ZMP
si:ch211-198b3.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate fibronectin type III domain containing 1 (FNDC1) [Source:UniProt
Human Orthologue:
FNDC1
Human Description:
fibronectin type III domain containing 1 [Source:HGNC Symbol;Acc:21184]
Mouse Orthologues:
CT485609.1, Fndc1
Mouse Description:
fibronectin type III domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1915905]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25140 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23734 | Nonsense | Available for shipment | Available now |
sa45706 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25140
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014163 | Nonsense | 599 | 1645 | 11 | 22 |
ENSDART00000136039 | None | None | 110 | None | 4 |
ENSDART00000139643 | None | None | 335 | None | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 31063827)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 31135040 |
GRCz11 | 20 | 31037919 |
KASP Assay ID:
554-7520.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAATCAAAACCCAGCAATTCTGACATTGTCCCTAAAACATCCGAGGAT[A/T]AACGTCCTCCTTGGACCCCTCGTACATCCTCAATTGTTGATATTAGTAGA
Long Flanking Sequence:
ATACTATCTTATATAAGACTTGCAATTTGTCTCCAGCTAGCAATACTCACACAAGAAACATGGACAGCCAAAGGACAAGCCAAAGTACCTCAAAAACATCATCCAACAATGAATCAGACTACCAGGAACCAGATGAAATGGAAGAGCCCAATACTCAGACCACAACTCAAGCTCCAAACACAAATAGACGTCGCCCTCTTTCGCAAACCAGATCTTATCACAGCATCTTCTCCTCTGTAAGAGGTTCAGTCAGAAACGGAGGCTCAAAATCAAACTTGCATACATCCTCCACTCATACCAAAGATAGAGAAGATGAGGAGAAGCCAACAGCAGACAGTCCAATAGAAGAGAAGACCGGAGCAAATGAGGCTACTGAGGACACAAATCCAGAGAGGAGTAACAATGCATCACCACAAACACAAGAGCATTCAAAATTGTCACCGGACACAAAGGAATCAAAACCCAGCAATTCTGACATTGTCCCTAAAACATCCGAGGAT[A/T]AACGTCCTCCTTGGACCCCTCGTACATCCTCAATTGTTGATATTAGTAGATTAAGAAGGCCTAGTTCTCGCAGTGGTTCTAGGTCAAGAATGCGGAGTGAAGATACTTCAAGTTCATCACTAAACCAAGAGTCTGCAGCTACAAGAAAGGACCTAACAGCGGTTTCCTATCCTGATGGACAAAAATCACACAACCAGATAACTGTCACTGATAGTATGCCTTCAGTTGCTTCACCTCAGGAAAACAGGCCTGAACCAGTAAAAGAATCAGAACCTTCTTCATCTATTTCTTCTTCTCCAACATATTCCTCCTCAGCATCCTCATCATCTTCTTCAGTGTCTTCCCCTTCATCATCCTTACCATCATCTTCTGGTACTAGAAGATTTTCCTCAGGAGCATCTGGAGCCAAGTATCCTAATGGAAGGAGAGTTGGTATTTCAACCAGAGGTCAAAGACTTCAAACAGGAAAGCCCAAACCTGATTCATCTTCATCTGCATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23734
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 |
---|---|---|---|---|---|
ENSDART00000014163 | Nonsense | 830 | 1645 | 11 | 22 |
ENSDART00000136039 | None | None | 110 | None | 4 |
ENSDART00000139643 | None | None | 335 | None | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 31063134)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 31134347 |
GRCz11 | 20 | 31037226 |
KASP Assay ID:
2261-4505.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGATTCCACTTCCCATTCTTCTTCAAGGACTAACCCTTCTACAACAGGA[C/T]GAAGTTCATCCTTTTCGTTACCAAACCGAAATTCTAGAATAGTTACAAGC
Long Flanking Sequence:
ACCAGATAACTGTCACTGATAGTATGCCTTCAGTTGCTTCACCTCAGGAAAACAGGCCTGAACCAGTAAAAGAATCAGAACCTTCTTCATCTATTTCTTCTTCTCCAACATATTCCTCCTCAGCATCCTCATCATCTTCTTCAGTGTCTTCCCCTTCATCATCCTTACCATCATCTTCTGGTACTAGAAGATTTTCCTCAGGAGCATCTGGAGCCAAGTATCCTAATGGAAGGAGAGTTGGTATTTCAACCAGAGGTCAAAGACTTCAAACAGGAAAGCCCAAACCTGATTCATCTTCATCTGCATCTTCACAATCCACATTGCCAACAGGAACCAGCACAGATAATCATGATACAACAGAAGTGCATGATACAAACCAAAAAATTACAAAGTTAAACACAGAGGAACTCCCAGTACCAAAGGAAAATGATGATAACGAAGAAAAGACAGTAGATTCCACTTCCCATTCTTCTTCAAGGACTAACCCTTCTACAACAGGA[C/T]GAAGTTCATCCTTTTCGTTACCAAACCGAAATTCTAGAATAGTTACAAGCAGTCGTAGGCAAGATGGCAGGATACCATGGAGTAGGTCTGCCTCATCTGTAGGTGCAGGAAGGCCAATTATCAAAGGATTTCCTTCTCGTTCTACTTCTGTCAGCTCTCAAGACACTAGTGATAAAAACAAAGTTTCACCCACTGTATACCCAAAGCATAAAGTTAATCCTGTCTCGAATAAACCAAGTCTACTAAATGTAAAAAGTAGTAATGATCATGAAGATGATTATCTATATGAGGGAAGCAAAGAGATCTGGGATAGGCAAACCAAAGATGTAGTCTCAACAACAGCACCAAAAACAACAACAGCTGTGAGCGAATCTCACAAACCTGTCCAGAATTTCGAGAATGAAAGTGTAGATAGGGAACAAAGTAGTATGAGTACAGGTTTTAAGACAGTTCCTTCAGTTCCCCATAAACTCCCTACTGTAACTTCTAATGGTCGGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45706
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 |
---|---|---|---|---|---|
ENSDART00000014163 | Essential Splice Site | 1361 | 1645 | 16 | 22 |
ENSDART00000136039 | Essential Splice Site | None | 110 | 2 | 4 |
ENSDART00000139643 | Essential Splice Site | 51 | 335 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 20 (position 31043810)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 31115023 |
GRCz11 | 20 | 31017902 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGACATTCTGAAACTCTTTTTTTCCTCTTATCTTTCCCTTCTGTCCTCA[G/A]CTCCATATGTAAACTACATTCAGAAAGACCCTGGAGCTCCCTGCTCCCTG
Long Flanking Sequence:
AAAATGGACAGATTGAGAGCCAAATCCAATTTGTGTACAGTAAGTTCAAGAGTATTTTTTTCTCTTACTCAGTTTCAAATTTTCAAAAAAAATATTACACACCACAACTGTTGAACATTGCTAACAATAAAAAAATGGATCACATGACACTAAAAACAGGAGTAAATAAATTGCACTTAAGCCTAATATTTGGTATATACAATACATACAATAGGGTTTAAACTGTGAGCCTTTATTTAATGTTTTGTCAATTGTTTTTACGTTGAAGGACTTTAGCCTTATATGGTCCACTTTTCCATCCATCATGAAACTCTTTCTGCAGGAATTCTTTTTTTCCATTGAAGATGCACTTTAAATCATCTAAAATCATGCTGGGAAACATTATCATCAGGTTTTACACAACTTGAAGTTCAATTGCCTGTGGCAAAATCAATGGCAAAACGATCCTTTCAGACATTCTGAAACTCTTTTTTTCCTCTTATCTTTCCCTTCTGTCCTCA[G/A]CTCCATATGTAAACTACATTCAGAAAGACCCTGGAGCTCCCTGCTCCCTGACTGAGGCTCTGGAGTATTTGCAAGTGGACGTTTTAGCAGACCTGATGGAGAAAGACCAACAGTCTTCCAATCAGAAGCAGCCACCCAAAAACAAGCCCCACAATGTGACTGTTGTTGCTATGGAGGGCTGTCACTCCTTTGTGATTTTGGACTGGGCGCGTCCACTAAAAGACGACATGGTGTCAGGTGAGTGAAAATCTTATATCATGAAGCAGTTCTTTTAAATAATTAAAAATGCTTGACGTTGCAGAACATCTTTTGTTCTTTTCAACACAAAGTTTGCTTAATATAATGTACTGTACAGCAACAAATATCTAAGGTAAACATTCTATTGCTTATTTTATCTTTTAAAGTTTGGAGTTGCAACACAGTGGTTTAGTGGTTAGCACTATCGCCTCACAGCAAGAAGGTTGCTGGTTCGAGTCCCAGCTGAGCCAGTTGAAATTTCT
Associated Phenotype:
Not determined