ZMP
zgc:173573
Ensembl ID:
ZFIN IDs:
Description:
Zgc:173573 [Source:UniProtKB/TrEMBL;Acc:A9JRM8]
Human Orthologues:
ZFP62, ZNF268, ZNF585A, ZNF585B, ZNF624
Human Descriptions:
zinc finger protein 268 [Source:HGNC Symbol;Acc:13061]
zinc finger protein 585A [Source:HGNC Symbol;Acc:26305]
zinc finger protein 585B [Source:HGNC Symbol;Acc:30948]
zinc finger protein 62 homolog (mouse) [Source:HGNC Symbol;Acc:23241]
zinc finger protein 624 [Source:HGNC Symbol;Acc:29254]
zinc finger protein 585A [Source:HGNC Symbol;Acc:26305]
zinc finger protein 585B [Source:HGNC Symbol;Acc:30948]
zinc finger protein 62 homolog (mouse) [Source:HGNC Symbol;Acc:23241]
zinc finger protein 624 [Source:HGNC Symbol;Acc:29254]
Mouse Orthologues:
5430403G16Rik, Gm13212, Gm14124, Gm14295, Zfp26, Zfp27, Zfp619, Zfp62, Zfp658, Zfp788, Zfp808, Zfp873
Mouse Descriptions:
RIKEN cDNA 5430403G16 gene Gene [Source:MGI Symbol;Acc:MGI:1924450]
predicted gene 13212 Gene [Source:MGI Symbol;Acc:MGI:3651014]
predicted gene 14124 Gene [Source:MGI Symbol;Acc:MGI:3652002]
predicted gene 14295 Gene [Source:MGI Symbol;Acc:MGI:3709624]
zinc finger protein 26 Gene [Source:MGI Symbol;Acc:MGI:99173]
zinc finger protein 27 Gene [Source:MGI Symbol;Acc:MGI:99174]
zinc finger protein 619 Gene [Source:MGI Symbol;Acc:MGI:1917477]
zinc finger protein 62 Gene [Source:MGI Symbol;Acc:MGI:99662]
zinc finger protein 658 Gene [Source:MGI Symbol;Acc:MGI:2652821]
zinc finger protein 788 Gene [Source:MGI Symbol;Acc:MGI:1914857]
zinc finger protein 80 Gene [Source:MGI Symbol;Acc:MGI:3704127]
zinc finger protein 873 Gene [Source:MGI Symbol;Acc:MGI:3040689]
predicted gene 13212 Gene [Source:MGI Symbol;Acc:MGI:3651014]
predicted gene 14124 Gene [Source:MGI Symbol;Acc:MGI:3652002]
predicted gene 14295 Gene [Source:MGI Symbol;Acc:MGI:3709624]
zinc finger protein 26 Gene [Source:MGI Symbol;Acc:MGI:99173]
zinc finger protein 27 Gene [Source:MGI Symbol;Acc:MGI:99174]
zinc finger protein 619 Gene [Source:MGI Symbol;Acc:MGI:1917477]
zinc finger protein 62 Gene [Source:MGI Symbol;Acc:MGI:99662]
zinc finger protein 658 Gene [Source:MGI Symbol;Acc:MGI:2652821]
zinc finger protein 788 Gene [Source:MGI Symbol;Acc:MGI:1914857]
zinc finger protein 80 Gene [Source:MGI Symbol;Acc:MGI:3704127]
zinc finger protein 873 Gene [Source:MGI Symbol;Acc:MGI:3040689]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2119 | Nonsense | F2 line generated | Not yet available |
sa38415 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11168 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa2119
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058719 | None | None | 305 | None | 3 |
ENSDART00000074170 | None | None | 309 | None | 4 |
ENSDART00000112516 | None | None | 305 | None | 3 |
ENSDART00000125238 | Nonsense | 215 | 1014 | 1 | 5 |
ENSDART00000058719 | None | None | 305 | None | 3 |
ENSDART00000074170 | None | None | 309 | None | 4 |
ENSDART00000112516 | None | None | 305 | None | 3 |
ENSDART00000125238 | Nonsense | 215 | 1014 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 62970756)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 62071861 |
GRCz11 | 3 | 62308491 |
KASP Assay ID:
554-3247.1 (used for ordering genotyping assays)
KASP Sequence:
AGAAACCATTCACATGCACTCATTGTGGGAAGAGTTTCGGCCAATCATCA[C/T]AATTTAATAATCACATGAGGATCCACACTGGAGAGAAACCRTTCACATGC
Long Flanking Sequence:
TTATTCAACACATGAGGAGCCACACTGGAGAGAAACCATACACATGCACTCAATGTGGGAAGAGTTTCAGCCAGTCATCAAACTTTAATTTACACATGATGAACCACACTGGAGAGAAACCATACACATGTACCCAATGTGGGAAGAGTTTCAGCCAATCATCACACCTTAATATACACATGAGGATCCACACTGGAGAGAAACCATTCACATGCACTCAGTGTGGGAAAAGTTTCAGCCAATCATCAAACCTAAATTATCACATGAAGATCCACACTGGAGAGAAACCATTCGCATGCACCCAATGTGGGAAGAGCTTTATCAGATCAAGACACCTTAATCTGCACATGAGGATCCACACTGGAGAGAAACCATTCACATGCACTCAGTGTGGGAAGAGTTTCAGCCAGTCATCAAACTTTAATTTACACATGATGAGCCACACCGGAGAGAAACCATTCACATGCACTCATTGTGGGAAGAGTTTCGGCCAATCATCA[C/T]AATTTAATAATCACATGAGGATCCACACTGGAGAGAAACCGTTCACATGCACTCAGTGTGGGAAGAGTTTCAGCCAATTATCCAACCTTAATAATCACATGAGGATCCACACTGGAGAGAAACCATACACATGCACTCAGTGTGGGAAGAGTTTCAGCCAATTATCTAACCTTAAAAATCACATGAAGATTCACACTGGAGAGAAACCATTTACATGCACTCAGTGTGGGAAGACTTTCAACTACTCATCAACCCTTAATCAACACATGAGGATCCACACTGGAGAGAAACCATTCACATGCACTCAGTGTGGGAGGGGTTTCAGCCAAATGTCATCCCTTAGTAAACACAAAAATATCCACACTTGAGAGAAACCATTCACTTGCACTTAAGCTGCGGTCACACTGGACTTTTCTCCCCATAGACTTCCATACTTACGCGCGGATCGGAAATGCAAGTTCATGCCTTAAGTTTCGCAGTTCACTGTGTTGCAAAGTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38415
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 |
---|---|---|---|---|---|
ENSDART00000058719 | None | None | 305 | None | 3 |
ENSDART00000074170 | None | None | 309 | None | 4 |
ENSDART00000112516 | None | None | 305 | None | 3 |
ENSDART00000125238 | Nonsense | 311 | 1014 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 62971044)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 62072149 |
GRCz11 | 3 | 62308779 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAACTACTCATCAACCCTTAATCAACACATGAGGATCCACACTGGAGAG[A/T]AACCATTCACATGCACTCAGTGTGGGAGGGGTTTCAGCCAAATGTCATCC
Long Flanking Sequence:
CATTCGCATGCACCCAATGTGGGAAGAGCTTTATCAGATCAAGACACCTTAATCTGCACATGAGGATCCACACTGGAGAGAAACCATTCACATGCACTCAGTGTGGGAAGAGTTTCAGCCAGTCATCAAACTTTAATTTACACATGATGAGCCACACCGGAGAGAAACCATTCACATGCACTCATTGTGGGAAGAGTTTCGGCCAATCATCACAATTTAATAATCACATGAGGATCCACACTGGAGAGAAACCGTTCACATGCACTCAGTGTGGGAAGAGTTTCAGCCAATTATCCAACCTTAATAATCACATGAGGATCCACACTGGAGAGAAACCATACACATGCACTCAGTGTGGGAAGAGTTTCAGCCAATTATCTAACCTTAAAAATCACATGAAGATTCACACTGGAGAGAAACCATTTACATGCACTCAGTGTGGGAAGACTTTCAACTACTCATCAACCCTTAATCAACACATGAGGATCCACACTGGAGAG[A/T]AACCATTCACATGCACTCAGTGTGGGAGGGGTTTCAGCCAAATGTCATCCCTTAGTAAACACAAAAATATCCACACTTGAGAGAAACCATTCACTTGCACTTAAGCTGCGGTCACACTGGACTTTTCTCCCCATAGACTTCCATACTTACGCGCGGATCGGAAATGCAAGTTCATGCCTTAAGTTTCGCAGTTCACTGTGTTGCAAAGTTCAAGCTTGGTGAACTGTCACCTGTGAAATTGCATCACTTGACGGTGACTTTCCAAGAACGCAGAGAACTGACTTGCGTTCTTGTGGAGAGCGGTCTTGCCAGGTGTCCTCGGAAGAACGAACTTGGGAGACCGCGAGGGCAGAGAACGCGTCCTCTGAGAAATGAGATGCTGCGTTCTTCCTGATGCTCACATGGCCTTCACATGTTTTTAATGGAAAATTATTTAAACATTACAGCATTCATACAACGATTCATTGTTTTTCCCCTTTTAAAAATTTATACAATGCTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11168
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058719 | None | None | 305 | None | 3 |
ENSDART00000074170 | None | None | 309 | None | 4 |
ENSDART00000112516 | None | None | 305 | None | 3 |
ENSDART00000125238 | Nonsense | 538 | 1014 | 2 | 5 |
Genomic Location (Zv9):
Chromosome 3 (position 62976815)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 62077920 |
GRCz11 | 3 | 62314550 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATCACACCTTAATGAYCACATGAAGATCCACACTGGTGTAAAAGAGTA[T/A]ATGTGCTTTGAGTGTGACAAGACTTTTATTAAAGCTGGAGAATTGAAAYA
Long Flanking Sequence:
TGCACTCAGTGTGGGAGGAGTTTTAGCCAATCACAAAATCTTCAAAAACACATGGTGATCCACACTGGAGAGAGACCATACACATGCATTCAGTGTGGGAAGAGTTTCAGCCAACCACCATCACTTTATACACACATGAGGATCCACACTGGAGAGAAACCATACACATGCACTCAGTGTGGGAAGAGTTTCAGCCAAACATCACACCTTATTAAACACATGAGGATCCACACTGGAGAGAAACCATTTCCATGCACTCAGTGTGGGAAGAGTTTTAGCCAATCACCATCACTTTATGCACACATGAGGATCCACACTGGCGAGAAGCCATTCACTTGCACTCAGTGTGGGAAGAGATTCAGCCAATCATCACACCTTATTAAACACATGAGGATCCACACTGGAGAAAAACCATTTCCATGCACTCGGTGTGGGAAGAGTTTCAGTCGATCATCACACCTTAATGACCACATGAAGATCCACACTGGTGTAAAAGAGTA[T/A]ATGTGCTTTGAGTGTGACAAGACTTTTATTAAAGCTGGAGAATTGAAACAGCACCAGAGGGTTCACACTGGAGAAAAACCGTACGAGTGTTCACACTGCAATAAGAGATTTGGTGGTTTAGGAACCCTGAAAAAACATGAGAGGATCCACACTGGAGAGAAACCGTACGAATGTTCACTCTGCAATAAGAGATTTAATTGCACAGGAACCCTGAAAAAACATGTGAGGACTCACACTGGAGAGAAACCGTACGAGTGTTCACACTGCAATAAGAGATTTAGTTGCTCAGGAACCCTGACAAAACATGAGAGAATTCACACTCGAGAGAAACAATAGACATGATCAGAATCTTTAGAGCAGGGGTCACCAATCTCGGTCCTGAAGGGCCGGTGTCCCTGCAGGGTTTAGCTCCAACTTGCCTCAACACACCTGCCTGGATGATTCAAGTATACGTAGTAAGAGCTTGATTAGCTTGTTCAGGTGTCTTTGATTAGGGTTGG
Associated Phenotype:
Not determined