ZMP
tapt1b
Ensembl ID:
ZFIN ID:
Description:
Transmembrane anterior posterior transformation protein 1 homolog [Source:UniProtKB/Swiss-Prot;Acc:A
Human Orthologue:
TAPT1
Human Description:
transmembrane anterior posterior transformation 1 [Source:HGNC Symbol;Acc:26887]
Mouse Orthologue:
Tapt1
Mouse Description:
transmembrane anterior posterior transformation 1 Gene [Source:MGI Symbol;Acc:MGI:2683537]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32664 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39607 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32664
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 |
---|---|---|---|---|---|
ENSDART00000086867 | Nonsense | 169 | 567 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 21560772)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 22095939 |
GRCz11 | 1 | 22786678 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCCTGCTCAGGTCTGTGATGTTCTGAAGGGTTTCATCATGGTTCTGTG[T/A]TATTTCATGATGCATTATGTGGATTATTCCATGATGTATCACCTGATCCG
Long Flanking Sequence:
TGAGCTTTAAAGCTCCTGTCATTTACACATACATGAGCATTTTTTCAATAATATTCATATTTAATTATGCATTGGATCATTTATATTGTTGTCATTTAATCTTTGTAATGGAATCATTATTGGTTCTGTTATTCACATTTTGTTATTAATAGTTAATAATAGGACTCAAGTAATATAAAGGTAAAGCGAATATTAATAAGCTCATTTTAAAAACTAATGAATATGTCATTGCTCTGCTTTATTTGATCATGTGTCTAATCTTTAGCATGATGCATGGACTGAGTGTGTGACATTAGTAACCCAATGGCTGTGTGTGAAGGAACCGTTTTATTATAATCGTCTATTCTTTCATTGTGTTAATCCAGATGTCTTTGAATCTTATTTAACCATTAAGATGTATTATTTTGTGTGTTGCTGTGTGTGTGTGTGCGCAGTGGGTCTCGCATCTTGCAGCCTGCTCAGGTCTGTGATGTTCTGAAGGGTTTCATCATGGTTCTGTG[T/A]TATTTCATGATGCATTATGTGGATTATTCCATGATGTATCACCTGATCCGGGGTCAGTCTGTCATAAAGCTCTACATCATCTACAACATGCTCGAGGTACAGTATCACAACGTTCACATTTATTGCTTTCTTTTCTTTTTTTTGCTATTAATAATAACAGTACAGGAAGATGGATGGACACTCTTTTTGTTTTTCCACTAGGTGGCAGATCGCTTGTTTTCATCTTTTGGTCAAGATATTTTGGATGCTTTGTACTGGACGGCCACCGAACCTAAAGAGAGAAAAAGAGCACACATAGGAGTCATCCCACATTTCTTCATGGCTGTTCTCTACGTCTGTATCCTTCTCACTAGCTTTGTTTCCAATGCCAAGTAGACCATGTAAGATAATATTATAAATTAAATGTTTTATAATGATTAATTATTTTAAAATATATAATATTTAAAGAATAACATAATTAGTAAAAATTTTTAGTCAGATTAAGTACTATGTACTTTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39607
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000086867 | Nonsense | 532 | 567 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 21546751)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 22081918 |
GRCz11 | 1 | 22772657 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAAATTCCAACCAGCGAATCAGATCAGTTCCTCACGACACCTGATGAAT[C/A]AGAAGAAAAAAGCCTTATTCAGGACGATTCCGAACTTAAACACAGGGCAC
Long Flanking Sequence:
GCAGAAGAAGCCTCCTTATGCAATGCACTGCTTTTTTGTGCTTTGAAATGCAACATTTGAATGTTTGTAAAAAAAACAAAAAAACAAAAGCTTATTCTACAATGCACTAATATTGTGTAGTTTCAAAATACAAAATATTATCATTTTTATTTAGAAAAAGTCAACATAAGTGTCTTAAGGAGCAAAAATACAACAAATGGGATCTTATGTGTAGTTGGATCATCACTCATGTTGCAAGTCATATCTCTCCGGCCCCTCATTTGGAATGCTTTTCATAAACTGGCCCTAAGACAAACTAATTGAATAGCCCTGATAAACACCATAAAGTTTATGATATTTTGTTCTGACTGACCAAGTGTGTCCAACCCCCCCTGAAGGTGATCCAGCAGAAGAGGGCATGTCTGCATCAGTCACCACTCAGCCCACACAACAGGACGAGTGTCCCGCCCCTCAAATTCCAACCAGCGAATCAGATCAGTTCCTCACGACACCTGATGAAT[C/A]AGAAGAAAAAAGCCTTATTCAGGACGATTCCGAACTTAAACACAGGGCACCCAAAAAAGACTTGCTGGAGATTGACCGCTTCACAATCTGCGGGAACCGTATTGACTGACATGAACCAGCTCCCTCAAGTTTAAGAGCCAGATGTGCACTGAAATGCCCGCTTTCTTCTGCCAGCCCGATTCGATTGACATTTGAACCTGAGCTTGTTGGAACGGGACAACAGGATATTTATTAATAAGTGATGCACCTAATTTATTTAAGACTTAAACATACTCACACACAGACAATCACACACATTTGACCCATTTGGATTCCACCCAAGAAAGAGGTTCAAGATCACCTGCAGAGGTCACAGCGATCTTATTTCATGGTGGCATTGAATAAAGAAGAAAAAAAAGCATGGATTATGTTCTGAAATGACAGGTTATGAGGATTCTGGTCATGTGTGGAAAAAGTGATTCAAAGTTTGTTTGATTTTATTTTTCCTGCAGTGCTCCAAG
Associated Phenotype:
Not determined