ZMP
trps1
Ensembl ID:
ZFIN ID:
Description:
trichorhinophalangeal syndrome I [Source:RefSeq peptide;Acc:NP_001171405]
Human Orthologue:
TRPS1
Human Description:
trichorhinophalangeal syndrome I [Source:HGNC Symbol;Acc:12340]
Mouse Orthologue:
Trps1
Mouse Description:
trichorhinophalangeal syndrome I (human) Gene [Source:MGI Symbol;Acc:MGI:1927616]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9881 | Nonsense | Available for shipment | Available now |
sa9617 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9881
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056809 | Nonsense | 957 | 1243 | 7 | 7 |
ENSDART00000098145 | Nonsense | 957 | 1243 | 8 | 8 |
ENSDART00000141851 | Nonsense | 329 | 615 | 3 | 3 |
ENSDART00000056809 | Nonsense | 957 | 1243 | 7 | 7 |
ENSDART00000098145 | Nonsense | 957 | 1243 | 8 | 8 |
ENSDART00000141851 | Nonsense | 329 | 615 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 47138963)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 45781028 |
GRCz11 | 19 | 45376854 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTATCACGAGCAGAGGCCCAAGTCAAATACGAGGCTTACGGCCCCTCT[G/T]GAACCAAAAGTCACCCCAGTCCCCGTTCCACACAYGCTTTCCTCGTCAAC
Long Flanking Sequence:
CATTTGTCATTGTATTGATGTGACAAACACATATTTAAAAACTGTAAAGGGGCTATTTGTTTATATTCATAAGTACAACAGAACAATATGTTTTTTTATAAAATTTGTAAAACTCTGCTTTGCAATAAAAAAAGTTGCTTTGTCTTTCCGATTCTTCTGTCAACACAACTGGCACATGTGAAAAAATATAGTGAATATATTAAAGCCTTATTCGGTTTATCAAGTGTGTTTTCTAATCTTAAATATTTCTCTTGCAGACCCCCAGACCGCTGAACATAATCAAGCAAAACAACGGTGAGCAGATCATCCGTCGACGGACACGAAAGCGCCTGAACCCCGACCCCATGCCATCAGAGCAGGTGGGCTCCAAACAGCAGCGGGTCAACAGCGAGGAACGTCTGAACGGGAGTCCCTTAGAAAGGAGGACAGAAGACAACGGATCCGACGGATCTCTATCACGAGCAGAGGCCCAAGTCAAATACGAGGCTTACGGCCCCTCT[G/T]GAACCAAAAGTCACCCCAGTCCCCGTTCCACACACGCTTTCCTCGTCAACCAGACGCTGGAGATCCACAAGCGTATGCCTCCGCTGCATATGCACAAGAGTCCAGTGGACGGAGGATCCGCCGAGGGGAACGGGCTCAGTTTAGGACCCCAAGGCGCAGATGGGAAAGGTGGATCAGAAAGAGGCAGTCCAATCGAGAAGTACATGCGTCCATCAAAACAAGCTAGCTACTCTCCGCCTGGAAGCCCCATCGAGAAATACCAGTATCCCATCTTCAGCCTGCCGTTTCTCCATAACGACCTGCAAAACGAAACAGACTGGCTGCGCTTCTGGACTAAATATAAGATGTCTGTTCCGGGAAACGCAGCAGGTCACTATTTGAGTGCTGGACTTCCTAATCCGTGCCAAAGCTTCGTGCCTTATCCTGCCTTCAGTTTACCGCCTCACTTTCCACCTCCGACAGCTTCTGGACCCGAAAGCGATACTCCTCTTGACCTGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9617
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056809 | Nonsense | 957 | 1243 | 7 | 7 |
ENSDART00000098145 | Nonsense | 957 | 1243 | 8 | 8 |
ENSDART00000141851 | Nonsense | 329 | 615 | 3 | 3 |
ENSDART00000056809 | Nonsense | 957 | 1243 | 7 | 7 |
ENSDART00000098145 | Nonsense | 957 | 1243 | 8 | 8 |
ENSDART00000141851 | Nonsense | 329 | 615 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 19 (position 47138963)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 45781028 |
GRCz11 | 19 | 45376854 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCTATCACGAGCAGAGGCCCAAGTCAAATACGAGGCTTACGGCCCCTCT[G/T]GAACCAAAAGTCACCCCAGTCCCCGTTCCACACAYGCTTTCCTCGTCAAC
Long Flanking Sequence:
CATTTGTCATTGTATTGATGTGACAAACACATATTTAAAAACTGTAAAGGGGCTATTTGTTTATATTCATAAGTACAACAGAACAATATGTTTTTTTATAAAATTTGTAAAACTCTGCTTTGCAATAAAAAAAGTTGCTTTGTCTTTCCGATTCTTCTGTCAACACAACTGGCACATGTGAAAAAATATAGTGAATATATTAAAGCCTTATTCGGTTTATCAAGTGTGTTTTCTAATCTTAAATATTTCTCTTGCAGACCCCCAGACCGCTGAACATAATCAAGCAAAACAACGGTGAGCAGATCATCCGTCGACGGACACGAAAGCGCCTGAACCCCGACCCCATGCCATCAGAGCAGGTGGGCTCCAAACAGCAGCGGGTCAACAGCGAGGAACGTCTGAACGGGAGTCCCTTAGAAAGGAGGACAGAAGACAACGGATCCGACGGATCTCTATCACGAGCAGAGGCCCAAGTCAAATACGAGGCTTACGGCCCCTCT[G/T]GAACCAAAAGTCACCCCAGTCCCCGTTCCACACACGCTTTCCTCGTCAACCAGACGCTGGAGATCCACAAGCGTATGCCTCCGCTGCATATGCACAAGAGTCCAGTGGACGGAGGATCCGCCGAGGGGAACGGGCTCAGTTTAGGACCCCAAGGCGCAGATGGGAAAGGTGGATCAGAAAGAGGCAGTCCAATCGAGAAGTACATGCGTCCATCAAAACAAGCTAGCTACTCTCCGCCTGGAAGCCCCATCGAGAAATACCAGTATCCCATCTTCAGCCTGCCGTTTCTCCATAACGACCTGCAAAACGAAACAGACTGGCTGCGCTTCTGGACTAAATATAAGATGTCTGTTCCGGGAAACGCAGCAGGTCACTATTTGAGTGCTGGACTTCCTAATCCGTGCCAAAGCTTCGTGCCTTATCCTGCCTTCAGTTTACCGCCTCACTTTCCACCTCCGACAGCTTCTGGACCCGAAAGCGATACTCCTCTTGACCTGGCC
Associated Phenotype:
Not determined