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 |
---|---|---|---|
sa42956 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10589 | Nonsense | Available for shipment | Available now |
sa15119 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42956
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000104224 | Nonsense | 199 | 1358 | 4 | 19 |
ENSDART00000133668 | Nonsense | 199 | 1308 | 4 | 19 |
ENSDART00000133971 | None | None | 978 | None | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 29369680)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 29293607 |
GRCz11 | 17 | 29310570 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGGTACTTCTGGTTTCATCCTATCAACGCTCAATGCTTTTCTACACA[C/T]AAGAGCAGTCGCATCAGCAGCTGGGCAGTAAACCACGTAAAAGGTACAGC
Long Flanking Sequence:
AAAGCATTGATAGACTTGTCGAATTGATAATGTGGTTATGTTGTGTTGTTGCAGCTGAGAAGGTTTGATGTGGTGGGTTTGCACAAAAGCACAATTACTGCATTAGCGTGGAGTGCTAATGGCATGAAACTCTTCTCTGGTGATGATAAAGGGAAGGTGGTGTACTCTGCTGTGGACCTGGACCAAGTAAGCCTTTAATAAGGAATTGATTGGAACTGTTTCAGGCACTGCGAGAGGCAATGATGCTATAAATATTAGGATAAAAGTATTTTTGACCTTGGATGGAATTAGAAAGATTTAAGACAGGATTATAAGGTCATGTTAACAACTTTGAGTTACTGTATTATGACTGAATCTCTGAATATATGTGTACATTGTTTCTTTAGGGAGTCTGTAATCCAGTGGTCCTCTTCGAAGAGCCTTCAGCAATAGTACAGTTAGAATATAGTCAAAAGGTACTTCTGGTTTCATCCTATCAACGCTCAATGCTTTTCTACACA[C/T]AAGAGCAGTCGCATCAGCAGCTGGGCAGTAAACCACGTAAAAGGTACAGCATCTTCAGTTCATCATAACATGAAAGAGATCTATTTTCGTCAGGGTTGAACTACTGAGTTTAAGCTCCATTTTTGATATGTGTCTTCATTTTTGTAGCAATGGCAAGTTTGGAGCCTGCTTCCAGCCAGCTCTGTGCAAGCAGAGTGATCTGGTGGTTTATGCAGCGAGGCCGGGGTTACGTCTGTGGAGGACAGATGTGCGAGGACGTGTCGGGGAGACTCATGTCTTAAAGCCCCTTTTTAATCAAGATGTACCTCACTTTGAGCTGTTCCCACGCTCAGGTCCCACTGGTGGATACAGACCTTCAGAAAGACAGTTAGGAATGATCAGCTGCTTCCTGAAGGAGGGCTGGGTCCTCAGCTGGAACGAATATAGTGTTTATGTTGTGGACTGCACCAATCAGGTGTGAATGGACACTTTTGGATTTATTTTATTTGCATAATTGAAAT
Associated Phenotype:
Not determined
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