ZMP
si:dkey-31j12.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate fibromodulin (FMOD) [Source:UniProtKB/TrEMBL;Acc:B0UYH4]
Human Orthologue:
FMOD
Human Description:
fibromodulin [Source:HGNC Symbol;Acc:3774]
Mouse Orthologue:
Fmod
Mouse Description:
fibromodulin Gene [Source:MGI Symbol;Acc:MGI:1328364]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21346 | Splice Site, Nonsense | Available for shipment | Available now |
sa34454 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21347 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21346
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:
A > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019822 | Splice Site, Nonsense | 52 | 418 | 2 | 3 |
ENSDART00000141516 | None | None | 362 | None | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 38601631)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37457046 |
GRCz11 | 8 | 37489480 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTAACATACATTTTATCATAAAGATATTTATATTTGTGTTCTGACAGG[A/T]AACCTGCAGTGAAAATGAGAGGCTGGATTTTACTGCTGATCCTGGCAAGG
Long Flanking Sequence:
AACCTTACTGGCGTTTCTGATGTTGCTACTTACAAGAAAGTGCTGGTCTGAGTGTGCAGTTGGGTCTCCGTACCTGCCGCTTAACCCAACCCAACAGCCGAGGACTGTGCTCGCAGATCTGAGCGTGCAGTTAGGTCTCCGGGCCTGCAGCTTCCCCTTACTCATGTGGATATGTTTTTGAACGGATTAGCAGCATCAGGCAAATATTGGGGGACAATAAGTGTTTTCTAGCACTAGGGGTTGCATGTGGTAGTGGAATCTTATAGGTGGGTTGCAGAAAAAAGGGTATGCGCTGGTAAAACAATTTCCAGCGTAATTGGCAGTACATTCCACTGACTGCGATGAGTCCTAACAAATAAGGGACTACAATTGTCAAACCTGGAAGAAAAATATATGTTATTTATGATTGATTCAAATTAAGTAATATTTATTTTACAGCTTTTGTGTGTGCATTAACATACATTTTATCATAAAGATATTTATATTTGTGTTCTGACAGG[A/T]AACCTGCAGTGAAAATGAGAGGCTGGATTTTACTGCTGATCCTGGCAAGGCTTGTCAATCTTTCCATGACACAACCAACCAACTCTTTAACCTGGCTAAGTTATCTTCGTAACCGAGCCTACAGTCATGGCTATGGTCGTAGTCACAACGGCAATTACGCTTCTCTAAGAAATGAGGATGAGCCTTCTGTGCTAGACTGCCCTTTGGAATGTGACTGCCCTCCTGCCTACCCCAAAGCAATGTACTGCAACAACCGCAAGCTACAACATGTGCCGTTTGTACCATCTCATATTAAATATGTATACTTGCAAAATAACCAGATCACAGGCATCACAAATGGGGTCTTTGATAATGCACCAAATTTAACTTGGATCATTATGCATGCAAATAAACTAACCTCTGACAAGATTGGTGATAAAGTTTTTGCCAAACTTCCAAACCTTCAGCGCCTCTTTTTACAAAACAACAACTTAAGTCGTGTTCCACAGGATTTACCACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34454
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000019822 | Essential Splice Site | 368 | 418 | 2 | 3 |
ENSDART00000141516 | Essential Splice Site | 312 | 362 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 38602583)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37457998 |
GRCz11 | 8 | 37490432 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCAGCACCAGCCTAGAGAATCTGTATCTCCAGGCCAACAAGATCAAAG[G/A]TACAGAGAAATTATTTGAAATGTTAAGCAAATGTCATAGGGCATGTCACA
Long Flanking Sequence:
CTTTTTACAAAACAACAACTTAAGTCGTGTTCCACAGGATTTACCACATTCCCTACGAGATCTACACCTGAATCACAATAATATCTCAGTGGTACCGCTTAATTCTTTCCATGGAATGAGCAACCTGACAGCTCTATATCTTCAAGCAAATGCTATAGAAGACCTAGGCAATGCACTCAAGGGTTTGCTTTCCTTGACCGTTTTAGACTTAAGAGGGAACCGATTGAAAATGATTCCACAAAGCCTGCCACCAAAGCTGAGCCAACTCTATCTTGAGTACAACTATATATCCAGCATTCCTGCTGACTTTCTGAGCCAACGGCCTGATTTGCGCTTTGTACGGCTGTCTCACAACCAGCTCACCAATGGGGGAATTCCAGCCAATGCTTTCAATGTCAGCACACTTGTTGAACTCGATTTGTCATTCAACAAGCTGGAGAGGATTCCGACTATCAGCACCAGCCTAGAGAATCTGTATCTCCAGGCCAACAAGATCAAAG[G/A]TACAGAGAAATTATTTGAAATGTTAAGCAAATGTCATAGGGCATGTCACAGCTACTCTATTTTTAAAGAAACACATTTAAGATTTCATTTGCATTCACATGCATACAATATTTAGGAGTAATTTACATTTAAGATATAATTGCTGGAAAATGTACTCATTATTTACTCACCCTTAAGAGGCTCCAAACATTTATGAGCTTTTTTCTTCTTCTGTTGAATACTAAACATATTTTAAAGAAACCTGTAATCATTGACTTTCATAATAGAAAAAAAGTAAATACTATGAAAGTCAATAGTTACAGGTTTTCAGCTTTCAATTTCAAATTAATTTAATTAATGTTTTTTTAATTTCCCCAGACCCAGATTTTCAGTTATAAATTGATAAAAAATAGAAATGTCACTAAAAGAGCAGAAAAAATCTATTGCTATCTATTGTAAATTTACACAGGAAAACAAAGTAACAACACATTAATGTTACAGTGTTACATTAACACCACTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21347
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 |
---|---|---|---|---|---|
ENSDART00000019822 | Nonsense | 400 | 418 | 3 | 3 |
ENSDART00000141516 | Nonsense | 344 | 362 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 38607878)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 37463293 |
GRCz11 | 8 | 37495727 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTATTCTAACCTGCGTGTACTGCGACTGGAGGCCAATGAAATTACCCCA[C/T]GAGATATACCCAATGAAGCGGTTCTCTGTCTGCGCCTGGCAACCAACATC
Long Flanking Sequence:
TGAATTTTCTCAAGTGAGTGGGCGGGTCAATCTGTGCTTTTTAAAAAAATACTATTGGTTGGGTTTAGGGAAAGAGGAAGGTGGGTCAGTTGATCGGTCAGTCAGTCAGTCATTCAGACAGTCAAACAGTCACTCGACAGTGGCCTCTGGTGGATTTACGCGAGAAGAGCAGGTACGAATGGCACTTACAAAAGAAATTTGAGATCTCAAAAAATGTACACAGCGGCCTCTGGGGGATTTGCAAAAACAAAAACTGCAAAAAAACGTAGCTCCTGGGACATATTTAGCGCACTCCAGAAATGTATATAGAGGTACGTTTTCAGAATGAGCCTGGGTTGAAGGAATTAATGTAAAGATTTATTCTCTGTACGTGCATGGACAAAGCAATATCTGCTTTTCATTTCCCAGAATTTTCAGTGAGCAGCTTCTGCAGAGTTGTGGACACAAACAATTATTCTAACCTGCGTGTACTGCGACTGGAGGCCAATGAAATTACCCCA[C/T]GAGATATACCCAATGAAGCGGTTCTCTGTCTGCGCCTGGCAACCAACATCGACCTGTAGGCCTGGCATCAAGCCTTCAACAGTGCATCAAATTATTGTCAGGCATGAGCTACATGTAATGAATCTATAGCTTTGCTTTGATTTGCAATTATGCTTAACAAAATTGTAAGTCTTGTGCTTTTTCTGAATTTACAACCAGTGTTAAAGTGTGAGATTAGGCTCTCTGATTCAGGAACACTAGCTATGTTTCCATCCAAAGATGTTAATTAAATTTATGCACAAAATTGAAATATTGCAGTAAAGATATGTGAATAAAGCACTAATTTAAAGTTTCCATCCAATGAGGCAAAGAGAACAAAATTGTCACTTATATCAATGATAAAATATCAGAACAAATATCCATAATAAAAACAGAATTTGCTAAGGTAGGAGAAGCTGCATGCAGAGGCGAACTGGCCATAGGGAGCACCAGGACATTTCTCGGTGGCCTGACAGTCAATC
Associated Phenotype:
Not determined