ZMP
si:ch211-113e8.10
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens ZFP91, zinc finger protein 91 homolog (Mouse) (ZFP91) [Source:Uni
Human Orthologues:
AP001350.3, ZFP91
Human Descriptions:
ZFP91-CNTF readthrough transcript (ZFP91-CNTF), non-coding RNA [Source:RefSeq DNA;Acc:NR_024091]
zinc finger protein 91 homolog (mouse) [Source:HGNC Symbol;Acc:14983]
zinc finger protein 91 homolog (mouse) [Source:HGNC Symbol;Acc:14983]
Mouse Orthologue:
Zfp91
Mouse Description:
zinc finger protein 91 Gene [Source:MGI Symbol;Acc:MGI:104854]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa10025 | Nonsense | Available for shipment | Available now |
| sa17953 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10025
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000113527 | Nonsense | 48 | 761 | 1 | 12 |
| ENSDART00000135647 | Nonsense | 48 | 663 | 1 | 13 |
| ENSDART00000146917 | None | None | 216 | None | 7 |
| ENSDART00000148234 | None | None | 13 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 40524883)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 39414292 |
| GRCz11 | 1 | 40132365 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGGCATCCAGAGGACGCGGAGACGGGTGCTTCAACACCGAAGTGACCTG[C/A]CCACCCGAAACCAAYGGAGCCGCGACAAGCGCCACGGGATCAGGAAGGGT
Long Flanking Sequence:
TTCGGCTTTATCTCGACTTAAAGGAGACGCAACAAAGAGCGACAGCGGAGGGCCCTGCTAACAGCGTGGCTTACTATAGCTTTAAGAACTTTAAATAGGCTCTGGGTCTTTAAAATGAATTTTGCACAGTTATTATAGGGAGAATAGACTAAGTTTAAGATTTACGCTACTTGCATTTTTGCACCAAATTTGCAAAGGAAGTACGAGCGTCCACTAAATATGTTTGTCAATCGTATCGGGGCGGTTAGCCAGCCAACATTTTTCATAATTAATGCCTCCTCTTTATTTCACACTACGATTCAATTTGTTGAGAATTTCTGAGGTTTTCGGAAATAAGAGGAAAAAACTTCGGTAGTGATGGAGCCGCAGCTCTCGAGCAACAAAGAGGAGACGGAGAGCGAGACGGCCATAGAGAAATCCGCGGGGCAGAGTACCGCATCCAGCCCGTGCAGGGCATCCAGAGGACGCGGAGACGGGTGCTTCAACACCGAAGTGACCTG[C/A]CCACCCGAAACCAATGGAGCCGCGACAAGCGCCACGGGATCAGGAAGGGTTTTACGGGACAGGTCAACGCGGACGATCCCCGTGTGGAGGCAGACTGACATCAGCGAGGACCTGGCTGAAGTGTCACGGGACGCGTCAGGGAACCGCCGGAGGAAAGCGAAGTGCCCGCGGCGCAGGAAGAGCCCAGCAGCCGCCGCAGCCTCATCGGATGCGGGCAAAGACAGCGGCGGAGACTGCGACCTGCTGGATGAGTACGTGCCGCTTCTGTGTATTTTAGTGCTAAATAACAAGGCCTCGTTTGTGCAGATCCTACTAATGATGCTTAGCAGTTTTGTGAGTGTGTTCCTGTCACACATTCAGTCGTAATGTTGACAGACTGCAGTGTTTACATTAGCCCCAGTGACAGCAGCTCTTTCTGAGCCACTAGTTAGTTGGGCTAAAGAAATCTCAAACGCCTCATCTTTGACACTGCAAGGAGAATGTTTCAAAGTAAATAAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17953
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 |
|---|---|---|---|---|---|
| ENSDART00000113527 | Nonsense | 382 | 761 | 10 | 12 |
| ENSDART00000135647 | Nonsense | 413 | 663 | 11 | 13 |
| ENSDART00000146917 | Nonsense | 137 | 216 | 5 | 7 |
| ENSDART00000148234 | None | None | 13 | None | 3 |
Genomic Location (Zv9):
Chromosome 1 (position 40512651)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 39402060 |
| GRCz11 | 1 | 40120133 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTACGTCTGCCCTCACCCCACCTGCGGAAGACTCTTTCGGCTGCAGAAA[C/T]AATTGCTCCGCCATGCCAAGCACCACACAGGTRAGATAGRAACGCTTAAT
Long Flanking Sequence:
CTGCAATCTGTGTCCATTTAAAAGGTGTTAATTGTGCTTGAATTGGTTTTGTGAATGGCACACTTGGCATCACTCGTGTACGTGGCGAGAACGCGGTTGTAGAGCGCACCATATGTTTGGCGAAAGAAACAAATTGCAAGGAAGAGTGGTAGAAAGGCCTTTTGTGGTGATCATTTGGGCATGTCTTAGGCAATCGATTGACTTAGTACAAATTTTGACTACTCCAAACTATTTTTGTAAAAAAAAAAATTCTGCTCAGGAAAAAACCACCAGTGCAGTATGTCCGTTGTGAAATGGAAGGATGTGGTACAGTTCTGGCTCATCCACGCTATTTACAGGTAAACCTAAACTAGTGTTTCCTTCACTGACTCTTGAAGTTAGACCAGATACATTCACATAATCATTCTCTCCTGCAGCATCACATTAAATACCAACACCTGATGAAGAAAAAGTACGTCTGCCCTCACCCCACCTGCGGAAGACTCTTTCGGCTGCAGAAA[C/T]AATTGCTCCGCCATGCCAAGCACCACACAGGTGAGATAGGAACGCTTAATGTGATGCTTAAAAAATGCTGAAGTATCTTCTGTTGAGTGGTTTTGTATAAAGTAAAATTTGTATTGCAGATCAGAGAGATTATATCTGTGAGTTTTGTGCTCGCGCCTTCAAGAGTTCTCATAACCTGGCTGTGCATCGCATGATACACACCGGAGAGAAGCCACTACAGTAAGTCAAATCTCTGCAGAGTAACCTGTTTATATTAATGCTGTAGTGTTGTACATAGCTACGTAGTGCACTATATGGCTGAATAGTATTAAGATATGTTTTCAGAATGAACTTTTCGTCTTTTCTGATTGTTCTTTTCAATTACTACAACGAAAATTAACATAAAACATGCAATTGTTCAGCTTTCCACAGCACAAGAATTGTACCCCTTTTCCACCAAGGCAGTTTGAGTGTTGATTCAGAGATGGATCCTAGTCCCTAATTGGTTCTTTAGGCTTTTC
Associated Phenotype:
Not determined