ZMP
si:dkey-220f10.4
Ensembl ID:
ZFIN ID:
Description:
Novel tub family member protein [Source:UniProtKB/TrEMBL;Acc:Q1L8C0]
Human Orthologue:
TULP2
Human Description:
tubby like protein 2 [Source:HGNC Symbol;Acc:12424]
Mouse Orthologue:
Tulp2
Mouse Description:
tubby-like protein 2 Gene [Source:MGI Symbol;Acc:MGI:1861600]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35277 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35278 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14354 | Essential Splice Site | Available for shipment | Available now |
sa1568 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa35277
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084007 | Nonsense | 58 | 556 | 3 | 13 |
ENSDART00000091452 | Nonsense | 76 | 503 | 3 | 17 |
ENSDART00000128160 | Nonsense | 76 | 456 | 3 | 14 |
The following transcripts of ENSDARG00000062902 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 21971511)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 20497092 |
GRCz11 | 12 | 20618966 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACACGCAAACAGAAACCTGAGTGTGACGATACTGTTTTATTGATAAGC[C/T]AATCTCAAAGCAATACTTCCCTCAATGGTTTGTACACACTTACACTATAT
Long Flanking Sequence:
ATGCATTATTTATTAATGCTAAAATGTTGATAATTGTATTTTTTCCAGCTAAAGAAATGGAAGATGCAGAGGTTCGACAACAGAAGCTGGACAATCAGGTAAGATTCTAATAGATGAGTATATTTTTATTAGACATTTTCTCAAATTTGTTTTAATGTTATAAGAATAAAATGAATTTTGATCATTATTATCGTAGGTTACTTCGTGCTTAAAGAATGGAATCTAAGCACAAATAATGTTGTGAGGAAAGAATAGAAACTATATTTTTATCATTGTTTTGGAGAAATGTGTCTATACTGATGCCATTATACTGTGATTGTAATGCATAAGTGGATGTGTAACAACAGTTCATATCTTGTCAACTCTCATAGCGTTCACTTTTAATCAAGAAACAACAAAGACGAAGGGCAGATGCCCGGATGGTTACAGCGAATCCTGACATCTGTTCCAAGACACGCAAACAGAAACCTGAGTGTGACGATACTGTTTTATTGATAAGC[C/T]AATCTCAAAGCAATACTTCCCTCAATGGTTTGTACACACTTACACTATATAAACCGGAACCTCATTGCTAACATAACATCCATCTATCTATCAATCTACACTCAACAAAATTGTAAACGCAACACCTGTTGAAATTGCACCCATTTTTCATGAGCTTGAATGGCCAATTTCAGATTATTGTTCACACATTTGTCAAAATCTATGATACAGTAGTTTGTGCTTCTTCTTTGTCAATCAGTCGATCCACCTTACAGGTGTGACATATCAAGATGTTGACAGCATTATGATCAATATATTCAATCCATATCAACAGCTCTGTTGGACATTCCTGCAGTCAGTGGTATCTCTCCCTCAAAAATTTTGACATCTGTGGCATTGTGCTGTGTTATAAGAGTTGCACATTTTAGAGTGGTCTTTTATTGTGGCCAACCTAAGGCACACCTGTGCAATAATCATGCTGTGTAATCAGCATCTTGATATGCCACAGCTGTGGGGCAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35278
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084007 | Nonsense | 60 | 556 | 3 | 13 |
ENSDART00000091452 | Nonsense | 78 | 503 | 3 | 17 |
ENSDART00000128160 | Nonsense | 78 | 456 | 3 | 14 |
The following transcripts of ENSDARG00000062902 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 21971517)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 20497098 |
GRCz11 | 12 | 20618972 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAACAGAAACCTGAGTGTGACGATACTGTTTTATTGATAAGCCAATCT[C/T]AAAGCAATACTTCCCTCAATGGTTTGTACACACTTACACTATATAAACCG
Long Flanking Sequence:
TATTTATTAATGCTAAAATGTTGATAATTGTATTTTTTCCAGCTAAAGAAATGGAAGATGCAGAGGTTCGACAACAGAAGCTGGACAATCAGGTAAGATTCTAATAGATGAGTATATTTTTATTAGACATTTTCTCAAATTTGTTTTAATGTTATAAGAATAAAATGAATTTTGATCATTATTATCGTAGGTTACTTCGTGCTTAAAGAATGGAATCTAAGCACAAATAATGTTGTGAGGAAAGAATAGAAACTATATTTTTATCATTGTTTTGGAGAAATGTGTCTATACTGATGCCATTATACTGTGATTGTAATGCATAAGTGGATGTGTAACAACAGTTCATATCTTGTCAACTCTCATAGCGTTCACTTTTAATCAAGAAACAACAAAGACGAAGGGCAGATGCCCGGATGGTTACAGCGAATCCTGACATCTGTTCCAAGACACGCAAACAGAAACCTGAGTGTGACGATACTGTTTTATTGATAAGCCAATCT[C/T]AAAGCAATACTTCCCTCAATGGTTTGTACACACTTACACTATATAAACCGGAACCTCATTGCTAACATAACATCCATCTATCTATCAATCTACACTCAACAAAATTGTAAACGCAACACCTGTTGAAATTGCACCCATTTTTCATGAGCTTGAATGGCCAATTTCAGATTATTGTTCACACATTTGTCAAAATCTATGATACAGTAGTTTGTGCTTCTTCTTTGTCAATCAGTCGATCCACCTTACAGGTGTGACATATCAAGATGTTGACAGCATTATGATCAATATATTCAATCCATATCAACAGCTCTGTTGGACATTCCTGCAGTCAGTGGTATCTCTCCCTCAAAAATTTTGACATCTGTGGCATTGTGCTGTGTTATAAGAGTTGCACATTTTAGAGTGGTCTTTTATTGTGGCCAACCTAAGGCACACCTGTGCAATAATCATGCTGTGTAATCAGCATCTTGATATGCCACAGCTGTGGGGCAGTGATGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14354
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 |
---|---|---|---|---|---|
ENSDART00000084007 | Essential Splice Site | 187 | 556 | None | 13 |
ENSDART00000091452 | Essential Splice Site | 146 | 503 | None | 17 |
ENSDART00000128160 | Essential Splice Site | 99 | 456 | None | 14 |
The following transcripts of ENSDARG00000062902 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 21973198)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 20498779 |
GRCz11 | 12 | 20620653 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAAGACAAATGGAACTAAAGGGAGAGCAAAGACAGGGGAACAGTCCTG[T/A]AAGTTTACCGGAGATGTGTGTCTATTGTTAGGCTTGACACAAGTTAAAGG
Long Flanking Sequence:
CTTTTGTGTGCATATAAATTGTCTATCTGTCTGTGTCTGTATCTGTCTTTTTTAATATCAGACACACAACCTGAGCATATTTATGAAAACACAGTGGAGGAGATTTGTTTGGGAGAACTGAGTGTTTCATCCAGGACAGAAGAGGCATCAGAGGAAATTGCTCAGACTGTCCCGGTCATCATTAAGAAAATCGATCTAGAGATCAGCCCGAAGCACAGCACTACAAGCACTTTAGACACAGACGGCCAGGCAGATGAAAAGAAAACAAAGAAGAAGGGTGTGAAAAAGGGACAAACTAAACGTAAGTAGTTTTTTTCTGTTTTCAATCACACCTGTTGTGTCTGCCTTAGTTTGATGAGTCTATTTTGTTGAATTCCAGTACTTGAACCAAAAGCTGCACTGGAGGTGGAGGAAAATGAAAAGAAAGAGAAGAAATCTGTGAAGAAGAAGGAAAAGACAAATGGAACTAAAGGGAGAGCAAAGACAGGGGAACAGTCCTG[T/A]AAGTTTACCGGAGATGTGTGTCTATTGTTAGGCTTGACACAAGTTAAAGGCCATTTCCTGAAGCGCAGCTATTCATAAATAGGAAATAATTGGACATTGGCATCGTTAACATTCCGATTTTTGTATTTGTCCTCCTAGCAGTTCAGACTGATTCAGTTGTGGATTTCTCCATTAATGAAGAGAAAAAACCTGAATCAGAGAGTGAAGATGAAGGAAAAGACTGGTCAAAGAGCCCTGTTCCTCCTACACCAAAGAAAAAACAAATGAAGCCAAGTAAACGAAAAAAAAGTAACTTTTTGTTAACGATAGTGGCCTGATTGGTAAAATGCTATTTCTGTCATTGCAGTGAGATGTCATCTCAGTGACAGTGAAGAAGAAAACGATGAGAAAGAGGAGAAGGACAAGAAGAAGGAAGCTAAAAAAACACCAAAAAAGTCTAAAAAAAACACAAAAAGTGTTAACAGTCTTGCCTCTTTGAACTCCAACTATAAGGAGCACTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1568
Status:
F2 line generated
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084007 | Nonsense | 279 | 556 | 7 | 13 |
ENSDART00000091452 | Nonsense | 214 | 503 | 10 | 17 |
ENSDART00000128160 | Nonsense | 167 | 456 | 7 | 14 |
The following transcripts of ENSDARG00000062902 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 12 (position 21973687)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 20499268 |
GRCz11 | 12 | 20621142 |
KASP Assay ID:
554-1511.1 (used for ordering genotyping assays)
KASP Sequence:
AAAAAAAACACAAAAAGTGTTAACAGTCTTGCCTCTTTGAACTCCAACTA[T/G]AAGGAGCACTCTTCTGACAGTGATTCTTCCGACATCGGAAAAGTGAGTAT
Long Flanking Sequence:
GAACAGTCCTGTAAGTTTACCGGAGATGTGTGTCTATTGTTAGGCTTGACACAAGTTAAAGGCCATTTCCTGAAGCGCAGCTATTCATAAATAGGAAATAATTGGACATTGGCATCGTTAACATTCCGATTTTTGTATTTGTCCTCCTAGCAGTTCAGACTGATTCAGTTGTGGATTTCTCCATTAATGAAGAGAAAAAACCTGAATCAGAGAGTGAAGATGAAGGAAAAGACTGGTCAAAGAGCCCTGTTCCTCCTACACCAAAGAAAAAACAAATGAAGCCAAGTAAACGAAAAAAAAGTAACTTTTTGTTAACGATAGTGGCCTGATTGGTAAAATGCTATTTCTGTCATTGCAGTGAGATGTCATCTCAGTGACAGTGAAGAAGAAAACGATGAGAAAGAGGAGAAGGACAAGAAGAAGGAAGCTAAAAAAACACCAAAAAAGTCTAAAAAAAACACAAAAAGTGTTAACAGTCTTGCCTCTTTGAACTCCAACTA[T/G]AAGGAGCACTCTTCTGACAGTGATTCTTCCGACATCGGAAAAGTGAGTATAAATTCTAAAACTCAGTTTATAATTATTCATTATATTGTTTTTGCGTATGCACTTTATTAGTTGTGGTCATTTGTAAATGTGATGTGGCTTACTTCATATGTCATCCACTTCAAGTTCATTCTTAGTTAAAAAAAAAAACTACTCATTCGGTGCTTGTCTTAAATATTAGCATAACATTTATATGTGTGTGTTTGTGTGTGTAAAATAATAAATGATAGTGTAAATAATATTCATCATTTTGAAGTGGATGCATGCATCTTCTCTCTTTAGTACAGGCTTAAAAAAGTGATTAAAGTGTATTTTTCGAGGGGGAAAGTCAGACTGCCACTCTCTGTTTCTTTAAAGACCTTCAATAAGGTGTGGTGCCGCTTTTAAGATTATTTGCTGGGTAACTTTTCTGATACTTAAATTGAGAATTTAAAAAAATATATATTTTTTATTCATGCCTT
Associated Phenotype:
Not determined