ZMP
col4a3bp
Ensembl ID:
ZFIN ID:
Description:
Collagen type IV alpha-3-binding protein [Source:UniProtKB/Swiss-Prot;Acc:Q5M7Y0]
Human Orthologue:
COL4A3BP
Human Description:
collagen, type IV, alpha 3 (Goodpasture antigen) binding protein [Source:HGNC Symbol;Acc:2205]
Mouse Orthologue:
Col4a3bp
Mouse Description:
collagen, type IV, alpha 3 (Goodpasture antigen) binding protein Gene [Source:MGI Symbol;Acc:MGI:191
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa26571 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9854 | Nonsense | Available for shipment | Available now |
sa18820 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40554 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33707 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa26571
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 |
---|---|---|---|---|---|
ENSDART00000035299 | Nonsense | 82 | 620 | 3 | 17 |
ENSDART00000092938 | Nonsense | 82 | 594 | 3 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 52614399)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50281595 |
GRCz11 | 5 | 50928188 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATCTGTTATGTTTGCTTTCTCTTTTAGCCTCATGAGTTTGATGAATGC[C/T]GATTTGACATCAGTGTGAACGACAGCATCTGGTACCTGAGGGCTGAACAT
Long Flanking Sequence:
TTAAATCTTCTTGTATTATTTATAACAAGGTGTTTGAGACATCTTTAATACTTGATCTGACAGTTAGATTCGCGTAGTTGACTTGACTCATGTATATTAATTTGCTAAAACTTCCAAGGTAGTACTTAAGCATGTACAAAACAGCGGTTTAGCAAATTGTTGAGCTGGCAAAGATGCAAGTTCGAAGATCTAATTTGTGCACTATACTTCAAGCTTATAGCTGTTGGTTTCCCCTAGATTTGTGGATGAGCTGGTCAGCAGTTTTTGTTTTACTGTTGTAATCTGCCATCCGCTGACCTATTCAATAGATGCAAATCTGTGGTTTTACGCGGAAGTTGTTAATCAGGAACAGCAGGAAAAGTAGCTCTAAAAATATGATCGTACACAATATTGATTACAAACTGCTCATACACTTTTTTTTTTTTTCATTTTCCGACTAGTTTTTTACTATAATCTGTTATGTTTGCTTTCTCTTTTAGCCTCATGAGTTTGATGAATGC[C/T]GATTTGACATCAGTGTGAACGACAGCATCTGGTACCTGAGGGCTGAACATCCTTTGCTCCGACAGCAGTGGATCGATACCATTGAACTGCATAAGGTGGGTCCCTCAGAAGAAGCTATACAGTGGCCCTTGCTGGATAATCTGCAGCTCAGCCCTAGTTTCTGTCTGATAGTGAGTGATCACATTTGGGTGGCAGAACCTGATTGGGTGTTTAATTTCCTTTGTAAAAGGAGAGGAGGGTGTTGAAGGCTCATTGCAATGAAATGTGCCCTGCATTTTTTTTTTTCAGCTGTCATTTCCTTGTGCTGTCATTAGAGTTCATAAAGAGCCACTGTATAGTACTTTACTGGATTGTTCAGTTTAGGTTGAATCTAAATATGTGTACTTTCACATGTCCTGCGTACATTAGGCAATACATTGGACAGAACTGTGTTATTAGACTGTCACATTAGAGTGATACAAACACAAACACAGTCTCCTTTTTTTATTTCCTGATGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9854
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 |
---|---|---|---|---|---|
ENSDART00000035299 | Nonsense | 273 | 620 | 7 | 17 |
ENSDART00000092938 | Nonsense | 273 | 594 | 7 | 16 |
ENSDART00000035299 | Nonsense | 273 | 620 | 7 | 17 |
ENSDART00000092938 | Nonsense | 273 | 594 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 52635990)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50303186 |
GRCz11 | 5 | 50949779 |
KASP Assay ID:
2259-6489.1 (used for ordering genotyping assays)
KASP Sequence:
TGTCCCACTGCATCGAYATTTTAGTCAAACGAGAGGAGAGCTGGCAGAAA[C/T]GACTCGATAAGGYAGTGTGCAGCAGACATTTAAAAGGATGTTTTGTCTAA
Long Flanking Sequence:
TTGTGGTCCTGTCTGAATGCAGTTTGATTACTTGGCAAAGTAGACTTTCTTTTTGTCATGTGATTACACTTTATATATACCCTTTGATCCTTTTACATCTGTTGTATAAGTGAATGTTCGCACAATGCTATAAGCCGCAAATGGTTACATAAGTTTATCTGTTTAAAGGCTAAGTGCTTTTTACTCCTTTAATGGTGGAAATCTTCCATGATGTCTATGACTGTTGTTGGGAAATAGCTTCTTTCATTCTGAGACTGAAAAGATTTCTATCTAGACTGATCACTAATTAAATCTGCATTAGTGTCTTTTATCAAAACACTTATTTGATGCTTATTTTACTTGATTTCCCCTCAGCGTTCTTTGTGAACACCCTCAAAGATCCTGCAGGCATTGATTTCAAGGGTGAAGCCATCACATTTAAAGCCACAACGGCAGGAATCCTGTCTACACTGTCCCACTGCATCGACATTTTAGTCAAACGAGAGGAGAGCTGGCAGAAA[C/T]GACTCGATAAGGTAGTGTGCAGCAGACATTTAAAAGGATGTTTTGTCTAAAAATAAACTTTCTGTTATCATTAATTTTGCAAACCTGCATGAATTTGTCTAACTAGAATACAAAAAAGGACATTTTTGACAGTTTGGGGTCAGTAAGATGTATTTTTAATAAAATTTAAAAAGTAATTTATAGTTCTATTAAACAGGGATACATAATTATCATCAAAATCAAATTGGGGATGTCAAGTTTTTATGAATTCTCTAAATTTGGTGAAAATGATGTTTATAACATTTATTTCAATATGTAATCGTTTGATAAGGTGTGGGAATGTAGGAAATCACTCACACACACACACACACACACAGACAATTTGAGAGTGTCTGAAGATATCTACATTTCGGCAAGGGCTGAGGTAAAAAAATTTTTTACATAAAGATCTGCCTTTTACTTCCTTTCCTTTTATGAAAAAAATCCGGGAGACTCCAGGATGTAAAAACAGAGATATAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18820
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 |
---|---|---|---|---|---|
ENSDART00000035299 | Nonsense | 273 | 620 | 7 | 17 |
ENSDART00000092938 | Nonsense | 273 | 594 | 7 | 16 |
ENSDART00000035299 | Nonsense | 273 | 620 | 7 | 17 |
ENSDART00000092938 | Nonsense | 273 | 594 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 52635990)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50303186 |
GRCz11 | 5 | 50949779 |
KASP Assay ID:
2259-6489.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCCCACTGCATCGACATTTTAGTCAAACGAGAGGAGAGCTGGCAGAAA[C/T]GACTCGATAAGGTAGTGTGCAGCAGACATTTAAAAGGATGTTTTGTCTAA
Long Flanking Sequence:
TTGTGGTCCTGTCTGAATGCAGTTTGATTACTTGGCAAAGTAGACTTTCTTTTTGTCATGTGATTACACTTTATATATACCCTTTGATCCTTTTACATCTGTTGTATAAGTGAATGTTCGCACAATGCTATAAGCCGCAAATGGTTACATAAGTTTATCTGTTTAAAGGCTAAGTGCTTTTTACTCCTTTAATGGTGGAAATCTTCCATGATGTCTATGACTGTTGTTGGGAAATAGCTTCTTTCATTCTGAGACTGAAAAGATTTCTATCTAGACTGATCACTAATTAAATCTGCATTAGTGTCTTTTATCAAAACACTTATTTGATGCTTATTTTACTTGATTTCCCCTCAGCGTTCTTTGTGAACACCCTCAAAGATCCTGCAGGCATTGATTTCAAGGGTGAAGCCATCACATTTAAAGCCACAACGGCAGGAATCCTGTCTACACTGTCCCACTGCATCGACATTTTAGTCAAACGAGAGGAGAGCTGGCAGAAA[C/T]GACTCGATAAGGTAGTGTGCAGCAGACATTTAAAAGGATGTTTTGTCTAAAAATAAACTTTCTGTTATCATTAATTTTGCAAACCTGCATGAATTTGTCTAACTAGAATACAAAAAAGGACATTTTTGACAGTTTGGGGTCAGTAAGATGTATTTTTAATAAAATTTAAAAAGTAATTTATAGTTCTATTAAACAGGGATACATAATTATCATCAAAATCAAATTGGGGATGTCAAGTTTTTATGAATTCTCTAAATTTGGTGAAAATGATGTTTATAACATTTATTTCAATATGTAATCGTTTGATAAGGTGTGGGAATGTAGGAAATCACTCACACACACACACACACACACAGACAATTTGAGAGTGTCTGAAGATATCTACATTTCGGCAAGGGCTGAGGTAAAAAAATTTTTTACATAAAGATCTGCCTTTTACTTCCTTTCCTTTTATGAAAAAAATCCGGGAGACTCCAGGATGTAAAAACAGAGATATAAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40554
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035299 | Nonsense | 403 | 620 | 12 | 17 |
ENSDART00000092938 | Nonsense | 377 | 594 | 11 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 52644953)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50312149 |
GRCz11 | 5 | 50958742 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTGGTTTTGTTCACAGGTTGAGGAGATGGTGCACAGTCACATGACGTA[T/A]TCTTTACAGGATGTTGGTGGAGATGCTAACTGGCAACTGGTTGTTGAAGA
Long Flanking Sequence:
CCCACTTTAACTGACTCCCCCACGCACACACGCACACTCCTACACACTTGCTCTGTCAAAGCACATTGGCTTCTTCGTGACTGATTATGCAATTTGTCTCATCGCTGATGGTGGATGCGCTCTGTCAAATCTTTGGAGCTTTTGTTTTTTTACATTTGTAAAATTGCCTTTGTTCCAGTTCCTCTCTCTGAAATGTGCTTTACAGTGGCAGTCTGCTCTGTATTCTCTGGGTGATGATCAGATTTTAATTTCCGTCTCGTTTCATTGAGCTCTTTCTCTCTGGCTTTCTGTCTCTTGGGTTCAGCCTCACAGTCACACGTCCTCCTTGTCCTCCGTCGACCTCATAAGTGCCTCAGATGACGTGCACAGGTTCAGTGCTCAGGTAGAGAGAGTTGGTGAACTTGACTTGAAATAATGCTTTTGTTGTCTTGTATACTTTTAGTGACCTCTCGGTGGTTTTGTTCACAGGTTGAGGAGATGGTGCACAGTCACATGACGTA[T/A]TCTTTACAGGATGTTGGTGGAGATGCTAACTGGCAACTGGTTGTTGAAGAAGGAGATATGAAGGTGAGAGGTTTATTGACCTTTAAAGGTGACTTCTGAAGCCATTGTGTTATATCTTAGAATAGAAAACGGCATTTATTAAAATAACAATTGTTTTCATTTGCTGTGATTTAAACATAAGAGTCAATCCATCAAACATTGTATAAAGATGTTTAAAAACATGGCATCCACTTGCCACTTTATTAGGTACACCTTACTAGAACCGGGTTGGACCCCATAGATTCAACAAGTAACTGGAAGTATTAGTTGAGATTTTGGTCCATACTGACATGATCACAGTTGCTGCAGATTTGTCAGCTGTCTTGTTCCACCACATTCCAAAGGAGCTCTATTGGATTGAGATCTAGTGACTGTGGAGGCCATTTGAGTACAGTGAACTCATTGTCATGTTTAAGAAACCAGTCTGAGATGATTTGCACTTTATGACATGGCACAATATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33707
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000035299 | Nonsense | 522 | 620 | 15 | 17 |
ENSDART00000092938 | Nonsense | 496 | 594 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 5 (position 52649215)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 50316411 |
GRCz11 | 5 | 50963004 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGTTATGCGTAAAATTCTGTCCACCAATGAGAACGATCCAGACACCTG[G/A]CTGGTCTGCAACTTCTCAGTGGATCATGATGGTTATCCAGTGAGTTCCTG
Long Flanking Sequence:
CCCAATGTCTGGGTGAAGGAGTAATAGAAATATATACAATAAAGACTTTTGTCTCTGATATTTTTTTTACAACAAATCAACACAAAATAATGCCTTAAGTATTGCCGAAATTTTTAAATAAAGCCACAGCAAAATCAGTTATTTTAGGCTGCAAAATTCAGAACAAAGTCTTACAATGTCCTGGAGGGACTGATTGAAGATCAGATAAGCTGAAGCATTTTGGATCATTTTTAGTGTCATAATAGTGCATGATGGTCCAGTCAGAAAAGCATGTTTTGGAGCATTGCTGTAAATAATGTTTCCAGTAATTGGCCTGATCTGAGTACCCTAACATGTTGCTTATTGTGTGATTTTTTTTTTTCTAAAATAATTTTATATATCCTTTTTTTTTCCTTTTCTGCTCTTTGACAGAGAGTGTGGCCTGCTTCCCAACGAGATGTGCTTTATGTGTCAGTTATGCGTAAAATTCTGTCCACCAATGAGAACGATCCAGACACCTG[G/A]CTGGTCTGCAACTTCTCAGTGGATCATGATGGTTATCCAGTGAGTTCCTGCTTTTGAAGCCATTTTTGATGTCATATAGCCTTTTTACTGCAAGCATATACACACAAATTGTACGTCAGGTTACTTTTTTCTGTTTTTCAGCCTTCTACTAGATGCATTCGTGCCAAAATCAACGTAGCCATGATCTGTCAAACACTAATCAGCCCACCAGAGGGAGACAAAGAAATCAGCAGAGACAACATCATCTGTAAAATCACATATGTCGCCAATGGTGAGTCTAGCAGTGCAATAATGGTGGTTGTTATCAGGGTTTGAGGTTTGCCTACATTCCACCACACAAAATACATATAATAAAATAATAAATAAAAAAAAAACTAATCTTCCAGCAGGGTTCTTAAAAGTGTATATGCTAATGTTCAAAAGTTTGGGGTCAGGATTCTTTTTTAAGCTGTTTATGTAATAAAGTATATAACAGTTACGGTTATAACAACTGCTTCAAA
Associated Phenotype:
Not determined