ZMP
si:rp71-15d4.2
Ensembl ID:
ZFIN ID:
Description:
zinc finger protein 692 [Source:RefSeq peptide;Acc:NP_001116748]
Human Orthologue:
ZNF692
Human Description:
zinc finger protein 692 [Source:HGNC Symbol;Acc:26049]
Mouse Orthologue:
Zfp692-ps
Mouse Description:
zinc finger protein 692, pseudogene Pseudogene [Source:MGI Symbol;Acc:MGI:2144276]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18471 | Nonsense | Available for shipment | Available now |
sa1641 | Nonsense | F2 line generated | Not yet available |
sa41179 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18471
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113340 | Nonsense | 192 | 503 | 3 | 11 |
ENSDART00000134124 | Nonsense | 192 | 503 | 4 | 12 |
The following transcripts of ENSDARG00000078434 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 20523121)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 19953018 |
GRCz11 | 8 | 19985103 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAGGAACCARTCACAGATACAGAAAGACAAGAAATGATGACTAGATTA[A/T]AAACCAGACAGCAACAGAGAGAAGATGCTGGCAMTRACACAAATAAAATG
Long Flanking Sequence:
TTCTTGCTGTGAAGCAATAGTACTACCCACTGAGCCACCGTGTCACCTGCTTTAAATCTTTGTGCACTTTTTTTTATTATTGTTTTTATCATTGATAATCTGTGGCATTAAATCAATTGAACTTAGGTGATGGGAAAGAAGAGACTGTATCAACTACAAAGGAGTCTTTGCAGGAACTCATCTTGATGGTCCACAACCATGGACAGACGTGTCCCCTTCCTCCTGTCCTGCAGTGTAGGCCTGTTCAAAAAACAAAACTATCAACACGCAGTCAGAGTGGAAGAATAGAGGCTGCTACTGAGCCCAAGAAATTAGCAGAAGCGGATGAGTGTTTTAAATATACATGTGAAGATGGACATCATTTTATGTGGTGTCCTTTTAACCTGGAGAAGGTACTGATTTCTAAAAATGAAGGAGATAAAATTACATCCGAACAAGGCAAGAGACAGATGAAGGAACCAGTCACAGATACAGAAAGACAAGAAATGATGACTAGATTA[A/T]AAACCAGACAGCAACAGAGAGAAGATGCTGGCACTAACACAAATAAAATGCTTGGACAAAATAAAAATGCAGGTGAATGCTTTTTCTTTAATAAATAATAATTAATAATAATAATATTTTTTTTTTCAAGGACTAACTATACACTGTAAAAAATTTGACCTTAAATTCACAGTAAATTACTGGCTAATAATTGCATTACTTTCACAGTAAATTACTGTATGTAAATTCACAGTAAATTATTGTGAGGTAGTTCACAGTAATTTACTGTGGTTTTGTCACATTAAATTATTGTGAAATTACAACCATATATTGTAACTTTACAGTAGATAATAAAGTCCGTTACTGTGATTTCACAGTATTATCTTGTAGAATTAACTATATTTTACTGTGAATTTGCAATATGATTACTGTGATTTAGCAGTAGGTTGCAGTTTAAATACCTGATTTAACTGTAAAGTTACAGTTATATCCCGGATTACTGTAATTTAACAGTTTGGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1641
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 |
---|---|---|---|---|---|
ENSDART00000113340 | Nonsense | 465 | 503 | 11 | 11 |
ENSDART00000134124 | Nonsense | 465 | 503 | 12 | 12 |
The following transcripts of ENSDARG00000078434 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 20535669)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 19965566 |
GRCz11 | 8 | 19997651 |
KASP Assay ID:
554-1581.1 (used for ordering genotyping assays)
KASP Sequence:
GAAAAGAGAGAYAATGTTACGGCTCACCGTAGCAAGAGTCACCCAGACTA[T/G]AATACAGGCACTCTGGAAAGATCTCTTCCCCTTCCTCCCTCTGACCCACT
Long Flanking Sequence:
TAATAGAGATGAGTTGATGTTTTTTTTCCTGCTGTTCCTGTTAATACGTTTTTCTCCCTGTGCTTCTTTATGTCTGTGAGATCAGCGAGACTATATCTGTGAGTTCTGTGCTCGGGCGTTTCGAACCAGCAGTAACCTGATCATCCACCGCAGGATACACACCGGAGAGAAGCCGCTGCAGTATGAGTTTCACCACATATTCATTAGGCCTTTTGTTTATGCCAAAGGATTGTGTAACTCCCAACTCATTTTTTAACAAACTTTCAATCAATATTGAACACAACTAGATTGCTCAAGGGTCTTTTATGACAGCTTTTTCTATCTTTCCTTTTGAGGTGTGAAGTGTGTGGCTTCACCTGTCGACAGAAAGCCTCTCTGAATTGGCACATGCGGAAACACAATGCTGAGAGCACCTACCAGTTCCCTTGTGAGATCTGCGGCCGTCGCTTTGAAAAGAGAGACAATGTTACGGCTCACCGTAGCAAGAGTCACCCAGACTA[T/G]AATACAGGCACTCTGGAAAGATCTCTTCCCCTTCCTCCCTCTGACCCACTCCTGCATCCCTCGAGGCACCGCGGATCTTCCCCTTCTGTTTCCAAGAATCAACCCACTGCAGAATAAGAGTTGTGACAACAGTTTGAACACTCTTGACCTCAAGCAATCTCTAATGTGGGATTGGTTGGTAAACAAAATCTCCATGCGGTGCCTTAATAATGTTGTTAGTTCTTATTTTGTTTTTGTTTTTTAGATTTTTTTCAGAGACCGTGAATAGACCATCAGTATACACAGGTCAGTATTTGACAAATTGAGTACGCTTACATGGACACCAATAATCTGATCTGAATACTATTAAGACAATACTCTGATTGATAGTCTACCATGTAAACAGCGAGTTTTGATTAATTTAATAAAATTAAGACATATGCTGATTTTAGCCGCATTATTGAAGTGCAGTACAGACATGTAAACTATGTCAAACTATTTTCATCATGTAGTTTTATCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41179
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 |
---|---|---|---|---|---|
ENSDART00000113340 | Nonsense | 499 | 503 | 11 | 11 |
ENSDART00000134124 | Nonsense | 499 | 503 | 12 | 12 |
The following transcripts of ENSDARG00000078434 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 20535769)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 19965666 |
GRCz11 | 8 | 19997751 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGCATCCCTCGAGGCACCGCGGATCTTCCCCTTCTGTTTCCAAGAAT[C/T]AACCCACTGCAGAATAAGAGTTGTGACAACAGTTTGAACACTCTTGACCT
Long Flanking Sequence:
GAGTTCTGTGCTCGGGCGTTTCGAACCAGCAGTAACCTGATCATCCACCGCAGGATACACACCGGAGAGAAGCCGCTGCAGTATGAGTTTCACCACATATTCATTAGGCCTTTTGTTTATGCCAAAGGATTGTGTAACTCCCAACTCATTTTTTAACAAACTTTCAATCAATATTGAACACAACTAGATTGCTCAAGGGTCTTTTATGACAGCTTTTTCTATCTTTCCTTTTGAGGTGTGAAGTGTGTGGCTTCACCTGTCGACAGAAAGCCTCTCTGAATTGGCACATGCGGAAACACAATGCTGAGAGCACCTACCAGTTCCCTTGTGAGATCTGCGGCCGTCGCTTTGAAAAGAGAGACAATGTTACGGCTCACCGTAGCAAGAGTCACCCAGACTATAATACAGGCACTCTGGAAAGATCTCTTCCCCTTCCTCCCTCTGACCCACTCCTGCATCCCTCGAGGCACCGCGGATCTTCCCCTTCTGTTTCCAAGAAT[C/T]AACCCACTGCAGAATAAGAGTTGTGACAACAGTTTGAACACTCTTGACCTCAAGCAATCTCTAATGTGGGATTGGTTGGTAAACAAAATCTCCATGCGGTGCCTTAATAATGTTGTTAGTTCTTATTTTGTTTTTGTTTTTTAGATTTTTTTCAGAGACCGTGAATAGACCATCAGTATACACAGGTCAGTATTTGACAAATTGAGTACGCTTACATGGACACCAATAATCTGATCTGAATACTATTAAGACAATACTCTGATTGATAGTCTACCATGTAAACAGCGAGTTTTGATTAATTTAATAAAATTAAGACATATGCTGATTTTAGCCGCATTATTGAAGTGCAGTACAGACATGTAAACTATGTCAAACTATTTTCATCATGTAGTTTTATCGCATTTTGTGACAGGATAGTCTATACACACACACGACTGTTTGACACTATTCTCTGCACCTACCAAGTCAGTGAAGGACCACAGACATCTGCATCGTGAAAT
Associated Phenotype:
Not determined