ZMP
gbp1
Ensembl ID:
ZFIN ID:
Description:
guanylate binding protein 1 [Source:RefSeq peptide;Acc:NP_001002343]
Human Orthologues:
GBP1, GBP2, GBP3, GBP4, GBP5, GBP6, GBP7
Human Descriptions:
guanylate binding protein 1, interferon-inducible, 67kDa [Source:HGNC Symbol;Acc:4182]
guanylate binding protein 2, interferon-inducible [Source:HGNC Symbol;Acc:4183]
guanylate binding protein 3 [Source:HGNC Symbol;Acc:4184]
guanylate binding protein 4 [Source:HGNC Symbol;Acc:20480]
guanylate binding protein 5 [Source:HGNC Symbol;Acc:19895]
guanylate binding protein 7 [Source:HGNC Symbol;Acc:29606]
guanylate binding protein family, member 6 [Source:HGNC Symbol;Acc:25395]
guanylate binding protein 2, interferon-inducible [Source:HGNC Symbol;Acc:4183]
guanylate binding protein 3 [Source:HGNC Symbol;Acc:4184]
guanylate binding protein 4 [Source:HGNC Symbol;Acc:20480]
guanylate binding protein 5 [Source:HGNC Symbol;Acc:19895]
guanylate binding protein 7 [Source:HGNC Symbol;Acc:29606]
guanylate binding protein family, member 6 [Source:HGNC Symbol;Acc:25395]
Mouse Orthologues:
AC113980.1, Gbp1, Gbp10, Gbp2, Gbp3, Gbp4, Gbp5, Gbp6, Gbp7, Gbp8, Gbp9
Mouse Descriptions:
Guanylate binding protein 11 [Source:UniProtKB/TrEMBL;Acc:A9YVJ5]
guanylate binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:95666]
guanylate binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:102772]
guanylate binding protein 3 Gene [Source:MGI Symbol;Acc:MGI:1926263]
guanylate binding protein 4 Gene [Source:MGI Symbol;Acc:MGI:97072]
guanylate binding protein 5 Gene [Source:MGI Symbol;Acc:MGI:2429943]
guanylate binding protein 6 Gene [Source:MGI Symbol;Acc:MGI:2140937]
guanylate binding protein 7 Gene [Source:MGI Symbol;Acc:MGI:2444421]
guanylate-binding protein 10 Gene [Source:MGI Symbol;Acc:MGI:4359647]
guanylate-binding protein 8 Gene [Source:MGI Symbol;Acc:MGI:1923324]
guanylate-binding protein 9 Gene [Source:MGI Symbol;Acc:MGI:3605620]
guanylate binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:95666]
guanylate binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:102772]
guanylate binding protein 3 Gene [Source:MGI Symbol;Acc:MGI:1926263]
guanylate binding protein 4 Gene [Source:MGI Symbol;Acc:MGI:97072]
guanylate binding protein 5 Gene [Source:MGI Symbol;Acc:MGI:2429943]
guanylate binding protein 6 Gene [Source:MGI Symbol;Acc:MGI:2140937]
guanylate binding protein 7 Gene [Source:MGI Symbol;Acc:MGI:2444421]
guanylate-binding protein 10 Gene [Source:MGI Symbol;Acc:MGI:4359647]
guanylate-binding protein 8 Gene [Source:MGI Symbol;Acc:MGI:1923324]
guanylate-binding protein 9 Gene [Source:MGI Symbol;Acc:MGI:3605620]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32993 | Nonsense | Available for shipment | Available now |
sa14292 | Essential Splice Site | Available for shipment | Available now |
sa9198 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32993
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056460 | Nonsense | 61 | 621 | 2 | 11 |
ENSDART00000140788 | Nonsense | 61 | 142 | 2 | 4 |
The following transcripts of ENSDARG00000038668 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 42133252)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42182716 |
GRCz11 | 2 | 42032134 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGACTCTACCGTACGGGGAAGTCTTACCTCATGAACCGACTAGCTGGA[C/T]AACAGACAGGTAAGGGAACCATCAAAACTTAAAGCGTTAGTTTACCCAAA
Long Flanking Sequence:
ATTAGAATAAAATAAATAAGTAAAATTAAAAACAATGTGAATAAATAAACCACCGTAATCATACAGTAGCATTTGTGTATAATCAAAGTAAAATATGATAACACTAATTTGTTGCTTTTTTAATTGTTAATCCTGTTGTGTGTTATTTTTTTAGCCCATACTGTAGTACCTACAGTAATCTATGTTTGTACATTTTTCAGACAATAAATTACAAGGAACATTAATTGTGGGAATGTTTGCATTTTTTTTCACAATAAACGAACTTTTTTGACAGGAAGGAAGAGCTAGAAAACAGACAGGAAGTGCTAGAAAGAACCAACATGTCTAAACCCACAATGATGCCTTCGCCCATTTGTTTGGTGGAGAATGTGAACGGATCACTCAGCATCTGTAAAGATGCCATAGATTTTCTCAGTAATATTAATGAGCCGGTGGTGGTGGTGTCTGTGGTGGGACTCTACCGTACGGGGAAGTCTTACCTCATGAACCGACTAGCTGGA[C/T]AACAGACAGGTAAGGGAACCATCAAAACTTAAAGCGTTAGTTTACCCAAAAGTGTAAAATATATGATTAATTACTCACTTCGTGACAACCTTGCCAAAGCTAACTGTGAGATATGTAAACGGGATTGCAAGAGGTGGAAATAAAAAGGCTACATTTAACTCAACAAACAGTTGTTGAATGTGAAATAAATAGAAAATAAGGAACGTCCTGGATCTGTTTCTTCACTCTTCTTTATTCTTTTTTATGTATGAAATATTGGATCGTGTTTCGGTATCGGTAGATACTCAAAATCAAATGACTCAGACTTGAAGGCAAAAAAAAAAAATTGATCAGGCCATCCCTAATTTTAGGTGAAAGCTCTCTCATCCACTCTAGTCAGCAATTGTCCCAACTCGTTTAAATTCCAGAAAGGTACCAAAAATATCTTTAAAACAGACCATACATTAACATGTGTTTCAAACAGAGGTATTTATGTGCGGACAATTAACAGGATAAACATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14292
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056460 | Essential Splice Site | 106 | 621 | 3 | 11 |
ENSDART00000140788 | Essential Splice Site | 106 | 142 | 3 | 4 |
The following transcripts of ENSDARG00000038668 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 42131867)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42181331 |
GRCz11 | 2 | 42030749 |
KASP Assay ID:
2259-2465.1 (used for ordering genotyping assays)
KASP Sequence:
GACACACTTTGGTTCTGCTGGACACAGAGGGACTGGGTGATGTTGACAAG[G/T]TGAGGACAAGGCCAGATTTGRTAGTTTTTTGTGWGCYGAAGTTGAAGCTG
Long Flanking Sequence:
CACACACCTGATCAAACTAATTGAGTGCTTTAGGCTTGTTTGATTCCTACAGGTAGATGTGTTGAAGCAGGGCTGAAACTAAACTCTGGAGAGCTGTGGCCCTCCCGGAATTGAGTTTGACACACTGCTTTAGCTACATCAGGGGTGTCCAAACTAGGTCCTCGAGTGCCGGTGTCCTGCAAATTTCATCTCCAACCTTAATCAAACACACCTGAACCAGCTAATCAAGCTCTTACTAGATATACTAGAAACATCCTGGCAGGTGTGTTGAAGCAAGTTGGAGCTAAACTCAGCAGGACACCGGCTTTCCAGGGCTGAGTTTGGACACCCCTGAGGTACATCATGCTAATTACAGAAATGTAATTGTCTCAGGCTTTGCTCTCGGCAACACTATTGAGTCAAAGACCAAAGGTATCTGGATGTGGTGTGTCCCTCACCCGAAAAAACAAGGACACACTTTGGTTCTGCTGGACACAGAGGGACTGGGTGATGTTGACAAG[G/T]TGAGGACAAGGCCAGATTTGATAGTTTTTTGTGAGCTGAAGTTGAAGCTGATCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCAGGGAGACTCTAAGAACGACGGCTGGATCTTCTGTTTGGCTGTTCTTCTCAGCAGTACTCTGGTGTACAACAGCCGTGGCACCATCGACAACAGCGCACTGGAGAAACTGCAGTATCCTTTAGCCTGCCAATTTCTCCTCCACATACTCCAAACTCAGTCCCGGAGGTCTGGTGTCCTGATGAGTTTATTTCAAACTGCCTTCAACACACCTGCCCGGAAGTCTCTAGTACAGGCATGTGCAAACTCGGTCCTGGAGGGCCAGTGTCCTGCAAAGTTTAGTTCCAACCCCAATCAGACACACCTGGGCTAGCTAATCAAGCTCTGACTAGGCTTTCTAGAAACATCCTTGCAGGTGTGTTGAAGCAAGTTGGAGCTAAAATCTGCAGGACACCAGCCCTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9198
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 |
---|---|---|---|---|---|
ENSDART00000056460 | Nonsense | 562 | 621 | 11 | 11 |
ENSDART00000140788 | None | None | 142 | None | 4 |
The following transcripts of ENSDARG00000038668 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 42122513)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 42171977 |
GRCz11 | 2 | 42021395 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGAGAAAGCCATCGACAGCAAACTRAAGGAGCAGGAGGAGATGCTGAAT[A/T]AAGGCTTTAAGGAGAGGGCTGATCTCCTRTCTGAGGARATCAATGATCTG
Long Flanking Sequence:
GGCGAAAATTACATGCTGTGCCTTTAAGGTGTGTCTGTATGTGTGTGTTTATGTGCAGGCCGAGGCCGTGCTGCATGAGTTTCTGAACGAACGAGGAGCTGAAGCAAACAGCATCCTCTACACAGATACAAAACTCACTGAAAACGATAAAAAGATTCAAGGTAAATCTTTGCAATGAAACGTTTGGCCCTGGAGCACTTGTAATTAAAAAAACACACACACAACATTTTAACCACATTTAAATCTTGATGTTTTTTTCTTCCTCAATCTTGATTAAACTTGCAGAGGAGAAGGAGAGGAATGCTTTGATGCAACAGAAGTGTGAGGAGGAACAGGAGAAACGAATAGAGAGCGAACGAATGATGGCGGCAGAAAAAGTGCGGCAGGATGACCAAATCAAGCAGATGCAGGAGAAGTTTGAGAAGGAACGAGAGCAAATGCAGCAGGAGACGGAGAAAGCCATCGACAGCAAACTAAAGGAGCAGGAGGAGATGCTGAAT[A/T]AAGGCTTTAAGGAGAGGGCTGATCTCCTATCTGAGGAAATCAATGATCTGAAAAAAGAGAAGAAAGGATTTATGGAAGAATACATCATGCCTATTGTTGGAGCTGCGGCACAAATCCTTCCTACAATTCTTGATTACAGAGTGATGATGAAAGGAATGAAATATGGAAAAGTAAAAATATAATTAATGTTTACATTTAAATCCCTGTTGTGACCAATTGATTGGCTGTTGACTGTTTATACAGCTTACCAGATGTAATCATGTTTATTTAGGAGCATAGTATTTAGTTTGATAAAAAGTGGTGTCCTAGATCACATAGGTGTGTACTGAAAGTATCTGCTTTGTTTCTGATGATGGAAAAATCAATGATATTAAGATTATTTCATAGCCCTTAATTGCACCTTGATTGCACATTCTGCCATATTATATGTATGGATTCAAGCATTATGTTCATTTTAATAAATTCATTAATAAAAAAAAATTCTGTTGTCACAAGTTTAT
Associated Phenotype:
Not determined