTTCTTTCCATTTTGTTGTGCTGCCCTTGTACAATGTGTACTAAACATTTTGCATGTATATTTAATTGTTTATCACTAAATGTTTTGTGCAGGTGAGCAGTAATGGGGCAGCTGCCTCTGGTCAGGTAGCTCAGACAGGTGCAACTGCACAGGACCCCCAACAACAGCAACAA[C/T]AACAGCCCAGTGCCTGGCAGGTGATTAAAGGTGTCCTCTTTAGGTGAGTTCAGATCTTGCAAATTTAAATTATGTGTAACTCATAACTATTTTCCCCCTGTTGTTCTCACTTTAAAGCTATAGTATGTAACTCACATCAAATCACTCAAATCATTTATATTGTCACATCATCAGCAGCATGTTTACTACGAGGAGTAAAAACGCTTAGGTGCTGACAGTGCAAACTGTAACTCGCTCTCTAGCAGTTAATAAAACAACAATTCATGTCTTTTTAAGTACTACTGTTTATTAAGTTGTAGGGATGAATTGAACACAGGTTCATAGCTACTCCACAGTATGGATTGAGCCAACAGATCTAAAATAATTTGAATATTAATACTTATTTTATTATTTTTGAATGTAAATTTTGTAGCCTTTTAGTGGTTTGTTGTGGGTTTGTTGTGATTTTAGAAAGTATATGCTAACATTTTAGATTATTAATGGTGATTGAGCTGTGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45533
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046648 | Essential Splice Site | 101 | 631 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 16100249)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17145212 |
GRCz11 | 15 | 17081234 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTCCGCGAGTGCCCAGCCGAAACCTCTTCCCTAAGGACACTCTTATGG[T/A]ATTCGTAGCTTTTCATGTATAACAACATAAGCAGAATATATAATCAAGCA
Long Flanking Sequence:
AACAACCCCAGTGTGAGTCCTGAGGGCTGCATTACTCGATGGACATCCCCTGAGGGGAAAACAACTAAACTCCAGAGCTGTTCTGACTGCTCTAATTGATGTCACGGGATTTGCATTCCTAATATTTCACACTTACGCAATATTTAAAGTGTATTGTCACAGTTACAGCATTTACCTTCTCCAGAGGTGTTTCTCAAAAATTGACTTTACTCTTATTTAAAGGGGCTGAAATAATATTAATATATATATTTTTTTTACTCTCACGTTATAGCTGATAGTTTAAAATAGCAATGTTGCATCATGAGATCTGGGAATACTCTTCTTAAACATCATAGGACTGACGTCTAAAGTTAACCCCCTCATGTTTTTACCCAGGATTTTTATCATCTGGGCTATTAGCAGCTGGTTTCGCAGAGGTCCATCAACCCCAGATCCCAACACTCCTGCTGGAGCTCCGCGAGTGCCCAGCCGAAACCTCTTCCCTAAGGACACTCTTATGG[T/A]ATTCGTAGCTTTTCATGTATAACAACATAAGCAGAATATATAATCAAGCACATAATGAAATTCAAAGTAGGTTCATGTTTGATAACCATCACCTGTCTGTTTACAGGATTTATATGTGTATATCTCAGAGAGCGAGATATTTACAGATTTTAACAATACAGAAGAACTGTTCTGGTACCAGCAAGATCTGGTTTATGGAGAGTGGACCACAGGGGACTCGGGAGATGGCTGCTATGAATATTACAAAGAGCTGGACCTCTCTGAGGTGAGACATGTTTGCTTGCTGTGAATGTGATGGGTCTGAGACATGCACAGTTTGAAAATGTATGAAGGCGTGTAATTGACTATTTATAACCACTTTGCACGGCGGTATTGTTTTGGTGCTTTTCAGTACATGTGCCTACTAAGCTTTGACGCACACTAGAACATGGTAAAACACAAGTATGTTAATAGCTTCACAACTCTTTTAGCATTTAATAAGATGTATCACTTTAAAAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14801
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046648 | Essential Splice Site | 376 | 631 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 16109798)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17154761 |
GRCz11 | 15 | 17090783 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAGYTTCCATCGTCCACAGCATTTTTGAGWTCCWGGCCTTTAAGAATGG[T/A]AAATAAATACTGTTTTGATTATTTGAGWCTTGTGGCTTCTGGGATCTGAG
Long Flanking Sequence:
GAAACGCTGCTTTATTCGCACGTCTTTTATACGATAATCCAGTTTTGTGCATAAAGTTAATTTGCATTTTTGGATGGAAACATACAGTAGCTAGTGGTTCCCAACCTTGTTCCTGGAGGCACACAAATAGTCCACATTTAAAACTTTTCCTAATCAAAGACGCCTGAATCAGCTCATCACATCATTAGAAGAGTCTACAAACCAAAAATGAATGGGTCCTCTGAAGGAGACATCCAAAACATGTACTGTTGGTGTGCCTTCAGGAACAGGGTTGGGAAACACTGCATTATGCTACAAATTAGACTCATGAATAGGTGAAATAATGTTAACGGTTCAACAAGCACAGTATTAAATGTCATTTACAAGTCTTTTTGTGTTTATATGCTTGCTTGTTTCTTTTAACAGGTGGCTCTGCTTGAAACCAACCCCTACCTCCTAGGCCTGACCATTGTAGTTTCCATCGTCCACAGCATTTTTGAGTTCCTGGCCTTTAAGAATGG[T/A]AAATAAATACTGTTTTGATTATTTGAGTCTTGTGGCTTCTGGGATCTGAGCAGTACCGTCTCATTTTATCTTCTCTGCAGATATCCAGTTCTGGAACAGCCGTCAGTCTCTGGAGGGACTCTCCGTACGCTCCATCATATTCGGAGTGTTCCAGTCTCTTGTAGTGCTGCTTTATATCCTGGACAACGAGACCAACTTTGTGGTCCAGGTCAGCGTATTCATTGGCCTGCTCATCGACTTCTGGAAGATCACCAAAGTCATGGACGTCAGGGTGAGATGAAGCCACTGCCAGACATTTTAGACCGCTTAAATGGCTAGGGCTAAATTGATGTTCATTCTTTTCTTTTCTTTTTTTTTCTAGCTGGACAGAGAGAACAGGATTGCTGGAATTGTCCCAAGATTAGTATTCAAAGACAAGTCCACATATGTGGAGTCTTCAACCAAAATCTATGATGATGTAAGAGTCACTTTTAAGCTGCATTAGAGCAAATTCAGATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17636
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000046648 | Nonsense | 493 | 631 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 15 (position 16110402)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 17155365 |
GRCz11 | 15 | 17091387 |
KASP Assay ID:
2260-8276.1 (used for ordering genotyping assays)
KASP Sequence:
CCTGTCCTGGCTGTTGTACCCTCTRTTTGGATGCTATGCAGTGTATAGCT[T/A]ATTATATGTGGAACACAAGGGCTGGTACTCRTGGGTGCTCAGTATGCTTT
Long Flanking Sequence:
CAGTCTCTGGAGGGACTCTCCGTACGCTCCATCATATTCGGAGTGTTCCAGTCTCTTGTAGTGCTGCTTTATATCCTGGACAACGAGACCAACTTTGTGGTCCAGGTCAGCGTATTCATTGGCCTGCTCATCGACTTCTGGAAGATCACCAAAGTCATGGACGTCAGGGTGAGATGAAGCCACTGCCAGACATTTTAGACCGCTTAAATGGCTAGGGCTAAATTGATGTTCATTCTTTTCTTTTCTTTTTTTTTCTAGCTGGACAGAGAGAACAGGATTGCTGGAATTGTCCCAAGATTAGTATTCAAAGACAAGTCCACATATGTGGAGTCTTCAACCAAAATCTATGATGATGTAAGAGTCACTTTTAAGCTGCATTAGAGCAAATTCAGATGAATTCATATTGTTCCATGATTAACATGTTTTTTTTCCCCAGATGGCCTTTAAGTACCTGTCCTGGCTGTTGTACCCTCTGTTTGGATGCTATGCAGTGTATAGCT[T/A]ATTATATGTGGAACACAAGGGCTGGTACTCGTGGGTGCTCAGTATGCTTTATGGGTTCTTGTTAACCTTTGGTAAGTAGAGCTTCACATCATGTTTGTTATGTCTTCATGCAATTGTGATTACCAAAAGCACGCTCCCAGACTGTGTCCACATCAAATAAGAACTAGATGCCTGAGGAAAACACTGCAAAGGGGAATTCAACTTATTAGCATTTAAGACTCAAATGATTTTCTACAGTGCTGTGAAATAGAATAAGAAAGAGCACTGTATGGTCTTTGTGAAATCCAGTTGTTAGCCCTGGGGATATGATTGCATGTTGAAATATATTCATGTTTAATGGATTTCATAATGAAAGTTACAGAGAAACGTTTTGTCAGATGTGGCTCTTTGGTATGGTTTAAATAGAGTTGCAGACAATTTTCCAAAAAAAATGATATTTAATTTAATTTTTTTATTTCATATATATATATATTTTTTTTTTTTTTTATGTTTTTATTTAT
Associated Phenotype:
Not determined