ZMP
trpc4apa
Ensembl ID:
ZFIN ID:
Description:
short transient receptor potential channel 4-associated protein [Source:RefSeq peptide;Acc:NP_57164
Human Orthologue:
TRPC4AP
Human Description:
transient receptor potential cation channel, subfamily C, member 4 associated protein [Source:HGNC S
Mouse Orthologue:
Trpc4ap
Mouse Description:
transient receptor potential cation channel, subfamily C, member 4 associated protein Gene [Source:M
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41839 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11819 | Splice Site, Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41839
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 |
---|---|---|---|---|---|
ENSDART00000019450 | Nonsense | 531 | 774 | 14 | 19 |
ENSDART00000128126 | Nonsense | 3 | 246 | 3 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 26106888)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24935713 |
GRCz11 | 11 | 25173329 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTGAGAGCTTTCTGAGAGGAGCCACATCATATGCAGACCAGATGTTTT[T/A]GCTGAAGAGAGGCTTGCTGGAGGTGAAGATCTTAATAGAACACATCAGAG
Long Flanking Sequence:
AACTCTGGGAGTCGATTTCTGAGTTCCAGTAATGGGTTCATTGACAGTTAAGGAATCAAGCCTTTTGGAGTCGACTCCCAACTTCAGAAAATTAGTTAACATTAGGGATTGGAACATAATTCTCAAGCTATTTTAAACAGATGTCTTTAATTTATTTTTTTTTTAAATGCACAAATTAGTTGTTGAATTTCTAATATATATTAGCCTTAATCATTTGCTTTCAGAAGGCAAATATTGTAATGCATCATGTCTGTGTTCTCTTGAAGGAGTTTAGTGTGTGATGGTAAAAAAGGGCTCCTCACGCGGCTCCTGACAGTTATGAAAAAAGAACCCCCAGACTCTTCCTTCAGGTGAGACACTAGATTTATAACAGTGTGTCTAAAGTTTTTTGCAATAACACATGAATAACGGCGACATATTTTCTCCCTGAAGATTCTGGCAGGCCAGAGCTGTTGAGAGCTTTCTGAGAGGAGCCACATCATATGCAGACCAGATGTTTT[T/A]GCTGAAGAGAGGCTTGCTGGAGGTGAAGATCTTAATAGAACACATCAGAGTGTCTGTATTTGGTTCGCAGAACTGGATGAGTCACTGAAATGTTGTCTTGTGATTGCAGCACATCCTCTTCTGCATCATTGACAGCGGCTGCAAGTCCAGAGATGTCCTGCAGAGCTACTTTGACCTGCTCGGGGAGCTTATGAAGTTCAATATTGATGCCTTCAAGAGATTCAACAAATATGTGAACACAGACGAAAAGGTACTTGTAGATGCTGTGGTATTGGAAAAAACTAAGGCTGTTGTTAACATTATGTGCTTGACTTTGTTGCCTCTTTTAGTTCCAGGTGTTCCTCACACAGATCAACAGCTCTCTGGTTGACTCCAACATGCTGGTCCGCTGTATTGTGCTCTCGCTGGATCGCTTCGAGAGCCAGACGGAGGATGTGAAAGGTGAATTCAGACACAGTGCTCTTGGATTGTTATTGAAAGTAATCTAAAATGTACAGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11819
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019450 | Splice Site, Nonsense | 660 | 774 | 17 | 19 |
ENSDART00000128126 | Splice Site, Nonsense | 132 | 246 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 11 (position 26110083)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24938908 |
GRCz11 | 11 | 25176524 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGYCCTTTCTTTTWAGGCTGGTCAACATCATCAACGTGCAGACCCTCACA[C/T]AGGCAAGACCACAGTGCACATCTTCTCCACCTGTTTGCCTCATTTCAGTC
Long Flanking Sequence:
TACCCCATTTGAAATCATTTCAATTAATTCTGCGGATATAATAGTACTTTTTTTTCTTAAAGCGTTGATATATATATTTCCTTGTTTAAGCTTTTGTCTTTAGTGCATGGAAACATTAAAATAGTTACATTGCTTTTTCATTTTAAGCATCCATGCACTTCAAATATGTCATAAGTGTGTAGTGTAGTAAAGAAAAATCATATGGAAATTTGCTTTAACTAGCTTTCTTGGGATTTTCTTTAAAAATCTGCTTGCTTTCAGTGATGTTGTAAATGGCTTAATCAGATGGATGGTCTGTCCAGAGCATTAGACGTGCATGTTTTCCTGGAAAATATTCTACTGGAAATAATGGCGTTGTCTATTTTGGTGGGTGTTTTTGCTTCTCTGCAGTGGTTGAAGTGCTCTCCGAGTGCTGTCTCCTGTCCTACATGGCTCGAGTGGAGAACAGGCTGTCCTTTCTTTTTAGGCTGGTCAACATCATCAACGTGCAGACCCTCACA[C/T]AGGCAAGACCACAGTGCACATCTTCTCCACCTGTTTGCCTCATTTCAGTCCTCTTGTGGTAATTATTCCTGTTTTTCTGGCTGCTATCCCAGGAGAACGTGAGTTGTCTTAACACCAGCCTGGTGATTCTGATGTTGGCCCGGAGGAGAGGCAAGCTCCCGTTTTACCTGAACGCCCTGCGGGAGAAGGAATATGCAGAGAAATATCCTGGATGCCTGCTCAACAACTTCCACAACCTGCTGCGCTTTTGGCAGCACCACTACCTCAACAAAGACAAGGACAGCACCTGCCTAGAGAATGTGAGTATTTGTAGGGTTTGGGGAACTCCGCACAATTTAGCAAATCGCAGTATGGATGTTTGGTAAATACATGTGCTACTGGTTTACCTTATGTGCTTCTTGTAAGCAGTAAACCAAATGTGCTTGAAAAGTAAAGTTGAAATCTTCACCCCCTGGTGGTGACCTGCAGTATAGGTCATATTTCTAGCCCTCTCCATGTAA
Associated Phenotype:
Not determined