ZMP
fam114a1
Ensembl ID:
ZFIN ID:
Description:
family with sequence similarity 114, member A1 [Source:RefSeq peptide;Acc:NP_001082947]
Human Orthologue:
FAM114A1
Human Description:
family with sequence similarity 114, member A1 [Source:HGNC Symbol;Acc:25087]
Mouse Orthologue:
Fam114a1
Mouse Description:
family with sequence similarity 114, member A1 Gene [Source:MGI Symbol;Acc:MGI:1915553]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24838 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa39588 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa11826 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24838
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 |
|---|---|---|---|---|---|
| ENSDART00000082063 | Essential Splice Site | 188 | 546 | 5 | 13 |
| ENSDART00000147228 | None | None | 254 | None | 6 |
The following transcripts of ENSDARG00000008287 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 17328276)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 17893444 |
| GRCz11 | 1 | 18586381 |
KASP Assay ID:
554-7812.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCACCATCATATTTATGTTCATACTAATTCATCCTTCTTGCTTTTTTTA[G/A]GGAAAGTCAGTAATAACTGGAGGTCTTGATGCTTTGGAGTTCATTGGAAA
Long Flanking Sequence:
TTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTGTACAAAACAAAACAATTGGGACTGTAAATTAGGTAATTTGACACTCTTTTGTGTGCATTATGCCTTGCAAAGCAAACAAAACATTAAATAATGAATTTTCTTTTTGTCGTCTTTAGGTCAAGGGTTTAGCTCTGTGAAAGAGAAGGCAGGTGTGGCGTTGCGGATACGTCAGAGCTCAACATGTGAGGAGGCAGAGGAGGCCCATGAGCATTCTGGGACGGAGCAGGCAGAACACGCTCATGCAGAGGAGACGCACAGAGGAGTACTGTCAACCATCAGCAGCGCTGTTCACAACACTGTGAGCCTGCACACATACAGTATTACACACAGCTTTACCATCACTGACAGGCAACAACATCAAACTCTCAACTTCATTCACTCAAGATATATTAATCTGTCATATCCACCATCATATTTATGTTCATACTAATTCATCCTTCTTGCTTTTTTTA[G/A]GGAAAGTCAGTAATAACTGGAGGTCTTGATGCTTTGGAGTTCATTGGAAAGAAGACCATGAATGTCTTAGCAGAGAGTGATCCAGGCTTTAAAAAGACTAAGATACTAATGCAAAGAACTGTCTCTCTGTCTCAGGTTAGATGCTCAGCAAATGATCAAATAACATTTTACACCATGATTACATGTCATGTGAAACACCAGGCTAATGCTAATTAATCATTAAAGGAACACTCAAATGACTTTTTCATACTTATTTTAAAATAGGCCCTTTTTTACAAGTTTGACCTTGAGTTTGACTATTGTGAATCTATTCAACCGATCTCCGGGTATGGCGGGAGTACTTTTAGCATAGCTTAGCATAAATCATTCAACTGGATTAGACCATTAGCATCTTGCTTATTAAAAGTTTCAATAATTAAGCTTGACCCCTCTGTATTTACATAATGTATCATATCGACGGAAAATTAAAAGTCACTATTTTCTTGGTTGATATTGCTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39588
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000082063 | Nonsense | 330 | 546 | 8 | 13 |
| ENSDART00000147228 | Nonsense | 97 | 254 | 3 | 6 |
The following transcripts of ENSDARG00000008287 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 17323341)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 17888509 |
| GRCz11 | 1 | 18581446 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCTTGGGCATAAAATTCATGTTATCTGTGTGTTTCAGCTGCTGATGGA[G/T]AGGAGTTTGTCAGTGTTCTTACCGAACTACTCTTTGAGCTCCACGTTGCC
Long Flanking Sequence:
TTTTTTTATTGTCTACAGAACAAGCCACTGTTATCCAATAAATCACCTAATTATCTTTACTTGCCTAGTTAACAGAATAACCTAATTAAGTCTTTAAATTACACTTTAAGCTGAATAATAGCATATTGCAAAAGAAGCAGAAAAATATTTTGCCCTGTCATGATAGCAAAAAAAGTTATTATAAATTAGTTATTAAAGTATTATGTTTAAAATTCTCTCTGTTAAACAACTATTGGGAAATATTTTTAAAAGAAAAAATAACAGAAGAGCAAATAATTTTGGCTTCGACTATAATTATTAAGCCTGTGAAATGATAATATAGTCTGTAATTCTGCTTTGAATCACTATGCTACAAGCCCAATATTGGCGAATCTCAATGAACAAACATTGATCTGATATGACAAGCGACTCAGTCAGAACGTTATAAATTTTTCAGTCCTCCCCATTTTTGCTCTTGGGCATAAAATTCATGTTATCTGTGTGTTTCAGCTGCTGATGGA[G/T]AGGAGTTTGTCAGTGTTCTTACCGAACTACTCTTTGAGCTCCACGTTGCCGCAACTCCAGACAAGCTGAACAAAGTATGGTCACACTTTTAAACACATTCATGTATATCCACTGTCAATGCAAATGTGTACTTTCTCTATCTTTCTAACACACAGACACACATGTTATTCACAAGCTACAACTCAAATCATACCATGTGCCCTGCAGGCCCGTATTAAAGCTCATGACTGGGTGCAAGAAGTGGAGAAGTCTCAGGAAGCTGTCAAGAGTGTAACGGATGAAGCTTGCCCTGCTCCAGAAAAGGAGGGACCAACAGATAAAAAGAAAGAGAAAGTTGAAGTGGGAGACAATGAGGAAAGTAATGCAAAGGATGTGAAAACAGATACTGTTGAGGTGAGATGTGTTGTCGTGTTATATATTTAGAGTGCTCAGCAAATATGAGTACACCTCATTTTGAAAATAAACATTTTTATCCATTTCTCAGTGAATATGAGTATGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11826
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 |
|---|---|---|---|---|---|
| ENSDART00000082063 | Essential Splice Site | 354 | 546 | 8 | 13 |
| ENSDART00000147228 | Essential Splice Site | 121 | 254 | 3 | 6 |
The following transcripts of ENSDARG00000008287 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 17323266)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 17888434 |
| GRCz11 | 1 | 18581371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AACTACTCTTTGAGCTCCAYGTTGCCGCAACTCCAGACAAGCTGAACAAA[G/A]TATGGTCACACTTTYAAACACATTCATGTATATCCACTGTYAATGCAAAT
Long Flanking Sequence:
AATAACCTAATTAAGTCTTTAAATTACACTTTAAGCTGAATAATAGCATATTGCAAAAGAAGCAGAAAAATATTTTGCCCTGTCATGATAGCAAAAAAAGTTATTATAAATTAGTTATTAAAGTATTATGTTTAAAATTCTCTCTGTTAAACAACTATTGGGAAATATTTTTAAAAGAAAAAATAACAGAAGAGCAAATAATTTTGGCTTCGACTATAATTATTAAGCCTGTGAAATGATAATATAGTCTGTAATTCTGCTTTGAATCACTATGCTACAAGCCCAATATTGGCGAATCTCAATGAACAAACATTGATCTGATATGACAAGCGACTCAGTCAGAACGTTATAAATTTTTCAGTCCTCCCCATTTTTGCTCTTGGGCATAAAATTCATGTTATCTGTGTGTTTCAGCTGCTGATGGAGAGGAGTTTGTCAGTGTTCTTACCGAACTACTCTTTGAGCTCCACGTTGCCGCAACTCCAGACAAGCTGAACAAA[G/A]TATGGTCACACTTTTAAACACATTCATGTATATCCACTGTCAATGCAAATGTGTACTTTCTCTATCTTTCTAACACACAGACACACATGTTATTCACAAGCTACAACTCAAATCATACCATGTGCCCTGCAGGCCCGTATTAAAGCTCATGACTGGGTGCAAGAAGTGGAGAAGTCTCAGGAAGCTGTCAAGAGTGTAACGGATGAAGCTTGCCCTGCTCCAGAAAAGGAGGGACCAACAGATAAAAAGAAAGAGAAAGTTGAAGTGGGAGACAATGAGGAAAGTAATGCAAAGGATGTGAAAACAGATACTGTTGAGGTGAGATGTGTTGTCGTGTTATATATTTAGAGTGCTCAGCAAATATGAGTACACCTCATTTTGAAAATAAACATTTTTATCCATTTCTCAGTGAATATGAGTATGTCGTAAATTCGACTTCTCATTAATTACAAATTATCAGACCGGAGGTTTTTGAATATCAGAAAATAGACTTTATTCTC
Associated Phenotype:
Not determined