ZMP
rassf7b
Ensembl ID:
ZFIN ID:
Description:
Ras association (RalGDS/AF-6) domain family (N-terminal) member 7b [Source:RefSeq peptide;Acc:NP_92
Human Orthologue:
RASSF7
Human Description:
Ras association (RalGDS/AF-6) domain family (N-terminal) member 7 [Source:HGNC Symbol;Acc:1166]
Mouse Orthologue:
Rassf7
Mouse Description:
Ras association (RalGDS/AF-6) domain family (N-terminal) member 7 Gene [Source:MGI Symbol;Acc:MGI:19
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1126 | Nonsense | F2 line generated | Not yet available |
| sa21058 | Nonsense | Available for shipment | Available now |
| sa41002 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1126
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 |
|---|---|---|---|---|---|
| ENSDART00000025451 | Nonsense | 141 | 427 | 3 | 6 |
| ENSDART00000131210 | Nonsense | 141 | 201 | 3 | 3 |
| ENSDART00000137059 | Nonsense | 141 | 232 | 3 | 3 |
| ENSDART00000141934 | None | None | 90 | None | 3 |
The following transcripts of ENSDARG00000003193 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 51138584)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 49408820 |
| GRCz11 | 7 | 49681596 |
KASP Assay ID:
554-1037.1 (used for ordering genotyping assays)
KASP Sequence:
CCCGAACTCGTGTGAAGCAGGTTGAAAAGCCACCTAAAGACTTCCAAGCA[C/T]GAGGTGCATCTCCATCGCCCTCTTTGTCACTTGCCCAAGCAGCTCCATCC
Long Flanking Sequence:
AAGGTGTGGGTGGATGGCATTCCCCGTGTCGTCTGTGGCCTCTCAGAAGACACATCTTGTCAGGATGTAGTCATCGCTCTTGCCCAGGCTATAGGTACGTTATAGAATACCTCTGTTTTTCTCTCTATTTTACCTTTTGACCAGCTGTATTTTAACATTTAACACTCGTAATGTCTTCTTCAGGGCAAACTGGTCGCTATGTTCTCATCCAGAAACTACGGGATAAGGAAAGGCAGCTTATGGCCAATGAATGTCCATTGGAGGCCCTTGCAAAACTTGGCCAGTTGGGCAATGAAGTGCAATTCATTCTACGTCGCACTGGCCCCACGACCAGTGAAGCACCAGACCAAAGTCGGGCCCCTAAAATACATAAACCTACAGATCCAGTTCCCATCAAACACAAAGAGCCCAAAAAAGCTCTTACGTTCAACTTGGGCCCCTCCACGTCTCCCCGAACTCGTGTGAAGCAGGTTGAAAAGCCACCTAAAGACTTCCAAGCA[C/T]GAGGTGCATCTCCATCGCCCTCTTTGTCACTTGCCCAAGCAGCTCCATCCAAAGACGCTCTCTATCAGCAGATTCTTCGACAACAAGGGCAGCTGCAGTCTTTGCAGGCGCAGCTGGAGGGATTCGAGAGGGAGCTGGGCGTTTGGGAGCGCTCTCCTCCTCCAGCACTTTCTCCTGAACTCCTTGAAGAAATGGACCGCTTACAGCAGGCTTTTAGACGGAGCGAGGCAGAGCTGGCCCATGCTAAGTTTTGGGAAGATGAGTTTCAGTCCGAGGTACAAAAAGAAAAGGACATCCTTCGGCAAAAAAATGAACTCAAAATTGCCCTAGATAAACAAAACCGAAGACTGCATGATACAGACAGCCAATCAGAGCAGCTACAGCGAGAGATTCAGGTGCTCATTGAAACCAAGAGAAATGGTATGCTTCAGGTCAAGCCCAGTGTTGAAGAATCTGTGGTTAAAGCCAAAGAGCAACTGGTCAACCATCAGCGCCACGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21058
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 |
|---|---|---|---|---|---|
| ENSDART00000025451 | Nonsense | 237 | 427 | 3 | 6 |
| ENSDART00000131210 | None | None | 201 | None | 3 |
| ENSDART00000137059 | None | None | 232 | None | 3 |
| ENSDART00000141934 | None | None | 90 | None | 3 |
The following transcripts of ENSDARG00000003193 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 51138872)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 49409108 |
| GRCz11 | 7 | 49681884 |
KASP Assay ID:
2259-9424.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCATGCTAAGTTTTGGGAAGATGAGTTTCAGTCCGAGGTACAAAAAGAA[A/T]AGGACATCCTTCGGCAAAAAAATGAACTCAAAATTGCCCTAGATAAACAA
Long Flanking Sequence:
GCAATGAAGTGCAATTCATTCTACGTCGCACTGGCCCCACGACCAGTGAAGCACCAGACCAAAGTCGGGCCCCTAAAATACATAAACCTACAGATCCAGTTCCCATCAAACACAAAGAGCCCAAAAAAGCTCTTACGTTCAACTTGGGCCCCTCCACGTCTCCCCGAACTCGTGTGAAGCAGGTTGAAAAGCCACCTAAAGACTTCCAAGCACGAGGTGCATCTCCATCGCCCTCTTTGTCACTTGCCCAAGCAGCTCCATCCAAAGACGCTCTCTATCAGCAGATTCTTCGACAACAAGGGCAGCTGCAGTCTTTGCAGGCGCAGCTGGAGGGATTCGAGAGGGAGCTGGGCGTTTGGGAGCGCTCTCCTCCTCCAGCACTTTCTCCTGAACTCCTTGAAGAAATGGACCGCTTACAGCAGGCTTTTAGACGGAGCGAGGCAGAGCTGGCCCATGCTAAGTTTTGGGAAGATGAGTTTCAGTCCGAGGTACAAAAAGAA[A/T]AGGACATCCTTCGGCAAAAAAATGAACTCAAAATTGCCCTAGATAAACAAAACCGAAGACTGCATGATACAGACAGCCAATCAGAGCAGCTACAGCGAGAGATTCAGGTGCTCATTGAAACCAAGAGAAATGGTATGCTTCAGGTCAAGCCCAGTGTTGAAGAATCTGTGGTTAAAGCCAAAGAGCAACTGGTCAACCATCAGCGCCACGGGGCTGAGCTGCTGACATCGTTTGAAGAGGTGGATAAGGCACTAAGGCTGGCGGAAGAAGAACTGCAGGTCAGTATTACTGAAACTATTACTCATAATCAAACATACTTTTTTTATTTCTTACAGCTGCATACATCAACCAAGGTGTACAGTAGATCAAGGTCTTGTGAAATTAAAATAAAAAAGTTTTTTAGATGTATCAATCAATATGTTCGTTTTAAGGATGTCTATAAGCCAATGGTCTCAAACTTAATTCCTGGAGGGCAGCAGCTTTGCATAGTTTAGCTCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41002
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 |
|---|---|---|---|---|---|
| ENSDART00000025451 | Nonsense | 421 | 427 | 6 | 6 |
| ENSDART00000131210 | None | None | 201 | None | 3 |
| ENSDART00000137059 | None | None | 232 | None | 3 |
| ENSDART00000141934 | None | None | 90 | None | 3 |
The following transcripts of ENSDARG00000003193 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 7 (position 51147379)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 49417615 |
| GRCz11 | 7 | 49690391 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCCTCATTCCATTGTGTATGTGTGTGTGTGTCTTGCAGTCCTGTCAT[C/A]AAGAGAGACATCATGGCGATAAAGTCCGGACTGCGACACAAGGAATTATT
Long Flanking Sequence:
ATGTCAATAAAGGCTTTTTAATAGTTTTTTCCACATTTTTTAAGTGTCTTGGATTGATTTTTGCTGTTTATTCAGATGAATCCCTTACCCAAAGGAATTATTAAAGCTACCACTGAGCACCTTTTGTTTCATTTTGAATTTTTACCTTTATTTTGAGCATTTATGCTGCCTTCATTGTAAAAATTCAGGTTCCACACAATTCATTCATGTTGTCTCAACACAAATCAATATATGGATAATAGTTCATTTAACAAATCTAAGTGGATTCAACATAAAACAAATCTCAAGAGTTGAGTTGTTTTAACTCATTCTAAATAGTGGCTTAACAAAATCCTTTTTTGGGTGTTTTCTTTCCTTTGTTTACACTTTCCACACCTTTTTCTCTCACGCACTCACCTTCATCCCATGTGTATTTAAAAACATGTATTAGGATCATTCTCCATAAAGGCCAGAGCCTCATTCCATTGTGTATGTGTGTGTGTGTCTTGCAGTCCTGTCAT[C/A]AAGAGAGACATCATGGCGATAAAGTCCGGACTGCGACACAAGGAATTATTCACTGTTCACTTTATATTATGTCTACTTCATTATGATTTTTTTTCTAAATATTTTAATTGTATATTCTTTTGTATGATACTCTGTGAAATGCATTCGTGAAAGTATAATACATTGATGTAAATACAGTGCTGTCTTTGTAATTATTAAATAGATTTTTTATTGTATTTTAACAACCTGCGTATATATTTCATTAGCTAAAAACATTCTGAAATAAAAAAAGATATGATTGAGAAATTTCTTGTGTCATGTTGTGTCTTGTTGATTTCCCACTCTAAATGTATTTGCTTTTATATCCATATACTTTTTATTGATTTTCATTTTAACACAATGAATGCACTAAGATAACAGACATAACATAACATAAAAAAAACATATTTAGCAAATTTTCTATACTTGTTTTTATTTTTTCCTGTTTATTTATCCTTTTGAATTGCATTACGGGACCTCAA
Associated Phenotype:
Not determined