Busch Lab

ZMP

col4a1

Ensembl ID:
ENSDARG00000055009
ZFIN ID:
ZDB-GENE-081105-114
Description:
Novel type IV collagen alpha chain protein [Source:UniProtKB/TrEMBL;Acc:B8JK27]
Human Orthologue:
COL4A1
Human Description:
collagen, type IV, alpha 1 [Source:HGNC Symbol;Acc:2202]
Mouse Orthologue:
Col4a1
Mouse Description:
collagen, type IV, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:88454]

Alleles

There are 12 alleles of this gene:

Allele Name Consequence Status Availability
sa21437 Essential Splice Site Available for shipment Available now
sa16923 Nonsense Available for shipment Available now
sa34560 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa21437
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000077296 None None 1601 None 50
ENSDART00000130442 Essential Splice Site 26 1644 2 52
Genomic Location (Zv9):
Chromosome 9 (position 8714870)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 8694713
GRCz11 9 8673043
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGCCTCCTAGTGTTTCAAAGCTGACATAATTTTTCATCTTTTTCTTTC[A/T]GGGTGGATGCTCGGGGTCTTCATGTGGTGGTTGTGACTGCAGCGGTGTTA
Long Flanking Sequence:
ATTGTGAGCATTCAGTAGCATTTTGTGTTATTATTAACACATTGTTCATCTCAAATAAATATAAAGTGCAGTTTTACTTGAGCCAACACAAAAAGTAACTTTTATATTGTAGTGAAATATTAAATCTCTGTCTTTAAAGCCTTTAGCTTATGTGTCTGTTTCAGACCCTGCACATATTAAATACATTTCTCGTAGCTGTCCTGGAGTAAAATATTGTTAAAAAAATGACTAATGTGGATCAATACTGTTCAACATGAAATCATGCCACTTTCTTCTATTAGCATTTTCTAAAAGCTTACATGTCCAAAATGATGTTGATTTATTCACGCTATCAACATTTTTCTGTTTAATTCTAAGCCATCAGTAGATTTTACCAGAATGTTCTCTTCATTGCCACCCTTGAGTCTCTGTACTCCATTAACCCATTTTGAATGCCTTTATCATGTATTTGCTGCCTCCTAGTGTTTCAAAGCTGACATAATTTTTCATCTTTTTCTTTC[A/T]GGGTGGATGCTCGGGGTCTTCATGTGGTGGTTGTGACTGCAGCGGTGTTAAAGGGGCAAAGGTGGGCATGTTTTCTTCTACTTCCTGCCATATTACCTATGTTGCATCATTTAAGATCAACAATAGTAAATATCTTTATTTGTTGTGATGGAAAATCAAGGATATTCCACCAAATATTATTATCTAAACCACTAATTATTATTGTTACCACACATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCATTCCTTCGTTCATTCGTTCATTTGTTCAATTAATCATAAATGAATGAATGAATGAATGAATGAATGAATAAATGAATGAAAGCATTATTTTATTTTAAATGTGGAAGAAATTGGATTTCTCCTTTATAGATAAAACGATTATTATCACTTTACTCAAACTCAATCCTACACAGTAGTATACACAGTAAAGAAAAATGATTAGCAAGTGATCTCCTTTCCCCACATAGCAATAAACATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16923
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000077296 Nonsense 765 1601 30 50
ENSDART00000130442 Nonsense 803 1644 32 52
Genomic Location (Zv9):
Chromosome 9 (position 8697648)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 8677491
GRCz11 9 8655821
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCTTGGTAATGTCCCAGGCCAGTCTGGAATAAAGGGTGACAAGGGTTA[T/A]CAAGGACTACCTGGTTTGGACATGCCTGGCCCTCCAGGAGACAGAGGTAG
Long Flanking Sequence:
TCACCCTGTCTATAAGAGTGTGCCCTGCCACCCTGCAAAGGAAACTCATTTCAGCCGCTTGTTTCCGAGATTTTGTTCTTTCGGTCATGACCCAAAGCTCATGACCATAGGGGAGAATAGGAACAAAGATTAGCAGTTAGGTACAGAAAGGTAGTTATATTATAATATATTATTATAGGACTGTGTATGATTGATGGCTTACACAAATGTAGGGGGTAATTAGAAGTGTTATAATAGCTCCTGATTAATTTTGTTACTTTTGCAGGTAACCCTGGACCACCTGGAGTCCATGGTGCACTAGGGCCACCAGGTCCTCCAGGACTGGGAGAACCTGGAGCTCCTGGACCAATGGGGCCACCTGGAGGCCCTGGACCTATTGGTGAGATGTTTCTATTGCCTAGCACCCACACTTACATGCCCAGATGTTCACATTTGACATAGTTTGTGACAAGTCTTGGTAATGTCCCAGGCCAGTCTGGAATAAAGGGTGACAAGGGTTA[T/A]CAAGGACTACCTGGTTTGGACATGCCTGGCCCTCCAGGAGACAGAGGTAGCCCTGGTGTCCCAGGTCTACCAGGATCAAAGGGTTTGCCTGGGCAACCAGGAGTTCCTGGAAAAGATGGCTTTCCTGGCGAACGTGGTGAGTGTTTACTCCTTGCCATCTAATAAAGCCTATTAGATGCTGATTTTTTGTTGCTCAAAAGAATTCATATTTGAATTTGTTTTTCAGGTCCAAAAGGAGAAATTGGAATCATGGGAATGGCAGGACCACCAGGATTTCAAGGTTTAGTTGGAAATCCTGGAGATCCTGGGCAAAAGGGTATGTGAACACACAATAGAAACAATTTCTATCATTCATTCATTCATTTTTTTTTTCGGCTAAGTCTCTTTATTAATATGGGATCACCACAGCGGAATGAACCACCAACTTATCCAGCATATGTTTTAAGCAGCGGAGGATCTTCCAGCCACAACCCAACACCCATACACTCTTGCATTCACAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34560
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000077296 Nonsense 923 1601 33 50
ENSDART00000130442 Nonsense 961 1644 35 52
Genomic Location (Zv9):
Chromosome 9 (position 8693177)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 8673020
GRCz11 9 8651350
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGTGACCCTGGTATGCCAGGAAAAGATGGAATGCCAGGGTCACCTGGA[C/T]AGCCAGGTTTGTCCCTAAAGCAATCATATGAAGTAAAAAAATAGTTGGAT
Long Flanking Sequence:
GTGAAATGGTCATTTTTTTCCACTTAGACTTACTTTGCATCCTGTAAATAGCGAATGCGCTTATGGCGCAACGCAGCTGGCTCTTAAAGGGAATGGGAGATGAGACTCTAATTGGTTTATTCTCAAAACACACCTATAACTCATAAAGAAAATAAACTCAACCCTTTAAGACCATGCGCCATGGCGCAAAGCAGATTTTCCCGTCCTTAAATTAACAAAAATGCGTTCTGACATGCCCTGAAAGCGTTTGCGCCCTGCGTTTTGCACTCTGCGCATGGACCGTCAAAATAGAGCCCTTGAAGTTGAAAGCCTTAATCATATATAAACCTGAGCACATTCAATTTCAGAGGCTTGTTGGGGCTCTAAAATTAAACTCATTAGACTTTGTGTTTTAACCTTGTTTTGCAGGTGATCCTGGTCCTACTGGAGAAAAGGGGTTTCCTGGAACATCTGGTGACCCTGGTATGCCAGGAAAAGATGGAATGCCAGGGTCACCTGGA[C/T]AGCCAGGTTTGTCCCTAAAGCAATCATATGAAGTAAAAAAATAGTTGGATATTAATTATCTTTATTTGATAATGTTAGTATTATGGGATCATACAGTTAAAGTCTGAATTATTAGCCTCCCCTTTATTTTTTATTTTTGTAATATTTCTCAAATGATTAACAGAGCAAGAAAATTTCACAGCATTTCTGATCATACTTTTTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCTGCTAAAATAAAAGCAGTTTAAAAATTTTTAAAAACCATTTTAAGGTCAAAATTATTAGCCCCTTTAAGCTATATTTATTTCGATAGTCTATAGAACAAACCATTGTTATACAATAATTTGCCTAATTACCCTAACCTGCCTGGTTAACTGAAAAAAAAAAAAAAAACTAGTTAAGCCTTTAAATATCACTTTAAGCTGTATAGAAGTGTCTTGAAAAATATCTAGTAAAATTTATTTACTGGCATCACGCAAAGGTAAAATAAATC
Associated Phenotype:
Not determined