ZMP
rasgef1ba
Ensembl ID:
ZFIN ID:
Description:
Ras-GEF domain-containing family member 1B-A [Source:UniProtKB/Swiss-Prot;Acc:Q6DHR3]
Human Orthologue:
RASGEF1B
Human Description:
RasGEF domain family, member 1B [Source:HGNC Symbol;Acc:24881]
Mouse Orthologue:
Rasgef1b
Mouse Description:
RasGEF domain family, member 1B Gene [Source:MGI Symbol;Acc:MGI:2443755]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20496 | Nonsense | Available for shipment | Available now |
| sa20495 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20496
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 |
|---|---|---|---|---|---|
| ENSDART00000097880 | Nonsense | 44 | 494 | 3 | 15 |
| ENSDART00000127123 | Nonsense | 23 | 473 | 2 | 14 |
| ENSDART00000137801 | Nonsense | 64 | 514 | 3 | 15 |
The following transcripts of ENSDARG00000033614 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 41337828)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39131720 |
| GRCz11 | 5 | 39731873 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTCCAGTGATGTATGGATCCACCAATGGATACAACAAGAATCTCTAC[A/T]AGGCCAAGGAAGAGGACTATGAAGGCTTGTATTACCATGACAACAACCTG
Long Flanking Sequence:
TTTACACGTCCACGTGAGGTAAAAGCACCATGAAGATTAATTTGTTGGTGTTTGTGAGTGAAATCCGCCAGCGGTACATTCAGCTGATATCTTGGTGGATTAGAGCCAGCGAGCGTGAGTCTGAAATTTTCACAGAATGGAGATTAAACTCAAGTTCTCACAAGCTCAATCATGAAAGGTGTTTGCACATTGAGATTAATCACGACATGTTAATCTCTGCGAGTCGTCCATCCGAAGAAGAGTAATTTTCCACTCAGCCTCCTGTAATGATACTGGGGACCTTTCGTTTTACGCAAAGGTAAACAATGTTCTAAGGAGGACCGAGGATTGGCATTAATGAAATGGTTATTGGTCTATATCAGTGTATGTTTTTCATTTGAGGTTTATCTGAGGCTTATCTGACCTGCCTTTCTTTATTTTCTCAACAGGACAAAATGCCTCAGACGCCACCCTTTCCAGTGATGTATGGATCCACCAATGGATACAACAAGAATCTCTAC[A/T]AGGCCAAGGAAGAGGACTATGAAGGCTTGTATTACCATGACAACAACCTGATATCTGGGTCCTTGGAAGCTCTTATTGAGCACTTGGTTCCTACAGTGGCGTACTATCCAGATGTGAGTGTGCAAATATTCAGCAGTTTCAGATATTGTTTTTTACTTTGAACTTTGTCAAAACATTGTAACCATAAAACACATTTAATAATTGAAGTCAGAATTATTAGCCCCCCTCTTTATTTTTTCCCCCAATTTCTGTTTAATGAAAGAAATATATATTTTTTCAACACATTTCTGAACATAATAGATTTAATAACTCATTTCTAATAACTGATTTATTTCATCTTTGCCATGATGACAATAAATAATATTTGCCTAGATATTTTTCAAGACACTTCTATACAGTTTAACGTGACATTTAAAGGCGTAACTAGGTTAATTGGGTTAACTAGGCAGGTTAAGGTAACTAGGCAAGTTATTGGAAAATTATGTTTTGTTCTGTAGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20495
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000097880 | Essential Splice Site | 264 | 494 | 7 | 15 |
| ENSDART00000127123 | Essential Splice Site | 243 | 473 | 6 | 14 |
| ENSDART00000137801 | Essential Splice Site | 284 | 514 | 7 | 15 |
The following transcripts of ENSDARG00000033614 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 41330832)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 39124724 |
| GRCz11 | 5 | 39724877 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGTTTGTTCAGGCGTTTGTTCAGAAAGACCCTCTTGATAATGACAAG[G/A]TAACACTTTCTTCCTGTTTATGGGCAGTTAAAAATACACACGGCACAAAT
Long Flanking Sequence:
GTAATTCTGGTCAATAAAAGCAGGGTTGTAAATCCTGATCTTGTGTGTGTCTTCAGCTGTATCGTAAGGCGGTGCAACAGATGACACAAACGCTGATCCGTAAGCTCACCACACTGAGTCAGTATGAAGAAGCGCTGGCCAAGATCAACTCCTCGGTGACGGACAGACTAACCGTGCTGAAGACCAAACCGCAGTCCATCCAGAGAGACATTCTGACCATCTGCAACGACCCCTTCACCCTGGCACAACAACTCACACACATTGAACTGGTGAGAGGAATTTCCTCAGTTTACACAACCTCACATTCCTCACCTCACCCTGTGCTTGGACTGATTTGTTTACTAAATCAATAATCTAGGGCTATTTTTAGGGTGACCATTTGGGCGAAATGCAAAGGTGACGTTGATCTCATGTTTGTTTTTCAGGAAAGGCTAAGCTACATCGGACCGGAGGAGTTTGTTCAGGCGTTTGTTCAGAAAGACCCTCTTGATAATGACAAG[G/A]TAACACTTTCTTCCTGTTTATGGGCAGTTAAAAATACACACGGCACAAATGTTATCTCTTGCACTTACAACAACAAATATCCAAATCAATAGTCGCCATGTTTACGTTAACCCTCGGGTTCAAAGTGGTGTCACCTTTTTCACGGCACATTCCTCTCCTAATCTGTCAGCGTCCAAGTTTCTCTCCTCACGTTCCACACACTGTCCTTTTGTAGCCAAAGCCTAGCAACTGGTTTCTCACAATAACCCGCCAAAAGTTTGCTCAGCCCTGCCTCGTAATGCCCATTGCTGTCTGGCTGCTAGGCAACAGCCTGTGTCGTGGCGGTACTGGTGCGATTTTTCTCTTTTGTTCTGGTCGTCGTCTCTCCAGAGGGTCCCTGTGCACGGCCGTGGCTCTCTGATGTTGTCCGTCAAAGGTGGTGTAGGGTGGATCGTGTATTGTGTGACGGACCGCACAGTCAGAGTGTAGGAATGCGAGGAATGAAGGGTTAGAGTGACCTA
Associated Phenotype:
Not determined