ZMP
si:ch211-1n9.11
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate tachykinin receptor family [Source:UniProtKB/TrEMBL;Acc:B8A5E6]
Human Orthologue:
TACR2
Human Description:
tachykinin receptor 2 [Source:HGNC Symbol;Acc:11527]
Mouse Orthologue:
Tacr2
Mouse Description:
tachykinin receptor 2 Gene [Source:MGI Symbol;Acc:MGI:98477]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42186 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17156 | Nonsense | Available for shipment | Available now |
sa11002 | Nonsense | Available for shipment | Available now |
sa22285 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42186
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 |
---|---|---|---|---|---|
ENSDART00000110745 | Nonsense | 41 | 376 | 1 | 5 |
ENSDART00000142129 | Nonsense | 17 | 329 | 1 | 5 |
The following transcripts of ENSDARG00000074509 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 23105402)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22834740 |
GRCz11 | 13 | 22965190 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCTGTTCGAGCAGCCGGACTGGCAGGTGGCATTATGGGCGATTGCATA[T/A]ACTTTGATCGTAATTATTTCCTTCATTGGCAATGTCACAGTTATTTGGAT
Long Flanking Sequence:
TGTCCACGGTTAGCGCGTCAAGTGCATGCCAATTAAATATTTTGATTATTGGCAGATTTTCGGAACGCAGGATGGATGCTGCGCGTCATTGCGCGCTGGCAAAGATGCTTTACTCAACGTCACTGCATTGGACCCGACACACCTCCAATACTTGGCACACATTCCTTCAGTTTTCCACCATCCCTGCAGGCGCAAAAACGCACTTCAGCCGGCAGTTTGGACATAAAGCGGCACATAGCGCACTGACCACTCACTGGAGAATGAACTGCTGCAAATGCCTAAAATACACAGTTTTACCATGCCATAGCATCAGAATAGTGAGTCATTCAATGGAATAAGCAAAAAGATTTATGTCTTGAGATTTTATGGACAATTACAATGGATACCACTTTGGACCCCCTTTCATCATCTCTTCTGTATTACGATGAAGATGGAAACGAAACATCCATTAATCTGTTCGAGCAGCCGGACTGGCAGGTGGCATTATGGGCGATTGCATA[T/A]ACTTTGATCGTAATTATTTCCTTCATTGGCAATGTCACAGTTATTTGGATCATTCTGGCGCATAAACGCATGAGGACAGTGACCAACTACTTCATTGTCAACCTCGCCTTCTCTGATGCCTCTATGGCAACTTTTAACACCGTTTTTAATTTCGTTTATGCTTTGCACAATGACTGGTATTTTGGTTTAGGATATTGTAAATTTCAAAACTTCTTCCCAATAACAGCAATGTTCTCAAGCATTTATTCAATGGCCGCTATTGCAGTTGACAGGTAAGCAGACTAAACAAATTATAAGGTGTGTGTTAATGTGCGTGTGCGTGTGCGTGTAATGTAATAGTGCTTTTACACCTTAACATGTTCCCCCAGTTTGGTAATAATAAATATTTATTGCACAACAATGAGATTATATGTTATAAATCATGTATTATAAAGACTGCAAGTTCCTAAAAAATAGCAGTGATAAAACACGTAAACTATAAGATTATGAAGTTCTGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17156
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 |
---|---|---|---|---|---|
ENSDART00000110745 | Nonsense | 104 | 376 | 1 | 5 |
ENSDART00000142129 | Nonsense | 80 | 329 | 1 | 5 |
ENSDART00000110745 | Nonsense | 104 | 376 | 1 | 5 |
ENSDART00000142129 | Nonsense | 80 | 329 | 1 | 5 |
The following transcripts of ENSDARG00000074509 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 23105590)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22834928 |
GRCz11 | 13 | 22965378 |
KASP Assay ID:
2260-6349.1 (used for ordering genotyping assays)
KASP Sequence:
CACMGTTTTTAATTTCGTTTATGCTTTGCACAATGACTGGTATTTTGGTT[T/A]AGGATATTGTAAATTTCAAAACTTCTTCCCAATAACAGCAATGTTCTCAA
Long Flanking Sequence:
GGCGCAAAAACGCACTTCAGCCGGCAGTTTGGACATAAAGCGGCACATAGCGCACTGACCACTCACTGGAGAATGAACTGCTGCAAATGCCTAAAATACACAGTTTTACCATGCCATAGCATCAGAATAGTGAGTCATTCAATGGAATAAGCAAAAAGATTTATGTCTTGAGATTTTATGGACAATTACAATGGATACCACTTTGGACCCCCTTTCATCATCTCTTCTGTATTACGATGAAGATGGAAACGAAACATCCATTAATCTGTTCGAGCAGCCGGACTGGCAGGTGGCATTATGGGCGATTGCATATACTTTGATCGTAATTATTTCCTTCATTGGCAATGTCACAGTTATTTGGATCATTCTGGCGCATAAACGCATGAGGACAGTGACCAACTACTTCATTGTCAACCTCGCCTTCTCTGATGCCTCTATGGCAACTTTTAACACCGTTTTTAATTTCGTTTATGCTTTGCACAATGACTGGTATTTTGGTT[T/A]AGGATATTGTAAATTTCAAAACTTCTTCCCAATAACAGCAATGTTCTCAAGCATTTATTCAATGGCCGCTATTGCAGTTGACAGGTAAGCAGACTAAACAAATTATAAGGTGTGTGTTAATGTGCGTGTGCGTGTGCGTGTAATGTAATAGTGCTTTTACACCTTAACATGTTCCCCCAGTTTGGTAATAATAAATATTTATTGCACAACAATGAGATTATATGTTATAAATCATGTATTATAAAGACTGCAAGTTCCTAAAAAATAGCAGTGATAAAACACGTAAACTATAAGATTATGAAGTTCTGATTTCAGCTGCTTTTTATTCTTTCTTGCTGGACATATATAGTTAGAATTTGGATATCAAACCAATTTATGTGATTGATCAGGTGGTCAGACATCTGGTTAAAGAGCTCTTTTTTCCCAATAGGAATGCAGAATTTTAGTACCATAGAAAGTATAAAAAATGCCACTAAACGTTTAGAATAAAATAATTAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11002
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 |
---|---|---|---|---|---|
ENSDART00000110745 | Nonsense | 104 | 376 | 1 | 5 |
ENSDART00000142129 | Nonsense | 80 | 329 | 1 | 5 |
ENSDART00000110745 | Nonsense | 104 | 376 | 1 | 5 |
ENSDART00000142129 | Nonsense | 80 | 329 | 1 | 5 |
The following transcripts of ENSDARG00000074509 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 23105590)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22834928 |
GRCz11 | 13 | 22965378 |
KASP Assay ID:
2260-6349.1 (used for ordering genotyping assays)
KASP Sequence:
CACMGTTTTTAATTTCGTTTATGCTTTGCACAATGACTGGTATTTTGGTT[T/A]AGGATATTGTAAATTTCAAAACTTCTTCCCAATAACAGCAATGTTCTCAA
Long Flanking Sequence:
GGCGCAAAAACGCACTTCAGCCGGCAGTTTGGACATAAAGCGGCACATAGCGCACTGACCACTCACTGGAGAATGAACTGCTGCAAATGCCTAAAATACACAGTTTTACCATGCCATAGCATCAGAATAGTGAGTCATTCAATGGAATAAGCAAAAAGATTTATGTCTTGAGATTTTATGGACAATTACAATGGATACCACTTTGGACCCCCTTTCATCATCTCTTCTGTATTACGATGAAGATGGAAACGAAACATCCATTAATCTGTTCGAGCAGCCGGACTGGCAGGTGGCATTATGGGCGATTGCATATACTTTGATCGTAATTATTTCCTTCATTGGCAATGTCACAGTTATTTGGATCATTCTGGCGCATAAACGCATGAGGACAGTGACCAACTACTTCATTGTCAACCTCGCCTTCTCTGATGCCTCTATGGCAACTTTTAACACCGTTTTTAATTTCGTTTATGCTTTGCACAATGACTGGTATTTTGGTT[T/A]AGGATATTGTAAATTTCAAAACTTCTTCCCAATAACAGCAATGTTCTCAAGCATTTATTCAATGGCCGCTATTGCAGTTGACAGGTAAGCAGACTAAACAAATTATAAGGTGTGTGTTAATGTGCGTGTGCGTGTGCGTGTAATGTAATAGTGCTTTTACACCTTAACATGTTCCCCCAGTTTGGTAATAATAAATATTTATTGCACAACAATGAGATTATATGTTATAAATCATGTATTATAAAGACTGCAAGTTCCTAAAAAATAGCAGTGATAAAACACGTAAACTATAAGATTATGAAGTTCTGATTTCAGCTGCTTTTTATTCTTTCTTGCTGGACATATATAGTTAGAATTTGGATATCAAACCAATTTATGTGATTGATCAGGTGGTCAGACATCTGGTTAAAGAGCTCTTTTTTCCCAATAGGAATGCAGAATTTTAGTACCATAGAAAGTATAAAAAATGCCACTAAACGTTTAGAATAAAATAATTAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22285
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110745 | Essential Splice Site | 197 | 376 | 2 | 5 |
ENSDART00000142129 | Essential Splice Site | 173 | 329 | 2 | 5 |
The following transcripts of ENSDARG00000074509 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 23106998)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 22836336 |
GRCz11 | 13 | 22966786 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGTATGGTGGAATGGCCTGACGATTATGGAGGGAAACATCAGCTCTC[G/A]TAAGAAATGACTTTGCATGTTGTGGTGGGATTTGTGCTCTGAAAAGTTTT
Long Flanking Sequence:
TGTGTTCTGATGACAGGAGTCTGATTTAGAGACCAACAAGAAGATGATAGTAATAAAACAGGGGAAAAAGTAACTCAACCAAATCAATCCTCTCTTTCTGGGTGGGCTCCAGTGTAAAATTATGCATGCAGTAATTCATGTTCAAAAGCAGCCCTGTAATGCATTGAATGTCTTTAGAAGGGAGAGTCACTAAAATGACATTGAGCCTATTTTGTTTTTTATAAACATATATCAAATTTATGGTGGGACATCAGTTAAAGGCATATAGTCACTTTCATTAAGATGTTGTTGGCTGAAATCCACAGATATATGGCCATAATCCATCCTCTGAAGCCCAGACTGTCCTCCACCACTACTAAACTTCTGATCGGGGTCATCTGGACCGTGGCTTTTTCTTTGGCATTTCCTCAGTGTTATTATGCCAGCACCAAGTTTTACTTCCCGCGGACTGTTTGTATGGTGGAATGGCCTGACGATTATGGAGGGAAACATCAGCTCTC[G/A]TAAGAAATGACTTTGCATGTTGTGGTGGGATTTGTGCTCTGAAAAGTTTTCACATTTTATATGTTTATGCACACACTGGCCCACTTCATTAAGCACATCTGTTGAGCTGTTTTTTCCCATATCTGAGGAATGAATGTAGTAGGTGTGGTAAAGGCAATCTGATGAAGTTCCAACAGAGCACCTGAATGAAAAGAAAGGTTATTAAAGTGATTTTAAACATGGCATTACAGATGACCTGGTCTGAGAATTTCAGATGTTCACTATCAGAGATTTAAAGAGTATTTAAAGTTGTAGTTTTGTGACCAAAAGTGTATTGTTGAGGTCAGAGGAGAATGACCAGACTGATTAAAGTCAAAAGAAGTTCAAACATTGTTAAAAATGAGGTCTGAAAAAGAGCTTCTCTGAATGCACAACAACACTATTAACACCTTGAAGCAGATGAGCTACAGCAGTAGAAAATCACACAGATGATTGTCAGTTTATCGATTATTGTCAGTTTA
Associated Phenotype:
Not determined