ZMP
zgc:123321
Ensembl ID:
ZFIN ID:
Description:
protein YIPF7 [Source:RefSeq peptide;Acc:NP_001032310]
Human Orthologue:
YIPF7
Human Description:
Yip1 domain family, member 7 [Source:HGNC Symbol;Acc:26825]
Mouse Orthologue:
Yipf7
Mouse Description:
Yip1 domain family, member 7 Gene [Source:MGI Symbol;Acc:MGI:1922831]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10273 | Essential Splice Site | Available for shipment | Available now |
sa22230 | Nonsense | Available for shipment | Available now |
sa31908 | Essential Splice Site | Available for shipment | Available now |
sa42143 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10273
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058064 | Essential Splice Site | None | 247 | 1 | 6 |
ENSDART00000130974 | None | None | 247 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 8797902)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 9100522 |
GRCz11 | 13 | 9432545 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAAWCAAACCAAGAACCTTCAACTCAAACTCAAGACYGGCGTAGAAAGG[T/A]AAGAGTATAACTTGATTGATGTCRCAGCTGAGATTKTGYACACACTCCTT
Long Flanking Sequence:
CAATAATTAACTGTAATCAGTTTCTAGTTACCGCTACTGCTACTATCACAGTAATTAACTGGCAACACTGTTGTTAGATACCTACTGTAATGGTTTGGTTGCAGTATTTAACTGGCAAAACTGTTGCCAGTAAGTCACTGTAATGGTTTGGTTACAGTAATGTACTGTTAAATACTGTAAACAAACCATTACAGTGACTAACTAGCAGCAGTGTTGCCAGTATTCTATTGTAAAATAGCCTGGTAAGGTCTAACAGTGTAGCAAAGTGTAAATAATAAAGTGGTCAGCACTACTTTAGTCAATTGGTCTTCAGTACATTTCCCAGATCTAGAGATCATCAGGATGGCTTTACAACTCAAGCTCATGGCCTGCAAGTAAATATAGAAAACTATTAATAGCATCACACACACAGCACAACAGCTGCTCAGTGACCAAGCAAAGCCTCAGTTCAAAAACAAACCAAGAACCTTCAACTCAAACTCAAGACTGGCGTAGAAAGG[T/A]AAGAGTATAACTTGATTGATGTCGCAGCTGAGATTTTGTACACACTCCTTCTTATTTTAAGCAGAATGGGAGACTTTCAGAACACTGAACAAGACTTCTATCAGTCTGGATATTATATTGATGGTCAACAGGAAGATGTGTATGGCTATGATCCAGCCTACCTCAATCCAGAATACAATGATGCGTAAGTGTAAAAACATCTGTGTGTGTTTGATATGCATACATATATCAGACTGTTGTTCTGTGTGCAGTTTGTATTGTTAGTTGTTCAGTTTAGTAATTAATTAAGTCATTGTATCCTGTCTGATTTTCAGGGATAATTCAGCACACTTAGCAGATGAATATGCAGCATCAGCACCTTATACTGGACAAGTGTATCAGCCTGTAGCTCAACCCGAGCAAACAGAATATACAGACTCCTATGAGGACGAACCACCTCTTTTAGAAGGTAATACAATCACTTGTTAGAAAATATCTTTAAGCTGAAATGTGTGAACAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22230
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058064 | Nonsense | 61 | 247 | 3 | 6 |
ENSDART00000130974 | Nonsense | 61 | 247 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 8798280)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 9100900 |
GRCz11 | 13 | 9432923 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTTAGCAGATGAATATGCAGCATCAGCACCTTATACTGGACAAGTGTA[T/G]CAGCCTGTAGCTCAACCCGAGCAAACAGAATATACAGACTCCTATGAGGA
Long Flanking Sequence:
ATATAGAAAACTATTAATAGCATCACACACACAGCACAACAGCTGCTCAGTGACCAAGCAAAGCCTCAGTTCAAAAACAAACCAAGAACCTTCAACTCAAACTCAAGACTGGCGTAGAAAGGTAAGAGTATAACTTGATTGATGTCGCAGCTGAGATTTTGTACACACTCCTTCTTATTTTAAGCAGAATGGGAGACTTTCAGAACACTGAACAAGACTTCTATCAGTCTGGATATTATATTGATGGTCAACAGGAAGATGTGTATGGCTATGATCCAGCCTACCTCAATCCAGAATACAATGATGCGTAAGTGTAAAAACATCTGTGTGTGTTTGATATGCATACATATATCAGACTGTTGTTCTGTGTGCAGTTTGTATTGTTAGTTGTTCAGTTTAGTAATTAATTAAGTCATTGTATCCTGTCTGATTTTCAGGGATAATTCAGCACACTTAGCAGATGAATATGCAGCATCAGCACCTTATACTGGACAAGTGTA[T/G]CAGCCTGTAGCTCAACCCGAGCAAACAGAATATACAGACTCCTATGAGGACGAACCACCTCTTTTAGAAGGTAATACAATCACTTGTTAGAAAATATCTTTAAGCTGAAATGTGTGAACAGCACTGCACACATGTACTTTCTAGACTTGAGTACACAATCCCGCCATTCACATGTACCATTTACTGTGTAGAAGCCATTTACCGTTGCTAGCCCCCTTGTCCCCCCCCCCACCCCAAATCAATGCATCAATTAAACTCACCAGAAAATCTGCTTAAAGGAAAACTGCATGTGTATTTTCATTGTTTCCCAGAGCTGGGCATTAACTTTGAGCACATCTGGCAGAAGACTCTGACTGTGTTGAATCCACTGAAGCCTGCTGATGGCAGCATCATGAACGAGACCGATCTCACCGGCCCTGTTCTCTTCTGCGTCGCTCTGGGAGCCACACTACTGATGGTACAAACTCCACCTTGAATCCATTAACTAGAGGTACATGGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31908
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 |
---|---|---|---|---|---|
ENSDART00000058064 | Essential Splice Site | 134 | 247 | 5 | 6 |
ENSDART00000130974 | Essential Splice Site | 134 | 247 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 8798865)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 9101485 |
GRCz11 | 13 | 9433508 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTCCAGAGCACATACCCGTGTGTGTGTGTGTTTATATTTGTTCCGCA[G/A]GCAGGAAAGGCACACTTTGGATATGTATACGGCATCAGTGCTCTGGGATG
Long Flanking Sequence:
TGTTAGAAAATATCTTTAAGCTGAAATGTGTGAACAGCACTGCACACATGTACTTTCTAGACTTGAGTACACAATCCCGCCATTCACATGTACCATTTACTGTGTAGAAGCCATTTACCGTTGCTAGCCCCCTTGTCCCCCCCCCCACCCCAAATCAATGCATCAATTAAACTCACCAGAAAATCTGCTTAAAGGAAAACTGCATGTGTATTTTCATTGTTTCCCAGAGCTGGGCATTAACTTTGAGCACATCTGGCAGAAGACTCTGACTGTGTTGAATCCACTGAAGCCTGCTGATGGCAGCATCATGAACGAGACCGATCTCACCGGCCCTGTTCTCTTCTGCGTCGCTCTGGGAGCCACACTACTGATGGTACAAACTCCACCTTGAATCCATTAACTAGAGGTACATGGTCTTTTGTATTGCACAGGGGACATGAAAACAGATGTAATGTCCAGAGCACATACCCGTGTGTGTGTGTGTTTATATTTGTTCCGCA[G/A]GCAGGAAAGGCACACTTTGGATATGTATACGGCATCAGTGCTCTGGGATGTGTCGGGATGTACATGTTGTTGAATCTGATGAGCATTTACAGTATATCCTGTGGAAGTGTGGCGAGTGTGCTGGGATACTCTCTGCTGCCAATGGTGGCGCTCTCTGCATTTGCTGTCGTTTATTCCCTTCAGTGAGTATCCAATAGTGTATGTAGAATTGGATTTTATTTTAGAATTGCACTTTTAGGCTACTGAATTTGTCCATTTTTATTTACAATCTCGATTATATGAACATTAATAGGCACTTTTAAAGGGAGAGTTCACCCAAAAATGAATATTACTCATGATTTACTTTCCCTCAAGTAAACCTTTGTTTACTCTCAGACAATCCTTGATCACGTTTACAGTCACTAGTTCATTTACAGTGCATGCGGAAAGTATTCGTAGCTTCCCTTCACTTTTTCCACATTTTGTTGTGACCGCTCCGTTATTACAAAATTGATTAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42143
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058064 | Nonsense | 238 | 247 | 6 | 6 |
ENSDART00000130974 | Nonsense | 238 | 247 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 8801776)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 9104396 |
GRCz11 | 13 | 9436419 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCATGAGCGGTCAGCAGCTGCTGGTGGCGTATCCATGTGCTCTTCTGTA[C/A]GGCGTCTTCGCTCTTCTCACTGTCTTCTGAAAATGCTCTGCAAAATCTGA
Long Flanking Sequence:
TCCACACAGAAATGCCAACTGACCCAGCTGAGGCTCGAACCATCGACCTTCTTGCTGTGAGGCGACAGCGCTACCCACTGTGCCACCCATGTATTTTTTTTTTACAAATAATACACATTAATTTAAGATTTTTTCAAGACTAAATAATGCTTGGATCAACTAAAGTTACAGAGATGTAATTATTTAATTAAGTGCATTTATATTTATAATAAACTAATTGTATGTATGTACTGTTCACTGCAAAGAGCCTAGAATTGTTCTTTTATAAGTGGTATTCGATGTGAAAATCATCTTTTAGAACTTATTTTTAAGAGTGAGTGTATAATTGAATTGCTTTTGAATAACGTGTGCTTTATATTTGAACACAGGGGTCTGCTGGGAACGCTGTTGGCCTTGATTGTGATTGGCTGGTGCAGTCTGTCTGCTTCTAAGATCTTCAGCTCCACTCTGGCCATGAGCGGTCAGCAGCTGCTGGTGGCGTATCCATGTGCTCTTCTGTA[C/A]GGCGTCTTCGCTCTTCTCACTGTCTTCTGAAAATGCTCTGCAAAATCTGAGCTAAGAAAGATTACTCTTTGATCAGATGACAATCCACTTTGCATTCAAAAGCACAGTCCACCCCAAAAATGAAAATGCTGTAATCATTTACTCGCCCTCCACTTGTTTATAAACTAGCCACATAGCTGAATTTCTCTGGCCCAGCTCTGGCCCACACAATCAGGTTCTGCTTGATGAATTACAGCACATGACTGGACCAAGTCTGGCCTCCAGACAAGGGCCAAACATGGCCAAGTCACAGCCAAGTTAATAACTCATAACTGGGCCAGATAAGTTGATGTTTTTCGATTGCAATTAAATTGATAAACACATGAAGCTTTGCGCTTTAGGCACACTGTAGGCATGTTTTTTTTAAAACAACCTCATAAGTAGAATTTTTTTCATTACTCAAAATTTATTTTAATATACAGTTAAAGTCAGAATTATTAGCCCCCCTTTGAATATTTGTT
Associated Phenotype:
Not determined