ZMP
tecpr2
Ensembl ID:
ZFIN ID:
Description:
tectonin beta-propeller repeat-containing protein 2 [Source:RefSeq peptide;Acc:NP_001038644]
Human Orthologue:
TECPR2
Human Description:
tectonin beta-propeller repeat containing 2 [Source:HGNC Symbol;Acc:19957]
Mouse Orthologue:
Tecpr2
Mouse Description:
tectonin beta-propeller repeat containing 2 Gene [Source:MGI Symbol;Acc:MGI:2144865]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10589 | Nonsense | Available for shipment | Available now |
sa15119 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10589
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 |
---|---|---|---|---|---|
ENSDART00000104224 | Nonsense | 740 | 1358 | 8 | 19 |
ENSDART00000133668 | Nonsense | 690 | 1308 | 8 | 19 |
ENSDART00000133971 | Nonsense | 360 | 978 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 29365327)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29289254 |
GRCz11 | 17 | 29306217 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTGAGCTTGCAGAGCTCATCTGCTGAGCAGAAGGAGGATGAAGAGACA[C/T]AGCTCCTCAAAGCTGACCAGGTCAGAGAGCATATCCRATTARGAGACCTA
Long Flanking Sequence:
CCATTCAGAGCCCATCAGAGCCCTTGCTGAACCAAGAGCCATGTCTGGTTGCAGTTAACCAAGCAGCACAGACCTCACCACCTTGCCCCGCGTCTCTGACACTAGACATGGAGTGTCAGTTGTACAGTGAAAATGTGTTTGCTGAAAATGAGCAAATCGCAGCTACACCTGATGTAGACATGCTGCTGGAATGTACCTTCTCGTACATGCAGGCATCTGACGAGCAGGACATCATGAAGAAATATGTGAAGGAGCACAAAGACGTCCTGGAGGATTCAGAGGAACATTTTAAGCAGAGTTTACATGAGGACTTTAATTTGGACTTGTCTTATGATCCCATTAGGCCGCTGGGTTACTCCCCTGAGCCTGAGCCATCGCCATCTAGTGACGAGGAGGACATCTATGCTCATGGAGTTCCATCCAGTGCAAGTCTTGGGGATGGACTGAATGCTCTGAGCTTGCAGAGCTCATCTGCTGAGCAGAAGGAGGATGAAGAGACA[C/T]AGCTCCTCAAAGCTGACCAGGTCAGAGAGCATATCCAATTAAGAGACCTACTTGGTTACCTTTACAATTTATAAGGCTGTGTAATATACACTACTGTTAAAAGAGTTTTAAAAGAGATTTCATATGTATCATGAAAATGAGGGTAAAAACAATAACAGTATAATGATGGAGCTAAATTTTCTACTGAATTACTTCAGGTGCCATATTTAAATGGTGCTACTGTAACCTTTTTAAATATTTATTTTTAGTCCTTTTGCTTTTATTATGACAGGACCAGTAGCTAGATCGGAAATGAAGATGAAGACAGACTAAGGGGCTGCGATTGGAAAAGGCCTGAAATGCATTGCCAGTATATGTCAGTAGGGTTTGGCTGCGGACTGCAAGACGGGCGTAGCATGAAGGGGCCTTAGGGGCTTGTAGTATGTTAGAGGTGTAGGAGCATGTCAAAACTATGTTGTCAGCAAGATGGTGCTGTACATCAGTTATTAACGGCTACACCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15119
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 |
---|---|---|---|---|---|
ENSDART00000104224 | Nonsense | 1216 | 1358 | 17 | 19 |
ENSDART00000133668 | Nonsense | 1166 | 1308 | 17 | 19 |
ENSDART00000133971 | Nonsense | 836 | 978 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 29347245)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29271172 |
GRCz11 | 17 | 29288135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGTGYTTTTCTTTTYCTGATGTTTWCTTTGAGCAGCCTGCWGGACAYTA[T/A]TTGGTGAAGAYTCAGACCAGTCCTAATGACCGCATGCTGTGGGCACTGGA
Long Flanking Sequence:
TTATTAGCAATTATGTATAATAAAATCAGTTTAAAATGTATATATTTAATTTTATACATTCATTCATTTTCTTTTCGGCTTAGTCGCCTTATTTGGACCTTACTGTAGCACAAACTAAAGTCATATTTAATGTGTACTTAGTATCAACCCTTGTGGAAAAAAAAATCCTCAAAAAGTATTTGTTTTATATAATTTCTAAACCAGATACACTGTTTACAAGAGACTTGGCAAATCCGATTCCACACTGAAATTCTGTTTAAAGCTACATTCCTACTGAAATTGAAAAAGATAAAAGTTTTGAAATGATATTCACTCATTAAGCAAATTTGGAACAAAAAAGTTTACATACTGCAACTTTAAATGTAATATTTTTAATACACAGGTCCTACAATGATCCAGTTCAGGATCATTTATGCCATTAAACACACCATATAATAGTTCACCTACCTGATGTGCTTTTCTTTTCCTGATGTTTTCTTTGAGCAGCCTGCTGGACATTA[T/A]TTGGTGAAGATTCAGACCAGTCCTAATGACCGCATGCTGTGGGCACTGGACAACAGAGGCAATGTGCTCGTACGTATCGGCATCACTGAGGAGATGCCTGTTGGGACGGCCTGGGAGCACATTCCAGGTAAGCCACCATTACATAATCCTATTCGCTGTTGTCATTTTTATTTTTTTTATTTTTTAAATAAAACTGTTAAATTTAAGTTCTTTTTTATAAGTGACTTTCTGATTGGTCATTGTTTTTTTGTTTTTTTTTTCCTGTAGGACTTCAGGCATGTCAGTTGGTTCTGAGCATGAGGACCGCTTGGGTTCGTCTTGCTAATGGGCAAGTGGCTCGTCGATACGGAATTACAGAGAAAAACCCTGCTGGAGATTACTGGAAGAAGATCCCTGGACTGGCCAGCTGCCTCGCAGGTGAGCTTTTAGGATCAATTAAGGCAAACATTAGTGTCAAAAAATAATTATAAGAATTTCTTGCTCCTCCATATTTTTTAGAT
Associated Phenotype:
Not determined