ZMP
atf7ip
Ensembl ID:
ZFIN ID:
Description:
Activating transcription factor 7-interacting protein 1 [Source:UniProtKB/Swiss-Prot;Acc:A0JME2]
Human Orthologue:
ATF7IP
Human Description:
activating transcription factor 7 interacting protein [Source:HGNC Symbol;Acc:20092]
Mouse Orthologue:
Atf7ip
Mouse Description:
activating transcription factor 7 interacting protein Gene [Source:MGI Symbol;Acc:MGI:1858965]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32740 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6602 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32740
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 |
---|---|---|---|---|---|
ENSDART00000101452 | Nonsense | 98 | 816 | 3 | 14 |
ENSDART00000135089 | Nonsense | 98 | 815 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 46048382)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 44885894 |
GRCz11 | 1 | 45577689 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCATCTCCATCCTTCCCAGTCTCTCGATCGCCCTCTCCACCCAACACA[C/T]AGACTACCTCACCTGCGATGGATTTGGAAGACCCCCTTGTGGCCACCGAG
Long Flanking Sequence:
GTGATCAAGGGGAAGAGAGAATTCTAGAACAGCAAGTAATATCTTTTAGATAAGTGACAGTGACACCTTGTGGTCACTCCCCTGTAAAGACATTTCTACTTGGTTAGATTAATCAGACTTGTTGAGTACCACACATAGTTTAGCTAACTAGCCTGGGATCTAGCATTTGTTTTGACATATTCTTCTGTATTTTTTTTTCACAGGTGAAAATGGAAGTAGCTGTACCTGAGGAACCTCAAAAGAAAATCTTTCGCGCACGGAAAACTATGAAGATGAGTGATCGACAGCAATTGGAAGTGCTGCACAACACCCTGGCAACCACCAACTCCAGCTTATCTTCCTCTCCACCTCAGACACCTCTGATGAACGGCACTCATACCGAGACGGAGAAAGACTTGAATAATAAGGAGGGTGACCTGATGGCACCTGCCACAGATTCAGCTCGCTGTTCCCCATCTCCATCCTTCCCAGTCTCTCGATCGCCCTCTCCACCCAACACA[C/T]AGACTACCTCACCTGCGATGGATTTGGAAGACCCCCTTGTGGCCACCGAGGAGAAAAAGGAGACAAGCAATAAAAGTTCATCCTCTTCACCTTCTGCTTCTCCTGCTGGGTTGAACTGTGACCCAGAGGTTAAAGAAGGATTTCTGTGCTTGAGCGAAGAAGATGAGACCCAAGCAGACAAAGATGAAAAAGACAGTAGTGAGGAGAAGATGAATGTAGATGCTGAGACTGAAGACCAAAAAGAGGAAAAGGATGAAAAAGATACTGATACACCTGAGAATGCAGAAGGTGAGGACATCCAACCACCCTGACATTAGAGGTTGACAGGGCTTCTCGATAGAGTTTCATTACAGAGATTGAAAAAATATGAGGTTTTGTTTACAACCTCTACGATGGACTTTCAAACAATTAAAGATCAACAATTCTGTTTCTCCAATTTGACAGAATTATCATTTTTTGTTAGCAAACTGAATATCTAAAGGAATTGTTTACAAAGAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6602
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 |
---|---|---|---|---|---|
ENSDART00000101452 | Nonsense | 593 | 816 | 10 | 14 |
ENSDART00000135089 | Nonsense | 592 | 815 | 10 | 14 |
Genomic Location (Zv9):
Chromosome 1 (position 46044439)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 44881951 |
GRCz11 | 1 | 45573746 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCATAATGTAATCNTTGTTTTATTTTTTNCTGTTGCAGMWAATCAGGCCT[C/A]GACACCAAAAACASCCTCTCAGGTAAGTCTCATTTTAAACCACGCTGGTG
Long Flanking Sequence:
CAGGATCAGCAGCAGCTGCGGCTGGTTCACCATCGGCTTCGGCATTGGCTTCTAAGACCGGTATGAGAAAATGTTTTGTGTAAAGTGTGTGTGTGTGTGTGTGTGTGTTTGTTATTTTGCTGGGGTTTTTTTTGGCCTAGGAAGGATTACAGATTTCAAAGATAAAATTTAAATCATGGAATTAATTAAATATTTTTCAAAAAACTGTTAGGTTTTCATTAATTATTATTGCAATTATTACAATTATTGCTGCTGCCTCTTTCAGTTGTTCTTCTTGTAATCACCGTTTCGTTGCATAATCCGGACACATTTGGATACATTGCCCCATTTTATTTATTTAAGTGCTTTGTAAGCTTATTTGACTTGTGTTTTAGTATACATTTTCTAGCACATTTGACTACTTTTATTATAAAGTAAGGTATAGTTTTATTTATTCTTCAGTATTTTTATTCCATAATGTAATCTTGTTTTATTTTTTTCTGTTGCAGATAATCAGGCCT[C/A]GACACCAAAAACAGCCTCTCAGGTAAGTCTCATTTTAAACCACGCTGGTGTGGAAAAAGTATTTGCCTCCTCACTGATTTTTATTTAGTTTTTCCTGAATATTAATTATCCTAATTTCAAAACTGAATGGATTACTTGTTATCTTTGACTAATATTTACATTTTGTTTGATTATCTAAAACCTAAAAGTGTGACAAACCTGCAAAAAATAAGAAATCAGTAAGGAGGCAAACTCTTTCACACCACTGTATGTGGTGATTTAAACTATATAATTGCAGGTTGCTCTATTGTAATGACTAAATTCTTCTTCTTCTCTACAGCCTGGGCGTCCTAAAGGTTCTGTGATTGATCTGACCGAAGATGATGATGATGTTCAAGGTAAAACCACTGTTGTTGATTTCTCTGTAGGTGTTCTCACATTTGCTGAAATTTAATGTCAATTAGCTAGCATTATATGAAGAACCATAATTTGCACTCAATTGAGAAACTGAGCAGCTTTGA
Associated Phenotype:
Not determined