ZMP

klf7l

Ensembl ID:

ENSDARG00000043821

ZFIN ID:

ZDB-GENE-041014-171

Description:

Kruppel-like factor 7 (ubiquitous), like [Source:RefSeq peptide;Acc:NP_001038231]

Human Orthologue:

KLF7

Human Description:

Kruppel-like factor 7 (ubiquitous) [Source:HGNC Symbol;Acc:6350]

Mouse Orthologue:

Klf7

Mouse Description:

Kruppel-like factor 7 (ubiquitous) Gene [Source:MGI Symbol;Acc:MGI:1935151]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa31721	Essential Splice Site	Available for shipment	Available now
sa8567	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa31720	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa31721

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000064343	None	None	195	None	3
ENSDART00000104317	Essential Splice Site	237	295	2	4
ENSDART00000142295	Essential Splice Site	203	261	1	3

Genomic Location (Zv9):

Chromosome 9 (position 29396025)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	28551971
GRCz11	9	28362717

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGTTTACACAAAAAGCTCCCACCTGAAGGCACACCAGAGGACACATACAG[G/A]TGATTGACTGCAGACATTATATTGTTAATTTTTATTCACATGTTGTTTTC

Long Flanking Sequence:

CGACGAGGACTTGATGGACCCTTTGCTGCCCAGTTTATCCGACGAGCCTAGCCCCCCACCTCTGCTTGTGTCCCTTCCCAAAACCCTCCACACCCCAGCCAACACTAAGAGTACTGATGCAGGGCTCAAAGAAGCCAGTGGAGGGGTTAATCCAGCCCAGTTAAATGCAGTCACGTCCCTCACGCCACCTTCTTCCCCAGAGTTGGGTCGCCATCTTGTTAAGCCCACACAGACTCTTACCGCCACAGCTGATGGCACACTCACACTAAAACTGGTGGCCAAGAAAGTCGGCCTTGGAGCGGCAAAGCTGGTTGCAACGCATTCGATACCTTCACCACCAAATCGTGGCACACAGAGTGATGGCGAAGGAGGACTTGGTACAGTAGGTGGAGGGGACATCCCAGAGAACAAAAAGAGGGTCCATCGCTGCCAGTTTAATGGCTGTCGGAAGGTTTACACAAAAAGCTCCCACCTGAAGGCACACCAGAGGACACATACAG[G/A]TGATTGACTGCAGACATTATATTGTTAATTTTTATTCACATGTTGTTTTCCTCGAGAGTGTATAGCAACTGTAGCTGTGCACGGAATGTGATGAAGTTTCAGAGTTTGGAAAATCTTCTTTGCCTAGGTTCCGTTACCATAGAAGGGTCACACAATATCTTGTGAAGCTAACTCGATTTCTGCAGCACAGCCCCAAAGCAAGATAGCTGGTTTTCTCTCCCTGCACCTTAATCTCAGACTAAAATGAGCCTAGCCACACCATTCAAAACCTGCCACTGCAGTCAGTAATTGCAAGATGATTGATAGACCGGCTAAGCTAAATCTCGTTTCCCAGCTAATTCAGGCTCGCACGCTCCGGTGCTGTCGTTGCTGCCCTCTCAATGAACCTGAGAGCATGTTGCACTCTGCCATGGCCCCGAAACCCACTGTGACAGTGGCCTCAATGCAGCGTATCTAGCCCCTGTGGCCAGCTGTTGACTAGCTTATAGAAGGCACTTTTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa8567

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000064343	None	None	195	None	3
ENSDART00000104317	Essential Splice Site	238	295	3	4
ENSDART00000142295	Essential Splice Site	204	261	2	3

Genomic Location (Zv9):

Chromosome 9 (position 29389226)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	28545172
GRCz11	9	28355918

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GTGTGTGTGAATGGTGAAGSGGGGATTAAATGATGTGTGTTTGTGCATGC[A/T]GGTGAGAAGCCTTACAAATGCYCCTGGGAAGGCTGTGAATGGCGTTTCGC

Long Flanking Sequence:

TGGAACAATTGGTATCTCCTTTCCCATCTGTTTAACTTCATTTGAATTTCAGAGCTCACTGGGAGGGTGGAGAACATTTAGCACAAATGGCTTCATTTTGGATACTTGACTTTGGGTTATGAATTCGTTCTGTTATGGTGACTGAGCACATTTATGCAGCCCCTCTTCAGTTTAAGAAAAAATGTAAAACAGTGATTTGATTGAATCAAAATCTGTTTCATTTTCTTTCTTTTCTATATATATTTTACGTTTGACTACTGAGAATGCAGGAGGTTTGAGCTACAGCGCTGTAATTTGGAGAACTGGGCAATAAATGGTGTGATCCGATTGGCTGGCTAGGATATGTGATTGAGAGAAACAGTAATGAATGATGTTGATAATGGAACTGCTGACTGTACTCGCAGTGGCACAGCAGCAGCCTCGCTCCAGAGGCGCACCATCTGTGTACAGGTGTGTGTGAATGGTGAAGCGGGGATTAAATGATGTGTGTTTGTGCATGC[A/T]GGTGAGAAGCCTTACAAATGCTCCTGGGAAGGCTGTGAATGGCGTTTCGCACGAAGCGACGAACTGACGAGGCACTACCGCAAACACACTGGTGCCAAACCTTTCAAGTGCAACCACTGCGACAGGTAAGAGAAGCACAGCAAAAGCTCCAAAACTAGCTTTCAATAAAAGTAAGCAAGCATGCATGCATTTAACCCTTTTTAATTCTGTAACGCTCCCACACACAAACTCAACCACGCTAGTCCACAGTCCTCAAGTGCCTATAAACAAATTCCTCCAGTTATGAGACCACAGGACTAAACTCTCTCCCTCTCAAAGAATCCATCGCACCCTCCCTTCGGCTCTTGTTTTCTTAAATTCTCTCTGATGGCATGCACATAGCAGTGCTGCATCGGGCTCATTGGAAGTTAGCACAGGCCCGGTTCCCTGCTGAATAACTCATTCACAGTCTGGTCCTGTGATACCCATTACCGAATTACTGCGAATATCTCATTCTCACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa31720

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000064343	None	None	195	None	3
ENSDART00000104317	Essential Splice Site	279	295	3	4
ENSDART00000142295	Essential Splice Site	245	261	2	3

Genomic Location (Zv9):

Chromosome 9 (position 29389099)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	28545045
GRCz11	9	28355791

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACCGCAAACACACTGGTGCCAAACCTTTCAAGTGCAACCACTGCGACAGG[T/C]AAGAGAAGCACAGCAAAAGCTCCAAAACTAGCTTTCAATAAAAGTAAGCA

Long Flanking Sequence:

TTCTGTTATGGTGACTGAGCACATTTATGCAGCCCCTCTTCAGTTTAAGAAAAAATGTAAAACAGTGATTTGATTGAATCAAAATCTGTTTCATTTTCTTTCTTTTCTATATATATTTTACGTTTGACTACTGAGAATGCAGGAGGTTTGAGCTACAGCGCTGTAATTTGGAGAACTGGGCAATAAATGGTGTGATCCGATTGGCTGGCTAGGATATGTGATTGAGAGAAACAGTAATGAATGATGTTGATAATGGAACTGCTGACTGTACTCGCAGTGGCACAGCAGCAGCCTCGCTCCAGAGGCGCACCATCTGTGTACAGGTGTGTGTGAATGGTGAAGCGGGGATTAAATGATGTGTGTTTGTGCATGCAGGTGAGAAGCCTTACAAATGCTCCTGGGAAGGCTGTGAATGGCGTTTCGCACGAAGCGACGAACTGACGAGGCACTACCGCAAACACACTGGTGCCAAACCTTTCAAGTGCAACCACTGCGACAGG[T/C]AAGAGAAGCACAGCAAAAGCTCCAAAACTAGCTTTCAATAAAAGTAAGCAAGCATGCATGCATTTAACCCTTTTTAATTCTGTAACGCTCCCACACACAAACTCAACCACGCTAGTCCACAGTCCTCAAGTGCCTATAAACAAATTCCTCCAGTTATGAGACCACAGGACTAAACTCTCTCCCTCTCAAAGAATCCATCGCACCCTCCCTTCGGCTCTTGTTTTCTTAAATTCTCTCTGATGGCATGCACATAGCAGTGCTGCATCGGGCTCATTGGAAGTTAGCACAGGCCCGGTTCCCTGCTGAATAACTCATTCACAGTCTGGTCCTGTGATACCCATTACCGAATTACTGCGAATATCTCATTCTCACATTCTGTTCCACTTTCCTCCGTCCTCCCATCGGTACGGCGTATGCCCACACTGTGGCTCGAGTGCAGGGAGAAAGAGAAGTTAGAGGCATGGGTATGCATTCCAAGGTAAGAGGAGTTACATAACAGT

Associated Phenotype:

Not determined